Transcriptional programming and T cell receptor repertoires distinguish human lung and lymph node memory T cells

Schoettler, Nathan; Hrusch, Cara L; Blaine, Kelly M; Sperling, Anne I; Ober, Carole

doi:10.1038/s42003-019-0657-2

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Published: 13 November 2019

Transcriptional programming and T cell receptor repertoires distinguish human lung and lymph node memory T cells

Nathan Schoettler ORCID: orcid.org/0000-0001-9851-6352^1,2,
Cara L Hrusch¹,
Kelly M Blaine¹,
Anne I Sperling¹^na1 &
…
Carole Ober²^na1

Communications Biology volume 2, Article number: 411 (2019) Cite this article

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Abstract

Antigen-specific memory T cells persist for years after exposure to a pathogen and provide effective recall responses. Many memory T cell subsets have been identified and differ in abundance throughout tissues. This study focused on CD4 and CD8 memory T cells from paired human lung and lung draining lymph node (LDLN) samples and identified substantial differences in the transcriptional landscape of these subsets, including higher expression of an array of innate immune receptors in lung T cells which were further validated by flow cytometry. Using T cell receptor analysis, we determined the clonal overlap between memory T cell subsets within the lung and within the LDLN, and this was greater than the clonal overlap observed between memory T cell subsets compared across tissues. Our results suggest that lung and LDLN memory T cells originate from different precursor pools, recognize distinct antigens and likely have separate roles in immune responses.

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Introduction

The hallmark of the adaptive immune system is the persistence of antigen-specific and long-lived memory cells capable of mounting recall responses. A number of CD4 and CD8 memory T cell subsets have been described and are distinguished by cell phenotypes and responses after peptide:MHC activation. Memory T cells are typically classified into effector memory (EM) or central memory (CM) populations. EM T cells are characterized by the ability to secrete cytokines and the capacity for cytotoxic activity^1,2, whereas CM T cells lack effector function but rapidly proliferate after stimulation and can activate other immune cell types and differentiate into EMs. More recently, tissue resident memory (TRM) T cells have been recognized as a separate subset that are able to quickly proliferate outside secondary lymphoid organs, and provide the most potent recall protection^3,4,5. Thus, an array of responses is mounted by activation of memory T cell subsets that generate expanded populations of antigen-specific T cells with specialized functions.

Memory T cell subsets are also present at varying frequencies in different anatomical sites. While CMs and EMs are present in the blood and tissues, TRMs are rare in the blood but constitute the predominant memory T cell subset in many tissues^6,7. Not surprisingly, T cell subsets also differ in their patterns of circulation with EMs trafficking through tissues, blood and secondary lymphoid organs, CMs circulating in the blood and secondary lymphoid organs, and TRMs residing mainly in tissues. However, it is becoming increasingly clear that memory T cell subsets may themselves be influenced by their local environment, and it is possible that phenotypically identical cells at different sites have independent ontogeny, antigen specificity and functional capacity.

In this study, we investigated the extent to which human T cell subsets from the lung and LDLN, two sites in close proximity but with different cellular compositions, share transcriptional profiles. Mucosal immunity imparted by T cell memory is particularly relevant at these sites given the exposure to inhaled pathogens and other stimuli. We found that a large number of genes are differentially expressed between phenotypically identical memory T cell subsets in the lung and LDLN and that there is limited clonal overlap of T cell receptor (TCR) repertoires between specific memory subsets in the lung and LDLN. These findings are consistent with lung and LDLN memory T cells recognizing different antigens and being poised for distinct responses after activation.

Results

Phenotypic analysis of lung and LDLN T cell subsets

We first evaluated the frequency of memory T cells in paired lung and LDLN T cell subsets from 11 human donors using an 11-color antibody panel (Supplementary Table 1) and a traditional gating strategy (Supplementary Fig. 1) that allowed phenotyping of CD4 and CD8 naive, CM, EM and TRM subsets in each tissue. The relative proportions of these subsets varied between donors (Fig. 1a). Comparisons between tissues revealed that the frequencies of CD4 TRMs, CD4 EMs and CD8 TRMs were higher in the lung than in the LDLN (P value = 0.0069, P value = 0.0013 and P value = 0.0018, respectively), and CD4 and CD8 naive cells were higher in the LDLN than in the lung (P value = 0.0004 and P value = 0.0283, respectively; Fig. 1a, b and Supplementary Fig. 2). No differences were observed in tissue-specific frequencies of CD4 CM, CD8 EM and CD8 CM subsets. The ratio of CD4 to CD8 T cells was also higher in the LDLN than in the lung (Supplementary Fig. 2). Because CD4 and CD8 TRMs have been described as populations of non-circulating T cells with tissue specific localization^4,5, we were surprised to observe appreciable numbers of cells with CD4 and CD8 TRM phenotypes in LDLNs (Fig. 1a, b).

To further characterize the phenotypic landscape of lung and LDLN T cells and identify discrete clusters of cells, we applied t-distributed stochastic neighbor embedding (t-SNE) to the multiparameter cytometry data. The majority of clusters were comprised of cells from all donors, indicating that most T cell subsets are shared between individuals (Fig. 1c). In contrast, each cluster was composed predominantly of cells from either the lung or LDLN, although cells from the non-dominant tissue were interspersed in every cluster (Fig. 1d). Cells in each cluster were also overwhelmingly either of naive or memory phenotypes based on expression levels of the cell surface markers CD45RA and CD45RO, respectively (Fig. 1e). Additionally, clusters were separated into those with cells expressing either CD4 or CD8 (Fig. 1f, g). Expression of CD69, a marker of TRMs, as well as other cell markers used for phenotyping (CCR7, CD11a, CD11b, CD103, and CD169), had more variable patterns (Fig. 1h and Supplementary Fig. 3). In summary, our analyses identified phenotypically identical memory T cell subsets in the lung tissue and the LDLNs using both a traditional gating strategy and an unsupervised approach.

Transcriptional programs in lung and LDLN T cell subsets

The presence of memory CD4 and CD8 subsets in both the LDLN and lung raised the question of whether memory subsets have identical transcriptional programming between these two sites. To address this question, we sorted CD4 and CD8 EM, CM and TRM T cell subsets from paired lung and LDLN for RNA sequencing (Supplementary Table 2, Supplementary Data 1 and Supplementary Fig. 1). 128 samples that passed QC (see Methods) were analyzed. As expected, CD4 and CD8 T cells at each site expressed high levels of either CD4 or CD8A, respectively (Supplementary Fig. 4). At a false discovery rate (FDR) of 5%, 128 genes were differentially expressed between lung CD4 TRMs and lung CD8 TRMs and 805 genes were differentially expressed between LDLN CD4 TRMs and LDLN CD8 TRMs. As expected, CD4, CD8A, and CD8B were the most differentially expressed genes between these two cell types from each site (Fig. 2).

Principal component analysis of the RNA sequences was performed to assess patterns of gene expression between tissues and samples. Surprisingly, however, the primary clustering along principal component 1 was based on tissue of origin and not by T cell type, subset or donor (Fig. 3 and Supplementary Fig. 5). Consistent with this clustering, we observed a large number of genes that were differentially expressed between phenotypically identical T cell subsets residing in the lung compared to the LDLN: 418 genes were differentially expressed between lung CD4 TRMs and LDLN CD4 TRMs, and 1,363 genes were differentially expressed between lung CD8 TRMs and LDLN CD8 TRMs (Table 1, Fig. 4a, b). In fact, differences in gene expression between lung and LDLN memory T cells were present in all memory subsets (Fig. 4c, d, Supplementary Fig. 6 and Supplementary Data 2–6). To more formally assess the effects of tissue and cell phenotype on gene expression, we compared the number of genes differentially expressed between tissues to the number of genes differentially expressed within tissues for 5 memory T cell subsets. Phenotypically identical subsets between tissues had a higher number of genes differentially expressed compared to subsets in the same tissue (Wilcoxon rank-sum test P value < 0.01). These findings demonstrate that not only do lung and LDLNs have different proportions of memory T cell subsets, as previously shown⁷, but phenotypically identical memory T cells from the lung and LDLN have different transcriptional programming.

Table 1 Number of differentially expressed genes between lung and LDLN (5% FDR)

Full size table

The majority of genes that are differentially expressed between memory T cell subsets from the lung and LDLN are not shared by other T cell subsets. Only 78 out of 801 genes that were differentially expressed by CD4 memory subsets were shared by CM, EM and TRM subsets, and CD8 EM and TRM subsets shared 127 of 1582 genes that were differentially expressed between lung and LDLN subsets (Fig. 5). Similarly, 168 out of 1813 differentially expressed genes were shared between CD4 TRM and CD8 TRM subsets. Specific examples of differentially expressed genes include higher expression of IL2, IL10, XCL2, GZMA, and GZMB in lung CD4 TRMs compared with lung CD4 EM, whereas none of these genes were differentially expressed in LDLN CD4 TRMs and EMs. Instead, the expression of other genes was higher in LDLN CD4 TRMs compared to LDLN EMs, including CXCL13 (Fig. 4e). Similarly, lung, CD8 EMs had higher expression of SELL and S1PR5 compared with lung CD8 TRMs, while LDLN, CD8 TRMs had higher expression S1PR1 compared to CD8 EMs (Fig. 4d). Thus, the overwhelming majority of tissue associated gene expression differences are subset specific.

Validation of gene expression results

We next asked whether the gene expression differences between lung and LDLN cells resulted in differences in protein levels that could be detected by flow cytometry. We tested 5 surface markers whose genes were differentially expressed between the tissues: FCGR3A (CD16) had higher gene expression in the lung for all CD4 and CD8 memory subsets; CD79 and CD9 had higher gene expression for all lung CD4 memory subsets; CXCR5 had higher gene expression in the LDLN for all CD4 memory subsets, especially in LDLN CD4 TRMs (Fig. 3a); and CD200 had higher gene expression in the LDLN for CD4 TRMs. Flow cytometry on paired lung and LDLN samples from the same 5 donors confirmed that the effect of tissue origin on gene expression is mirrored with cell mean fluorescence intensity (MFI) for FCGR3A (CD16), CD79, CD9, and CD200 (Fig. 6). The proportion of cells positive for each of these markers mirrored results with gene expression data for most of these markers (Supplementary Fig 7). Therefore, including these additional markers to the established memory cell surface markers will allow further classification of T cell subsets that reflects lung or LDLN localization.

Gene ontogeny of differentially expressed genes

Gene ontogeny (GO) analyses were performed on sets of genes with differential expression shared by certain T cell subsets. Among the 78 genes differentially expressed between tissues by all CD4 memory T cell subsets, GO identified enrichment for a number of processes, and the top processes related to immune response, immune effector processes, cellular activation and leukocyte migration (Supplementary Data 7). Similarly, the 127 genes shared by CD8 EM and CD8 TRM subsets were enriched for leukocyte immunity, leukocyte activation and immune effector process (Supplementary Data 8). Gene ontogeny analysis of genes that were differentially expressed between tissues by both CD4 TRM and CD8 TRM subsets identified highly enriched pathways that were also related to immune responses, immune effector responses, immune regulation and leukocyte degranulation (Supplementary Data 9). Collectively, this GO analysis highlights that gene expression differences between lung and LDLN that are shared by memory T cell subsets result in differences in activation status, effector capacity and migration.

Differences between lung and LDLN TRM T cells

We focused subsequent analyses on TRMs because these cells are non-circulating, reside in the tissue and have been shown to have unique responses in a number of tissues^5,7,8. We first defined genes with tissue-specific expression as those that were differentially expressed between the lung and LDLN for CD4 and CD8 subsets at a 5% FDR. We then performed pathway analysis separately on the 241, 177, 899, and 464 genes with tissue-specific expression in TRM subsets in the lung and LDLNs (lung CD4, LDLN CD4, lung CD8, LDLN CD8 TRMs, respectively). Genes with higher expression in lung CD4 TRMs compared to LDLN CD4 TRMs were enriched in pathways regulated by cytokines such as IFNG, TGFB1, TNF and IL-4 (Supplementary Data 10), which were also highly connected in gene networks (Fig. 7 and Supplementary Fig. 8). These networks connected genes involved in specific immune pathways such antibody binding Fc receptor family (FCGR2A, FCGR3A, FCGR3B and FCER1G), a complement receptor gene (C5AR1), as well as cytokines and chemokines (IL17A, IL1B, IL1G, CCL20, CXCL2, and CXCL3). Therefore, these genes and pathways distinguish lung CD4 TRMs from LDLN CD4 TRMs. Among the genes with lung-specific expression in CD8 TRMs, IFNG, TNF, IL13, TCL1A, and TGFB1 were the most promising upstream regulators. These genes formed several highly connected networks, including one with TLR4 and MYD88 as hubs (Fig. 7, Supplementary Fig. 7 and Supplementary Data 11). Innate sensing and signaling appears to be a prominent feature in lung CD8 TRMs, and these molecules coordinate with other differentially expressed genes, including chemokines, cytokines and IRF3, a transcriptional regulator of interferon genes. Differential expression of TLR4 and MyD88 is not associated with classical T cell subsets, however, we also observe higher expression of one or both of these genes in lung CD4 CMs and lung CD4 EMs compared with these populations in the LDLN (Supplementary Data 3 and 4). Overall, the transcriptional profiles of lung CD4 TRMs and lung CD8 TRMs revealed higher expression of genes involved in innate immune processes in the lung compared to phenotypically similar cells in the LDLN. These genes were also enriched for inflammatory, infectious and hematologic diseases, as well as respiratory conditions, including “inflammation of the lung”, “damage of lung”, “infection of respiratory tract”, “severe acute respiratory distress syndrome”, “fibrosis of the lung” and “lung injury” (all P value < 1 × 10^–8, Supplementary Data 12). Therefore, focusing on lung T cell subsets revealed their important relationship with lung pathologies and innate immune processes.

To assess for tissue-specific processes relevant to lung TRM subsets, we analyzed the ontogeny of genes that were differentially expressed between the lung and LDLN in CD4 TRMs but not differentially expressed in other CD4 memory subsets. The top processes associated with the 255 CD4 TRM-specific genes were “regulation” functions related to stress, defense, cellular processes and signaling responses (Supplementary Data 13), which contrasts from the more immune-related GO processes described above for the set of genes with differential expression shared by all memory CD4 subsets. This is consistent with CD4 TRMs playing a pivotal role in coordinating immune and inflammatory responses in a tissue-specific manner. When CD8 TRMs were similarly analyzed, the most promising GO terms were broader, including “cellular processes”, “biological process”, “cell activation” and “metabolic process” (Supplementary Data 14), possibly indicating that CD4 TRMs and CD8 TRMs modulate immune responses by distinct mechanisms.

TCR repertoires of lung and LDLN memory T cell subsets

T cell receptor specificity is determined by the recombination of TCR V, D and J gene segments that results in a vast TCR repertoire. While the TCR repertoires of memory T cell subsets are derived from the naive TCR repertoire, memory TCR repertoires are also shaped by antigen recognition and clonal proliferation resulting in a less diverse TCR repertoire memory subsets. To characterize the TCR repertoires in the sorted T cells from the lung and LDLNs, we aligned RNA sequencing reads to the TCR β chain CDR3 gene sequence. This yielded 1.12 × 10⁶ functional (in-frame) TCR β CDR3 sequences, which was used to assess the extent of clonality within a given sample. In addition, comparisons were made of the clonal overlap between memory subsets in the lung and LDLN, and independent of clonality, whether particular V gene segments were more commonly used than others.

Our sample included 110,123 unique TCR clones. Rarefaction analysis indicated that we captured a large majority of the repertoire for nearly all samples (Supplementary Fig. 9). TCR repertoire diversity differed between samples (Supplementary Fig. 10), but only 5.3% of the 110,123 unique clones were identified in more than one sample. We focused our analysis on the 6 of 11 donors with TCR repertoire data in at least 3 CD4 subsets from both the lung and LDLN and with more than 150 clones present in more than one subset. None of CD8 datasets from any donor met these criteria, and therefore, CD8 subsets were not analyzed (Supplementary Data 1). We first assessed the clonal overlap of CD4 memory T cell subsets from the lung and LDLN separately for each donor using clones that showed the most overlap between subsets (Fig. 8a and Supplementary Fig. 11). While several patterns of clonal overlap were observed, phenotypically identical subsets from the lung and LDLN had lower overlap than overlap of subsets within the lung or LDLN, and the most clonal overlap was between lung subsets, as indicated by more sharing of clones on the right side of the heatmaps in Fig. 8a and Supplementary Fig. 11. Next, we performed hierarchical clustering using the repertoire data from CD4 subsets for these same 6 individuals and observed clustering of subsets by tissue of origin and not CD4 subset membership (Fig. 8b and Supplementary Fig. 12). Indeed, we did not observe any instances where memory subset pairs across tissues were most closely related, and among all 6 donors, 32 of 35 memory subsets clustered according to tissue (binomial test P value = 4.2 × 10^-7, Fig. 8b and Supplementary Fig. 12). To further investigate clonal relationships, we applied multidimensional scaling (MDS) to the combined dataset of all subsets and all donors (Supplementary Fig. 13). The advantage of using MDS is that distance measurements are scaled and can be quantitatively compared between all samples and individuals. Comparisons of the average pairwise distances between CD4 subsets within and between tissues, revealed low overlap (small MDS distance) between naive and memory TCR repertoires but significantly larger overlap (large MDS distance) of the TCR repertoire of memory populations in the LDLN and in the lung (Wilcoxon rank-sum test P value = 0.000175 and 0.0421, respectively, Fig. 8c). While the TCR repertoire overlap between phenotypically identical T cell subsets from the LDLN and lung was larger than the overlap of naive and memory CD4 subsets (Wilcoxon rank-sum test P value = 0.00354), it was not larger than the overlap of different memory T cell subsets within the LDLN or lung (Wilcoxon rank-sum test P value = 0.116 and 0.879, respectively, Fig. 8c). These results show that clonal overlap of CD4 memory T cell subsets within the lung or within the LDLN is greater than the clonal overlap between phenotypically identical subsets in the lung and LDLN. Therefore, memory subsets in each of these tissues are each derived from a separate pool of progenitors with little overlap, as reflected in the modest sharing between the tissues.

We next asked whether there were particular patterns of V gene segment and J gene segment usage that occur for reasons other than clonal expansion, such as differences in V and J gene segment recombination frequencies. For this analysis, we counted each clone as a single count regardless of its frequency. Complex patterns of V gene segment and J gene segment usage were observed (shown for CD4 subsets from two individuals in Supplementary Fig. 14), but there were no prominent donor-specific patterns (Supplementary Fig. 15). We therefore pooled data from all individuals and evaluated over- or under-represented V gene or V-J gene combinations in each T cell subset. In all memory CD4 and CD8 subsets, unequal V gene usage was apparent (Fig. 9, Supplementary Fig. 15 and Supplementary Fig. 16). For example, in CD4 memory subsets from both the lung and LDLN, V5–1, V7–2, and V20–1 were over-represented (Fig. 9a, b, Supplementary Fig. 15 and Supplementary Fig. 16). These same V gene segments were overrepresented in CD8 T cell subsets from both lung and LDLN (Fig. 9c, d). Conversely, we observed that some V gene segments, including V5–2, V22–2, and V26, were rarely used in CD4 or CD8 T cells. Over and under-representation of particular V genes in memory subsets could be due to antigen selection, although we observed the same patterns in naive CD4 and CD8 subsets (Fig. 9). Taken together, these observations suggest that mechanisms biasing V gene usage occur before antigen encounter and influence CD4 and CD8 T cells equivalently in the lung and LDLN.

Discussion

In this study, we investigated the relationship between memory T cell subsets from human lungs and LDLNs and demonstrated how they differ with regard to cellular frequency, transcriptional programming, cell surface marker expression, and clonality. Our results established that memory T cell subsets are distinct between these two sites, despite the close proximity of lung tissue and LDLNs and the fact that both antigen and lung T cells drain into the LDLN. Therefore, differences between cells that are phenotypically identical using classical markers from these tissues likely result from independent roles during immune responses.

Although it is well known that lymphocyte proportions vary between tissues and typically do not reflect cell proportions in the blood, the majority of studies on human immune cell types have been conducted on whole blood or cells isolated from blood. Non-circulating memory T cell subsets, and in particular TRMs, have been reported to have tissue-specific responses and be abundant in human tissues, including the skin, gastrointestinal tract and lung^7,8,9. While all of these tissues have highly specialized function, the lung’s dedicated role in gas exchange necessarily juxtaposes a highly vascular pulmonary circulation with the environment. This constant exposure to the inhaled environment results in regular encounters and re-encounter with pathogens and other stimuli. In mouse models, specific lung memory T cell subsets are essential for recall responses to specific pathogens, and they are presumed to play crucial roles in humans as well^10,11,12. As such, the biology of lung memory T cell subsets is highly relevant to vaccine responses and likely an array of respiratory diseases such as asthma, acute lung injury and cystic fibrosis. We have now determined that differentially expressed genes in lung memory T cell subsets are enriched in a number of inflammatory and fibrotic lung diseases as well as innate immune processes.

Our observations of greater proportions of CD4 and CD8 TRMs in the lung compared to the LDLN and the lower proportions of lung CMs, and particularly CD8 CMs, is consistent with previous reports^7,13. The gene expression data described here is also consistent with other studies of CD4 and CD8 memory T cell subsets in humans. For example, IL2 expression is higher in lung CD4 TRMs compared with lung CD4 CMs in our study, and previous studies have demonstrated high IL2 expression in human lung and liver TRMs^14,15. One previous study showed gene expression differences between human CD69 + and CD69- CD4 and CD8 TRM subsets, but this study was limited to analysis of three donors and to a combined analysis of blood, spleen and lung samples¹⁴. Another group reported gene expression differences between blood and lung CD4 + cells with the TRM phenotype¹⁶. Another study identified lymphoid tissue memory CD8 T cells with similar phenotypic and gene expression patterns as CD8 TRMs and these may be particularly relevant for protection against HIV¹⁷. In mice, gene expression differences have been reported between TRMs isolated from the spleen and TRMs isolated from the female reproductive tract after viral infection¹⁸. In contrast to these earlier studies, our work revealed large differences in transcriptional programs between T cells that are identical using classical phenotypes from two different sites in humans.

We confirmed that at least some of the observed transcriptional differences are biologically meaningful as all 5 of the genes we selected for further studies showed similar protein expression differences between the lung and LDLN by flow cytometry. CD9 is a tetraspanin protein that is present on many immune cells and has recently been reported to be present on memory and CD4 TRMs in the skin¹⁹. Increased levels of CD200 (also called OX40) on LDLN memory CD4 T TRMs plays a crucial role in costimulation of T cells. We also confirmed by flow cytometry that lung memory T cells have higher levels of proteins involved in antigen presentation, including the low-affinity Fc receptor, CD16, and the MHC class II invariant chain, CD74. Although T cells are not considered classical antigen presenting cells, induced expression of these antigen presenting surface markers in T cell subsets has been reported previously^20,21. To our knowledge, this is the first demonstration of antigen presenting cell surface markers in human lung memory T cells.

Pathway and network analyses of genes more highly expressed in lung CD4 TRMs compared with LDLN CD4 TRMs suggest that inflammatory and regulatory cytokines are differentially expressed between these tissues, including IL1B, IL10, IL17A, IFNG, and TGFB. Compared with LDLN CD8 TRMs, lung CD8 TRMs also had higher expression of cytokine genes such as IL10, IL6, IL17A. Interestingly, CD8 + T cell subsets present in blood and several tissues express IL17A, and IL-17 secreting cells have been associated with tissue infiltration and inflammation²². We also observed higher expression of receptors typically associated with innate immune responses. As an example, CD14, MYD88 and other toll like receptor genes were expressed at higher levels in lung CD8 TRMs than LDLN TRMs, and a number of innate receptors were present in lung CD4 memory subsets. While innate function is not typically attributed to classical T cell subsets, human T cells have been reported to express these genes²³, suggesting that innate sensing in the tissue may be highly relevant to these memory subsets. Our observation that gene expression of both cytokine and innate receptor genes differ between lung and LDLN subsets suggests either that these tissue-specific subsets have tremendous plasticity that is influenced by the tissue environment or that these populations are more diverse than suggested by current phenotyping by cell surface markers.

Taken together, the results of our study raise the question of whether differences in gene expression are induced in T cells by exposure to the lung and LDLN environments or whether the expression of specific genes in T cells contributes to their homing to a specific location. For example, it may be that the lung environment drives cellular characteristics of T cells. Alternatively, specific subsets may express genes and receptors that promote preferential residence in the lung. A limitation of the current study is that we cannot differentiate between these two possibilities.

We sequenced over 1 million TCRB CDR3 regions, revealing several insights about the TCR repertoires in the lung and LDLN. First, particular TCRB V gene segments are overrepresented and others are underrepresented across all T cell subsets, consistent with previous reports in other T cell subsets^24,25,26. Because biased TCRB V gene usage occurred independent of clonal selection, it must be influenced by factors that affect individual V gene segment recombination and/or selection of particular gene segments during development; several of these mechanisms have been described previously^27,28,29. Here, we show that the factors that globally influence V gene usage persist across a number of lung and LDLN T cell subsets, even after antigen selection into the memory pool.

Comparison of CD4 TCR repertoires revealed sharing of antigen specificity across memory CD4 T cell subsets in the lung, and the same was true of TCR repertoires of memory CD4 T cell subsets in the LDLN. It was previously demonstrated in mice that the same clone can be found in both skin TRMs and LN CMs following skin immunization³⁰. However, to our knowledge, the extent of clonal overlap of human memory CD4 T cell subsets within the same tissue, and in particular between the lung and LDLN, has not been previously recognized.

While features of TCR repertoires in CD8 T cell subsets were similar to CD4 T cell subsets, we focused only on evaluating clonal overlap in CD4 T cells because some CD8 subsets were not available from most of the donors. Therefore, while it is likely that clonal overlap of CD8 T cell subsets mirrors that of CD4 T cell subsets, we did not assess this directly. A second limitation of our TCR repertoire analysis is that while we optimized our experimental strategy to recover as many cells as possible from each T cell subset, we sampled only a fraction of the overall T cells in each subset. Therefore, our analysis, while powered to identify clonal overlap between T cell subsets, does not comprehensively capture the entire TCR repertoire of each of these subsets. Additional clones are likely present in each of the subsets, and it is also possible that some of the unique clones are actually shared at low frequencies between other subset(s). Our accounting of clones also assumes that identical CDR3 nucleotide sequences arise due to clonal expansion rather than independent TRB rearrangement events. This assumption is reasonable and supported by our observation of lower clonality in naive compared with memory T cell subsets and that there is a low probability of independent TRB rearrangements generating identical CDR3 nucleotide sequences.

Models of memory T cell subset formation propose that the duration of antigen exposure and recognition drives differentiation from the naive T cell pool, with CM progeny emerging prior to the development of EM progeny^31,32. More recently, it has been proposed that human CD8 T cell memory after yellow fever virus vaccination is maintained by quiescent cells, challenging a strictly linear differentiation³³. In linear models of differentiation, clonal fate is determined predominantly by the antigen and TCR recognition, implying that repertoires of T cell subsets are independent. In these models, clonal overlap between T cell subsets would be low. However, we find that overlapping clones were typically shared between memory subsets in the same tissue, and therefore, a strict linear model of memory T cell differentiation does not fit with our observations. Rather, our results are consistent with a model whereby clonal progenitors can differentiate into multiple memory T cell phenotypes, and possibly whereby residence in the lung or LDLN is imparted based on TCR specificity. The TCR repertoire findings support the observed gene expression patterns in our study, namely, that phenotypically identical T cell subsets in the lung and LDLN are independent populations.

We studied 8 different T cell subsets in human lungs and LDLN and the principal difference we identified was not whether cells were CD4 or CD8 or a particular memory subset, but rather, whether they resided in the lung or the LDLNs. This was consistent across phenotypic, transcriptional and TCR repertoire analyses. While memory T cell subsets are known to have distinct roles during immune responses, our results suggest that T cell location may be more relevant, underscoring the need for further studies of human lung T cells.

Methods

Human tissue procurement

Human lung samples were obtained from organ donors whose lungs were not used for transplantation through the Gift of Hope Regional Organ Bank of Illinois. Donors with >10 pack-years of tobacco use were excluded from this study. Because samples from this study were from deceased donors, they do not qualify as “human subjects” (confirmed by the Institutional Review Board at the University of Chicago).

Leukocyte isolation

Cells were processed as previously described³⁴. Briefly, lung tissue was perfused with sterile fetal bovine serum and phosphate-buffered saline. Paratracheal, hilar, interlobular and palpable interlobar LNs were dissected and pooled. LDLNs were mechanically dissociated into a single cell suspension and cryopreserved. The right lower lobe was minced and digested. Separately, LDLN and lung tissue mononuclear cells were enriched using density gradient centrifugation and cryopreserved.

Cell staining and sorting

A panel of 11 antibodies was established to discriminate leukocyte and specific T cell subsets and stained according to manufactures’ recommendations. Antibody details are in Supplementary Table 1. Each paired sample (lung leukocytes and LN leukocytes from the same individual) was processed and sorted on the same day, and a minimum of two individuals had samples processed on a given day. Cells were sorted using a FACSAria Fusion (Becton Dickinson, Franklin Lakes, NJ) at the University of Chicago with the same sort template. Purity checks were performed on at least one sorted population during each day of sorting, and rarely, minor changes in compensation were made to maintain a sort purity > 98%. Cells were sorted directly into lysis buffer, immediately frozen on dry ice and stored at −80 °C.

Flow cytometry analysis

Flow cytometric data was analyzed using BD FACSDiva software (BD Biosciences) to determine the frequency of defined populations. Additionally, the flow cytometric data was randomly down-sampled to 2,500 CD45 + CD3 + events for each donor and analyzed using t-distributed stochastic neighbor embedding (t-SNE)³⁵ with the Rtsne package³⁶.

Flow cytometry validation of gene expression

Based on the results of RNA sequencing, 5 cell surface markers, CD16, CXCR5, CD9, CD74 and CD200, were chosen to be tested by flow cytometry (details on the antibodies used are shown in Supplementary Table 1). Paired lung and LDLN samples from same 5 donors used for gene expression studies were stained according to the manufacture’s recommendations. Samples were run on a Fortessa X20 cytometer (Becton Dickinson). The results were analyzed using FlowJo software (Becton Dickinson) to calculate the MFI and percent of cells that were positive with gates set according to florescent-minus one controls. Memory CD4 T cells were defined as the population that was CD3+CD11b-CD4+CD8-CD45RO+CD45RA-, and similarly, memory CD8 T cells were defined as the population that was CD3+CD11b-CD8+CD4-CD45RO+CD45RA-.

RNA sequencing

Samples were randomized by individual, T cell subset and source (lung versus lymph node) prior to RNA extraction. RNA was extracted using All Prep DNA/RNA Mini Preparation Kit (Qiagen, Hilden, Germany). RNA quality, concentration and RNA integrity number (RIN) was assayed using an Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA). cDNA was synthesized using the SMART-Seq v4 Ultra Low Input RNA Kit (Takara Bio Company, Mountain View, CA) and libraries generated using Nextera XT DNA Library Preparation Kit (Illumina, San Diego, CA). Individual libraries were pooled and sequenced at the University of Chicago using a HiSeq 4000 (Illumina, San Diego, CA) with 100 base-pair paired-end reads. Reads were aligned to Genome Reference Consortium Human Build 38 and gene counts were calculated using STAR 2.5.0³⁷. Samples with less than 10 million mapped reads were removed. Analysis of CD8 CM subsets was not performed because fewer than 4 samples from each tissue met this threshold. Genes were filtered for those with more than one count per million in at least 10 samples, which included 14,820 genes. Principal component analysis was used to identify technical covariates.

Statistics and reproducibility

All statistical analyses were performed using R (version 3.3.3). Differentially expressed genes were identified using linear regression with the Limma package;³⁸ each donor was included as a random variable³⁹ while amplification cycles, age, gender and race were included as fixed variables. We controlled the false discovery rate according to the Benjamini and Hochberg method⁴⁰ with a threshold of 5%.

Gene networks and regulators

Ingenuity Pathway Analysis (IPA) was used to identify gene networks and regulators of genes differentially expressed in the lung and LDLN for CD4 TRM and CD9 TRM subsets. Analysis was performed using databases that included all leukocyte types, immune cell lines, bone marrow, spleen, lymph node and lung tissues.

Gene ontology

Gene lists were tested for enrichment in GO pathways using PANTHER version 14.2 (release 04–2018)^41,42. The “Statistical overrepresentation test” was performed using default settings. Enrichment in the GO biological process complete annotation data set was tested using Fisher’s exact test and an FDR p-value threshold of 0.05 was used.

T cell receptor repertoire analysis

RNA sequencing reads described above were aligned to TCR genes using MiXCR⁴³. Sequences aligning to TCR β CDR3 regions that were productively rearranged (without stop codons) were included in further analysis. Clones were determined based on nucleotide sequence. Multi-dimensional scaling was calculated for all samples using clones that were present in two or more samples. For most individuals, at least one CD4 memory T cell subset was not available or did not pass quality control for sequencing. Therefore, MDS distances between memory subsets from the same individual were averaged to allow for comparison between tissues and between naive and memory subsets (Fig. 8c). For hierarchical clustering of CD4 subsets, Euclidean distances of clones present in more than one subset was calculated separately for each donor. Donors with less than 150 shared clones were excluded in this analysis.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

Data availability

RNA sequences generated and analyzed in the current study are available in Gene Expression Omnibus (www.ncbi.nlm.nih.gov/geo/) with an accession number GSE137967. Source data are presented in Supplementary Data.

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Acknowledgements

This research was supported by the National Institutes of Health Grants: NHLBI T32 HL007605, NHLBI R01 HL122712 and NIAID U19 AI095230. Human lung tissue was generously provided by the Gift of Hope Regional Organ Bank of Illinois, We appreciate contributions from Dr. Steve White and Janel Huffman to this work, and thank the following University of Chicago core facilities: Cytometry and Antibody Technology; Genomics Facility and Center for Research Informatics.

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These authors contributed equally: Anne I Sperling, Carole Ober.

Authors and Affiliations

Department of Medicine, The University of Chicago, Chicago, USA
Nathan Schoettler, Cara L Hrusch, Kelly M Blaine & Anne I Sperling
Department of Human Genetics, The University of Chicago, Chicago, USA
Nathan Schoettler & Carole Ober

Authors

Nathan Schoettler
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Cara L Hrusch
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Kelly M Blaine
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Anne I Sperling
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Carole Ober
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Contributions

N.S., C.L.H, A.I.S., and C.O. conceived the study. C.L.H. and K.M.B. collected and processed samples. N.S. conducted the experiments. N.S. and C.O. performed the data analysis. N.S., A.I.S., and C.O. contributed to manuscript writing; all authors read and approved the final version.

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Correspondence to Nathan Schoettler.

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Schoettler, N., Hrusch, C.L., Blaine, K.M. et al. Transcriptional programming and T cell receptor repertoires distinguish human lung and lymph node memory T cells. Commun Biol 2, 411 (2019). https://doi.org/10.1038/s42003-019-0657-2

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Received: 25 March 2019
Accepted: 16 October 2019
Published: 13 November 2019
DOI: https://doi.org/10.1038/s42003-019-0657-2

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