Giacomo Mulinacci1,2†
Andrea Palermo1,2†
Alessio Gerussi1,2
Rosanna Asselta3,4
Merrill Eric Gershwin5
Pietro Invernizzi1,2*- 1Division of Gastroenterology, Center for Autoimmune Liver Diseases, Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy
- 2European Reference Network on Hepatological Diseases (ERN RARE-LIVER), San Gerardo Hospital, Monza, Italy
- 3Department of Biomedical Sciences, Istituti di Ricovero e Cura a Carattere Scientifico (IRCCS) Humanitas Research Hospital, Milan, Italy
- 4Department of Biomedical Sciences, Humanitas University, Milan, Italy
- 5Division of Rheumatology, Allergy and Clinical Immunology, University of California, Davis, Davis, CA, United States
Primary Biliary Cholangitis (PBC) is a rare autoimmune cholangiopathy. Genetic studies have shown that the strongest statistical association with PBC has been mapped in the human leukocyte antigen (HLA) locus, a highly polymorphic area that mostly contribute to the genetic variance of the disease. Furthermore, PBC presents high variability throughout different population groups, which may explain the different geoepidemiology of the disease. A major role in defining HLA genetic contribution has been given by genome-wide association studies (GWAS) studies; more recently, new technologies have been developed to allow a deeper understanding. The study of the altered peptides transcribed by genetic alterations also allowed the development of novel therapeutic strategies in the context of immunotolerance. This review summarizes what is known about the immunogenetics of PBC with a focus on the HLA locus, the different distribution of HLA alleles worldwide, and how HLA modifications are associated with the pathogenesis of PBC. Novel therapeutic strategies are also outlined.
Introduction
Primary biliary cholangitis (PBC) is a rare pathology that can evolve to cirrhosis and liver failure. Although the etiology has not been completely explained, there is evidence supporting that autoimmunity targeting intrahepatic biliary ducts plays a central role in the pathogenesis (1).
PBC presents features that makes it a typical autoimmune condition. Firstly, it is characterized by the presence of specific autoantibodies, i.e. antimitochondrial autoantibodies (AMAs), which have a central role in diagnosis; secondly, the intense infiltrations of lymphocytes damaging bile ducts is a typical histological finding; finally, PBC patients have a high prevalence of concurrent autoimmune disorders (2). Like other autoimmune diseases, environmental and genetic factors have been called in action to explain its pathogenesis. PBC onset is thought to follow the interaction of an environmental trigger(s) with a predisposing genetic background. Concerning environmental factors, recurrent urinary tract infections, cigarette smoking, hair dyes, and the use of hormone replacement therapies have all been associated with increased risk of PBC (3). Furthermore, a growing number of studies have reported a higher prevalence in urban and polluted areas (4).
Genetic predisposition has a significant role in the onset of PBC too (5). The observation of clustering of cases within families and the high concordance rate between monozygotic twins support this claim. Örnolfsson et al. used a nationwide genealogical database and defined the relative risk for first-, second-, and third-degree relatives of PBC patients as 9.13, 3.16, and 2.59, respectively (6). The odds ratio for PBC of an individual with a sibling affected by the same condition is 10.5, in line with other autoimmune disorders (7). Further, the concordance rate for PBC in monozygotic twins is estimated to be 63%, among the highest reported in autoimmune conditions (3). From a genetic perspective, PBC is a complex trait, defined by Lander et al. as “any phenotype that does not exhibit classic Mendelian recessive or dominant inheritance attributable to a single gene locus” (8). This means that multiple gene variants increase or decrease the genetic risk with a relatively small effect size (9). A strong contribution in the advancement of the knowledge of PBC and its genetics has been given by the genome-wide association studies (GWAS). GWAS employ a large scanning of the entire genome for specific genetic variants (typically single nucleotide polymorphisms, SNPs) to identify alleles statistically associated with the disease (10). The strongest statistical association with PBC has been mapped in the human leukocyte antigen (HLA) locus. The HLA region is a highly polymorphic area of the genome located on chromosome 6p21 covering 6.7 Mb (11), and encoding hundreds of loci related to adaptive immune response, including histone and tRNA genes, several key immune response genes, as well as those of the major histocompatibility complex (MHC). The extended MHC region can be subdivided into three classes: class I (extended and classical, respectively, containing the A, B, C as well as MICA and MICB loci); class II (extended and classical, respectively, containing the DPA1/DPB and DQA1/DQB1 loci); class III (containing the DRA1/DRB1 loci).
Apart from the HLA region, a significant number of non-HLA genes have been identified, and many of the alleles involved genes implicated in innate immunity. In particular, studies have found alterations in genes and pathways involved in antigen presentation and production of interleukin (IL)-12 (IRF5, SOCS1, TNFAIP3, NF-κB, and IL-12A), activation of T cells, and interferon γ (IFN-γ) production (TNFSF15, IL12R, TYK2, STAT4, SOCS1, NF-κB, and TNFAIP3), as well as activation of B cells and production of immunoglobulins (POU2AF1, SPIB, PRKCB, IKZF3, and ARID3A) (Table 1) (12–20).
Table 1 List of PBC-related non-HLA associations.
This review outlines the current evidence about the genetic association between HLA variants and PBC, the link between HLA haplotypes and clinical manifestations in various populations worldwide, the alleged role in disease pathogenesis, and novel therapeutic strategies.
Genetic studies for HLA variants
From a methodological point of view, it is possible to separate genetics studies regarding HLA in PBC by identifying pre-GWA-, GWA- and post-GWA-studies. A summary of the most significant HLA variants associated with PBC can be found in Table 2.
Table 2 List of PBC-related HLA associations.
Pre-GWAS era
Before the advent of the GWAS era (approximately from 1992 up to 2009), several candidate studies pointing to the HLA region were performed. The analysis of the HLA region identified a relatively small number of alleles associated with PBC in several independent studies (21–26); these results were more reliable than similar studies on non-HLA alleles, that were mostly underpowered and resulted in several signals not validated in following GWAS (27).
First studies on HLA in PBC were conducted in the early ‘90 on UK population, revealing the presence of DR8 as predisposing factor for disease onset (21). Donaldson and Invernizzi associated the HLA loci DRB1*08 with an increased risk of PBC in British and Italian individuals respectively, and DRB1*11 and B1*13 with a protective effect in Italians (28, 29). Despite these consistent findings, we should bear in mind that these studies suffered from relatively weak statistical power, a strong potential for type 1 statistical error, and were criticized for their a priori approach.
GWAS era
In GWAS, the frequency of genetic variants (SNPs) is compared between cases and controls. If there is a statistical association sufficiently divergent from the distribution seen in a control group (typically a p-value < 5*10-8), variants are considered associated with the phenotype (30). The strength of the association is typically evaluated by the Odds Ratio (OR), calculated based on the allele frequencies in cases and controls. Most of human multifactorial diseases have a complex genetic architecture, with several risk variants contributing little to the disease per se and tagging mostly regulatory regions of the genome.
From 2009 up to the present date, GWAS in PBC have included individuals of European origin (Italy, United Kingdom, USA, Canada) and East Asians (China, Japan), and further analyses, including fine-mapping studies and genome-wide meta-analysis have expanded the list identifying up to 50 genome-wide significant associated variants (12–19, 31–33). Genome wide association studies confirmed that the MHC region remains by far the strongest genetic contributor to PBC susceptibility in terms of OR (Figure 1). The HLA-DRB1 genes (alleles *08, *11, and *14) have been reported for most of the DRB1 association signal; DRB1*08 is the strongest predisposing allele, whereas DRB1*11 is the protective one (34). A more recent meta-analysis from Li et al. (35) identified HLA DR*07 as risk factor in Asian and European populations, and HLA DR*08 associated with PBC in Asian, American and European subgroups; on the contrary, a protective role of HLA DR*11 and *13 was described in Asian and European populations, while HLA DR*12 decreased risk of PBC in Asian and *15 in European and Americans populations. It is of note that the HLA signals DR*08, DRB1*11, and *13 have been confirmed across different populations, except in Sardinians (36). Furthermore, studies based on UK PBC consortium confirmed the results of the pre-GWAS era. Strong associations were found for HLA-DQA1 (alleles *04:01), conferring an approximately threefold increased disease risk, HLA-DQB1 (alleles *04:02, *03:02) and HLA-DRB1 (alleles *04:04). Conversely, HLA-DQB1 (alleles *06:02, *03:01), HLA-DRB1 (alleles *15:01, *11:01, *11:04), HLA-DQA1 (alleles *01:02, *05:01) have been reported as protective ones (18).
Figure 1 The complex milieux of HLA alleles and its association with PBC (increased vs protective risk).
Subsequently, HLA-DPB1 (alleles *03:01, *06:01, *10:01, *17:01 as causative and alleles *04:01 as protective), HLA-C (allele *04:01) and HLA-DPA (allele *02:01) were found to be significantly associated within the same cohort (37). In a Chinese cohort, Qiu et al. found 179 SNPs in the MHC region and described the most significant association with the HLA-DRA locus, while a SNP in the HLA-DRPB1 was the second most significant locus in the MHC region (16).
GWAS allow to associate genetic variants with any phenotype of interest. PBC is typically characterized by the positivity for AMA and/or PBC-specific anti-nuclear antibodies (against the gp210 and sp100 proteins) (38). Positivity for these autoantibodies may occur even before the presence of overt disease and be an isolated laboratory finding. In a Chinese cohort, Wang et al. studied the genetic predisposition to sp100 positivity and identified HLA-DRB1*03:01, DRB1*15:01, DRB1*01 and DPB1*03:01 alleles as the most associated ones (38).
Generally speaking, since association does not mean causation, the region where the leading SNP has been found is usually dissected by the so-called “fine mapping strategy”, that aims to identify the potential biological role of the genetic variant associated with the disease (39). Fine-mapping of the MHC region in Han Chinese court confirmed that HLA-DRB1 and/or HLA-DQB1 contributed the strongest signals, and that HLA-DPB1 was a separate independent locus (40). In addition, the authors performed logistic regression to identify independent associations with amino acid polymorphisms in MHC genes. Three residues (HLA-DRβ1-Ala74, HLA-DQβ1-Pro55 and HLA-DPβ1-Asp84) were found to be independently associated with PBC and all three were located in the peptide-binding groove of MHC II molecules. The 3D protein structure model and electrostatic potentials calculation revealed alternations in antigen-binding affinity leading to an instability of the MHC proteins, that has been proposed as a pathogenetic mechanism in HLA-mediate autoimmune disease (41).
Post-GWAS era
GWAS have some intrinsic limitations. First of all, GWAS results only account for few percent of the whole genetic risk (the remaining being called “missing heritability”) (42). One reason is that diseases are likely to have some of their genetic risk determined by rare genetic variants that are not included in GWAS (43). Second, GWAS generate hypotheses but require fine-mapping downstream approaches to put their results in the right biological context. Third, many ethnic groups have not been included in GWAS for decades, leaving out a huge number of underserved populations (44). On top of the ethical concerns, when GWAS have been performed on populations with different genetic backgrounds only partial overlap with historical ones has been found, revealing novel variants and generating novel candidates for further dissection.
For all of these reasons, several “post-GWAS” strategies have been developed (45). As far as the study of HLA is concerned, there is mounting interest in studying how genetic alterations result in altered peptides. This is becoming more and more relevant also for clinical purposes, since typing HLA at the amino acid level can tease apart different proteins that can lead to allogeneic responses. For example, as previously described, amino acid alterations located in the antigen-binding site of MHC molecules can lead to instability of the molecule that more likely might form MHC-self-epitope complexes, conferring a risk for autoimmunity (41).
Nonetheless, precise HLA typing remains very challenging due to the high density of polymorphisms in HLA genes, sequence similarity among these genes, and to the extreme level of linkage disequilibrium of the locus (46). High resolution HLA typing is possible with various technologies that are becoming more and more efficient with an increasing reduction in cost. Next-generation sequencing (NGS) methods have been increasingly replacing previous technologies (such as DNA-based typing and sequence-based typing methods) allowing an increasingly precise HLA typing, bringing many advancements to the field of HLA genotyping within relatively few years (47).
Other promising approaches have been under development. For example, the PCR-NGS approach implies the use of standard polymerase chain reaction (PCR) to capture regions of interest, and the resultant amplicons are then subjected to NGS (48). More recently, a new technology called HLAscan has been proposed. HLAscan is a typing multi-step method based on alignment approach, in which short selected sequence reads are aligned with reference HLA alleles obtained from a database and then allele types are determined based on the numbers and distribution patterns of the reads on each reference target. HLAscan demonstrated not only to outperform the established NGS-based methods but also to complete other sequencing-based typing methods (49).
World-wide efforts in developing NGS technologies have dramatically increased the availability of whole-genome sequencing (WGS) and whole-exome sequencing (WES) data. WES and WGS have proved to be effective strategies in discovering rare variants that produce large effects, even in non-monogenic rare disease (50) and in isolated population (51). Li et al. applied WES in three PBC families and associated three new HLA variants (HLA-DRB1*07:01, *14:01 and *14:05) to PBC (52). The authors of this study also describe the amino acid variants located in the peptide-binding site of the MHC molecule and found that DRB1*07:01 was strongly associated with clinical manifestations. Of note, Wang et al. used WES on 90 individuals including 30 PBC probands and identified 19 unreported genes harboring validated de novo mutations (DNMGs) (53). Subsequently, the authors interrogated the co-expression dynamics of the DNMGs utilizing a published transcriptome dataset of the CD4+ T cells, since they play a critical role in PBC (54). In addition, they found that transcription factor MEF2D and the DNA repair gene PARP2 were highlighted as hub genes and identified to be up- and down-regulated respectively in peripheral blood data. This transcription alteration seems to be the trigger of a series of molecular and cellular processes that have pivotal roles in PBC pathophysiology (53). This represents a small example of the potential of WES/WGS to further improve the understanding of the genetic predisposition to the disease.
Geoepidemiology
PBC presents different prevalence and incidence rates across populations and geographical areas. Geo-epidemiology has focused on potential environmental and socioeconomic risk factors (55, 56). Studies from the North-East of England have identified a higher prevalence of PBC in urban areas that have a strong coal-mining heritage (55), whereas a study in New York City found clusters of PBC patients in zip codes that contained, or were adjacent to, superfund toxic waste sites (56).
Other environmental factors associated with increased risk of PBC were cigarette smoking, hair dyes, the use of hormone replacement therapies, and recurrent urinary tract infections (UTI) (3). As it concerns the latter molecular mimicry analysis has shown that PBC autoantigene pyruvate dehydrogenase complex E2 subunit (PDC‐E2) has common structure with the Escherichia coli E2 subunit of the 2‐oxo‐acid dehydrogenase complexes (57). This suggested that the infection with E. coli, a predominant pathogen in most cases with UTI, is a key factor in breaking immunological tolerance in PBC (58).
In addition to environmental factors, there is known variation in allele frequencies among different ethnic groups. Unfortunately, PBC GWAS have mostly been performed on subjects of European ancestry and more recently on east-Asians (Han Chinese and Japanese). At the time of writing, genetic studies on “neglected population” such as African, Latin American or Australian population are still lacking.
The role of HLA in PBC pathogenesis: Imperfect HLA interactions
The most recent model of PBC pathogenesis comprises two phases: an initiation phase, characterized by autoimmune phenomena driven by defects in biliary homeostasis and aberrant antigen presentation; and a progression phase, driven by the retention of bile acids (2). Based on this model, one would expect that HLA would play its major pathogenetic role at the initiation phase. Despite the association between HLA and autoimmune diseases have been known since 1970s (59), the exact pathogenic mechanism that links HLA and disease onset remains largely elusive (60). The scientific progress in genetic and molecular profiling technologies represents a big hope for the future, since it is gradually unveiling the complex interaction between HLA, peptides and TCR (61). Several structural and associated functional studies were conducted, with more than 50 unique TCR-peptide-HLA structures recognized (62).
A variety of physiologic and steric factors can affect the TCR-peptide-HLA interface (61). Further, several mechanisms of imperfect HLA interactions were identified as potential disease triggers in several autoimmune disorders. They include: i) molecular mimicry and mechanical binding alterations (HLA–peptide–TCR binding orientation, low-affinity peptide binding), ii) post-translational epitope modification or iii) generation of hybrid peptides (63) (Figure 2). As for the latter, no data are available in PBC. We will thus briefly focus on the first two mechanisms.
Figure 2 Imperfect HLA interactions and autoimmunity: (A) Molecular mimicry: Foreign antigens (i.e. either from infecious or chemical agents) with similarities to self-antigens are primed by T and B cells, that autoreactive and trigger autoimmunity. (B) Immunological synapse and autoimmunity: several mechanisms of the complex interplay between APC, B- and T- cells might lead to the activation of autoimmune B and T cells. Among them, mechanical binding alterations (atypical binding orientation, altered docking) and TCR stabilization of weak peptide. Weak HLA binding of self-peptides might contribute to autoimmunity by allowing the escape of autoreactive T-cellsfrom the thymus. (C) Post translational modifications (PTM): they are spontaneous or enzymatically induced modifications of one or more amino acids occuring after protein biosynthesis. After PTM, these proteins become modified self-antigens, and they do not “tolerize” developing thymocytes. Consequently, modified self-antigens can be taken and processed by APC, that will present them to autoreacitve T and B cells. (D): Generation of hybrid peptides: proteasomal-mediated degradation and splicing of intracellular self-peptides can promote the generation of non-self-hybrid peptides. This mechanism occurs with high protein concentrations in a confined environment, that favours protease-mediated peptide fusion.
Molecular mimicry and mechanical binding alterations
Molecular mimicry is a well-accepted mechanism linking infections and autoimmunity onset. It consists in the antibody- and cellular-mediated immune response against self-protein(s) sharing a sufficient degree of similarity with epitopes of infectious agents (64). Almost all patients with PBC have autoantibodies recognizing the E2 subunit of the pyruvate dehydrogenase complex (PDC-E2) or other related mitochondrial enzymes complexes. Thus, cross reactivity should not be a surprise since such mitochondrial enzymes have conserved sequences shared across different species (65). Shimoda et al. nicely demonstrated the mechanism of molecular mimicry of AMA and antinuclear autoantibodies in PBC, and also showed that the mimicry peptide can become the immunodominant T-cell epitope (57, 66). Different bacterial strains and xenobiotics were considered as possible causative of cross reaction in PBC. Among them, E. coli and Novosphingobium aromaticivorans are considered among the best candidates for the induction of PBC (67–71).
Along with molecular mimicry, mechanical binding alterations were considered among the triggers of autoimmune disorders (63). Somatic hypermutation (SHM) is a process occurring within germinal centres, aimed at producing high-affinity antibodies via the introduction of somatic mutations in the rearranged region of the Ig genes. Activation-induced cytidine deaminase (AID) is required for SHM to occur, and it leads to DNA mutations by conversion of cytosine into uracil (72). While some studies showed that AID can contribute to the loss of self-reactivity in mice and humans (73–76), other have attributed a role of AID and SHM deficiencies in autoimmune disease onset and severity (77–81). As for PBC, a single work assessed a limited SHMs in class-switched isotypes in PBC patients, which may be indicative of low-affinity Ag binding (82). To the best of our knowledge, data on HLA–peptide–TCR binding orientation in PBC are still lacking.
Post-translational epitope modification
Post-translational modification refers to the addition of a functional group to a protein or to the proteolytic processing and folding necessary its functional maturation. Acetylation, methylation, phosphorylation, ubiquitination and sumoylation are among the most common functional group additions. These modifications have fundamental roles in chromatin structure and function.
Reduced methylation levels of the cluster of differentiation 40 ligand (CD40L) promoter were described in peripheral CD4 T cells in PBC patients, and this correlated to increased immunoglobulin M (IgM) serum concentration, a typical serological finding of PBC (83). An increased variety of methylation patterns were on chromosome X of a small cohort of monozygotic twins with PBC (84). A scan of the X chromosome revealed a hypomethylation of the promoter of a C-X-C motif chemokine receptor 3 (CXCR3) (85). CXCR3 plays a key role in dysimmunity, and increased levels of this receptor were described among PBC patients (86).
T cells from PBC patients showed an increased concentration of β-arrestin 1, a protein involved in CD4+ T cells histone acetylation, and its overexpression correlated to hepatic disease severity (87). Upregulated βarr1 in PBC associated to decreased levels of TNF-related apoptosis-inducing ligand (TRAIL), involved in autoimmunity prevention through cell cycle arrest (87). The role of non-coding RNAs (ncRNAs) was largely studied in PBC. They are RNAs not translated into proteins. Scientific focus was directed towards microRNAs (miRNAs), a specific class of ncRNA with the ability to regulate gene expression (88). Among miRNAs, MiR-506 overexpression was described in PBC. This specific miRNA targets the anion exchanger 2 (AE2), an important protein involved in biliary epithelium homeostasis (89). Of note, miR-506 targeted cholangiocytes showed an higher expression of pro-inflammatory and pro-fibrotic markers (90). A novel and interesting topic in PBC is represented by the connection between epigenetic alterations and X chromosome monosomy/inactivation abnormalities (91). Deep investigation on the impact of epigenetic modifications in X chromosome alterations in PBC might reveal important insights on disease specific sex imbalance and pathogenesis.
The role of biliary epithelial cells in PBC pathogenesis
The recognition of self-peptides selectively presented by susceptible HLA has gained scientific interest for a long time. Specific HLA loci, when combined with certain molecules, may confer either protection or susceptibility to develop autoimmunity. In rheumatoid arthritis, variants at 71β position of certain HLA haplotypes are responsible for the presentation of citrullinated peptides, recognized as non-self by T cells (92). Similarly, the presentation of the reduced form of insulin to specific DRB1 protein haplotypes correlated to insulin autoimmune syndrome (93). As for PBC interesting data are emerging on the role of biliary epithelial cells [BECs, aka cholangiocytes (CC)] as possible triggers of autoimmunity. Cholangiocytes line the biliary tree from the small intrahepatic Hering canals to the large extrahepatic bile ducts (94). They are endowed with the ability to regulate bile production, fluidity, and homeostasis (95). Evidence showed that CC actively participate in the innate and adaptive immune responses, acting as innate immune cells, antigen presenting cells, and expressing cytokines, chemokines, and adhesion molecules (96). In this way, they protect hepatocytes from potentially toxic bile acids, microbial products, and the direct translocation of gut-derived microbes (97). BECs constitutively express HLA class I associated to CD8 cytotoxic activity, as it occurs for all mammalian epithelial cells. However, differently from other epithelial cells, they are capable of antigen-uptake and can upregulate HLA class II peptides in response to the local release of inflammatory cytokines, in particular IFN-γ and IL-2 (98).
This process was described in several autoimmune cholangiopathies, including PBC (99–102). Despite this, several studies failed to demonstrate that HLA class II expressed by BECs can directly present peptide antigens to T cells (54, 101, 103). This might occur secondary to the lack of B7-1 (CD80) and B7-2 (CD86) co-stimulatory ligands, required for T cell activation. The inefficient peptide antigen presentation, together with the expression of inhibitory molecule such as PDL1 and PDL2, result in T-cell anergy. This suggested a possible role of BECs as accessory cells rather than proper antigen presenting cells, at least for peptide antigen presentation (104–106).
A breakthrough in the recent history of immunology was the discovery of CD1-restricted T cells, capable of a subset of HLA I-like molecules with the ability to present self and microbial lipid antigens to T cells (107). The scientific excitement associated with this discovery grew dramatically with the recognition of CD1d-restricted NKT cells, a subset of T-lymphocytes bridging innate and adaptive immunity (108). Most NKT can recognize self-lipid antigens, but the antigen capability to activate NKT and trigger cytokine release depends largely on TCR signalling strength and the presence of co-stimulatory signals (109). NKT can rapidly express pro- and anti-inflammatory cytokines and are endowed with split roles in several pathologic conditions, including autoimmune disorders and malignancies. They can inhibit or exacerbate autoimmunity, and this feature makes them an interesting target for treatment (110, 111).
Cholangiocytes can present lipid antigens through CD1d and the HLA-related receptor MR1, respectively (112–114). In particular, MR1 activates a specific subset of T cells, the mucosal associated invariant T cells (MAIT), that are located in the peribiliary sinusoids close to the portal tracts, thus being in straight contact with gut bacteria antigens. Peribiliary MAIT localization was described in several hepatic disorders including PBC, autoimmune hepatitis and primary sclerosing cholangitis (115).
As for PBC, MAIT cells seem to have a protective, since their levels is reduced as compared to healthy livers (116).
CD1d is upregulated on biliary epithelial cells during the early stages of PBC (113). In vitro models showed the ability of CD1d to activate natural killer T cells through the presentation of endogenous and microbiome-derived lipid antigens (112). Whether the expression of HLA class II molecules might represent an epiphenomenon of BECs activation, or it might link cholangiocytes and autoimmunity is unknown, and further studies are awaited.
The strength of unity in autoimmunity: Shared HLA recognition
Specific HLA subtypes are shared among different autoimmune disorders (117). This feature has attracted the scientific interest in the search for molecular mechanisms behind this correlation (63). Conversely, several MHC−I-pathies share immunopathogenic basis despite different HLA genotypes (118). The ability to compare HLA commonalities and differences among autoimmune diseases can translate into the recognition of shared or distinct pathophysiological pathways, thus increasing the understanding of disease aetiology and therapy. As for HLA class II, different allele interactions were identified for multiple sclerosis, rheumatoid arthritis, type 1 diabetes, and coeliac disease (119). However, large data collection and sharing enabled by technological advances will ease the process of common disease pattern recognition.
The role of HLA-mediated antigen recognition
The pool of endogenous and exogenous antigens presented by each HLA molecule varies enormously not only among different subjects but also within different tissues of the same subject. The rapid pace of epitope recognition fostered by novel quantitative mass spectrometry technologies enabled the recognition of millions of peptide repertoires, collected from blood and target tissue samples (120). In chronic autoimmune disorders, epitope heterogeneity coupled with HLA polymorphisms leads to a continuous competition of T cells for the most immunodominant epitopes. This resulted in the development of a large T cell clonotypes repertoire, consequence of lifetime modifications occurring from the early thymic T-cell development to specific events occurring in peripheral tissues (121). In liver tissues derived from PBC patients, disease-associated clonotypes were detected irrespectively of the presence of DRB1*08:01/DRB1*04:04 susceptibility alleles, with three clonotypes detected in 40% of the cases. Further, antigen-driven clonal selection and expansion was evidenced, with HLA restricted autoreactive T cells specific for the PDC-E2 (122). In addition, T-cell repertoires differ among autoimmune liver diseases (123), and this observation led to the concept of disease-specific imprinting from antigenic repertoires.
To conclude, the recognition of PBC-specific HLA susceptibility can translate into specific T-cell repertoires. This might consequently lead to the recognition and selective targeting of disease-specific T-cells, with possible treatment implications for the future.
The imperfect HLA-antigen-TCR binding behind autoimmunity
It has been long recognized that the strength of HLA-peptide-TCR interaction can influence the thymic fate of a TCR (124). In particular, weaker interactions promote positive selection and T cell survival, while stronger ones drive clonal deletion and differentiation into Treg phenotype.
The study of highly polymorphic TCR sequences and HLA alleles was enabled only in recent years, thanks to technological advances in deep-sequencing technologies (125). TCR receptors consist of an α- and a β-chain. They include three highly variable peptide loops, each encoded by a specific gene, that protrude toward the pMHC complex. Of them, the complementarity-determining region (CDR3β) in the β chain is the most variable, and it mediates antigen recognition (126). Hydrophobicity at specific positions of the β−chain CDR3β was demonstrated to promote reactivity to self-peptides (127, 128). Recent evidence highlighted the role of TCR β variable gene (TRBV), encoding for a region of CDR3β, in the mechanism of autoimmunity. In particular, TRBV shapes the TCR affinity to conserved HLA sites, thus altering their propensity towards self vs non-self-activation (129). A study of peptide-HLA libraries coupled to deep-sequencing analysis attested a higher tolerance for substitutions to peptide residues that are located distally to the TCR-binding site, and some of them were identified through computational analysis (130). The TCR-peptide-HLA docking mechanism is not always perfect, and engagement of homologous antigens via distinct docking geometries was described. TCR-antigen cross reaction might lead to the breakdown of immune tolerance, potentially triggering autoimmunity (131, 132). A recent study used NGS to characterize and compare the TCRβ chain of peripheral T cells in PBC patients vs controls (68). Results showed that PBC patients carried TCRβ with reduced CDR3 length and that TCRβs bearing shorter CDR3 loops, which are associated with abnormal insertion length at the variable, diversity and joining gene segments in the β-chain locus. The functional outcome of this structural alteration is yet to be demonstrated.
Exploiting the HLA-peptide-TCR binding to modulate autoimmunity: Antigen specific immunotolerance
Antigen-specific immunotolerance (ASI) represents one of the most promising therapeutic approaches for autoimmune disorders. It has been long practiced in the field of allergy (133, 134), and it consists in the promotion of antigenic specific tolerance by inhibiting autoantigen-specific immune response, while sparing the rest of the immune system. In fact, despite the revolutionary potential of immune suppressive treatments in autoimmune and inflammatory disorders, those are predominantly symptomatic approaches not acting on disease cause and associating to several side effects. The inhibition of autoantigen-specific immune response though ASI represents a clever, innovative, and safer approach. It mainly relies on the administration of antigenic epitopes derived from the same proteins targeted by the autoreactive lymphocytes. Prior to antigen administration, specific antigenic conditioning is required to induce a regulatory response capable to restore homeostasis and to aid the deletion of autoreactive cones. The HLA background has a strong influence on the efficacy of ASI, since HLA heterogeneity largely shapes the antigen-specific immune responses. Individual HLA background should be considered in clinical trials exploiting ASI, and early tolerization should be encouraged to reduce the likelihood of epitope spreading.
The use of ASI recently increased also in autoimmune disorders, after a preliminary success in experimental models (135). So far, ASI focused on antigen presenting cells (APC), in particular dendritic cells (DC), and CD4 T cells, responsible for the onset and perpetuation of most autoimmune-related processes (136). Tolerogenic vaccines represent the mainstay of ASI, and several vaccines platforms were built throughout the years (Figure 3). Since APC represent the main actors of antigen specific tolerance, strong efforts were directed towards the recognition and delivering of autoantigens to specific APC subtypes (136–138). There are several mechanisms of action behind the induction of antigen-specific tolerance, each with a specific antigen delivery approach (139). A major limit of ASI in most autoimmune disorders is the poor knowledge of the whole autoantigen panel involved and the uncertainty of whether tolerance towards the recognized autoantigen/s is enough to reverse autoimmunity, since several autoimmune disorders have autoantibodies associated with disease but without a role in disease pathogenesis (140). ASI should rely on antigens capable of modulating CD4 T cells without engaging pathogenic B or T cells. In this way, a correct balance between efficacy and safety is guaranteed.
Figure 3 Tolerogenic vaccine platforms: The goal of NPs-, peptides-, and DNA/RNA-based platformes is to stimulate tolerogenic DCs to suppress CD4+ T cell-mediated autoimmunity. NPS, nanoparticles; DC, dendritic cells.
Among the different antigen delivery approaches, the use of nanoparticles seems promising, with great interest for tolerogenic nanoparticles (tNPs). A particular subtype of tNPs, called tolerogenic immune modifying nanoparticles (TIMP) were designed to achieve antigen-specific and site-specific immune tolerance (141).
TIMP use has steeply increased, emerging from cell-based to synthetic antigen carriers and from animal models to clinical trials. In particular, the role of TIMP was studied in some autoimmune disorders, such as experimental autoimmune encephalomyelitis (the mouse model for multiple sclerosis), type 1 diabetes, systemic lupus erythematosus and multiple sclerosis (142–149). Of note, up to 99% of nanoparticles pass through the liver, and most of them are taken up and internalized by scavenger receptors of hepatic Kupffer cells (150, 151).
The tolerogenic nature of liver fosters the induction of antigen-specific regulatory T cells (Tregs), a subset of CD4+ T cells with a critical role in maintaining immune system homeostasis and immune tolerance. The contact between nanoparticles carrying autoantigens and Tregs favours the induction and activation of latter (152). PBC represents an ideal target disease for nanotechnology, since autoantibodies are disease- and organ-specific, thus increasing the specificity of nanoparticles-delivery. The major actors of PBC immunopathogenesis are AMA, T cells and biliary epithelial cells, while the inner lipoyl domain of PDC-E2 is the dominant autoepitope (153). The recognition of the correct timing and dosing of antigen delivered by nanoparticles are limiting steps in the process of immunogenicity, and research is ongoing at an exciting pace. TIMP is a potentially safe approach, and it represents a potential shift from immunosuppressive to tolerance inducing therapies in autoimmune disorders (154–156). As mentioned above, Tregs orchestrate the immune system homeostasis. They express high levels of transcription factor Forkhead box protein P3 (FOXP3), critical for their thymic development and activity (157). FOXP3+ Tregs exert a suppressive activity for autoreactive T and B cells (158), and its absence results in severe autoimmune and immune-related disorders (159, 160). Treg dysfunction might be responsible for the uncontrolled T cell reaction against cholangiocytes, as showed by Jeffrey et al. (161). PBC patients showed a reduced level of peripheral Tregs (162, 163), and the silencing or reduced activity of FOXP3 in murine models led to peri-biliary immune damage and AMA production (164, 165). Of interest, reduced levels of Tregs were recorders also in the peripheral blood of daughters and sisters of PBC patients (162, 163). The expansion of Tregs represents a promising treatment approach in autoimmune disorders, even if several barriers need to be overcome to achieve a high quality Treg cell therapy. Among them, mentions should be done to the difficulty of Treg expansion and the lack of Treg-exclusive markers (136).
Conclusions
PBC is a complex autoimmune disorder with high inter- and intra- individual variability. HLA has long been studied in PBC, and associations were first described in the pre-GWAS era and largely expanded thanks to the rapid spread of GWAS platforms. However, such platforms are not informative on the causal genes or the disease mechanisms, explain only a small fraction of the missing heritability, do not allow to assess rare disease variants, and were not implemented for several populations worldwide. The rapid pace of technological innovation, with the development of novel sophisticated sequencing technologies will gradually unveiling the “hidden” genomic signatures, possibly enabling a complete disease HLA (and non-) mapping. The role of HLA in PBC, as it occurs for most autoimmune disorders, is still to be determined and detailed. The HLA-peptide-TCR interaction has been the focus for long time, but we are far from an exhaustive explanation on how it might be involved in autoimmunity. While PBC pathogenesis remains far from being determined, there is a rapid and constant surge of novel treatment approaches aimed at limiting the autoimmune clones to guarantee antigen specific immunotolerance. Among them, scientific excitement surrounds the discovery of tolerogenic vaccine platforms aimed at the expansion of Tregs.
Author contributions
GM and AP equally searched the literature and contributed to the first draft of the manuscript. All authors provided critical feedbacks and helped to shape the research, analysis and manuscript. PI, MEG, RA and AG reviewed for important intellectual contents. All the authors approved the final version of the manuscript.
Funding
This research was partially supported by the Italian Ministry of University and Research (MIUR)—Department of Excellence project PREMIA (PREcision MedIcine Approach: bringing biomarker research to clinic).
Acknowledgments
The authors thank AMAF Monza ONLUS and AIRCS for the unrestricted research funding.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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References
1. Gerussi A, Carbone M. Primary biliary cholangitis. Autoimmune Liver Dis (2020), 123–41. doi: 10.1002/9781119532637.CH7
2. Tanaka A, Leung PSC, Bowlus CL, Gershwin ME. Primary biliary cholangitis. Liver Immunol (2020) 335–57. doi: 10.1007/978-3-030-51709-0_22
3. Selmi C, Mayo MJ, Bach N, Ishibashi H, Invernizzi P, Gish RG, et al. Primary biliary cirrhosis in monozygotic and dizygotic twins: Genetics, epigenetics, and environment. Gastroenterology (2004) 127(2):485–92. doi: 10.1053/J.GASTRO.2004.05.005
4. Dyson JK, Blain A, Foster Shirley MD, Hudson M, Rushton S, Jeffreys Jones DE. Geo-epidemiology and environmental co-variate mapping of primary biliary cholangitis and primary sclerosing cholangitis. JHEP Rep (2021) 3(1):100202. doi: 10.1016/J.JHEPR.2020.100202
5. Tanaka A, Leung PSC, Gershwin ME. The genetics of primary biliary cholangitis. Curr Opin Gastroenterol (2019) 35(2):93–8. doi: 10.1097/MOG.0000000000000507
6. Örnolfsson KT, Olafsson S, Bergmann OM, Gershwin ME, Björnsson ES. Using the icelandic genealogical database to define the familial risk of primary biliary cholangitis. Hepatology (2018) 68(1):166–71. doi: 10.1002/HEP.29675
7. Jones DEJ, Watt FE, Metcalf JV, Bassendine MF, James OFW. Familial primary biliary cirrhosis reassessed: A geographically-based population study. J Hepatol (1999) 30(3):402–7. doi: 10.1016/S0168-8278(99)80097-X
8. Lander ES, Schork NJ. Genetic dissection of complex traits. Sci (80-) (1994) 265(5181):2037–48. doi: 10.1126/SCIENCE.8091226
9. Gerussi A, Carbone M, Asselta R, Invernizzi P. Genetics of autoimmune liver diseases BT - liver Immunology : Principles and practice. Liver Immunol (2020), 69–85. doi: 10.1007/978-3-030-51709-0_5
10. Manolio TA. Genomewide association studies and assessment of the risk of disease. N Engl J Med (2010) 363(2):166–76. doi: 10.1056/NEJMRA0905980/SUPPL_FILE/NEJMRA0905980_DISCLOSURES.PDF
11. Dendrou CA, Petersen J, Rossjohn J, Fugger L. HLA variation and disease. Nat Rev Immunol (2018) 18(5):325–39. doi: 10.1038/NRI.2017.143
12. Juran BD, Hirschfield GM, Invernizzi P, Atkinson EJ, Li Y, Xie G, et al. Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. Hum Mol Genet (2012) 21(23):5209. doi: 10.1093/HMG/DDS359
13. Hirschfield GM, Liu X, Han Y, Gorlov IP, Lu Y, Xu , et al. Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis. Nat Genet (2010) 42(8):655–7. doi: 10.1038/ng.631
14. Mells GF, Floyd JAB, Morley KI, Cordell HJ, Franklin CS, Shin SY, et al. Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. Nat Genet (2011) 43(4):329–32. doi: 10.1038/ng.789
15. Nakamura M, Nishida N, Kawashima M, Aiba Y, Tanaka A, Yasunami M, et al. Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population. Am J Hum Genet (2012) 91(4):721–8. doi: 10.1016/J.AJHG.2012.08.010/ATTACHMENT/29F94F23-B32C-4D78-9BF2-4256A188D92E/MMC1.PDF
16. Qiu F, Tang R, Zuo X, Shi X, Wei Y, Zheng X, et al. A genome-wide association study identifies six novel risk loci for primary biliary cholangitis. Nat Commun 2017 81 (2017) 8(1):1–8. doi: 10.1038/ncomms14828
17. Liu X, Invernizzi P, Lu Y, Kosoy R, Lu Y, Bianchi I, et al. Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. Nat Genet (2010) 42(8):658–60. doi: 10.1038/ng.627
18. Liu JZ, Almarri MA, Gaffney DJ, Mells GF, Jostins L, Cordell HJ, et al. Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. Nat Genet (2012) 44(10):1137–41. doi: 10.1038/ng.2395
19. Cordell HJ, Han Y, Mells GF, Li Y, Hirschfield GM, Greene CS, et al. International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways. Nat Commun (2015) 6:8019. doi: 10.1038/NCOMMS9019
20. Kawashima M, Hitomi Y, Aiba Y, Nishida N, Kojima K, Kawai Y, et al. Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population. Hum Mol Genet (2017) 26(3):650–9. doi: 10.1093/HMG/DDW406
21. Underhill J, Donaldson P, Bray G, Doherty D, Portmann B, Williams R. Susceptibility to primary biliary cirrhosis is associated with the HLA-DR8-DQB1*0402 haplotype. Hepatology (1992) 16(6):1404–8. doi: 10.1002/HEP.1840160616
22. Morling N, Dalhoff K, Fugger L, Georgsen J, Jakobsen B, Ranek L, et al. DNA Polymorphism of HLA class II genes in primary biliary cirrhosis. Immunogenet (1992) 35(2):112–6. doi: 10.1007/BF00189520
23. Onishi S, Sakamaki T, Maeda T, Iwamura S, Tomita A, Saibara T, et al. DNA Typing of HLA class II genes; DRB1*0803 increases the susceptibility of Japanese to primary biliary cirrhosis. J Hepatol (1994) 21(6):1053–60. doi: 10.1016/S0168-8278(05)80617-8
24. Begovich AB, Klitz W, Moonsamy PV, Van de Water J, Peltz G, Gershwin ME. Genes within the HLA class II region confer both predisposition and resistance to primary biliary cirrhosis. Tissue Antigens (1994) 43(2):71–7. doi: 10.1111/J.1399-0039.1994.TB02303.X
25. Donaldson P, Agarwal K, Craggs A, Craig W, James O, Jones D. HLA and interleukin 1 gene polymorphisms in primary biliary cirrhosis: Associations with disease progression and disease susceptibility. Gut (2001) 48(3):397–402. doi: 10.1136/GUT.48.3.397
26. Stone J, Wade JA, Cauch-Dudek K, Ng C, Lindor KD, Heathcote EJ. Human leukocyte antigen class II associations in serum antimitochondrial antibodies (AMA)-positive and AMA-negative primary biliary cirrhosis. J Hepatol (2002) 36(1):8–13. doi: 10.1016/S0168-8278(01)00237-9
27. Mells GF, Kaser A, Karlsen TH. Novel insights into autoimmune liver diseases provided by genome-wide association studies. J Autoimmun (2013) 46:41–54. doi: 10.1016/J.JAUT.2013.07.004
28. Donaldson PT, Baragiotta A, Heneghan MA, Floreani A, Venturi C, Underhill JA, et al. HLA class II alleles, genotypes, haplotypes, and amino acids in primary biliary cirrhosis: A large-scale study. Hepatology (2006) 44(3):667–74. doi: 10.1002/HEP.21316
29. Invernizzi P, Selmi C, Poli F, Frison S, Floreani A, Alvaro D, et al. Human leukocyte antigen polymorphisms in italian primary biliary cirrhosis: A multicenter study of 664 patients and 1992 healthy controls. Hepatology (2008) 48(6):1906–12. doi: 10.1002/HEP.22567
30. Webb GJ, Hirschfield GM. Using GWAS to identify genetic predisposition in hepatic autoimmunity. J Autoimmun (2016) 66:25–39. doi: 10.1016/J.JAUT.2015.08.016
31. Almasio PL, Licata A, Maida M, Macaluso FS, Costantino A, Alessi N, et al. Clinical course and genetic susceptibility of primary biliary cirrhosis: Analysis of a prospective cohort. Hepat Mon (2016) 16(11):31681. doi: 10.5812/HEPATMON.31681
32. Hirschfield GM, Liu X, Xu C, Lu Y, Xie G, Lu Y, et al. Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants. N Engl J Med (2009) 360(24):2544–55. doi: 10.1056/NEJMOA0810440/SUPPL_FILE/NEJM_HIRSCHFIELD_2544SA1.PDF
33. Cordell HJ, Fryett JJ, Ueno K, Darlay R, Aiba Y, Hitomi Y, et al. An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs. J Hepatol (2021) 75(3):572. doi: 10.1016/J.JHEP.2021.04.055
34. Invernizzi P, Ransom M, Raychaudhuri S, Kosoy R, Lleo A, Shigeta R, et al. Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis. Genes Immun (2012) 13(6):461. doi: 10.1038/GENE.2012.17
35. Li M, Zheng H, Tian Qb, Rui M, Liu D. HLA-DR polymorphism and primary biliary cirrhosis: Evidence from a meta-analysis. Arch Med Res (2014) 45(3):270–9. doi: 10.1016/J.ARCMED.2014.03.002
36. Clemente MG, Frau F, Bernasconi M, Macis MD, Cicotto L, Pilleri G, et al. Distinctive HLA-II association with primary biliary cholangitis on the island of Sardinia. United Eur Gastroenterol J (2017) 5(4):527. doi: 10.1177/2050640616665030
37. Darlay R, Ayers KL, Mells GF, Hall LS, Liu JZ, Almarri MA, et al. Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitis. PLoS Genet (2018) 14(12):e1007833. doi: 10.1371/journal.pgen
38. Wang C, Zheng X, Jiang P, Tang R, Gong Y, Dai Y, et al. Genome-wide association studies of specific antinuclear autoantibody subphenotypes in primary biliary cholangitis. Hepatology (2019) 70(1):294–307. doi: 10.1002/HEP.30604
39. Soskic B, Cano-Gamez E, Smyth DJ, Ambridge K, Ke Z, Matte JC, et al. Immune disease risk variants regulate gene expression dynamics during CD4+ T cell activation. Nat Genet (2022) 54: 1–10. doi: 10.1038/s41588-022-01066-3
40. Wang C, Zheng X, Tang R, Han C, Jiang Y, Wu J, et al. Fine mapping of the MHC region identifies major independent variants associated with han Chinese primary biliary cholangitis. J Autoimmun (2020) 107:102372. doi: 10.1016/J.JAUT.2019.102372
41. Miyadera H, Ohashi J, Lernmark Å, Kitamura T, Tokunaga K. Cell-surface MHC density profiling reveals instability of autoimmunity-associated HLA. J Clin Invest (2015) 125(1):275–91. doi: 10.1172/JCI74961
42. Tang R, Chen H, Miao Q, Bian Z, Ma W, Feng X, et al. The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk. Genes Immun (2015) 16(3):193. doi: 10.1038/GENE.2014.76
43. Young AI. Solving the missing heritability problem. PloS Genet (2019) 15(6):e1008222. doi: 10.1371/JOURNAL.PGEN.1008222
44. Rotimi CN, Jorde LB. Ancestry and disease in the age of genomic medicine. N Engl J Med (2010) 363(16):1551–8. doi: 10.1056/NEJMra0911564
45. Tam V, Patel N, Turcotte M, Bossé Y, Paré G, Meyre D. Benefits and limitations of genome-wide association studies. Nat Rev Genet (2019) 20(8):467–84. doi: 10.1038/s41576-019-0127-1
46. Dunn PPJ. Human leucocyte antigen typing: techniques and technology, a critical appraisal. Int J Immunogenet (2011) 38(6):463–73. doi: 10.1111/J.1744-313X.2011.01040.X
47. Hosomichi K, Shiina T, Tajima A, Inoue I. The impact of next-generation sequencing technologies on HLA research. J Hum Genet (2015) 60(11):665–73. doi: 10.1038/JHG.2015.102
48. Danzer M, Niklas N, Stabentheiner S, Hofer K, Pröll J, Stückler C, et al. Rapid, scalable and highly automated HLA genotyping using next-generation sequencing: A transition from research to diagnostics. BMC Genomics (2013) 14(1):221. doi: 10.1186/1471-2164-14-221
49. Ka S, Lee S, Hong J, Cho Y, Sung J, Kim HN, et al. HLAscan: Genotyping of the HLA region using next-generation sequencing data. BMC Bioinf (2017) 18(1):1–11. doi: 10.1186/S12859-017-1671-3/FIGURES/3
50. Turro E, Astle WJ, Megy K, Gräf S, Greene D, Shamardina O, et al. Whole-genome sequencing of patients with rare diseases in a national health system. Nat (2020) 583(7814):96–102. doi: 10.1038/s41586-020-2434-2
51. Southam L, Gilly A, Süveges D, Farmaki AE, Schwartzentruber J, Tachmazidou I, et al. Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Nat Commun (2017) 8(1):1–11. doi: 10.1038/ncomms15606
52. Li Y, Liu X, Wang Y, Zhou Y, Hu S, Yang H, et al. Novel HLA-DRB1 alleles contribute risk for disease susceptibility in primary biliary cholangitis. Dig Liver Dis (2022) 54(2):228–36. doi: 10.1016/J.DLD.2021.04.010
53. Wang L, Li J, Wang C, Tang R, Liang J, Gong Y, et al. Mapping of de novo mutations in primary biliary cholangitis to a disease-specific co-expression network underlying homeostasis and metabolism. J Genet Genomics (2022) 49(2):145–54. doi: 10.1016/J.JGG.2021.07.019
54. Leon MP, Bassendine MF, Wilson JL, Ali S, Thick M, Kirby JA. Immunogenicity of biliary epithelium: Investigation of antigen presentation to CD4+ T cells. Hepatology (1996) 24(3):561–7. doi: 10.1002/HEP.510240317
55. Dyson JK, Blain A, Foster Shirley MD, Hudson M, Rushton S, Jeffreys Jones DE. Geo-epidemiology and environmental co-variate mapping of primary biliary cholangitis and primary sclerosing cholangitis. JHEP Rep Innov Hepatol (2020) 3(1):100202. doi: 10.1016/J.JHEPR.2020.100202
56. Ala A, Stanca CM, Bu-Ghanim M, Ahmado I, Branch AD, Schiano TD, et al. Increased prevalence of primary biliary cirrhosis near superfund toxic waste sites. Hepatology (2006) 43(3):525–31. doi: 10.1002/HEP.21076
57. Shimoda S, Nakamura M, Shigematsu H, Tanimoto H, Gushima T, Gershwin ME, et al. Mimicry peptides of human PDC-E2 163-176 peptide, the immunodominant T-cell epitope of primary biliary cirrhosis. Hepatology (2000) 31(6):1212–6. doi: 10.1053/JHEP.2000.8090
58. Tanaka A, Leung PSC, Gershwin ME. Pathogen infections and primary biliary cholangitis. Clin Exp Immunol (2019) 195(1):25. doi: 10.1111/CEI.13198
59. Mcdevitt HO, Bodmer WF. Hl-a, immune-response genes, and disease. Lancet (1974) 303(7869):1269–75. doi: 10.1016/S0140-6736(74)90021-X
60. Miyadera H, Tokunaga K. Associations of human leukocyte antigens with autoimmune diseases: Challenges in identifying the mechanism. J Hum Genet (2015) 60(11):697–702. doi: 10.1038/JHG.2015.100
61. Miles JJ, Mccluskey J, Rossjohn J, Gras S. Understanding the complexity and malleability of T-cell recognition. Immunol Cell Biol (2015) 93(5):433–41. doi: 10.1038/ICB.2014.112
62. Rossjohn J, Gras S, Miles JJ, Turner SJ, Godfrey DI, McCluskey J, et al. T cell antigen receptor recognition of antigen-presenting molecules. Annu Rev Immunol (2015) 33:169–200. doi: 10.1146/annurev-immunol-032414-112334
63. Dendrou CA, Petersen J, Rossjohn J, Fugger L. HLA variation and disease. Nat Rev Immunol (2018) 18(5):325–39. doi: 10.1038/nri.2017.143
64. Oldstone MBA. Molecular mimicry and autoimmune disease. Cell (1987) 50(6):819–20. doi: 10.1016/0092-8674(87)90507-1
65. Boore JL. Animal mitochondrial genomes. Nucleic Acids Res (1999) 27(8):1767–80. doi: 10.1093/NAR/27.8.1767
66. Shimoda S, Nakamura M, Ishibashi H, Kawano A, Kamihira T, Sakamoto N, et al. Molecular mimicry of mitochondrial and nuclear autoantigens in primary biliary cirrhosis. Gastroenterology (2003) 124(7):1915–25. doi: 10.1016/S0016-5085(03)00387-1
67. Selmi C, Gershwin ME. Bacteria and human autoimmunity: The case of primary biliary cirrhosis. Curr Opin Rheumatol (2004) 16(4):406–10. doi: 10.1097/01.BOR.0000130538.76808.C2
68. Hou X, Yang Y, Chen J, Jia H, Zeng P, Lv L, et al. TCRβ repertoire of memory T cell reveals potential role for escherichia coli in the pathogenesis of primary biliary cholangitis. Liver Int (2019) 39(5):956–66. doi: 10.1111/liv.14066
69. Selmi C, Balkwill DL, Invernizzi P, Ansari AA, Coppel RL, Podda M, et al. Patients with primary biliary cirrhosis react against a ubiquitous xenobiotic-metabolizing bacterium. Hepatology (2003) 38(5):1250–7. doi: 10.1053/JHEP.2003.50446
70. Bogdanos DP, Baum H, Sharma UC, Grasso A, Ma Y, Burroughs AK, et al. Antibodies against homologous microbial caseinolytic proteases p characterise primary biliary cirrhosis. J Hepatol (2002) 36(1):14–21. doi: 10.1016/S0168-8278(01)00252-5
71. Bogdanos DP, Baum H, Grasso A, Okamoto M, Butler P, Ma Y, et al. Microbial mimics are major targets of crossreactivity with human pyruvate dehydrogenase in primary biliary cirrhosis. J Hepatol (2004) 40(1):31–9. doi: 10.1016/S0168-8278(03)00501-4
72. Dominguez PM, Shaknovich R. Epigenetic function of activation-induced cytidine deaminase and its link to lymphomagenesis. Front Immunol (2014) 5:642(DEC). doi: 10.3389/FIMMU.2014.00642
73. Detanico T, St. Clair JB, Aviszus K, Kirchenbaum G, Guo W, Wysocki LJ. Somatic mutagenesis in autoimmunity. Autoimmunity (2013) 46(2):102. doi: 10.3109/08916934.2012.757597
74. Kuraoka M, Snowden PB, Nojima T, Verkoczy L, Haynes BF, Kitamura D, et al. BCR and endosomal TLR signals synergize to increase AID expression and establish central b cell tolerance. Cell Rep (2017) 18(7):1627–35. doi: 10.1016/J.CELREP.2017.01.050
75. Sabouri Z, Schofield P, Horikawa K, Spierings E, Kipling D, Randall KL, et al. Redemption of autoantibodies on anergic b cells by variable-region glycosylation and mutation away from self-reactivity. Proc Natl Acad Sci USA (2014) 111(25). doi: 10.1073/PNAS.1406974111
76. Cantaert T, Schickel JN, Bannock JM, Ng YS, Massad C, Oe T, et al. Activation-induced cytidine deaminase expression in human b cell precursors is essential for central b cell tolerance. Immunity (2015) 43(5):884–95. doi: 10.1016/J.IMMUNI.2015.10.002
77. McDonald G, Medina CO, Pilichowska M, Kearney JF, Shinkura R, Selsing E, et al. Accelerated systemic autoimmunity in the absence of somatic hypermutation in 564Igi: A mouse model of systemic lupus with knocked-in heavy and light chain genes. Front Immunol (2017) 8:1094/BIBTEX(SEP). doi: 10.3389/FIMMU.2017.01094/BIBTEX
78. Jiang C, Foley J, Clayton N, Kissling G, Jokinen M, Herbert R, et al. Abrogation of lupus nephritis in activation-induced deaminase-deficient MRL/lpr mice. J Immunol (2007) 178(11):7422–31. doi: 10.4049/JIMMUNOL.178.11.7422
79. Snir O, Mesin L, Gidoni M, Lundin KEA, Yaari G, Sollid LM. Analysis of celiac disease autoreactive gut plasma cells and their corresponding memory compartment in peripheral blood using high-throughput sequencing. J Immunol (2015) 194(12):5703–12. doi: 10.4049/JIMMUNOL.1402611/-/DCSUPPLEMENTAL
80. Jiang C, Zhao ML, Scearce RM, Diaz M. Activation-induced deaminase-deficient MRL/lpr mice secrete high levels of protective antibodies against lupus nephritis. Arthritis Rheumatol (2011) 63(4):1086–96. doi: 10.1002/ART.30230
81. Quartier P, Bustamante J, Sanal O, Plebani A, Debré M, Deville A, et al. Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to activation-induced cytidine deaminase deficiency. Clin Immunol (2004) 110(1):22–9. doi: 10.1016/J.CLIM.2003.10.007
82. Tan Y, Wang Y, Zhang M, Han YX, Huang CY, Zhang HP, et al. Clonal characteristics of circulating b lymphocyte repertoire in primary biliary cholangitis. J Immunol (2016) 197(5):1609–20. doi: 10.4049/JIMMUNOL.1600096/-/DCSUPPLEMENTAL
83. Lleo A, Liao J, Invernizzi P, Zhao M, Bernuzzi F, Ma L, et al. Immunoglobulin m levels inversely correlate with CD40 ligand promoter methylation in patients with primary biliary cirrhosis. Hepatology (2012) 55(1):153–60. doi: 10.1002/HEP.24630
84. Selmi C, Cavaciocchi F, Lleo A, Cheroni C, De Francesco R, Lombardi SA, et al. Genome-wide analysis of DNA methylation, copy number variation, and gene expression in monozygotic twins discordant for primary biliary cirrhosis. Front Immunol (2014) 5:128/BIBTEX(MAR). doi: 10.3389/FIMMU.2014.00128/BIBTEX
85. Lleo A, Zhang W, Zhao M, Tan Y, Bernuzzi F, Zhu B, et al. DNA Methylation profiling of the X chromosome reveals an aberrant demethylation on CXCR3 promoter in primary biliary cirrhosis. Clin Epigenet (2015) 7(1):61. doi: 10.1186/S13148-015-0098-9
86. Chuang YH, Lian ZX, Cheng CM, Lan RY, Yang GX, Moritoki Y, et al. Increased levels of chemokine receptor CXCR3 and chemokines IP-10 and MIG in patients with primary biliary cirrhosis and their first degree relatives. J Autoimmun (2005) 25(2):126–32. doi: 10.1016/J.JAUT.2005.08.009
87. Hu Z, Huang Y, Liu Y, Sun Y, Zhou Y, Gu M, et al. β-arrestin 1 modulates functions of autoimmune T cells from primary biliary cirrhosis patients. J Clin Immunol (2011) 31(3):346–55. doi: 10.1007/S10875-010-9492-4
89. Banales JM, Sáez E, Úriz M, Sarvide S, Urribarri AD, Splinter P, et al. Up-regulation of microRNA 506 leads to decreased cl-/HCO3- anion exchanger 2 expression in biliary epithelium of patients with primary biliary cirrhosis. Hepatology (2012) 56(2):687–97. doi: 10.1002/HEP.25691
90. Erice O, Munoz-Garrido P, Vaquero J, Perugorria MJ, Fernandez-Barrena MG, Saez E, et al. MiRNA-506 promotes primary biliary cholangitis-like features in cholangiocytes and immune activation. Hepatology (2018) 67(4):1420. doi: 10.1002/HEP.29533
91. Gerussi A, Paraboschi EM, Cappadona C, Caime C, Binatti E, Cristoferi L, et al. The role of epigenetics in primary biliary cholangitis. Int J Mol Sci (2022) 23(9):4873. doi: 10.3390/IJMS23094873
92. Scally SW, Petersen J, Law SC, Dudek NL, Nel HJ, Loh KL, et al. A molecular basis for the association of the HLA-DRB1 locus, citrullination, and rheumatoid arthritis. J Exp Med (2013) 210(12):2569. doi: 10.1084/JEM.20131241
93. Eerligh P, Van Lummel M, Zaldumbide A, Moustakas AK, Duinkerken G, Bondinas G, et al. Functional consequences of HLA-DQ8 homozygosity versus heterozygosity for islet autoimmunity in type 1 diabetes. Genes Immun (2011) 12(6):415–27. doi: 10.1038/GENE.2011.24
94. Tabibian JH, Masyuk AI, Masyuk TV, O’Hara SP, LaRusso NF. Physiology of cholangiocytes. Compr Physiol (2013) 3(1):541–65. doi: 10.1002/CPHY.C120019
95. Banales JM, Huebert RC, Karlsen T, Strazzabosco M, LaRusso NF, Gores GJ. Cholangiocyte pathobiology. Nat Rev Gastroenterol Hepatol (2019) 16(5):269–81. doi: 10.1038/S41575-019-0125-Y
96. Ronca V, Mancuso C, Milani C, Carbone M, Oo YH, Invernizzi P. Immune system and cholangiocytes: A puzzling affair in primary biliary cholangitis. J Leukoc Biol (2020) 108(2):659–71. doi: 10.1002/JLB.5MR0320-200R
97. Atif M, Warner S, Oo YH. Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells. Hepatol Int (2018) 12(4):305–14. doi: 10.1007/S12072-018-9882-X
98. Schurich A, Berg M, Stabenow D, Böttcher J, Kern M, Schild HJ, et al. Dynamic regulation of CD8 T cell tolerance induction by liver sinusoidal endothelial cells. J Immunol (2010) 184(8):4107–14. doi: 10.4049/JIMMUNOL.0902580
99. Ayres RCS, Neuberger JM, Shaw J, Joplin R, Adams DH. Intercellular adhesion molecule-1 and MHC antigens on human intrahepatic bile duct cells: Effect of pro-inflammatory cytokines. Gut (1993) 34(9):1245–9. doi: 10.1136/GUT.34.9.1245
100. Broomé U, Scheynius A, Hultcrantz R. Induced expression of heat-shock protein on biliary epithelium in patients with primary sclerosing cholangitis and primary biliary cirrhosis. Hepatology (1993) 18(2):298–303. doi: 10.1002/HEP.1840180212
101. Barbatis C, Woods J, Morton JA, Fleming KA, McMichael A, McGee JO. Immunohistochemical analysis of HLA (A, b, c) antigens in liver disease using a monoclonal antibody. Gut (1981) 22(12):985–91. doi: 10.1136/GUT.22.12.985
102. Chapman RW, Kelly PMA, Heryet A, Jewell DP, Fleming KA. Expression of HLA-DR antigens on bile duct epithelium in primary sclerosing cholangitis. Gut (1988) 29(4):422–7. doi: 10.1136/GUT.29.4.422
103. Barnes BH, Tucker RM, Wehrmann F, Mack DG, Ueno Y, Mack CL. Cholangiocytes as immune modulators in rotavirus-induced murine biliary atresia. Liver Int (2009) 29(8):1253–61. doi: 10.1111/J.1478-3231.2008.01921.X
104. Savage COS, Brooks CJ, Harcourt GC, Picard JK, King W, Sansom DM, et al. Human vascular endothelial cells process and present autoantigen to human T cell lines. Int Immunol (1995) 7(3):471–9. doi: 10.1093/INTIMM/7.3.471
105. Lombardi G, Sidhu S, Batchelor R, Lechler R. Anergic T cells as suppressor cells in vitro. Science (1994) 264(5165):1587–9. doi: 10.1126/SCIENCE.8202711
106. Iwai Y, Terawaki S, Ikegawa M, Okazaki T, Honjo T. PD-1 inhibits antiviral immunity at the effector phase in the liver. J Exp Med (2003) 198(1):39–50. doi: 10.1084/JEM.20022235
107. Barral DC, Brenner MB. CD1 antigen presentation: How it works. Nat Rev Immunol 2007 712 (2007) 7(12):929–41. doi: 10.1038/nri2191
108. Bendelac A, Lantz O, Quimby ME, Yewdell JW, Bennink JR, Brutkiewicz RR. CD1 recognition by mouse NK1+ T lymphocytes. Science (1995) 268(5212):863–5. doi: 10.1126/SCIENCE.7538697
109. Hegde S, Fox L, Wang X, Gumperz JE. Autoreactive natural killer T cells: promoting immune protection and immune tolerance through varied interactions with myeloid antigen-presenting cells. Immunology (2010) 130(4):471–83. doi: 10.1111/J.1365-2567.2010.03293.X
110. Subleski JJ, Jiang Q, Weiss JM, Wiltrout RH. The split personality of NKT cells in malignancy, autoimmune and allergic disorders. Immunotherapy (2011) 3(10):1167. doi: 10.2217/IMT.11.117
111. Torina A, Guggino G, La Manna MP, Sireci G. The janus face of NKT cell function in autoimmunity and infectious diseases. Int J Mol Sci (2018) 19(2):440. doi: 10.3390/IJMS19020440
112. Schrumpf E, Tan C, Karlsen TH, Sponheim J, Björkström NK, Sundnes O, et al. The biliary epithelium presents antigens to and activates natural killer T cells. Hepatology (2015) 62(4):1249–59. doi: 10.1002/HEP.27840
113. Tsuneyama K, Yasoshima M, Harada K, Hiramatsu K, Gershwin ME, Nakanuma Y. Increased CD1d expression on small bile duct epithelium and epithelioid granuloma in livers in primary biliary cirrhosis. Hepatology (1998) 28(3):620–3. doi: 10.1002/HEP.510280303
114. Kjer-Nielsen L, Patel O, Corbett AJ, Le Nours J, Meehan B, Liu L, et al. MR1 presents microbial vitamin b metabolites to MAIT cells. Nature (2012) 491(7426):717–23. doi: 10.1038/NATURE11605
115. Zhang Y, Kong D, Wang H. Mucosal-associated invariant T cell in liver diseases. Int J Biol Sci (2020) 16(3):460. doi: 10.7150/IJBS.39016
116. Jeffery HC, Van Wilgenburg B, Kurioka A, et al. Biliary epithelium and liver b cells exposed to bacteria activate intrahepatic MAIT cells through MR1. J Hepatol (2016) 64(5):1118–27. doi: 10.1016/J.JHEP.2015.12.017
117. Gough SC, Simmonds M. The HLA region and autoimmune disease: Associations and mechanisms of action. Curr Genomics (2007) 8(7):453. doi: 10.2174/138920207783591690
118. McGonagle D, Aydin SZ, Gül A, Mahr A, Direskeneli H. ‘MHC-i-opathy’-unified concept for spondyloarthritis and behçet disease. Nat Rev Rheumatol (2015) 11(12):731–40. doi: 10.1038/NRRHEUM.2015.147
119. Lenz TL, Deutsch AJ, Han B, Hu X, Okada Y, Eyre S, et al. Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases. Nat Genet (2015) 47(9):1085–90. doi: 10.1038/NG.3379
120. Bassani-Sternberg M, Coukos G. Mass spectrometry-based antigen discovery for cancer immunotherapy. Curr Opin Immunol (2016) 41:9–17. doi: 10.1016/J.COI.2016.04.005
121. Vader W, Kooy Y, Van Veelen P, De Ru A, Harris D, Benckhuijsen W, et al. The gluten response in children with celiac disease is directed toward multiple gliadin and glutenin peptides. Gastroenterology (2002) 122(7):1729–37. doi: 10.1053/GAST.2002.33606
122. Van de Water J, Ansar A, Prindiville T, Coppel RL, Ricalton N, Kotzin BL, et al. Heterogeneity of autoreactive T cell clones specific for the E2 component of the pyruvate dehydrogenase complex in primary biliary cirrhosis. J Exp Med (1995) 181(2):723–33. doi: 10.1084/JEM.181.2.723
123. Liaskou E, Henriksen EKK, Holm K, Kaveh F, Hamm D, Fear J, et al. High-throughput T-cell receptor sequencing across chronic liver diseases reveals distinct disease-associated repertoires. Hepatology (2016) 63(5):1608–19. doi: 10.1002/HEP.28116
124. Moran AE, Hogquist KA. T-Cell receptor affinity in thymic development. Immunology (2012) 135(4):261–7. doi: 10.1111/J.1365-2567.2011.03547.X
125. Stubbington MJT, Lönnberg T, Proserpio V, Clare S, Speak AO, Dougan G, et al. T Cell fate and clonality inference from single-cell transcriptomes. Nat Methods (2016) 13(4):329–32. doi: 10.1038/NMETH.3800
126. Garcia KC, Teyton L, Wilson IA. Structural basis of T cell recognition. Annu Rev Immunol (1999) 17:369–97. doi: 10.1146/ANNUREV.IMMUNOL.17.1.369
127. Stadinski BD, Shekhar K, Gómez-Touriño I, Jung J, Sasaki K, Sewell AK, et al. Hydrophobic CDR3 residues promote the development of self-reactive T cells. Nat Immunol (2016) 17(8):946–55. doi: 10.1038/NI.3491
128. Daley SR, Koay HF, Dobbs K, Bosticardo M, Wirasinha RC, Pala F, et al. Cysteine and hydrophobic residues in CDR3 serve as distinct T-cell self-reactivity indices. J Allergy Clin Immunol (2019) 144(1):333–6. doi: 10.1016/J.JACI.2019.03.022
129. Lagattuta KA, Kang JB, Nathan A, Pauken KE, Jonsson AH, Rao DA, et al. Repertoire analyses reveal T cell antigen receptor sequence features that influence T cell fate. Nat Immunol (2022) 23(3):446–57. doi: 10.1038/S41590-022-01129-X
130. Birnbaum ME, Mendoza JL, Sethi DK, Dong S, Glanville J, Dobbins J, et al. Deconstructing the peptide-MHC specificity of T cell recognition. Cell (2014) 157(5):1073–87. doi: 10.1016/J.CELL.2014.03.047
131. Borbulevych OY, Santhanagopolan SM, Hossain M, Baker BM. TCRs used in cancer gene therapy cross-react with MART-1/Melan-A tumor antigens via distinct mechanisms. J Immunol (2011) 187(5):2453–63. doi: 10.4049/JIMMUNOL.1101268
132. Beringer DX, Kleijwegt FS, Wiede F, van der Slik AR, Loh KL, Petersen J, et al. T Cell receptor reversed polarity recognition of a self-antigen major histocompatibility complex. Nat Immunol (2015) 16(11):1153–61. doi: 10.1038/NI.3271
133. Loon L. Prophylactic inoculation against hay fever. Int Arch Allergy Appl Immunol (1953) 4(4):285–8. doi: 10.1159/000228032
134. Valenta R. The future of antigen-specific immunotherapy of allergy. Nat Rev Immunol (2002) 2(6):446–53. doi: 10.1038/NRI824
135. Sabatos-Peyton CA, Verhagen J, Wraith DC. Antigen-specific immunotherapy of autoimmune and allergic diseases. Curr Opin Immunol (2010) 22(5):609–15. doi: 10.1016/J.COI.2010.08.006
136. Moorman CD, Sohn SJ, Phee H. Emerging therapeutics for immune tolerance: Tolerogenic vaccines, T cell therapy, and IL-2 therapy. Front Immunol (2021) 12:657768/BIBTEX. doi: 10.3389/FIMMU.2021.657768/BIBTEX
137. Mannie MD, DeOca KB, Bastian AG, Moorman CD. Tolerogenic vaccines: targeting the antigenic and cytokine niches of FOXP3+ regulatory T cells. Cell Immunol (2020) 355:104173. doi: 10.1016/J.CELLIMM.2020.104173
138. Willekens B, Cools N. Beyond the magic bullet: Current progress of therapeutic vaccination in multiple sclerosis. CNS Drugs (2018) 32(5):401–10. doi: 10.1007/S40263-018-0518-4
139. Richardson N, Ng STH, Wraith DC. Antigen-specific immunotherapy for treatment of autoimmune liver diseases. Front Immunol (2020) 11:1586/BIBTEX. doi: 10.3389/FIMMU.2020.01586/BIBTEX
140. Ganesan V, Ascherman DP, Minden JS. Immunoproteomics technologies in the discovery of autoantigens in autoimmune diseases. Biomol Concepts (2016) 7(2):133–43. doi: 10.1515/BMC-2016-0007
141. Kishimoto TK, Maldonado RA. Nanoparticles for the induction of antigen-specific immunological tolerance. Front Immunol (2018) 9:230/BIBTEX(FEB). doi: 10.3389/FIMMU.2018.00230/BIBTEX
142. LaMothe RA, Kolte PN, Vo T, Ferrari JD, Gelsinger TC, Wong J, et al. Tolerogenic nanoparticles induce antigen-specific regulatory T cells and provide therapeutic efficacy and transferrable tolerance against experimental autoimmune encephalomyelitis. Front Immunol (2018) 9:281/BIBTEX(MAR). doi: 10.3389/FIMMU.2018.00281/BIBTEX
143. Hunter Z, McCarthy DP, Yap WT, Harp CT, Getts DR, Shea LD, et al. A biodegradable nanoparticle platform for the induction of antigen-specific immune tolerance for treatment of autoimmune disease. ACS Nano (2014) 8(3):2148–60. doi: 10.1021/NN405033R
144. Lemos H, Huang L, Chandler PR, Mohamed E, Souza GR, Li L, et al. Activation of the STING adaptor attenuates experimental autoimmune encephalitis. J Immunol (2014) 192(12):5571–8. doi: 10.4049/JIMMUNOL.1303258
145. Cappellano G, Woldetsadik AD, Orilieri E, Shivakumar Y, Rizzi M, Carniato F, et al. Subcutaneous inverse vaccination with PLGA particles loaded with a MOG peptide and IL-10 decreases the severity of experimental autoimmune encephalomyelitis. Vaccine (2014) 32(43):5681–9. doi: 10.1016/J.VACCINE.2014.08.016
146. Al-Ghobashy MA, Elmeshad AN, Abdelsalam RM, Nooh MM, Al-Shorbagy M, Laible G. Development and pre-clinical evaluation of recombinant human myelin basic protein nano therapeutic vaccine in experimental autoimmune encephalomyelitis mice animal model. Sci Rep (2017) 7:46468. doi: 10.1038/SREP46468
147. Neef T, Miller SD. Tolerogenic nanoparticles to treat islet autoimmunity. Curr Diabetes Rep (2017) 17(10):84. doi: 10.1007/S11892-017-0914-Z
148. Sharabi A, Mozes E. The suppression of murine lupus by a tolerogenic peptide involves foxp3-expressing CD8 cells that are required for the optimal induction and function of foxp3-expressing CD4 cells. J Immunol (2008) 181(5):3243–51. doi: 10.4049/JIMMUNOL.181.5.3243
149. Obreque J, Vega F, Torres A, et al. Autologous tolerogenic dendritic cells derived from monocytes of systemic lupus erythematosus patients and healthy donors show a stable and immunosuppressive phenotype. Immunology (2017) 152(4):648–59. doi: 10.1111/IMM.12806
150. Zhang YN, Poon W, Tavares AJ, McGilvray ID, Chan WCW. Nanoparticle-liver interactions: Cellular uptake and hepatobiliary elimination. J Control Release (2016) 240:332–48. doi: 10.1016/J.JCONREL.2016.01.020
151. Violatto MB, Casarin E, Talamini L, et al. Dexamethasone conjugation to biodegradable avidin-Nucleic-Acid-Nano-Assemblies promotes selective liver targeting and improves therapeutic efficacy in an autoimmune hepatitis murine model. ACS Nano (2019) 13(4):4410–23. doi: 10.1021/ACSNANO.8B09655
152. Carambia A, Freund B, Schwinge D, et al. Nanoparticle-based autoantigen delivery to treg-inducing liver sinusoidal endothelial cells enables control of autoimmunity in mice. J Hepatol (2015) 62(6):1349–56. doi: 10.1016/J.JHEP.2015.01.006
153. Moteki S, Leung PSC, Rolland Dickson E, et al. Epitope mapping and reactivity of autoantibodies to the E2 component of 2-oxoglutarate dehydrogenase complex in primary biliary cirrhosis using recombinant 2-oxoglutarate dehydrogenase complex. Hepatology (1996) 23(3):436–44. doi: 10.1002/HEP.510230307
154. Kishimoto TK, Maldonado RA. Nanoparticles for the induction of antigen-specific immunological tolerance. Front Immunol (2018) 9:230(FEB). doi: 10.3389/FIMMU.2018.00230
155. Gharagozloo M, Majewski S, Foldvari M. Therapeutic applications of nanomedicine in autoimmune diseases: from immunosuppression to tolerance induction. Nanomedicine (2015) 11(4):1003–18. doi: 10.1016/J.NANO.2014.12.003
156. Cappellano G, Comi C, Chiocchetti A, Dianzani U. Exploiting PLGA-based biocompatible nanoparticles for next-generation tolerogenic vaccines against autoimmune disease. Int J Mol Sci (2019) 20(1):204. doi: 10.3390/IJMS20010204
157. Hori S, Nomura T, Sakaguchi S. Control of regulatory T cell development by the transcription factor Foxp3. Science (2003) 299(5609):981–5. doi: 10.1126/SCIENCE.1079490
158. Eggenhuizen PJ, Ng BH, Ooi JD. Treg enhancing therapies to treat autoimmune diseases. Int J Mol Sci (2020) 21(19):1–18. doi: 10.3390/IJMS21197015
159. Bennett CL, Christie J, Ramsdell F, et al. The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3. Nat Genet (2001) 27(1):20–1. doi: 10.1038/83713
160. Ramsdell F, Ziegler SF. FOXP3 and scurfy: how it all began. Nat Rev Immunol (2014) 14(5):343–9. doi: 10.1038/NRI3650
161. Jeffery HC, Braitch MK, Brown S, Oo YH. Clinical potential of regulatory T cell therapy in liver diseases: An overview and current perspectives. Front Immunol (2016) 7:334(SEP). doi: 10.3389/FIMMU.2016.00334
162. Rong G, Zhou Y, Xiong Y, et al. Imbalance between T helper type 17 and T regulatory cells in patients with primary biliary cirrhosis: the serum cytokine profile and peripheral cell population. Clin Exp Immunol (2009) 156(2):217. doi: 10.1111/J.1365-2249.2009.03898.X
163. Lan RY, Cheng C, Lian ZX, et al. Liver-targeted and peripheral blood alterations of regulatory T cells in primary biliary cirrhosis. Hepatology (2006) 43(4):729–37. doi: 10.1002/HEP.21123
164. Wakabayashi K, Lian ZX, Moritoki Y, et al. IL-2 receptor alpha(-/-) mice and the development of primary biliary cirrhosis. Hepatology (2006) 44(5):1240–9. doi: 10.1002/HEP.21385
Keywords: primary biliary cholangitis, human leukocyte antigens complex, HLA haplotypes, genetics, immunotolerance
Citation: Mulinacci G, Palermo A, Gerussi A, Asselta R, Gershwin ME and Invernizzi P (2022) New insights on the role of human leukocyte antigen complex in primary biliary cholangitis. Front. Immunol. 13:975115. doi: 10.3389/fimmu.2022.975115
Received: 21 June 2022; Accepted: 11 August 2022;
Published: 31 August 2022.
Edited by:
Nanda Kerkar, University of Rochester, United StatesReviewed by:
Dimitrios Petrou Bogdanos, University of Thessaly, GreeceJohn Vierling, Baylor College of Medicine, United States
Copyright © 2022 Mulinacci, Palermo, Gerussi, Asselta, Gershwin and Invernizzi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Pietro Invernizzi, cGlldHJvLmludmVybml6emlAdW5pbWliLml0
†These authors share first authorship