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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Annu Rev Med. Author manuscript; available in PMC 2010 January 1.
Published in final edited form as:
PMCID: PMC2716400
NIHMSID: NIHMS126293

Emerging Concepts in the Immunopathogenesis of AIDS

Abstract

There is an intense interplay between HIV and the immune system, and the literature is replete with studies describing various immunological phenomena associated with HIV infection. By definition, HIV is the cause of the immunologic findings, for without HIV there is no AIDS. However, many of the phenomena that have been described seem too broad in scope to be attributable to either direct infection of cells by HIV, or the HIV-specific immune response. Recently, a more fundamental understanding of how HIV impacts upon various T cells and T cell compartments has emerged. This review will cover the role of immune activation in HIV immunopathogenesis, how that activation could be mediated directly by HIV replicating within and damaging the gut mucosal barrier, how HIV affects multiple T cell functions and phenotypes, and how chronic HIV replication induces immune modulatory pathways to negatively regulate certain functions in HIV-specific T cells.

Keywords: human immunodeficiency virus, T lymphocyte, Th17 cells, cytokines, PD-1

Introduction

The interplay between HIV and the immune system that ultimately leads to loss of immune control of multiple pathogens and cancers has been termed the immunopathogenesis of AIDS. While many basic concepts of how HIV is able to damage the immune system are unquestioned – HIV infects and destroys CD4 T cells, neutralizing antibodies have little effect on virus replication, cytotoxic T lymphoctes (CTL) limit, but do not stop HIV replication completely – other concepts are more controversial. Many have questioned how HIV can infect such an apparently small proportion of CD4 T cells (estimated at 1 in 100 to 1 in 1,000) and yet still overwhelm the T cell renewal capacity of the immune system. Others question what is driving the chronic immune activation in HIV infection; the virus, the virus-specific immune response, or another mechanism. Within this context, controversy remains over whether the virus drives immune activation, immune activation drives virus replication, or both. Finally, while it is known that CTL can help control virus replication, why HIV-specific CTL fail to do a better job than they do remains an intense area of investigation.

Recent discoveries allow some unifying hypotheses to emerge. What has become clear is that in the balance between viral replication and immune activation, chronic high level virus replication is fundamental to the process of HIV immunopathogenesis. If virus replication is blocked with antiretroviral therapy (ART), most immunologic defects will revert towards normal (some more rapidly than others). However, blocking immune activation has proven much less successful in restoring normalcy to the immune system. The literature on the immunopathogenesis of AIDS, 25 years into the epidemic, is too vast to allow a comprehensive review of this topic. Therefore we will touch on some of the newer findings which help address some of the outstanding questions of how HIV, by infecting certain CD4 T cells, is able to wreak such wide havoc upon the immune system, and how HIV is able to subvert the T cell response that is mobilized against it.

Immune activation in HIV infection

Chronic systemic immune activation is an almost pathognomonic feature of progressive HIV infection. Indeed, it is one of the strongest predictors of disease progression (1-4), is associated with impaired immune reconstitution with antiretroviral therapy (ART) (5) and is a critical factor that distinguishes pathogenic from non-pathogenic non-human primate SIV infection (6). Such immune activation is manifest in many ways including polyclonal B-cell activation (7), increased T-cell turnover (8), increased frequencies of T-cells with an activated phenotype (9), and increased serum levels of proinflammatory cytokines and chemokines (10).

While immune activation may have some beneficial consequences such as T cell proliferation and, by inference, the partial restoration of tissue memory CD4 T cells (11), there is general agreement that it is overwhelmingly detrimental to the HIV-infected person. High turnover of CD4 and CD8 T cells imposes a strain on their homeostatic mechanisms (12) resulting in a decrease in the overall half-life of T cells (13) and clonal exhaustion of T cells may ultimately result in drainage of memory T cell pools (14, 15). Inflammatory damage to lymphoid tissues may underlie thymic dysfunction (16, 17) and TGF-β-mediated fibrosis of lymph nodes (18, 19) which are, in turn, associated with abnormal retention of effector type T cells (20) and poor immune reconstitution with ART (21). Furthermore, and perhaps most importantly, immune activation results in the generation of activated T cell targets for the virus itself, further driving viral replication (22, 23). Hence HIV is a virus that, through the induction of immune activation, generates its own substrate for replication. Critically, it is the activation, infection and depletion of central memory CD4 T cells that are viewed, under normal circumstances, as a “self-renewing” source for tissue effector memory CD4 T cells which may correlate most closely with progression to AIDS (11).

Thus, constant damage to the cellular sources of, and anatomical niches that maintain, the CD4 T cell compartments caused by a quasi self-perpetuating relationship between the virus and immune activation further exacerbates the progressive net loss in CD4 T cell numbers and function and inevitably leads to AIDS. However, even though HIV has been shown to activate dendritic cells and NK cells of the innate immune system in vitro via TLR7/8 (24-26), its replication cannot alone account for the extent of systemic immune activation in HIV-infected individuals. For example, elite controllers who spontaneously control viral loads to very low or undetectable levels may have high immune activation, which also correlates with progressive CD4 T cell loss (3). Furthermore, individuals treated with ART who suppress virus but have incomplete restoration of CD4 T cells also have increased immune activation (5). Finally, in non-pathogenic SIV infection of natural non-human primate hosts such as sooty mangabeys and African green monkeys, while there is high systemic immune activation in the acute phase of the infection, this is rapidly attenuated in the chronic phase, even in the presence of persistently high viral loads (27-29). Thus, defining the factors that underlie systemic immune activation would appear to be critical to understanding the pathogenesis of progressive HIV infection. Recent studies have provided a direct link between immune activation in chronic HIV infection and catastrophic pathogenic events that occur at the mucosal surfaces during acute infection.

The gut mucosa and immune activation

The mucosal surface of the gastrointestinal (GI) tract forms a unique anatomical and physiological niche, serving as a structural and immunological barrier against the microorganisms of the outside world. In fact, the majority of the body's lymphocytes are contained in the GI tract (30, 31). It has long been known that HIV infection causes damage to this critical organ. In 1984, Kotler and colleagues observed that HIV-infected individuals had histological abnormalities of the GI mucosa, malabsorption, and lymphocyte depletion (32). More recently, a number of groups have examined this systematically and have shown that during the acute phase of HIV infection in humans or pathogenic SIV infection in rhesus macaques the majority of GI tract CD4 T cells are depleted, likely as a result of direct viral infection (20, 33-39). Moreover, this depletion continues throughout the entire disease course and represents a considerable assault to the immune system, neither the tempo nor extent of which is reflected in peripheral blood CD4 T cell counts. In addition to the loss of CD4 T cells, gene expression profiles of GI tract biopsies reveal that genes associated with cell cycle regulation, lipid metabolism, and epithelial cell barrier and digestive functions are down-regulated in HIV-infected individuals (40). The enteropathy, which can occur from the acute phase of the infection through to advanced disease, involves diarrhea, increased GI inflammation, increased intestinal permeability and malabsorption (41, 42).

Histologically, the enteropathy involves inflammatory infiltrates of lymphocytes and damage to the GI epithelial layer including villous atrophy, crypt hyperplasia, and villous blunting (43). Importantly these pathological changes occur in the absence of detectable bacterial, viral or fungal enteropathogens often associated with enteropathy (43). SIV-infected rhesus macaques also manifest enteropathy (44), the cause of which may be in part attributed to virus-mediated enterocyte apoptosis and occurs very early in the acute phase of infection (45). A number of investigators recently identified a preferential loss from the GI tract of a subset of T cells that are defined by their secretion of the cytokine IL-17 (46, 47). These Th17 cells are thought to be critical in the defense against bacteria and fungi, particularly at mucosal surfaces, and also contribute to the homeostasis of enterocytes. Importantly, although this loss is observed in HIV infection and pathogenic SIV infection of rhesus macaques (wherein it correlates with progression to AIDS (47)), it is not observed in non-pathogenic SIV infection of sooty mangabeys (46). Thus, it has become apparent that the GI mucosal barrier suffers a serious immunological and structural insult very early in HIV and pathogenic SIV infection and that this damage may adversely affect the barrier function of the gut in the defense against luminal microbes. In fact, it has long been known that damage to the barrier function of the GI tract, such as in inflammatory bowel disease or after chemo/radiotherapy for hematopoietic cell transplantation, results in the translocation of microbial products such as lipopolysaccharide (LPS) into the systemic circulation, in the absence of overt bacteremia, which correlates with systemic immune activation (48-50). Recent studies have shown that chronically HIV-infected individuals have significantly increased levels of plasma LPS compared to uninfected individuals (51). The increased levels of LPS are at a level commensurate with those capable of inducing an acute phase inflammatory response (52) and are associated with increased levels of soluble CD14 and lipopolysaccharide binding protein, and decreased levels of antibodies directed against LPS core antigen indicating bioactivity of LPS in vivo. Moreover, LPS levels are associated with both the frequency of activated memory CD8 T cells and plasma levels of the proinflammatory cytokine IFNα. Importantly, neither of these measures of activation could be directly attributed to LPS. These findings suggest that plasma LPS, in addition to its potent immunostimulatory activity through TLR-4 is also an indicator of the translocation of additional microbial products that stimulate the immune system through other receptors. Notably, in those elite controllers whose disease course nevertheless progresses, the degree of CD4 T cell depletion is closely associated with the level of T cell activation which is, in turn, associated with significantly raised levels of plasma LPS (3). These findings implicate microbial translocation as a cause of immune activation in chronically HIV-infected individuals, thus providing a direct link between the damage to the GI tract during the acute phase of infection and progression to immunodeficiency.

Depletion of GI tract CD4 T cells alone is clearly not sufficient to result in mucosal translocation and immune activation. While pathogenic SIV infection of rhesus macaques is also associated with microbial translocation and immune activation, recent studies have shown that African green monkeys (29) and sooty mangabeys (28), both natural hosts for SIV, lose a significant fraction of their GI tract CD4 T cells during acute SIV infection, yet typically have low levels of immune activation and plasma LPS even in the presence of high viral loads, and do not progress to AIDS (28, 29, 51). Importantly, both species manifest significant immune activation in the acute phase (27-29), with measurable microbial translocation in sooty mangabeys (28) but differ from pathogenic SIV/HIV infection in that the immune activation and microbial translocation is transient and is controlled as the infected animals enter the chronic phase. These observations suggest that natural host species may have evolved immunological mechanisms for control of mucosal pathogens that are less dependent upon CD4 T cells and may also be able to attenuate potentially harmful inflammatory responses in the face of ongoing viral replication.

Thus, in HIV and pathogenic SIV infection the GI tract is a site of massive CD4 T cell depletion, viral infection, enterocyte apoptosis and structural damage to the epithelial surface. New therapeutic directions might aim to prevent or reduce the propagation of HIV at mucosal surfaces and to restore the immunological and epithelial integrity of the mucosal barrier thereby circumventing the associated immune activation and disease progression (53). However, with such emphasis on immune activation as a cause of disease progression and its attenuation in chronic non-pathogenic SIV infection even in the presence of high viral loads, one should not be left with the impression that the virus plays a minor role in disease progression in pathogenic infection. Indeed, it plays a central role at all stages of disease; the relationship between immune activation and the virus may not always be a direct one, but clearly without the virus there is no immune activation. The efficacy of ART in reducing immune activation bears witness to this contention.

T cell function in HIV pathogenesis

Subsets of T cells can be defined by their specificity, surface phenotype, degree of maturation, location, or functions they express upon stimulation, and any and all of these parameters can be affected by HIV infection. Which of these changes are a cause, and which a consequence, of HIV infection has been the focus of intense study for many years. Gross changes in the representation of different T cell subsets have been described (54). Besides the loss of CD4 T cells, a destruction consequential to the infection of this subset by the virus, general patterns were seen that are true of all T cells, including CD8 and gamma-delta subsets. In general, untreated individuals show a progressive loss of resting subsets (with a preferential loss of resting naïve T cells during chronic disease), and elevated levels of activated T cells – for example, those expressing HLA-DR and CD38. Seminal studies by Giorgi and colleagues showed that these activated phenotypes of CD8 T cells were reasonably predictive of subsequent progression rates, in that high expression of CD38 was particularly poor prognostic, whereas HLA-DR expression in the absence of CD38 was favorable (4).

Further studies showed that ART reversed, at least to some extent, many (but not all) of the changes described in chronic HIV infection (55-59). Individuals in whom treatment was halted (STI trials) showed that these reversals were only temporary – suggesting that the remodeling of the T cell compartment accompanying HIV infection was largely a consequence of high viral loads, and that therapeutic control of virus would allow the immune system to partially heal. In general, the substantial phenotypic changes described for CD4 and CD8 T cells during HIV disease rarely correlate with disease progression and are probably more indicative of an immune system under duress.

With the advent of assays to identify antigen-specific T cells (intracellular cytokine staining, or ICS), attention shifted to characterizing those cells actively involved in controlling the virus, i.e., HIV-specific CD4 and CD8 T cells. ICS assays can enumerate the fraction of T cells (or absolute number) that respond by making one or more functional responses following stimulation with antigen; this is referred to as the magnitude of the response. In addition, by considering the types of different responses that are elicited by the stimulation, the quality of the response may be defined (60).

A number of studies demonstrate that the magnitude of the CD8 T cell response to HIV does not correlate with (nor predict) progression (61, 62). Indeed, the magnitude of this response is largely correlated to the viral load; successful control of viremia leads to a diminution of the T cell response (63-65). The failure to find a correlation between the CD8 T cell response to virus and pathogenesis came as a disappointment; there was every expectation that a vigorous T cell response to the virus would be associated with better control and clinical outcome.

Nonetheless, over the past few years it has become clear that the quality, if not the magnitude, of the T cell response may provide such a correlate. Initially, studies quantified the fractions of T cells that made IFNγ, IL2, or both on a cell-by-cell basis. While there was no difference between progressors and nonprogressors in terms of the magnitude of the IFNγ response, the fraction of the cells that made IL2 (alone or in combination with IFNγ) was elevated in nonprogressors (66-69). In other words, the quality of the response varied from an IFNγ-dominated response (progressors) to a more balanced, IL2-producing response (non-progressors) (Figure 2).

Figure 2
Functionally-defined T cell differentiation and HIV disease progression

A seminal paper by Betts et al. dramatically extended this paradigm (70). In this study, T cell quality was defined by the independent measurement of five different functions on a cell-by-cell basis; the concept of polyfunctional T cells (those cells capable of making a majority of measured functions) was born. By comparing clinically-defined progressors to nonprogressors, a substantial difference in the quality of the HIV-specific response was apparent: nonprogressors have a much larger fraction of their response comprised of polyfunctional T cells. Indeed, even within the progressor cohort, there was a correlation between the level of polyfunctionality and viral load – a correlation that had never before been seen with any functional measurement. This has been confirmed in a number of studies (67, 71-73).

Recent studies in HIV-2 infected adults provide additional support for the role of functionally, as opposed to phenotypically, defined T cell subsets in viral control (74, 75). HIV-2 is typically a far less pathogenic infection than HIV-1. As such, there are far more CD4 T cells preserved, and a detailed analysis of HIV-2-specific CD4 and CD8 T cells was possible. HIV-2 specific T cells were found to be more polyfunctional, akin to the HIV-1-specific T cells in nonprogressors. There was no correlation to be found with the phenotypes of these cells. Remarkably, the phenotypes of the antigen-specific T cells showed little correlation with function at all. Indeed, the only associations that were found were that more differentiated subsets produced less IL2 and more MIP1β; there was no association with IFNγ, TNF, or degranulation, and differentiation stage (defined phenotypically).

The potential role of polyfunctional T cells has been extended in a number of studies. Indeed, these cells appear to be relevant even in primary infection: patients with improved resolution of viral load had more polyfunctional responses (72, 76). Even within a single individual's response, there is heterogeneity that follows this pattern. First, responses to different HIV epitopes can be individually characterized; those epitopes that induced more polyfunctional responses also induced proliferative responses, in contrast to epitopes that induced only IFNγ production (68). And second, heterogeneity exists at the level of anatomical location: it appears that mucosal responses are more polyfunctional than those found in the blood. While rectal T cell responses were mildly more polyfunctional (77), T cell responses obtained from bronchoalveolar lavage (BAL) were far more polyfunctional (34). Interestingly, the BAL shows a far better preservation of CD4 T cells than the blood of these same individuals, indicating that pathogenesis is anatomically distinct (and correlates with the degree of polyfunctionality of the compartment).

Numerous studies now show that a higher level of T cells capable of IL2 production (or, more generally, that are polyfunctional) is associated with better outcome in HIV disease. However, to date these studies leave open the question of cause vs. effect. Polyfunctionality did not immediately increase in progressors undergoing ART (69, 70); however, long-term changes have not been well-defined. Nonetheless, there are good reasons to believe that polyfunctional T cell responses are superior and can directly lead to better control of virus. First, in an animal model, vaccine-elicited polyfunctional CD4 T cells were far better at providing protection against challenge with L. Major; indeed, the same number (magnitude) of monofunctional T cells provided essentially no protection (78). Second, each polyfunctional cell by definition elicts a wider repertoire of functions, both measured and unmeasured (for example, greater expression of CD40L, required for licensing dendritic cells) (67). Third, each polyfunctional T cells produces as much as 10-fold more of each cytokine than monofunctional T cells, bringing to bear a far larger effector response directly at the effector site (75, 78, 79). Finally, through the production of IL2, these cells are better equipped to proliferate and extend the response. In sum, these cells appear to be optimized effector cells that are also in the pivotal differentiation stage between central and effector memory T cells (60).

PD-1 and T cell dysfunction in HIV

Despite evidence that HIV- and SIV-specific CD8 T cells (CTL) are involved in the control of viral replication (80-82), there are intrinsic functional defects in these cells including decreased cytokine production, decreased proliferation, lack of polyfunctionality (described above), and lack of full effector differentiation which could at least partially explain their failure to clear the infection fully (83, 84). Similar defects in SIV-specific CTL also exist (85, 86). While chronic high-level antigen stimulation is associated with the generation of many of these defects, it is unclear if there is a central unifying mechanism that regulates all these functions, or whether the different defects, while all resulting from chronic antigen stimulation, are regulated through different pathways. Multiple surface molecules can transmit both positive and negative regulatory signals to T cells, any of which could be responsible for some or all of the observed defects in HIV-specific T cells (87).

Programmed death-1 (PD-1) has recently been identified as a crucial negative regulator of T cell function in HIV infection. PD-1 is a member of the CD28 family and was originally identified as a surface receptor involved in the apoptosis of cancer cells (88, 89). The role of PD-1 in regulating T cell function in chronic viral infection comes from studies of chronic LCMV infection in mice where the resultant CTL exhaustion mimics the defects seen in HIV infection of humans. In an elegant study, recovery from exhaustion of LCMV-specific CTL was accomplished in vivo by blocking the interaction between PD-1 and its ligand PD-L1 (90). This recovery of T cell function was accomplished even in CD4-depleted mice, making the findings relevant to HIV infection. This led to a flurry of activity to determine the role of PD-1 in T cell exhaustion in HIV infection.

Three near-simultaneous publications helped define the role of PD-1 in HIV infection (91-93). All three groups showed that PD-1 was highly expressed on HIV-specific CTL, and that CTL specific for less chronic or acute viruses had lower expression of PD-1. Trautmann et al and Day et al showed that there was an inverse relationship between viral load and PD-1 expression on HIV-specific CTL (91, 93), and a separate publication showed that HIV-specific CTL from long-term non-progressors have lower expression of PD-1 than progressors (94). All three groups showed that proliferation of virus-specific CTL could be improved by blocking the interaction of PD-1 with PD-L1 during antigen stimulation. However, there are some discrepancies in the literature over which CTL functions are directly controlled by PD-1. While expression of PD-1 on CTL has been linked by some to impaired production of cytokines (90, 91, 93) others have emphasized the predominant role of this receptor in regulating the survival of these cells (92, 95-98). Specifically, while blocking PD-1 increases the number of HIV-specific CTL that make cytokine in a multi-day assay, it is unclear if this is secondary to a direct effect of PD-1 on cytokine expression, or a reflection of the better proliferation/survival of HIV-specific CTL over the course of the assay. Petrovas et al were unable to demonstrate a direct effect of PD-1 on cytokine expression in HIV-specific CTL in short-term assays, suggesting a lack of direct linkage between PD-1 and cytokine production (92). Despite these minor differences, these findings collectively support the conclusion that PD-1 expression on HIV-specific CTL, and its engagement by PD-L1 on antigen presenting cells during chronic antigen stimulation, is responsible for at least some of the defects in CTL function.

What is the mechanism by which PD-1 engagement impairs CTL function? Petrovas et al investigated the association between PD-1 expression and apoptosis and concluded that PD-1 is a primary determinant of apoptosis sensitivity in CTL (92). Within any CTL population defined by any other set of surface markers, the PD-1+ population was always more sensitive to apoptosis than the PD-1 population. In addition, the level of PD-1 expression determined the sensitivity to apoptosis, and ligation of PD-1 was sufficient to induce apoptosis, indicating that PD-1 is not just a marker of, but a direct participant in, the apoptotic pathway. Therefore, PD-1 expression leads to a profound (but potentially reversible) survival defect.

There is evidence that chronic antigen stimulation drives the expression of PD-1. First, PD-1 expression decreases when viral replication is suppressed by antiretroviral therapy (91, 93). Second, within both HIV and SIV infections, PD-1 expression decreases on epitope-specific CTL once the epitope has escaped, while CTL specific for epitopes that have not escaped maintain high PD-1 expression (98, 99). Therefore, the PD-1-mediated impairment in CTL function is a direct consequence of high HIV-specific antigen stimulation and not general immune activation.

PD-1 is also expressed on CD4+ T cells. HIV-specific CD4+ T cells express high levels of PD-1 when compared to CMV-specific CD4+ T cells, and this expression correlates with viral load (91). As was seen with CD8+ CTL, PD-1 blockade significantly increased CD4+ T cell proliferation in vitro, suggesting a similar impact of chronic antigen stimulation, PD-1 expression, and functional impairment in both the CD4+ and CD8+ T cell arms of the immune response to HIV (91).

Collectively these findings define PD-1 as a potential therapeutic target for restoring the functional capacity of HIV-specific CTL (Figure 3). However, it should be appreciated that PD-1 expression attenuates potentially harmful T cell responses to many self antigens and other chronic pathogens. Given that many T cells express PD-1, it is likely that interventions which release all CTL from PD-1-mediated suppression will have untoward effects. That said, initial safety and tolerability studies of a PD-1 blocking antibody have been completed in monkeys, and clinical trials in cancer patients have begun. In addition, anti-PD-1 antibodies are being tested in SIV-infected monkeys. These initial studies will provide a foundation upon which decisions to move into human trials in HIV-infected subjects can be based. Use of anti-PD-1 interventions may be much easier in a vaccine setting, where one could target the intervention to T cells specific for a given antigen, thereby avoiding release of harmful responses from appropriate negative regulatory control. This could be accomplished by limiting the use of any anti-PD-1 intervention to either the time or location of the vaccination. While much needs to be done to better define the mechanisms and direct impact of PD-1 on T cell function, the recent discovery of a cell surface molecule that can be manipulated to reverse crucial T cell dysfunctions in HIV infection provides a very promising lead for further therapeutic development.

Figure 3
Model of PD-1 activity and therapeutic intervention

Summary

Because of the complexity of the interactions between HIV and the immune system, many differing and often competing hypotheses of how HIV causes AIDS have been put forth. In order to avoid emulating a group of blind men describing an elephant, specific findings need to be interpreted within the context of multiple other findings, and take into account not only what is observed in blood, but also at multiple other sites throughout the body. When such a view is taken, some unifying conclusions can be made. Among these are that HIV is the proximate cause of AIDS and that immune activation, while underlying the pathogenesis of ongoing viral replication, inhibition of T cell function, and impairment in immune reconstitution, only does this within the context and as a result of HIV infection itself. Recent data clearly demonstrate that the gut mucosal surface and the events that lead to its damage are crucial to the process by which generalized immune activation is established. This then drives further viral replication leading to more tissue destruction and a vicious cycle is established. Within this context, the major antiviral T cells which would normally control viral replication are negatively impacted upon first by the generalized immune activation and second by the high antigen loads and chronic T cell stimulation. This leads to T cell functional impairments that further impact upon the ability of the immune response to curtail HIV replication.

There are several bits of good news within this doomsday scenario. First, we know that potent anti-retroviral therapy, by shutting down HIV replication, leads to an often slow and incomplete but deliberate return of the immune system towards normality. Second, many of the processes described in this review are potential targets for new therapeutic or vaccine interventions. Finally, while there is still much to learn, our better understanding of how HIV causes AIDS will ultimately translate into better treatment options for HIV-infected people.

Figure 1
Central role of HIV in immunopathogenesis

Acronyms

HIV
Human immunodeficiency virus
AIDS
Acquired immunodeficiency syndrome
CTL
cytotoxic T lymphocyte
ART
Antiretroviral therapy
SIV
simian immunodeficiency virus
LPS
lipopolysaccharide
ICS
intracellular cytokine staining
PD-1
programmed death 1
PD-L1
ligand for programmed death 1
LCMV
lymphocytic choriomeningitis virus

Footnotes

Terms/Definitions

Immunopathogenesis of AIDS: interaction between HIV and the immune system leading to AIDS

Microbial translocation: process by which gut microbial products gain access to the systemic circulation in the absence of overt bacteremia

Polyfunctional T cells: individual antigen-specific T cells that respond to cognate antigen by liberating more than one or two functions simultaneously: ie they simultaneously make IL2, IFNγ, and TNF

T cell exhaustion: functional characteristic of CTL often seen in chronic viral infections where CTL proliferate, kill, and liberate cytokines poorly in response to stimulation

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