Front Immunol.
2019; 10: 3039.doi:
10.3389/fimmu.2019.03039PMCID:
PMC6987473
PMID: 32038613
1Department of Medicine II, Gastroenterology, Hepatology, Endocrinology, and Infectious Diseases, Faculty of Medicine, University Medical Center Freiburg, Freiburg, Germany
2Faculty of Biology, University of Freiburg, Freiburg, Germany
Find articles by Frances Winkler
1Department of Medicine II, Gastroenterology, Hepatology, Endocrinology, and Infectious Diseases, Faculty of Medicine, University Medical Center Freiburg, Freiburg, Germany
3Signalling Research Centres BIOSS and CIBSS, University of Freiburg, Freiburg, Germany
Find articles by Bertram Bengsch
Author information Article notes Copyright and License information PMC Disclaimer1Department of Medicine II, Gastroenterology, Hepatology, Endocrinology, and Infectious Diseases, Faculty of Medicine, University Medical Center Freiburg, Freiburg, Germany
2Faculty of Biology, University of Freiburg, Freiburg, Germany
3Signalling Research Centres BIOSS and CIBSS, University of Freiburg, Freiburg, Germany
Edited by: Helen Marie McGuire, University of Sydney School of Medicine, Australia
Reviewed by: Esaki M. Shankar, Central University of Tamil Nadu, India; Douglas Clayton Palmer, National Cancer Institute (NCI), United States
*Correspondence: Bertram Bengsch ed.grubierf-kinilkinu@hcsgneb.martreb
This article was submitted to Cancer Immunity and Immunotherapy, a section of the journal Frontiers in Immunology
Copyright © 2020 Winkler and Bengsch.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.
Mass cytometry has become an important technique for the deep analysis of single cell protein expression required for precision systems immunology. The ability to profile more than 40 markers per cell is particularly relevant for the differentiation of cell types for which low parametric characterization has proven difficult, such as exhausted CD8+ T cells (TEX). TEX with limited effector function accumulate in many chronic infections and cancers and are subject to inhibitory signaling mediated by several immune checkpoints (e.g., PD-1). Of note, TEX represent considerable targets for immune-stimulatory therapies and are beginning to be recognized as a major correlate of successful checkpoint blockade approaches targeting the PD-1 pathway. TEX exhibit substantial functional, transcriptomic and epigenomic differences compared to canonical functional T cell subsets [such as naïve (TN), effector (TEFF) and memory T cells (TMEM)]. However, phenotypic distinction of TEX from TEFF and TMEM can often be challenging since many molecules expressed by TEX can also be expressed by effector and memory T cell populations. Moreover, significant heterogeneity of TEX has been described, such as subpopulations of exhausted T cells with progenitor-progeny relationships or populations with different degrees of exhaustion or homeostatic potential that may directly inform about disease progression. In addition, TEX subsets have essential clinical implications as they differentially respond to antiviral and checkpoint therapies. The precise assessment of TEX thus requires a high-parametric analysis that accounts for differences to canonical T cell populations as well as for TEX subset heterogeneity. In this review, we discuss how mass cytometry can be used to reveal the role of TEX subsets in humans by combining exhaustion-directed phenotyping with functional profiling. Mass cytometry analysis of human TEX populations is instrumental to gain a better understanding of TEX in chronic infections and cancer. It has important implications for immune monitoring in therapeutic settings aiming to boost T cell immunity, such as during cancer immunotherapy.
Keywords:
T cell differentiation, systems immunology, mass cytometry (CyTOF), T cell exhaustion, chronic infections, cancer, immune checkpoint blockade, immunotherapy
Mass cytometry has become a transformative technology for human immune cell profiling. The use of purified metal isotopes as labels for specific antibodies to stain individual cells and detection of these label isotopes on ionized cells by time-of-flight mass spectroscopy allows the analysis of the protein expression of >40 insightful markers on single cells. The lack of relevant spectral overlap of metal isotopes is a major advantage over traditional fluorescence-based flow cytometry, in which multiplexing of reagents is frequently limited by the need to compensate for overlapping emission spectra of different fluorophores. The ability to integrate the information from more than 40 detection channels for single-cell profiling has been particularly valuable for comprehensive immune monitoring (i.e., analysis of many immune cell lineages) in the setting of translational studies that involve patient cohorts with limited sample access. However, in addition to this “horizontal” profiling approach, mass cytometry also represents a key tool suitable for deep “vertical” profiling of a given immune cell population and may reveal previously unknown heterogeneity within this population, such as complexity within CD8+ T cells (1). In this review, we will discuss how deep immune profiling of exhausted CD8+ T cells by mass cytometry has led to significant insights into their heterogeneity and role in pathophysiology across chronic infections and disease. Characterization of exhausted T cells using mass cytometry is of particular relevance in many immuno-oncologic trials that aim to enhance T cell function.
Exhausted T cells (TEX) are increasingly recognized as a distinct T cell population with a key role in many chronic infections and cancer. TEX were initially described in chronic viral infection, and many subsequent reports have highlighted the accumulation of TEX in the context of ongoing bacterial and parasitic infection, as well as cancer and autoimmunity (2). TEX are characterized by the co-expression of inhibitory receptors and reduced effector function preventing optimal control of viral infection or tumor progression. Targeting inhibitory signaling, such as by interference with inhibitory receptor PD-1 signaling or other immune checkpoints, can reinvigorate TEX function and contribute to disease control or elimination. Consequently, TEX have recently been identified as a major correlate of the clinical response of patients undergoing checkpoint therapy (3, 4), highlighting the need for better immune profiling of TEX as a relevant biomarker for immune therapy trials.
Based on the reduced effector function due to inhibitory signaling in TEX compared to canonical effector T cells (TEFF), TEX have been perceived long-term as a population of suppressed effector T cells according to a “loss-of-function” model (5–7). However, in recent years, it has become clear that the signals inducing T cell exhaustion following T cell activation can drive these cells dynamically into a distinct differentiation fate compared to TEFF and memory T cells (TMEM) that is characterized by massive changes in their metabolism, transcriptome, and epigenome (8–16) ( ).
Open in a separate windowExhausted T cells as well as functional effector and memory T cell differentiation are most thoroughly characterized in the Lymphocytic choriomeningitis virus (LCMV) models of acute and chronic viral infection. In these models, genetic differences between acute and chronic LCMV strains are minimal and immunodominant T cell epitopes are identical, facilitating cross-comparison of T cell phenotypes at the level of endogenous responses or by analysis of transferred virus-specific T cells sharing the same T cell receptor. During acute resolving viral infection, viral clearance after induction of functional effector T cells is followed by the establishment of a pool of memory T cells (17, 18) ( ). In sharp contrast, antigen-specific T cells during chronic infection progressively develop major features of exhaustion, including the up-regulation of inhibitory receptor expression and functional impairment (e.g., consecutive loss of IL-2, TNF and IFN-γ production) (6, 7, 19, 20). While in the first week of chronic infection, the exhaustion program appears to remain flexible and can be altered, as evidenced after transfer of T cells into non-chronically infected hosts, exhaustion appears to become more fixed following the second week of infection (21, 22). Notably, at later time points, the global differentiation program of TEX assessed on the transcriptional and epigenetic level remains stable even after checkpoint blockade intervention and functional reinvigoration (12).
Many insights into TEX have been obtained by the study of antigen-specific T cells in chronic infection and cancer, and multiplexed tetramer analysis together with surface and intracellular markers by mass cytometry has allowed important insights into antigen-specific T cells (1, 23). Identification of TEX without prior knowledge of antigen specificity has remained challenging and is a major obstacle for immune phenotyping in human disease—in particular in cancer—where many tumor antigens especially neoantigens are unknown and tools for assessment of antigen-specific T cell populations are limited. Moreover, established models for T cell differentiation in humans based on markers such as CCR7/CD62L, CD45RA/CD45RO, or CD27/CD28 that allow assessment of naïve T cells (TN), TEFF, and TMEM and additional subpopulations (e.g., central and effector memory T cells) cannot reliably distinguish TEX from the effector or effector memory T cell phenotype (24). A likely explanation is that TEX, similar to TEFF, initially undergo T cell activation programs that include the downregulation of markers of naïvety (such as lymph node homing markers CCR7 and CD62L or preferential CD45RA to CD45RO alternative splicing linked to activation and memory programs), while activation markers, such as CD38 are also induced.
Many investigators have therefore turned to the profiling of inhibitory receptors with a relevant role in TEX biology, such as PD-1 (alone or in combination with other inhibitory receptors such as CTLA-4, Tim-3, Lag-3, 2B4, CD160, TIGIT, and others) for the assessment of exhausted T cells in chronic infections and cancer (20, 25–35). However, it has become clear that those inhibitory receptors can also be expressed by functional effector T cells and may also be present on memory T cell populations and therefore lack specificity (36–39). Moreover, heterogeneous subpopulations of TEX exist for which progenitor-progeny relationships or partial expression of memory-related programs has been described that present further challenges for phenotypic characterization (40–44). Nevertheless, while no single phenotypic marker can reliably assess TEX in humans, the utility of combining several inhibitory receptors for the analysis of differences in antigen-specific exhausted T cells suggests that a combinatorial strategy integrating several exhaustion markers might overcome the limitations for immune profiling.
Markers convenient for the identification of TEX and discrimination from TN, TEFF, and TMEM cells display different levels of expression on TEX compared to these canonical functional T cell populations and across several disease models. To identify such appropriate exhaustion-specific markers, differences in the transcriptional and epigenomic programs between canonical T cell populations and exhausted T cells from the well-controlled LCMV model can be harnessed as specific candidate genes.
Following such an approach, sets of epigenomically regulated exhaustion-specific genes have been recently identified, including 313 genes specifically up-regulated in TEX compared to TN, TEFF, and TMEM that displayed higher gene expression by transcriptome analysis and concomitant changes in enhancer accessibility (45). Moreover, 182 genes down-regulated in TEX were identified that were specifically suppressed on a transcriptional level and lacked accessibility of adjacent enhancers. These exhaustion-specific genes identified in the LCMV infection model were thus predicted as sufficient markers of TEX. The authors then validated individual genes by comparing them for their enrichment in other murine and human settings of infection and cancer, for which T cell exhaustion has been described. Specific genes for exhaustion-directed immune profiling with strong enrichment of gene expression in multiple settings of exhaustion for which suitable reagents were available for cytometry were then selected for further analysis ( ).
This approach confirmed several markers of exhausted T cells frequently used for the profiling of TEX, such as inhibitory receptors PD-1, 2B4, Lag-3, TIGIT, or transcription factor Eomes. Interestingly, CD38 and CD39, which are also frequently used as activation markers due to their induction on TEFF cells, displayed further exhaustion-specific up-regulation and enhancer changes compared with functional T cell populations. These observations suggest that the interpretation as activation markers indicative for TEFF cells may need to be reevaluated. Furthermore, this analytic approach also identified additional exhaustion markers induced on TEX, such as surface proteins CD7, CXCR5, cytotoxic molecule granzyme K or transcription factors Helios and TOX, many of which are also found enriched in tumor-infiltrating lymphocytes by single-cell transcriptomics (46, 47). In agreement with the high levels of TOX on exhausted T cell populations, TOX was recently identified as a master regulator of exhaustion required for the longevity and persistence of exhausted T cells that acts via epigenetic mechanisms facilitating the expression of exhaustion-related gene programs (48, 49). In addition to these novel markers of TEX, it has to be noted that other molecules which are also frequently expressed by TEX were not identified as exhaustion-specific candidates by this approach, including inhibitory receptors Tim-3, KLRG1, CD160, or transcription factor T-bet. This was due to lack of significant differences to canonical T cell subsets at the level of gene expression or associated enhancer changes. Similarly, additional immunoregulatory molecules such as CD72 and CD100 which have been previously described as linked to T cell exhaustion have not been identified by this pipeline, suggesting reduced specificity across T cell populations or context-dependent roles (50). It has to be noted that in this analysis of the specific expression patterns on exhausted cells, individual “exhaustion-specific” molecules can still be expressed to some degree on other T cell subsets (although with a significantly different expression level). Moreover, this strategy also predicted down-regulation of markers associated with naïve and/or memory T cells, such as CCR7, CD73, CD127 and transcription factor TCF-1 on TEX ( ). The integration of a high number of phenotypic “exhaustion-specific” markers into mass cytometry analysis is expected to allow a better discrimination of TEX populations from TN, TEFF, or TMEM.
Functional impairment is a key characteristic of exhausted T cells. Indeed, the term exhaustion was initially used to describe complete loss of effector function and disappearance of the antigen-specific CD8+ T cell response (5, 51). However, it has since become clear that in comparison to functional effector and memory T cells, TEX frequently experience a more gradual loss of effector function that can range from mild impairments in antiviral cytokine production to complete deletion. Typically, mildly exhausted cells exhibit impaired ability to produce IL-2, followed by loss of TNF production in more severe exhaustion, while the ability to produce IFN-γ is frequently maintained and lost usually only in severe exhaustion (52). Reduced expression of anti-apoptotic molecules (i.e., Bcl2) and higher levels of pro-apoptotic Bim have been reported in TEX and might be linked to a pre-apoptotic phenotype in more severely exhausted cells (53–55). Moreover, reduced cytotoxicity and impaired proliferation have been announced for TEX, and successful reinvigoration by checkpoint blockade is frequently measured using metrics of cell cycle activity and proliferation (7). However, it has to be noted that T cell exhaustion is not simply a “loss-of-function” phenotype affecting all T cell functions. On the contrary, higher induction of some chemokines, such as CCL3 and XCL-1, and higher message of other cytokines, such as IL-10 or IL-21, by TEX has been reported (8, 45, 56).
Mass cytometry has been instrumental in the comprehensive characterization of TEX function. For example, differences in the cytotoxic program of TEX with an increased expression of granzyme K, but reduced granzyme B and perforin can be readily assessed in combination with phenotypic profiling (57). Similarly, cell cycle activity assessed by Ki-67 combined with exhaustion marker phenotyping has been pivotal in mass cytometry analysis of responding TEX during checkpoint therapies (3). Nevertheless, the unbiased per-cell assessment of complex exhaustion-related patterns of impaired cytokine production with phenotypic analysis has remained challenging. For example, analyses focusing on the ability of T cells to express effector cytokines frequently struggle to differentiate between cells that never expressed those molecules (i.e., antigen-naïve T cells) or those that lost expression (including TEX). To address these challenges, the characteristic impairment of polyfunctionality with regards to cytokine (e.g., IFN-γ, TNF, IL-2) but increased chemokine production (e.g., CCL3/4, XCL-1) can be used to rate individual T cells for their functional chemokine/cytokine exhaustion profile on a single-cell level using a function-passed exhaustion score. Combined with a comprehensive phenotypic exhaustion profiling possible through the use of mass cytometry, the integration of TEX function as a separate metric of T cell exhaustion was able to reliably discriminate TEX from TEFF, TN, and TMEM (45). The combination of high-parametric functional and phenotypic exhaustion profiling may thus represent a helpful tool for the assessment of individual TEX populations but also for the general degree of CD8+ T cell immune dysfunction in chronic disease.
The integration of a larger set of exhaustion markers in mass cytometry panels creates novel challenges in data evaluation. In flow cytometry-based studies with few exhaustion markers, data evaluation relies heavily on manual gating and boolean analysis of inhibitory receptor co-expression or polyfunctionality (e.g., using SPICE software analysis) (29, 58, 59). These approaches remain valuable for the assessment of TEX using mass cytometry, but have disadvantages compared to bioinformatics algorithm-aided pipelines suitable for the higher data dimensionality generated by mass cytometry. Several bioinformatic strategies have been developed that allow more intuitive visualization of the high-dimensional data using dimension reduction approaches [most prominently based on visualization of “t stochastic neighborhood embedding,” tSNE (60)], and cluster identification strategies in high-dimensional data [e.g., SPADE (61), FlowSOM (62), PhenoGraph (63) and many more] or trajectory inferences that are reviewed elsewhere (64–66). For example, tSNE can be used to generate an “exhaustion map” by calculating a two-dimensional representation of the high-dimensional complexity of TEX phenotypes based on exhaustion marker expression ( ). This approach helps in the identification of TEX heterogeneity and points toward differences of the exhaustion landscape in clinical settings ( ), including the detection of specific populations of exhausted T cells enriched in the tumor microenvironment (45). Moreover, one-dimensional tSNE implementation (“OneSense”) has been used to reduce high-dimensional exhaustion phenotypes to a single parameter and compare them with other sets of marker categories (such as “function”) (67, 68). However, despite the advantages of tSNE-based analysis and high accuracy regarding local neighborhood relationships, tSNE performs different transformations on different regions of a map, resulting in possible challenges regarding interpretation of distance relationships on a tSNE map. Thus, use of tSNE for the discovery of discrete high-dimensional clusters as a crucial correlate of subsets with distinct biology is challenging. Other dimension reduction strategies with manifold approximation, such as uMAP, may address some of these limitations, but loss of information inherent to dimension-reduction strategies cannot be completely avoided (69). As a consequence, cluster identification based on the complete high-dimensional data is often preferred. For example, 25 high-dimensional clusters of CD8+ T cells were identified using PhenoGraph analysis based on the analysis of exhaustion markers in a large and diverse cohort of patients with chronic HIV infection, lung cancer and healthy controls (45). These clusters often projected to discrete regions of a tSNE exhaustion map that was calculated using the same exhaustion parameters but also displayed cluster affiliations that were not obvious from a tSNE map ( ). Clearly, such an exhaustion marker-based clustering approach will also identify functional T cells, such as TN, TEFF, or TMEM cells, but will have increased granularity for TEX subset identification.
Open in a separate windowThe characterization of discrete T cell clusters in high-dimensional “exhaustion data space” thus serves as a foundation that requires further detailed analysis of their functional and clinical role. In particular, a combination with functional profiling following short term stimulation is valuable to assess the extent of cellular exhaustion and can be used to determine the single-cell chemokine or cytokine pattern necessary for calculation of a “functional exhaustion score” discussed above. Such a functional profiling combined with a scaffold of phenotypic markers allowed appropriate mapping of chemokine/cytokine functionality to the high-dimensional exhaustion clusters, suggesting that 9–12 of the 25 phenotypically defined discrete CD8+ T cell subpopulations fit functional properties of T cell exhaustion (45).
Several of the identified exhausted clusters enriched in severe disease contexts, such as severe HIV infection with possible AIDS, or in the tumor microenvironment of lung cancer patients. Phenotypically, these disease-associated exhausted T cells displayed co-expression of exhaustion-specific receptors such as PD-1, CD38 and a transcription factor signature characterized by high Eomes and TOX but low TCF-1 expression ( ). Interestingly, disease-associated TEX in chronic infection were further characterized by co-expression of inhibitory receptors TIGIT and 2B4 (as well as some KLRG1 and CD160) while in cancer, TEX more frequently exhibited higher expression of CTLA-4, Lag-3, and CD39. These data suggest a conserved biology of exhausted T cells in chronic infection and cancer but also highlight specific differences in exhaustion programs with potentially large translational relevance. For example, the altered co-expression patterns of immuno-regulatory molecules on different TEX populations across different disease entities or even across different stages of disease suggest that the therapeutic efficacy of combination therapies (i.e., combined targeting of PD-1 and CTLA-4) could vary according to the TEX subset composition. Importantly, not all subsets of functionally exhausted T cells enrich with disease progression. For example, subsets with expression of PD-1 and co-expression of CD127, TCF-1, and CXCR5 were found enriched in HIV patients with relatively good disease control (i.e., high CD4 counts, CD4/CD8 ratio and low viral load) and these “health-associated” TEX subsets were also detected in large amounts in tumor-surrounding macroscopically non-infiltrated lung compared to the tumor tissue.
Open in a separate windowThese TEX subpopulations identified by high-dimensional analysis using mass cytometry are in agreement with reports about severely exhausted T cells co-expressing several inhibitory receptors being linked to severe disease in chronic infection and cancer in HIV, HCV, HBV, and melanoma patients (29–32, 70–75). They are also in agreement with findings of progenitor and progeny relationships within exhausted T cell populations based on PD-1, Eomes and T-bet expression and the enrichment of TEX populations with high homeostatic potential expressing TCF-1 and CD127 in scenarios of disease control (e.g., clearance of HCV infection) (40, 44, 76). Moreover, TEX expressing CXCR5 have been linked to better control of HIV infection and are thought to constitute a major subset responding to checkpoint therapy (41, 42, 77). Precursor populations of exhausted tumor-infiltrating T cells with higher TCF-1 and CXCR5 expression were also identified to be linked to better clinical outcomes after checkpoint blockade therapy (78).
Thus, mass cytometry is perfectly suited for the interrogation of the clinically significant TEX heterogeneity. A model of TEX heterogeneity including potential lineage relationships and the suggested markers required for minimal TEX immunoprofiling via mass cytometry is displayed in and .
TEX are emerging as a central correlate and useful biomarker of successful immune checkpoint blockade therapies. In clinical trials with patients receiving checkpoint therapies, special attention has to be directed to immune-profiling panels, as therapeutic antibodies and staining reagents may compete for the same epitope. While combination stainings with secondary antibodies against the checkpoint reagents are established, these remain to provide challenges for bioinformatic analysis. Moreover, transient permeabilization protocols frequently used for intracellular barcoding in mass cytometry trials can reduce anti-PD-1 staining. Despite these challenges, mass cytometry has been successfully applied in multiple studies profiling CD8+ T cells. Reinvigoration of TEX compared to tumor mass was identified as a major correlate of the clinical response of patients with malign melanoma receiving checkpoint therapy with anti-PD-1 antibodies (3). Similar observations have been made using flow cytometry and in patients with non-small cell lung cancer (4). In a study comparing the differential effects of PD-1 and CTLA-4 checkpoint therapies, PD-1 blockade was found to preferentially induce a response in the CD8+ TEX compartment, while anti-CTLA-4 therapy caused more profound changes in CD4+ T cells (79). These reports also highlight the utility of combining TEX-directed panels with markers focusing on other immune cell populations. Indeed, further evidence for the on-treatment role of TEX reinvigoration during anti-PD-1 checkpoint blockade therapies came from a study that also identified a pre-treatment biomarker for checkpoint response on the level of a CD14+ CD16− HLA-DR+ monocyte population (80). However, improved and more focused exhaustion-directed profiling of the heterogeneity of TEX subsets will be required for a detailed understanding of TEX dynamics during checkpoint therapies and personalized medicine approaches for combination therapies.
The inability to discriminate TEX from TEFF and TMEM using conventional phenotyping approaches has been a longstanding problem, preventing optimal monitoring and understanding of the relevance of TEX in disease. The use of high-parametric mass cytometry has been instrumental in addressing this issue and advanced the characterization of TEX. The combinatorial information from several exhaustion markers is required to distinguish TEX from TEFF and TMEM and has also informed our understanding of the heterogeneity of TEX. One advantage of mass cytometry—the ability to integrate the higher parametric expression profile of TEX with readouts for functional profiling allows the fine characterization of TEX subpopulations and their involvement in human diseases. Induction of several molecular programs linked to recent T cell activation remains a shared feature of many TEX populations with effector T cells (e.g., CD38, CD39, PD-1), while programs of homeostasis and access to anatomic niches can be shared by other TEX populations (including those linked to disease control) with memory T cells. Heterogeneous TEX subsets with different clinical roles have now been described in several translational settings of human chronic infection and cancer and are implied in differential responsiveness to immune checkpoint blockade.
Other strategies that allow an in-depth profiling of the heterogeneity of exhausted T cell populations have been described, such as scRNA-Seq, which allows the analysis of T cell transcriptomes with single cell resolution. However, currently, these approaches have several limitations over the described mass cytometry approach as they are limited by the limited sensitivity for lowly expressed genes; low cell numbers that can be practically analyzed and therefore limited ability to identify rare populations and limited scaling toward cohort analysis; lack of information on protein expression missing potential post-transcriptional regulation; and, importantly, lack of testing for T cell function. It is further unclear whether excessively larger datasets of mRNA transcripts on a single cell level will reveal more relevant heterogeneity of TEX populations, as the profiling approach outlined above already was designed to maximize utilization of markers informative for differences between TEX and functional T cell subsets. Of note, the combinatorial complexity of high dimensional data generated during immunome analysis by mass cytometry is different from other omics approaches. For example, simultaneous analysis of mass cytometric immune profiling together with transcriptome, microbiome, proteome and metabolome analysis during pregnancy indicated that the mass cytometry dataset was more informative based on modularity analysis (as measured by the number of principal components needed to account for 90% variance of each dataset) compared to the other omics datasets assessing significantly larger numbers of parameters (81).
To date the most detailed profiling of TEX has been performed in murine models of chronic infection or cancer. With detailed resolution of TEX heterogeneity in humans now accessible through the use of specialized mass cytometry analysis, more detailed identification of TEX features associated with specific types of diseases and anatomical locations that will guide understanding of changes in TEX cell populations in chronic infections, cancer and even autoimmunity is expected. The expression of many exhaustion-related proteins involved in many immuno-regulatory pathways amenable to therapeutic intervention also suggests that TEX profiling might be required for adequate selection of combination therapies and could become indispensable for the rational design of personalized therapeutic treatments.
In sum, deep immune profiling of TEX using mass cytometry is expected to provide further insights into the biology underlying this special T cell differentiation stage and its role in pathogenesis and response to immune therapies in cancer, viral infection and autoimmunity.
FW and BB conceived and wrote the manuscript, revising it critically for important intellectual content.
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.
We thank the members of the Bengsch, Thimme, and Wherry labs for the fruitful discussions. We thank F. Gherardini for the help with Phenograph visualization.
Funding. This work was supported by grants from the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)—Projektnummer 272983813—TRR179 and BE5496/5-1, and under Germany's Excellence Strategy—EXC-2189—Project ID: 390939984.
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