Abstract
T cell immunity relies on the generation and maintenance of a diverse repertoire of T cell antigen receptors (TCRs). The strength of signaling emanating from the TCR dictates the fate of T cells during development, as well as during the immune response. Whereas development of new T cells in the thymus increases the available TCR repertoire, clonal selection during the immune response narrows TCR diversity through the outgrowth of clonotypes with the fittest TCR. To ensure maintenance of TCR diversity in the antigen-selected repertoire, specific mechanisms can be envisaged that facilitate the participation of T cell clonotypes with less than best fit TCRs. Here, we summarize the evidence for the existence of such mechanisms that can prevent the loss of diversity. A number of T cell-autonomous or extrinsic factors can reverse clonotypic hierarchies set by TCR affinity for given antigen. Although not yet complete, understanding of these factors and their mechanism of action will be critical in interventional attempts to mold the antigen-selected TCR repertoire.
Introduction
Adaptive immunity provides formidable defense against an antigenically unpredictable array of infectious microbes and transformed cells. Recognition of diverse antigens relies on the generation and maintenance of a correspondingly diverse repertoire of antigen receptors, generated somatically and distributed clonally on lymphocytes (1).
Both chains of the heterodimeric αβ T cell receptor (TCRαβ, referred to here as TCR) are generated by a recombinatorial process of variable (V) and junctional (J), and in the case of the TCR β chain, also diversity (D), gene segment rearrangement. This process can create a conservatively estimated diversity of 1015 different TCRs (1), which recent studies suggest may be even higher (2–5). However, owing to the finite size of the T cell compartment, far fewer TCRs will ever be made in the life-time of an individual and even fewer will be successfully selected in the thymus. For example, TCR diversity in the mouse has been estimated in the order of 2 × 106, a number that may be considered relatively small (5, 6). Nevertheless, this “practical” or “realized” TCR diversity appears sufficient to ensure that most, if not all, individuals will respond to most, if not all, antigens, a response perhaps facilitated by the cross-reactive nature of the TCR. Indeed, the mouse TCR repertoire contains on average ~100 naïve CD4+ T cells that bind a given antigenic peptide-MHC II (pMHCII) tetramer, most of which represent distinct clonotypes, each with a unique TCR (7–9). These different TCRs that share antigen reactivity are likely to recognize antigenic pMHCII complexes in different ways, receiving varying degrees of TCR signal strength.
The intrinsic ability of each TCR to recognize antigenic pMHCII complexes is largely responsible for the disparate behavior of distinct CD4+ T cell clonotypes during the immune response, both in terms of expansion (10–12) and T helper subset differentiation (13). This disparity, in turn, underlies the enrichment of the TCR repertoire in clonotypes that display the optimum TCR signal strength under the specific conditions. Indeed, fast outgrowth of clonotypes receiving the strongest TCR signal has been observed during CD4+ T cell priming in various systems (9, 14–18).
In addition to its involvement during priming, the available evidence suggests that TCR signal strength contributes to clonotypic selection during memory formation and recall responses. Several studies have demonstrated selection for CD4+ T cell clonotypes with stronger pMHCII tetramer binding or functional avidity during memory formation in response to immunization or infection (14, 19–22). In contrast, increased amount or potency of a given immunizing antigen (23, 24) or different models of infection or immunization (25–27) have been shown to favor lower-affinity CD4+ T cell clonotypes for entry into the memory pool. Moreover, individual CD4+ T cells transferred in separate hosts exhibit substantial variance in clonal expansion, even if they express identical TCRs (9). Thus, although these studies collectively support a role for TCR signal strength in clonotypic selection during both priming and memory formation, they also highlight the potential influence of factors other than TCR affinity.
Which parameters of immunization or infection can affect TCR clonotypic composition independently of TCR affinity, and indeed to what degree they can overcome TCR affinity-based hierarchies, remains poorly understood. It is clear, however, that such parameters have the potential to reduce the gap in TCR signal strength between high- and low-affinity clonotypes. This property may be critical in ensuring the necessary clonotypic diversity in the CD4+ T cell response. Here, we focus on CD4+ T cells (as the significant amount of knowledge on CD8+ T cells is reviewed elsewhere) and review the current knowledge of the factors that can modify the response of distinct T cell clonotypes that would otherwise be set by TCR affinity.
A T Cell’s Behavior Altered by Other T Cells
The cell-autonomous effect of intrinsic TCR affinity on CD4+ T cell clonal expansion and selection is often taken to imply that CD4+ T cells responding to antigen are oblivious to other CD4+ T cells, including those with shared reactivity. However, the behavior of a given CD4+ T cell may be strongly affected by other CD4+ T cells, either through competition or regulation.
Competition between clonotypes with shared reactivity
The advent of TCR-transgenic T cells permitted the artificial increase of the precursor frequency of T cell clones reactive with a given antigen. At unphysiologically high precursor frequencies, memory development of antigen-specific monoclonal CD4+ T cells was found to be severely compromised due to intraclonal competition (28–31).
Starting at more physiological precursor frequencies, monoclonal CD4+ T cells responding with relatively low functional avidity to an H2-Ab-restricted epitope from the lymphocytic choriomeningitis virus (LCMV) glycoprotein (GP), failed to enter the memory pool when the GP epitope was expressed recombinantly in Listeria monocytogenes, but successfully competed with the host response following LCMV infection (32). The results of this study indicate that the fate of low-avidity monoclonal LCMV-specific CD4+ T cells, and their ability to compete with other clonotypes, is not simply intrinsically determined, but context-dependent.
In another TCR-transgenic system, low-avidity CD4+ T cell clonotypes in a semipolyclonal TCRβ-transgenic population reactive with an epitope from the surface glycoprotein (SU), encoded by the envelope (env) gene of Friend murine leukemia virus (F-MLV) were outcompeted by high-avidity clonotypes if they all were present even at low frequencies (18). However, removal of the high-avidity competitors permitted the full expansion of the low-avidity F-MLV-reactive CD4+ T cell clonotypes (18). Thus, the behavior of low-avidity CD4+ T cell clonotypes is modified by the relative composition of the antigenic pMHCII-reactive pool, and a given low-avidity CD4+ T cell will either clonally expand or not, depending on the absence or presence, respectively, of higher-avidity competitors.
Competition between clonotypes with shared antigen reactivity may drive even more extreme differences in outcome if we consider the composition of the antigen-naïve TCR repertoire. Although current estimates suggest that reactivity for a given antigenic pMHCII complex is shared by, on average, 100 CD4+ T cells in the preimmune repertoire, this number varies substantially for different antigenic pMHCII complexes in the same individual from a theoretical one to experimentally observed several hundred (8). Moreover, owing to the random nature of repertoire formation, the preimmune pool of CD4+ T cells reactive with a given antigenic pMHCII complex will also vary between individuals, both in terms of numbers and clonotypic composition. For, example, the same low-avidity CD4+ T cell may have to compete with only one other similarly low-avidity CD4+ T cells in one individual, but with five other higher-avidity CD4+ T cells in another individual, and therefore, its behavior is expected to vary accordingly (Figure 1).
Figure 1
Although CD4+ T cell clonotypes with shared ability to recognize a particular antigenic pMHCII complex will compete for access to it, there are a number of additional factors that have been proposed to determine the outcome of clonotypic competition. These include multiple costimulatory factors, such as members of the B7 or TNF families of cytokines and costimulatory molecules and their receptors (33–35). In principle, limiting availability of costimulatory signals would render T cells more reliant on antigenic signals for their expansion, thus amplifying the advantage of those clonotypes that are more sensitive to antigen. Indeed, costimulation of virus-specific CD8+ T cells by CD27 was shown to permit the recruitment of lower-affinity clonotypes, promoting diversity in the response (36). A role for CD27 in maintaining clonotypic diversity in the CD4+ T cell response has not been directly demonstrated, but is supported by findings linking loss of CD27 expression in antigen-reactive effector CD4+ T cells with shortened half-life and inability to persist as memory (37). However, given the complex regulation of immune responses by both the B7 and TNF families, the overall effect of a particular costimulatory or inhibitory pathway on the clonotypic composition of a T cell response is often difficult to predict. For example, inclusion of multiple costimulatory pathways in the design of vaccine vectors was shown to favor higher affinity CD8+ T cells, rather than permitting recruitment of lower affinity CD8+ T cells (38). Moreover, engagement of the inhibitory molecule CTLA-4 was shown to increase the breadth of the CD4+ T cell response to immunization, likely by increasing, rather than decreasing clonotypic diversity (39). Nevertheless, these studies further support the notion that the particular constellation of costimulatory or inhibitory pathways seen in infection or immunization help shape the clonotypic diversity of antigen-reactive T cells.
Competition at the level of costimulation operates among T cell clonotypes with shared antigen reactivity, but may not be restricted to them. Expression of the receptors for many costimulatory or inhibitory molecules is typically induced on effector CD4+ T cells (33–35), and it is possible that through modulation of these pathways, T cells responding to a particular antigen affect other T cells concurrently responding to an unrelated antigen. Examples include depletion of costimulatory ligands on APCs by CTLA-4 on effector CD4+ T cells, thus depriving other effector CD4+ T cells of essential costimulation through CD28, the shared receptor for these ligands (40). Competition among CD4+ T cells irrespective of antigen specificity is akin to “quorum sensing,” a density-dependent mechanism that can adjust T cell numbers and maintain T cell homeostasis (41, 42). Although some evidence for “quorum sensing” operating at the T cell population level has been provided (41, 42), to what degree it determines the clonotypic hierarchy in the response to a particular antigen is not currently known.
Clonotypic molding by regulatory T (Treg) cells
The preimmune CD4+ T cell pool also contains a significant proportion of regulatory T (Treg) cells, characterized by the expression of the transcription factor Foxp3, and naturally endowed with suppressive activity (43). Although originally thought to suppress autoimmune T cells, their suppressive activity against T cell responses to foreign antigens in now well established (43).
A generally suppressive environment created by Treg cell action would raise the activation threshold for all clonotypes indiscriminately. However, the effect of Treg cells would block the activation of lower avidity clonotypes preferentially, as their threshold may fall below that for effective participation in the response. Indeed, Treg cell activation by IL-2 secreted by the first few effector T cell clonotypes may, in principle, prevent further recruitment of other clonotypes (42). Studies of the CD8+ T cell response to L. monocytogenes demonstrated that Treg cells inhibit priming selectively of low-avidity CD8+ T cell clonotypes, thus improving the overall avidity of the response (44). Studies of the effect of Treg cells on CD4+ T cell clonotypes are limited. However, vaccination of a small number of ovarian cancer patients with a peptide from the germ cell protein NY-ESO-1 was shown to induce low-avidity CD4+ T cell clonotypes that were insensitive to Treg cell-mediated suppression, suggesting that Treg cells act mostly against high-avidity CD4+ T cell clonotypes (45). Although, together these studies highlight the potential of Treg cells to affect the clonotypic composition of an antigen-specific T cell response, additional studies will be required before a consensus emerges.
Another layer of complexity regarding Treg cell-mediated modulation of clonotypic diversity is shared antigen reactivity between Treg cells and effector CD4+ T cells. Although high-avidity effector CD4+ T cell clonotypes can be efficiently suppressed by Treg cell that do not share antigen reactivity (46), the concomitant presence of Treg cells and effector T cells with the same pMHCII reactivity can often occur (47, 48). It is conceivable that Treg cells have a stronger effect of clonotypic diversity of effector CD4+ T cells when their pMHCII reactivity is identical, thus including Treg cells in intra-clonotypic competition.
Clonotypic Composition According to Antigen Presentation
The overall strength of TCR signal a T cell receives is determined by the TCR affinity for a given pMHCII complex, but it is also affected by the amount or nature of the pMHCII complex itself. Increasing amounts of antigenic pMHCII complexes will prime an increasing number of clonotypes as the activation threshold of lower avidity clonotypes is progressively reached (23, 49). Excessive amounts of antigenic pMHCII complexes or use of higher potency antigenic peptides can lead to the elimination of high-avidity clonotypes, likely through activation-induced cell death (24). Similarly, changes in pMHCII complex as a result of escape mutations in the antigenic peptide will also alter the clonotypic composition of the ensuing T cell response (50). These observations emphasize the potential effect on T cell clonotypic composition of antigen dose and mutability, which in turn affect the relative TCR signal strength each clonotype receives. There are, however, observations where antigen delivery or presentation has been shown to affect the clonotypic composition in ways that are either not fully understood or do not seem to follow simple models of TCR affinity.
An effect of antigen delivery mode on clonotypic diversity
Early work by Malherbe et al. first demonstrated the powerful effect of the co-administered adjuvant on the overall avidity and clonotypic composition of the CD4+ T cell response to immunization with a fixed amount of purified pigeon cytochrome c (PCC) protein (51). The capacity of adjuvants to induce a high-avidity CD4+ T cell response was associated with their ability to disperse from the site of injection (51). In addition to different adjuvants in protein immunization, different viral or bacterial vectors used for vaccination of mice against the HIV-1 env were found to induce distinct fine antigen specificities and TCR usage in vaccine-elicited CD8+ T cells (52). More recently, the F-MLV env was shown to induce fundamentally different outcomes upon immunization with either the retrovirus or vectors based on recombinant human adenovirus 5 (Ad5) (18). In this study, higher-avidity CD4+ T cell responses were linked with faster overall kinetics of the response (18).
Although the choice of adjuvant or vaccine vector can have a profound effect on the clonotypic composition of the elicited T cell response, the underlying mechanisms remain unclear and thus the outcome is not always predictable. Nevertheless, some shared properties of vaccines that induce high-avidity CD4+ T cells can be postulated (53). These will undoubtedly include the amount and conformation of antigenic pMHCII complexes produced, the cell type that is presenting them and the inflammatory setting that is generated (53). A common feature of vaccine adjuvants or vectors that elicit higher-avidity CD4+ T cell responses seems to be that they also elicit numerically larger responses. Indeed, in the PCC protein immunization system, the adjuvants that induced the highest response magnitude also induced the highest proportion of high-avidity CD4+ T cells (51). The same correlation was also observed in the F-MLV env system encoded by either F-MLV or Ad5, and when the vaccine doses were adjusted to ultimately induce a comparable numerical peak in the CD4+ T cell response, the response that was faster to reach the peak also contained the highest proportion of high-avidity CD4+ T cells (18).
If we consider the speed and numerical size of the response as an indicator of the efficiency of antigenic pMHCII presentation, the results of these studies would suggest that fast and strong antigen presentation kinetics result in preferentially high-avidity CD4+ T cell responses. This observation would be consistent with a model where the outcome of competition between clonotypes is determined by at least two parameters: first, timing of recruitment, with the higher-avidity clonotypes starting their response earlier; and second; the duration of the response as a whole (Figure 2). The magnitude of the response, counting high- and low-avidity clonotypes collectively, is restricted to a maximum, set by additional T cell-extrinsic parameters. These parameters are not entirely delineated and may include finite availability of growth factors and other factors, collectively described as niche space (54–56). Indeed, comparisons of acute and chronic LCMV or retroviral infection have indicated that virus-specific CD4+ T cell numbers achieve comparable magnitudes, following which contraction is initiated, irrespective of viral persistence (57, 58). T cell responses where niche space is filled, and therefore clonal expansion ceases, before low-avidity clonotypes are recruited, will consist entirely of high-avidity clonotypes. In contrast, slower T cell responses, where despite their delayed recruitment, low-avidity clonotypes are allowed time to expand before the total response peaks, will be more diverse (Figure 2). Experimental evidence supporting this notion has been provided in a murine system of CD4+ T cell priming to retroviral envelope (18).
Figure 2
The contribution of APC type to T cell clonotypic composition
Any effect of antigen delivery, production, and presentation will inevitably also depend on the type of APC. The potential of distinct APC types to instruct fundamentally different fates in T cells is perhaps best exemplified by thymic selection, where developing T cells interact with diverse subsets of thymic APCs in discrete thymic microenvironments, resulting in positive and negative selection (59). It is therefore conceivable, that antigen presentation to mature T cells in the periphery may heavily influence the clonotypic composition, according to the particular APC type (53).
Professional APCs, including dendritic cells (DCs), macrophages, and B cells, differ wildly in terms of absolute numbers, anatomical location as well as the way they capture and process exogenous antigen (60–63). In addition to receptors shared with other APCs, B cells can also concentrate limiting amounts of available antigen by virtue of their antigen-specific BCR (64, 65). Nevertheless, antigen can also be captured by non-specific B cells by complement-mediated mechanisms (66–69).
In addition to capturing antigen administered as a vaccine or produced in other cell types, professional APCs may also synthesize antigenic proteins for loading onto MHC II molecules, particularly in the setting of infection. Numerous infectious microbes have been documented to infect professional APCs, including the notable examples of LCMV infection of mouse DCs, Epstein–Barr virus (EBV) infection of human B cells, and Mycobacterium tuberculosis infection of mouse and human macrophages (70–72). Importantly, direct infection of professional APCs has, in many cases, been linked to a certain degree of immune subversion or suppression (70–75). Thus, the outcome of presentation by a given APC type may vary depending on whether or not the APC is directly infected.
As well as professional APCs, a variety of hematopoietic and non-hematopoietic cell types are increasingly implicated in MHC II-mediated antigen presentation (76). The overall effect of such atypical APCs on the composition of the CD4+ T cell response is not currently understood, but they may favor expansion of unusual clonotypes. Of note, a rhesus cytomegalovirus (RhCMV) vector that was adapted in vitro to fibroblast cells and was engineered to express simian immunodeficiency virus (SIV) proteins induced highly unusual SIV-specific CD8+ T cells that also reacted with epitopes presented by MHC II molecules (77).
These studies collectively support a role for the type of APC in shaping the clonotypic composition of the CD4+ T cell response. However, given the large number of variables potentially dictating the quantity and quality of antigen presentation by different APC types, it is perhaps unsurprising that a clear correlation with the clonotypic composition of the induced T cell response has not yet been made.
TCR Levels and Signaling Capacity
Besides the affinity of the TCR for pMHCII complexes, the total amount of TCR signaling a CD4+ T cell will receive will vary according to the amount of TCR molecules expressed on the T cell surface, as well as the relative capacity of the TCR signaling complex to initiate the signaling cascade. Both of these parameters can change during the course of the immune response and may therefore affect the clonotypic hierarchy.
Antigen-induced TCR downregulation and clonotypic composition
At steady-state, numbers of surface TCR molecules are maintained at constant levels by balancing production, recycling, and degradation of individual components of the TCR-CD3 signaling complex (78). Upon engagement, surface TCR-CD3 complexes are internalized and recycled or degraded, largely depending on the quality of pMHCII complexes presented by APCs (79, 80). Although antigen-induced TCR internalization may prolong or even amplify TCR signaling from triggered TCR in the immunological synapse, the relative loss of surface TCR reduces new triggering events (79, 80).
The molecular details of TCR downregulation have been elucidated using short in vitro assays. However, several infections can cause dramatic downregulation of surface TCR, which can persist for weeks (17, 81–83). In these longer term settings, persistent TCR-CD3 downregulation is thought to render T cells refractory to further antigenic stimulation, thereby contributing to pathogen persistence and the prevention of excessive immune pathology (84).
To what extend TCR downregulation reduces the ability of a T cell to receive further antigenic stimulation, particularly in chronic in vivo responses, is not entirely clear. Relative loss of surface TCR levels per se may not necessarily compromise TCR signaling capacity. This is due to organization of the surface TCR into oligomers of different sizes prior to antigenic stimulation, which in turn affect sensitivity to antigen (85). Although memory CD4+ T cells generally express lower TCR levels than naïve CD4+ T cells, TCR signaling is more efficient in memory CD4+ T cells as a result of organization of the TCR into larger oligomers in these cells, than in naïve CD4+ T cells (86). Moreover, the density of antigenic pMHCII complexes on individual APCs will also modify the degree of TCR downregulation experienced by CD4+ T cells, with higher density pMHCII complexes inducing greater loss of surface TCR. Thus, the combined effect of TCR downregulation and TCR oligomerization could either reduce or magnify differences in overall TCR signal strength between clonotypes with high- or low-affinity TCRs.
TCR signaling settings imprinted prior to antigen encounter
Other than changes in levels and organization of the surface TCR-CD3 complex, accumulating evidence suggests that the TCR signaling capacity in response to antigenic stimulation is modified by the strength of TCR signaling received prior to antigenic encounter. Such signaling originates from recognition of self pMHCII complexes, but may also include environmental antigens from ubiquitous sources or unrelated infections, and has the ability to tune the TCR signal strength (87).
A major function of self pMHCII interaction is to desensitize or eliminate, through negative selection, strongly autoreactive CD4+ T cells (87). However, self pMHCII interaction also ensures that CD4+ T cells have a fully functional TCR. The latter function is not restricted to passive selection for thymocytes with successfully rearranged TCR; self pMHCII recognition appears to play an active role in setting and maintaining CD4+ T cell functionality. Indeed, continuous self pMHCII interaction is necessary for peripheral CD4+ T cells to retain full functionality and reactivity with antigenic pMHCII complexes (88, 89). Higher than average affinity for self pMHCII complexes during successful selection of thymocytes establishes in mature T cells a modified naïve phenotype characterized by elevated expression of CD5 and reduced expression of Ly6C (90, 91). Recent studies have highlighted the importance of self pMHCII interaction during thymocyte development and later in the periphery in determining the relative success of mature CD4+ and CD8+ T clonotypes during subsequent responses to antigenic stimulation (92–94).
The precise relationship between affinity for self or antigenic pMHCII complexes and clonal expansion in response to antigen is not fully delineated and may depend on additional parameters. In a simple model, clonotypes with the strongest reactivity with self pMHCII complexes will also display the strongest reactivity with antigenic pMHCII complexes, likely as a result of stronger TCR binding to the latter complexes (93). Alternatively, clonotypes with stronger reactivity with self pMHCII complexes will react stronger with antigenic pMHCII, not due to increased affinity of the selected TCR for antigenic pMHCII, but due to more efficient TCR signaling in these cells (92). Moreover, reactivity with self pMHCII complexes does not always predict which clonotype will dominate the CD4+ T cell response (82, 92, 93).
The proposed dominant effect of self-reactivity on CD4+ T cell responsiveness to antigenic stimulation (92, 93) seemingly contrasts the evidence supporting a role for affinity to antigenic pMHCII driving clonotypic competition. The relative importance of either self or antigenic pMHCII complexes in determining the clonotypic composition of the CD4+ T cell response will depend on multiple factors. These will include the relative abundance of self and antigenic pMHCII complexes at various stages of the response. For example, whereas self pMHCII complexes shape T cell repertoires and TCR responsiveness already in the thymus and they are assumed constitutively present in the periphery, antigenic pMHCII complexes will exhibit dramatic changes in abundance in the course of an infection. At the peak of infection, the effect of antigenic pMHCII complexes may be stronger and overshadow that of self pMHCII complexes. In contrast, as infection is controlled and antigenic pMHCII complexes become limiting, the role of self pMHCII complexes may become increasingly dominant.
In the same way, relative importance of either self or antigenic pMHCII complexes will also depend on the affinity of individual clonotypes for either type of TCR stimulation (Figure 3). When the affinity of two distinct clonotypes for the same antigenic pMHCII complex is comparable, the difference in clonal expansion will derive from differences in self-reactivity, thus emphasizing the contribution of the latter. Conversely, when self-reactivity of two distinct clonotypes is comparable, then differences in clonal expansion will depend on affinity for antigenic pMHCII complexes. In a polyclonal repertoire, where clonotypes with equally high affinity for a foreign antigen can be drawn from CD4+ T cell pools with either low or high self-reactivity, the fraction with higher self-reactivity may win the competition. The use of CD5 as a marker for self-reactivity has provided strong evidence that self-reactivity optimizes reactivity to foreign antigen (93). However, if as a result of self-tolerance, the fraction with high self-reactivity contained clonotypes with only low affinity for a particular antigenic pMHCII complex, then clonotypes with high affinity for that antigen in the fraction with low self-reactivity may win the competition (Figure 3). Antigens with significant similarity to self proteins may fall in the second category. Indeed, the presence of endogenous retroviruses in the germ-line has been shown to create partial tolerance to exogenous retroviral proteins, resulting in a repertoire where clonotypes with higher reactivity with endogenous retroviral antigens display lower reactivity with exogenous antigen and are outcompeted during retroviral infection (95).
Figure 3
TCR Signals during Priming Affecting T Cell Maintenance
An overwhelming amount of data supports a role for strong TCR signaling in CD4+ T cell expansion and differentiation during priming. Continuous TCR signals also contribute to successful CD4+ T cell memory formation (22, 96–98) and homeostatic competition between memory CD4+ T cell clonotypes (99). However, settings can also be considered where the same strong TCR signals that promote CD4+ T cell expansion during the early phases of the response compromise the ability of T cells to maintain their presence. In analogy to the antagonistic pleiotropy hypothesis, first proposed to explain how a given gene product can increase fitness early in life, but cause aging later in life (100), what drives early fitness of a particular CD4+ T cell clonotype may lead to its demise later in the response.
Negative feedback pathways tuning the T cell response
Central to the ability of the host to mount a strong T cell response is also the ability to regulate potential over-reactivity and many cell-autonomous layers of negative regulators have been described. The most extreme form of negative regulation is death of T cells as a direct result of strong or persistent TCR signaling (101), a mechanism that has been incriminated in the loss of high-affinity CD4+ T cell clonotypes following immunization with high potency agonists (24). However, there are less extreme negative feedback pathways that may not lead to the complete elimination of the highest affinity clonotypes, but rather curtail their dominance. CTLA-4 can regulate T cell responses both cell-intrinsically and -extrinsically (40, 102). Notably, CTLA-4 accumulation at the immunological synapse is proportional to the strength of TCR signaling and, by extension, to TCR affinity (103). As a result, cell-intrinsic T cell inhibition by CTLA-4 is expected to affect higher affinity CD4+ T cell clonotypes more than lower-affinity ones. Similarly, strong TCR activation also induces PD-1 expression, which in turn inhibits TCR signaling (104). Thus, a direct link between TCR signal strength and expression of inhibitory receptors such as CTLA-4 and PD-1 can be considered as a negative feedback mechanism preserving clonotypic diversity by limiting the expansion of higher affinity CD4+ T cell clonotypes.
Clonotypic composition according to clonotypic Th subset differentiation
TCR signal strength can heavily skew Th differentiation to or away from particular Th subsets (13). Strong and weak TCR signals are generally inducing Th1 and Th2 differentiation, respectively (105–108). Strong TCR signals can also promote T follicular helper (Tfh) cells in certain responses (9, 109), although efficient Tfh differentiation of clonotypes receiving weak TCR stimulation has also been observed in other responses (17, 110, 111). Moreover, clonotypes with higher self-reactivity show a bias in Treg cell conversion (90).
The relative ability of different Th subsets to form a stable memory population has not been systematically compared and may vary according to the infection or immunization. For example, maintenance of Tfh cells is thought to require persistent antigen and germinal center B cells (112), and consequently Tfh cell numbers would be expected to decline when the germinal center reaction ceases. Nevertheless, Tfh cell numbers have also been reported to increase in the chronic phase of LCMV infection (113, 114) or to stably persist as memory in other settings (115–118). Th1, Th2, Th17, and Treg cells can also display variable kinetics, stability, or plasticity depending on infection and antigen parameters (54, 119–122).
Thus, CD4+ T cell clonotypes will, to a certain degree, assort into distinct Th functional subsets, each of which may exhibit differential capacity to persist into memory, in turn shifting the clonotypic composition of the CD4+ T cell response over time. For instance, a low-affinity clonotype may be preferentially enriched in a chronic response due to its skewed differentiation into a Th subset with increased numerical stability.
The relative stability of Th subsets, and by extension of the clonotypes that preferentially differentiate into those subsets, can additionally be affected by extrinsic infection-related factors. CD4+ T cells clonotypes with the highest affinity for antigenic pMHCII complexes will outcompete other lower-affinity clonotypes, but may be lost due to preferential infection in the case of T cell-tropic viruses (123, 124). Similarly, high-affinity CD4+ T cell clonotypes skewed to Th1 differentiation will preferentially migrate to the inflamed tissue in the case of granulomatous bacterial infections, where they are more likely to die than clonotypes that do not show this behavior (125).
Concluding Remarks
The energetically costly generation of a diverse TCR and BCR repertoire underpins the evolutionary success of adaptive immunity as it is critical for its function (5, 126). The obvious advantage of TCR repertoire diversity is to allow the selection of at least one T cell clonotype, best fit to respond to a particular antigen. Clonal expansion of such a T cell clonotype ensures effective immunity and contributes to immunological memory. However, the potential advantage of TCR repertoire diversity in the response to a particular antigen may be more difficult to quantify. In principle, sufficient numbers of a single T cell clonotype with the optimal TCR affinity could competently provide immune protection. However, there may be distinct advantages of preserving diversity in the antigen-selected TCR repertoire.
Although a single naïve T cell can give progeny that differentiates into multiple functional subsets (9, 127), distinct CD4+ T cell clonotypes will generate different Th subset ratios (9). Thus, the maximum Th subset diversity can only be achieved by sufficiently large TCR diversity.
As the number of available TCRs is finite and relatively small in comparison to the number of potential antigens, TCR cross-reactivity is essential to broaden immune coverage by the naïve repertoire (5). This property will remain essential in the antigen-selected TCR repertoire. As different TCR that share reactivity with a given antigen display varying amounts of cross-reactivity with altered variants of this antigen, TCR diversity in the antigen-specific response will expand the number of antigenic variants that can be recognized by antigen-selected T cells. This will be particularly important in infections where the speed of escape mutations present a challenge to the adaptability of the immune response (128).
Another potential advantage of diversity in the CD4+ T cell response to a particular antigen relates to the clonal nature of TCR distribution. Even if sufficient for protective immunity, a single clonal T cell family may inherit the characteristics of the single thymic selection event imprinted onto the founder cell of that family. A polyclonal response will comprise clones from separate thymic selection events, life-histories and likely different patterns of TCR responsiveness, self-reactivity, and survival potential.
The emerging picture is of numerous factors that maximize diversity in the CD4+ T cell response, by alleviating any disadvantage of lower-affinity clonotypes. Some of these factors are extrinsic to T cells and can be manipulated in our attempts to induce protective CD4+ T cell immunity or prevent autoimmunity. However, any intervention toward TCR repertoire “engineering” will necessitate deeper understanding of the type of TCR diversity that best fits a particular response, and this should be the focus of future investigation.
Statements
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.
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Summary
Keywords
CD4 T cell, TCR repertoire, TCR affinity, T cell response, clonotypic diversity
Citation
Merkenschlager J and Kassiotis G (2015) Narrowing the Gap: Preserving Repertoire Diversity Despite Clonal Selection during the CD4 T Cell Response. Front. Immunol. 6:413. doi: 10.3389/fimmu.2015.00413
Received
15 June 2015
Accepted
28 July 2015
Published
11 August 2015
Volume
6 - 2015
Edited by
Eric Huseby, University of Massachusetts Medical School, USA
Reviewed by
Ross M. Kedl, University of Colorado Denver, USA; Salvatore Valitutti, INSERM, France
Copyright
© 2015 Merkenschlager and Kassiotis.
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) or licensor 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: George Kassiotis, Mill Hill Laboratory, The Francis Crick Institute, London NW7 1AA, UK, george.kassiotis@crick.ac.uk
Specialty section: This article was submitted to T Cell Biology, a section of the journal Frontiers in Immunology
Disclaimer
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