Jennifer A. Juno
Stephen J. Kent- 1Department of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, VIC, Australia
- 2Department of Infectious Diseases, Melbourne Sexual Health Centre, Alfred Health, Central Clinical School, Monash University, Clayton, VIC, Australia
- 3ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, The University of Melbourne, Melbourne, VIC, Australia
Elimination of the latent HIV reservoir remains a major barrier to achieving an HIV cure. In this review, we discuss the cytolytic nature of human gamma delta T cells and highlight the emerging evidence that they can target and eliminate HIV-infected T cells. Based on observations from human clinical trials assessing gamma delta immunotherapy in oncology, we suggest key questions and research priorities for the study of these unique T cells in HIV cure research.
Introduction
Efforts to eliminate the latent HIV reservoir have, to date, been unsuccessful, outside of aggressive chemotherapy and stem cell transplants from genetically resistant donors (Hutter et al., 2009; Gupta et al., 2020). Killing of infected cells with minimal viral replication, or killing of infected cells after latency reversal, is likely to be critical in the long-term containment or eradication of HIV. Novel approaches to clear infected cells now include the study and manipulation of highly cytotoxic lymphocyte subsets beyond traditional CD8+ CTL (Garrido et al., 2018a,b). It has become apparent from both in vitro studies and human clinical trials in oncology that gamma delta T (γδT) cells exhibit remarkable cytotoxicity (Simoes et al., 2018) and the potential for safe clinical use in human immunotherapy (Silva-Santos et al., 2019). A number of excellent reviews have recently described the use of human γδT cells in clinical trials for cancer treatment (Lo Presti et al., 2017; Godfrey et al., 2018; Pauza et al., 2018; Silva-Santos et al., 2019). Here, we will discuss how advances in gdT immunology have identified these cells as potential anti-HIV effectors, and what remains to be established regarding the efficacy of γδT cells as components of an HIV cure intervention.
Human Gamma Delta T Cell Subsets
Human γδT cells are typically classified on the basis of their TCR delta chain, of which there are 8 variants (Hayday, 2000). In peripheral blood, up to 90% of γδT cells express the Vδ2 chain (Triebel et al., 1988). The majority of Vδ2 cells pair with Vγ9 and form the well-studied population of phosphoantigen-reactive γδT cells (Tanaka et al., 1995). In contrast, Vδ2-negative γδT s dominate at many mucosal sites, including the gut (Lundqvist et al., 1995). These Vδ2- γδT cells tend to express either the Vδ1 or Vδ3 chain, with a variety of Vγ chain pairings (Groh et al., 1998). Vδ1 cells typically, but not always (Hviid et al., 2000), form a minor population of the circulating γδT cell compartment.
Vδ2Vγ9 cells (herein referred to as Vδ2 cells) form a polyclonal T cell population that rapidly expands postnatally, most likely due to persistent antigen exposure or other inflammatory stimuli (Pauza and Cairo, 2015; van Der Heiden et al., 2020). The Vδ2Vγ9 TCR recognizes pyrophosphate antigens, which include isopentenyl pyrophosphate (IPP) and the potent microbial metabolite (E)-4-Hydroxy-3-methyl-but-2-enyl pyrophosphate (HMB-PP) (Triebel et al., 1988). Like other unconventional T cells, however, Vd2 cells can also respond to TCR-independent stimuli, including cytokines such as IL-12 and IL-18, and various NK cell receptor ligands (Provine et al., 2018). Interestingly, phosphoantigen-reactive γδT cells are found only in humans, non-human primates, and alpacas, with no γδT cells in mice recognizing similar antigens (Fichtner et al., 2020). Owing in part to the ease with which they can be expanded in vitro, Vδ2 cells have been well characterized in human health and disease, and many of their defining features have been recently reviewed (Tyler et al., 2015; Davey et al., 2018). Notably, Vδ2 cells are commonly depleted during chronic HIV infection, with incomplete restoration among ART-treated cohorts (Hinz et al., 1994; Poccia et al., 1996; Wesch et al., 1998; Enders et al., 2003; Poles et al., 2003; Li et al., 2014, 2015; Cimini et al., 2015; Strbo et al., 2016; Bhatnagar et al., 2017). We have recently reviewed the impact of HIV infection and treatment on both circulating and tissue-resident γδT cells (Juno and Eriksson, 2019).
In contrast to Vδ2 cells, the antigen specificity of Vδ1 cells remains largely unknown. The Vδ1 cell population includes cells with specificity for R-phycoerythrin and EphA2 (Willcox and Willcox, 2019), CD1c- and CD1d-restricted lipid antigens (Uldrich et al., 2013; Roy et al., 2016; Willcox and Willcox, 2019), and the antigen presenting molecule MR1 (Le Nours et al., 2019). Vδ1 phenotype and frequency is markedly altered by infections such as malaria (Hviid et al., 2019) and human cytomegalovirus (HCMV) (Pitard et al., 2008; van Der Heiden et al., 2020). HCMV seropositivity is typically associated with substantial clonal expansion within the Vδ1 population, and differentiation toward a terminally differentiated (CD27-CD45RA+) phenotype (Davey et al., 2017; van Der Heiden et al., 2020). In contrast to Vδ2 cells, the Vδ1 cell population is significantly expanded during HIV infection and ART (De Paoli et al., 1991; De Maria et al., 1992; Rossol et al., 1998; Wesch et al., 1998; Poles et al., 2003; Poggi et al., 2004; Fausther-Bovendo et al., 2008; Li et al., 2014; Cimini et al., 2015; Olson et al., 2018; Chevalier et al., 2019), the implications of which are largely unknown (Juno and Eriksson, 2019).
Anti-HIV Activity of Gamma Delta T Cells
Efforts to eliminate the HIV reservoir following latency reversal have traditionally focused on the utility of antigen-stimulated conventional CD8+ T cells to kill HIV-infected cells (Shan et al., 2012; Deng et al., 2015). Limitations to this approach include the requirement for autologous CD8+ T cells to be collected and pre-stimulated for each individual (Shan et al., 2012), as well as a high burden of CTL escape variants in the latent reservoir (Deng et al., 2015). More recently, other lymphocyte subsets have been considered for use in HIV cure approaches. Evidence suggests that cytokine-treated NK cells can eliminate HIV-infected T cells following ex vivo latency reactivation, although IL-15 treatment downregulates the expression of the key NK cell receptor NKp46, which may be undesirable in vivo (Garrido et al., 2018a). With a transcriptional phenotype that blends characteristics of both NK and CD8+ T cells (Gutierrez-Arcelus et al., 2019; Pizzolato et al., 2019), γδT cells are intriguing candidates to mediate anti-HIV effector functions. Indeed, γδT-mediated inhibition of HIV replication has been recognized for more than 20 years (Poccia et al., 1999).
Like NK cells (Fehniger et al., 1998; Oliva et al., 1998), stimulated γδT cells can produce sufficient β-chemokines to block HIV entry into either CCR5+ or CXCR4+ CD4+ T cells (Poccia et al., 1999; Omi et al., 2014). In the context of HIV cure approaches, however, it is the potent cytolytic function of γδT cells that makes them strong candidates for immunotherapy. Early reports suggested that direct cytotoxicity toward HIV-infected cells was largely restricted to Vδ2 cell clones (Wallace et al., 1996; Poccia et al., 1997), with little to no cytotoxicity observed among Vδ1 cell lines (Wallace et al., 1996). More recently, Vδ1 recognition and killing of HIV-infected CD4+ T cells has been demonstrated (Fausther-Bovendo et al., 2008). Although it is challenging to determine the extent to which γδT cells contribute to natural control of HIV infection in cross-sectional studies, elite/viral controllers do exhibit higher frequencies of Vδ2 cells than untreated or antiretroviral treated normal progressors (Riedel et al., 2009; Chevalier et al., 2019). A study in non-human primates identified a relationship between cervical Vδ2 frequency and simian immunodeficiency virus (SIV) viral load (Tuero et al., 2016), which supports the possibility of a protective role for these cells during infection.
Perhaps the strongest proof-of-concept evidence for Vδ2-mediated elimination of infected CD4+ T cells following latency reversal in vitro was reported by Garrido et al. (2018b). Despite low frequencies of Vδ2 cells in ART-treated donors ex vivo, pamidronate + IL-2 treatment successfully expanded the Vδ2 population in a manner comparable to that of uninfected donors in vitro (i.e., a similar fold-increase). The expanded cells expressed CD56 and CD16, as well as relatively low levels of the inhibitory markers PD-1 and CTLA-4. Interestingly, both ex vivo isolated and in vitro expanded Vδ2 cells were equally capable of inhibiting HIV replication in autologous superinfected CD4+ T cells, with a level of inhibition comparable to that of CD8+ CTL. More importantly, however, expanded Vδ2 cells degranulated in response to co-culture with HIV-infected, but not uninfected, CD4+ T cells. These results were further extended to a latency clearance assay, which demonstrated that expanded Vδ2 cells cleared infected CD4+ T cells derived from ART-treated donors following in vitro reactivation with vorinostat. This study provides promising evidence for the ability of Vδ2 cells to contribute to an HIV cure approach that relies on eliminating reactivated virally infected target cells. A number of important questions remain, however, particularly regarding the mechanisms of Vδ2 recognition of HIV-infected cells as well as the optimal conditions for expansion Vδ2 cells with the most potent cytotoxicity. The need to address these gaps in knowledge is evidenced in a recent study by James et al. (2020) which found that the presence of gamma delta T cells in a viral outgrowth assay impacted viral replication in 4 of 15 donors. CD16 expression on Vδ2 cells correlated with a reduction in HIV recovery, but the key receptors involved in recognition of CD4 target cells and the reason for the heterogeneity in responses among the cohort remains unknown. Below, we explore the potential mechanisms that could be exploited in a gamma delta T-mediated HIV cure strategy (summarized in Figure 1).
Figure 1. γδT cell recognition of target cells. Relevant receptors that may facilitate γδT cell recognition of HIV-infected CD4 T cells are indicated for Vδ2, Vδ1, and in vitro-expanded Vδ1 cells.
Receptors Mediating Direct Cytotoxicity
Vδ2 cells express a number of receptors that might facilitate recognition of HIV-infected T cells. A critical receptor for the detection and killing of transformed and virally infected is NKG2D, which is commonly expressed on NK cells. NKG2D is widely expressed by Vδ2 cells both ex vivo and following in vitro expansion, and can mediate direct killing of target cells (Rincon-Orozco et al., 2005; Wrobel et al., 2007). The NKG2D ligands ULBP-1,−2, and−3 are absent on uninfected CD4+ T cells, but are highly upregulated upon HIV infection and mediate NK-cell killing of HIV-infected cells (Ward et al., 2007). NKG2D is therefore a strong candidate for Vδ2-mediated direct recognition and killing of reactivated HIV-infected cells. NK cells can also recognize infected CD4+ T cells through 2B4-CD48 binding (Ward et al., 2007). Although 2B4 is highly expressed on Vδ2 cells ex vivo, triggering of 2B4 in isolation is insufficient to activate γδT effector functions (Nakajima et al., 1999). Whether phosphoantigen-expanded Vδ2 cells can be activated through 2B4 signaling and/or recognition of CD48 on HIV-infected T cells is currently unknown. Similarly, there is a potential for Vδ2-expressed DNAM-1 to recognize its ligand PVR on infected CD4+ T cells, although NK cell killing of infected cells through this mechanism seems to require signaling through both NKG2D and DNAM-1, rather than DNAM-1 alone (Cifaldi et al., 2019). In general, it will be important for future studies to consider the impact of activating receptor ligation both among ex vivo-derived Vδ2 cells, as well as in vitro expanded cells. For example, NKG2D ligation on resting Vδ2 cells is reported to have either no or minimal functional impact (Rincon-Orozco et al., 2005; Nedellec et al., 2010), but in the context of TCR stimulation can provide robust co-stimulatory activity and effector function (Nedellec et al., 2010).
Expression of cytotoxicity receptors on Vδ1 cells differs substantially from those described on Vδ2 cells. Vδ1 cells commonly express CD94 paired with either the inhibitory receptor NKG2A (CD159a) or the activating receptor NKG2C (CD159c). Chronic HIV infection is associated with a significant increase in NKG2C expression on Vδ1 cells, which can substantially boost Vδ1 cell cytotoxicity when triggered by binding to its ligand HLA-E (Fausther-Bovendo et al., 2008). Interestingly, Vδ1 cells derived ex vivo from HIV-infected participants can lyse autologous HIV-infected CD4+ T cells in a manner which is partially dependent on Vδ1 NKG2C expression (Fausther-Bovendo et al., 2008), suggesting a currently unrealized potential for Vδ1 cells in anti-HIV immunotherapy. The in vitro expansion of Vδ1 cells is less commonly reported or standardized compared to Vδ2 cells, largely due to the lack of an antigen that can easily stimulate the majority of Vδ1 cells ex vivo. Several groups, however, have reported protocols to expand these cells using a combination of γδ TCR stimulus and cytokines. Almeida et al. reported on the production of “Delta One T (DOT)” cells using isolated γδT cells, CD3 engagement and a cocktail of cytokines, which resulted in a 60,000-fold expansion of Vδ1 cells in culture (Almeida et al., 2016). Vδ1 expansion can also be induced through the culture of isolated γδT cells with PHA and IL-7 (Wu et al., 2015). In both studies, expanded Vδ1 cells expressed a number of surface markers related to cytotoxic function, including NKp30, NKp44, NKp46, NKG2D, 2B4, DNAM-1, and CD94. Other approaches to expand Vδ1 cells include the use of artificial APCs (aAPCs) presenting CMV-derived peptides (Polito et al., 2019). Vδ1 cells expanded by this approach recognize an array of tumor cells and virally infected cell lines, but the mechanism underlying this recognition was not assessed. Although the translational potential of DOT cells and other expanded Vδ1 cells are currently focussed on cancer immunotherapy, the expression of traditionally NK cell-associated markers such as NKp44, NKG2D, and 2B4 on expanded Vδ1 cells may also mediate recognition of HIV-infected CD4+ T cells (Ward et al., 2007).
Antibody-Dependent Cytotoxicity
In addition to direct recognition and killing of HIV-infected target cells, HIV-specific antibodies can mediate antibody-dependent cellular cytotoxicity (ADCC) via Fc receptor-expressing cells such as NK cells. Naturally occurring anti-HIV ADCC antibodies decline following ART (Madhavi et al., 2015, 2017) and are not boosted following panobinostat administration (as a latency-reversing agent, LRA) and subsequent analytical treatment interruption (ATI) (Lee et al., 2017). This suggests such antibodies may be insufficient to mediate the level of ADCC needed to clear the latent reservoir. The infusion of more potent broadly neutralizing antibodies (BnAbs), however, may be sufficient to allow FcR-expressing cells to recognize Env expression on reactivated infected cells (Bruel et al., 2016). HIV-specific ADCC has been widely studied in the context of NK cells, but less so in relation to unconventional T cells. Both Vδ1 and Vδ2 cells can express FcgRIIIA (CD16) (Angelini et al., 2004; Couzi et al., 2012; He et al., 2013), making them potential mediators of ADCC in the context of latency reactivation and BnAb therapy.
Despite depletion of Vδ2 cells during chronic HIV infection, ART-treated individuals exhibit similar frequencies of CD16+ Vδ2 cells compared to uninfected controls (although there is intra-donor variability in steady-state CD16 expression) (He et al., 2013). As such, ex vivo CD16-mediated degranulation responses are comparable between these groups (He et al., 2013), suggesting that primary Vδ2 cells from ART-treated individuals are capable of performing ADCC. Poonia and Pauza (2012) demonstrated that zoledronate can expand Vδ2 cells in vitro from both HIV-uninfected and HIV-infected donors, with expression of CD16 detectible on a subset of the expanded cells. Although expanded Vδ2 cells from HIV-infected donors exhibited lower ADCC than those from uninfected donors, they remained capable of degranulation and cytokine expression following CD16 cross-linking.
The expression of CD16 on Vδ1 cells has been studied in the context of HCMV infection (Couzi et al., 2012; Bachelet et al., 2014) and cancer immunotherapy (Fisher et al., 2014), but despite the high prevalence of HCMV seropositivity among HIV-infected populations (Gianella and Letendre, 2016), there has been little study of Vδ1 ADCC in the context of HIV infection. The expanded population of Vδ1 cells in HIV-infected individuals exhibits high expression of perforin (Boullier et al., 1997), but whether this translates into antibody-mediated cytotoxicity is unknown. Similar gaps in knowledge exist for in vitro-expanded Vδ1 cells. There is no data available to describe CD16 expression on DOT cells (Almeida et al., 2016), while PHA/IL-7-expanded Vδ1 cells express moderate levels of CD16 and high levels of GzmB and Perforin, though they have not been assessed for ADCC activity (Wu et al., 2015).
Approaches for Gamma Delta Immunotherapy
As described above, there are many in vitro protocols that result in Vd2 or Vd1 T cell expansion from bulk PBMC. To translate these ideas to the clinic, there are two major approaches that can be considered: in vivo gamma delta T cell expansion, or adoptive transfer of in vitro-expanded cells. Currently, in vivo expansion has only been demonstrated for human Vd2 T cells. This method involves the administration of zoledronate and recombinant IL-2, and has successfully expanded Vd2 T cells in HIV-infected participants in a small clinical trial (Poccia et al., 2009). An advantage of this approach is that it is relatively simple and involves an existing, clinically approved drug (under the brand name Zometa). It would not, however, likely be suitable for individuals with substantial Vd2 T cell depletion/exhaustion or Vd2 T cell phenotypes that lack the receptors determined to be key in recognizing HIV-infected target cells. In such instances, it may be more attractive to consider the use of “off-the-shelf,” in vitro-expanded gamma delta T cells derived from HIV uninfected donors. Such cells could be expanded by any of the protocols described above, and could include both Vd2 and Vd1 T cell subsets. This approach has been tested in clinical trials for cancer patients (Lo Presti et al., 2017) and also used in studies of non-human primate Vd2 T cells (Qaqish et al., 2017).
Accessing the Latent HIV Reservoir
While in vitro studies can provide an important assessment of cytotoxic capacity and recognition of infected T cells, they largely ignore one of the major barriers to achieving an HIV cure: the anatomical localization of the latent reservoir. Recent evidence suggests that the B cell follicle is a key site of HIV replication, even during ART (Bronnimann et al., 2018). Germinal center (GC) T follicular helper (Tfh) cells are highly permissive to HIV infection (Kohler et al., 2016; Aid et al., 2018), while follicular dendritic cells (FDCs) can capture HIV virions and maintain an infectious virus reservoir even during ART (Smith et al., 2001; Bronnimann et al., 2018). A major barrier to the clearance of virus from the B cell follicle is the fact that the follicle is partially protected from CTL activity. Of the few CTLs found in the follicle, many may be exhausted or exhibit a regulatory phenotype (Bronnimann et al., 2018). Similarly, there are few NK cells found in the human lymph node, and a high proportion of LN NK cells in HIV-infected individuals exhibit an anergic CD56-CD16+ phenotype (Luteijn et al., 2011). Given these limitations, expanded γδT cells may be strong candidates for B cell follicle targeting and elimination of infected cells. Vδ2 cells can acquire a Tfh-like phenotype, complete with expression of the GC-homing marker CXCR5 (Caccamo et al., 2006; Bansal et al., 2012), and such cells have been described both in vitro and in vivo in human lungs (Caccamo et al., 2006). Furthermore, γδT cells have been visualized within GCs in the gastrointestinal mucosa, lymph nodes, tonsil and spleen, likely due to the induction of a LN migration program that occurs following Vδ2 TCR triggering (Brandes et al., 2003). Functional studies of Vδ2 Tfh cells have largely focused on their capacity to provide B cell help, leaving open the question of their cytotoxic potential and expression of cytotoxicity receptors. Nonetheless, the fact that γδT cells appear to access the B cell follicle merits further study of their potential to eliminate HIV-infected cells in this unique environment (Bronnimann et al., 2018).
Beyond the B cell follicle, many other tissues serve as HIV reservoir sites, including the spleen, bone marrow, liver, gut, nervous system, lung, and male and female reproductive tracts (Wong and Yukl, 2016; Cantero-Perez et al., 2019). Infection of tissue-resident T cells may be particularly important, given their longevity and capacity for self-renewal (Cantero-Perez et al., 2019). Both expanded Vδ1 and Vδ2 cells appear to be excellent candidates for tissue trafficking in vivo. When administered to mice, human-derived DOT cells seeded, and then further expanded in, various tissues including the spleen, lung, bone marrow, and liver (Almeida et al., 2016). The tissue-resident cells retained function, as assessed by IFNg and TNF production, and exhibited evidence of ongoing proliferation. Similarly, the adoptive transfer of expanded Vδ2 cells has been studied in non-human primates. Infusion of zoledronate-expanded Vδ2 cells resulted in trafficking to and persistence in the airway for at least 7 days (Qaqish et al., 2017).
Potential Advantages and Disadvantages of γδT Cell Immunotherapy
As with any immune-based intervention, there are both key advantages offered by γδT cells over other T cell therapies and issues that will need to be addressed prior to clinical testing.
Advantages of γδT cell-based immunotherapy include:
1) Lack of MHC restriction: GMP-compliant protocols have been developed to generate large banks of expanded γδT cells, allowing for an “off-the-shelf” allogeneic product that is not reliant on MHC matching (Deniger et al., 2014; Almeida et al., 2016; Polito et al., 2019). The lack of MHC-restriction of γδT cells is a major advantage that should avoid issues of graft-vs.-host disease in γδT -based immunotherapy. Indeed, adoptive transfer of haploidentical expanded γδT cells from the family members of cancer patients proved to be safe and highly effective toward achieving complete remission (Wilhelm et al., 2014).
2) Safety: Clinical trials of human γδT cell therapy, either using in vivo Vδ2 expansion or adoptive transfer of expanded Vδ2 cells, have proven to be safe and well-tolerated (Lo Presti et al., 2017). A major disadvantage to current αβ T cell-based chimeric antigen receptor (CAR)-T cell therapies is the potential for serious and/or fatal side effects, including cytokine release syndrome (van Den Berg et al., 2015), off-target effects due to antigen cross-reactivity (Linette et al., 2013), or transgenic TCR mispairing with endogenous TCR (Zhang et al., 2004). Several studies suggest that γδT-based immunotherapy is less likely to result in cytokine release syndrome (CRS) or off-target effects than αβ T cells (Harrer et al., 2017; Pauza et al., 2018; Rotolo et al., 2019). Indeed, expanded γδ T cells can mediate potent cytotoxicity but simultaneously produce lower levels of cytokines than αβ T cells (Harrer et al., 2017).
3) HIV-associated expansion and differentiation of Vd1 cells: As discussed in the introduction, Vδ1 cell frequency and absolute counts increase in the circulation during HIV infection. This increase persists during suppressive ART, resulting in a pool of terminally differentiated Vδ1 cells (Olson et al., 2018) that express NCRs such as NKG2C (Fausther-Bovendo et al., 2008). To date, we are not aware of any studies that have assessed the expansion and subsequent anti-HIV cytotoxicity of Vδ1 cells specifically derived from HIV-infected individuals. If expansion of Vδ1 cells from healthy donors does not induce the expression of NKG2C or other NCRs that are upregulated during HIV infection, then it may be advantageous to isolate and expand Vδ1 cells expressing these markers from people living with HIV. Care must be taken, however, to characterize the pro-inflammatory nature of these cells, as discussed below.
Potential challenges to γδT cell-based immunotherapy include:
1) In vivo potency: One of the major challenges facing the implementation of γδT cell therapy in cancer is a discrepancy between in vitro and in vivo γδT cell potency (Pauza et al., 2018). In vitro, γδT cell cytotoxicity can be achieved with effector:target ratios of <1, but results of human clinical trials show considerably more heterogeneity in objective responses to γδT immunotherapy (Pauza et al., 2018). Pre-clinical animal studies are hindered by the fact that Vδ2Vg9 phosphoantigen-reactive T cells are found only in humans and non-human primates (NHP). Studies in mouse models are therefore less informative and have more caveats than studies of other lymphocyte subsets. In the context of HIV infection, it will be critical to move studies into NHPs and SIV infection prior to human clinical trials.
2) γδT cell infection by HIV: Typically, both Vδ1 and Vδ2 cells lack expression of the HIV co-receptor CD4, seemingly rendering them refractory to direct infection. Concerningly, however, Soriano-Sarabia et al. (2015) reported that replication-competent HIV could be recovered from purified Vδ2 cells in 14 of 18 long-term ART recipients. Thus, the use of expanded autologous Vδ2 cells from HIV-infected patients may risk the reactivation and replication of a latent reservoir. This could be mitigated by the use of haploidentical or third-party Vδ2 cells from HIV-uninfected donors. Even in that scenario, though, consideration must be given to whether large numbers of adoptively transferred Vδ2 cells could be infected by HIV, since γδ immunotherapy would be reliant on the use of LRAs to reactivate the latent reservoir. Several reports now suggest that Vδ2 cells can transiently express CD4 during activation (Imlach et al., 2003; Soriano-Sarabia et al., 2015; Strbo et al., 2016) and can be productively infected with HIV (Wallace et al., 1997), which likely mediates the establishment of the latent reservoir detected by Soriano-Sarabia. For that reason, in vitro Vδ2 expansion and adoptive transfer may be preferable compared to in vivo Vδ2 expansion using aminobisphosphonate drugs.
3) Depletion of Vδ2 cells: In contrast to Vδ1 cells, Vδ2 cells are depleted during HIV infection and do not fully recover following ART (as discussed previously). Most data suggest that Vδ2 cells expand in vitro to a similar extent regardless of the HIV status of the donor, but individuals who exhibit low Vδ2 frequencies ex vivo will produce fewer absolute numbers of Vδ2 cells after expansion (Garrido et al., 2018b). Furthermore, the observation that the ADCC activity of Vδ2 cells derived from ART-treated donors was reduced compared to uninfected donors (Poonia and Pauza, 2012) suggests that further attention needs to be paid to functional defects of Vδ2 cells in HIV-infected donors.
4) Contribution to immune activation: While the causes of Vδ1 expansion during HIV infection are not conclusively known, it is likely that microbial translocation and loss of epithelial barrier integrity in the gut mucosa drive activation and differentiation of this subset (Harris et al., 2010; Olson et al., 2018). Some studies have shown that Vδ1 cells exhibit proinflammatory cytokine production that correlates with CD8+ T cell activation (Olson et al., 2018) or killing of bystander CD4+ T cells (Sindhu et al., 2003) during HIV infection. Thorough assessment of the characteristics of expanded Vδ1 cells derived from HIV-infected donors will be required to determine the potential pathogenic impact of these cells if adoptively transferred.
Concluding Thoughts and Future Directions
Intense interest in γδT cell-based immunotherapy for cancer is continually driving innovative and novel approaches to harness γδT cell cytotoxicity, which should be considered in the context of HIV cure strategies. For example, despite substantial differences in antigen specificity, NK cell receptor expression, and tissue tropism between Vδ1 and Vδ2 cells, it may be more effective to non-specifically expand a diverse population of γδT cells than to focus on the development of pure Vδ1 or Vδ2 populations. Using aAPCs engineered to express a number of co-stimulatory molecules, Deniger et al. (2014) demonstrated the expansion of a mixed population of Vδ1, Vδ2, and Vδ1-Vδ2- cells that recognized tumor cells via NKG2D, DNAM-1, and the γδ TCR. In an in vivo murine model, this mixed population was more effective at eliminating ovarian cancer xenografts than any of the individual γδT subsets alone. Similar results were obtained with mixed γδT cells in a model of neuroblastoma, where Vδ2 cells mediated CD16-dependent ADCC and Vd1 cells exhibited direct cytotoxicity (Fisher et al., 2014). Given the utility of both ADCC-based and direct recognition of HIV-infected T cells in cure strategies, mixed γδT expansion may be a potent method by which to generate effector γδT cells. More complex approaches could also engineer such cells to express a CAR, providing an additional mechanism by which to recognize infected cells (Rotolo et al., 2019).
Regardless of the nature of the γδT cells chosen for study, the path forward for γδT immunotherapy in HIV cure is clear: First, incisive mechanistic studies are needed to establish the most efficient mechanisms of γδT recognition of reactivated HIV-infected target cells. Despite the intriguing results of Garrido et al. (2018b), the latency-clearing capacity of Vδ2 cells needs to be replicated and the mechanism of recognition defined. With this information, it may be possible to identify γδT cell subsets whose selective expansion would generate better effector cell populations compared to bulk expansion protocols. Second, in vivo animal studies using non-human primates will be critical to addressing questions of tissue targeting and assessment of in vivo potency. Reagents exist to characterize both Vδ1 and Vδ2 cells in NHPs, and studies confirm that these cells recapitulate many aspects of human immunology including expression of CD16 (Hodara et al., 2014), NKG2D, NKG2A, GzmB, and CD107a (Tuero et al., 2016), as well as the ability to kill SIV-infected cells (Malkovsky et al., 1992; Wallace et al., 1994). SIV-infected macaques also recapitulate important aspects of HIV-infected human cohorts, including inversion of the Vδ1:Vδ2 ratio and microbial translocation-induced expansion of Vδ1 cells (Harris et al., 2010). Critically, translational studies of immunity to Mycobacterium tuberculosis have demonstrated the feasibility of both expanding macaque Vδ2 cells in vivo (Ali et al., 2007) or adoptively transferring in vitro expanded cells (Qaqish et al., 2017). With these goals in mind, the application of γδT-based immunotherapy to HIV cure strategies represents an exciting and informative research avenue.
Author Contributions
JJ and SK wrote and edited the manuscript.
Funding
JJ and SK were supported by NHMRC Fellowships (APP1123673 and APP1136322).
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.
Acknowledgments
The authors would like to acknowledge Wen Shi Lee and Kathleen Wragg for providing feedback on the manuscript.
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Keywords: gamma delta T cell, Vδ2, Vδ1, HIV, immunotherapy
Citation: Juno JA and Kent SJ (2020) What Can Gamma Delta T Cells Contribute to an HIV Cure? Front. Cell. Infect. Microbiol. 10:233. doi: 10.3389/fcimb.2020.00233
Received: 05 February 2020; Accepted: 23 April 2020;
Published: 19 May 2020.
Edited by:
Alfredo Garzino-Demo, University of Maryland, United StatesReviewed by:
Natalia Soriano-Sarabia, George Washington University, United StatesRedmond Patrick Smyth, Helmholtz-Institut für RNA-basierte Infektionsforschung (HIRI), Germany
Copyright © 2020 Juno and Kent. 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: Jennifer A. Juno, jennifer.juno@unimelb.edu.au