Abstract
The frequency of CD4+CD8+ double-positive (DP) T cells is highly associated with a variety of diseases. Recently, we used high-throughput single-cell RNA sequencing to show that circulating DP T cells in cynomolgus monkeys comprise nine heterogeneous populations. To better understand the characteristics of DP T cells, we analyzed 7601 cells from a rhesus monkey and detected 14,459 genes. Rhesus monkey DP T cells comprised heterogeneous populations (naïve, Treg-, Tfh-, CCR9+ Th-, Th17-, Th2-, Eomes+ Tr1-, CTL-, PLZF+ innate- and Eomes+ innate-like cells) with multiple potential functions. We also identified two new subsets using aggregated scRNA-seq datasets from the rhesus and the cynomolgus monkey: CCR9+ Th-like cells expressing ICAM2 and ITGA1, and PLZF+ innate-like cells that display innate-associated gene signatures such as ZBTB16, TYROBP, MAP3K8, and KLRB1. Trajectory inference of cell differentiation status showed that most DP T cells in the rhesus monkey were found in the mid-to-late pseudotime, whereas DP T cells from the cynomolgus monkey were found in early pseudotime. This suggests that DP T cells in rhesus monkeys may exhibit more diverse differentiation states than those in cynomolgus monkeys. Thus, scRNA-seq and trajectory inference identified a more diverse subset of the circulating DP T cells than originally thought.
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Introduction
Single-cell RNA sequence (scRNA-seq) profiling has enabled high-resolution mapping of cellular heterogeneity, development, and activation status in diverse immune systems1,2. Furthermore, trajectory inference has radically enhanced scRNA-seq research by enabling the study of dynamic changes in gene expression3. This approach can achieve a more detailed single-cell level characterization of a limited T cell subset present in peripheral blood.
Recently, we reported that CD4+CD8+ double-positive (DP) T cells from cynomolgus monkeys comprise nine heterogeneous cell populations4. Notably, we found that in terms of the presence of a substantial number of the naïve DP T cells expressing CD8αα, along with high expression of PECAM1(CD31; a thymic emigrant marker), this population might be one of the mature T cell lineages of thymic origin4,5. In addition, identification of Eomes+ innate-like cells also has important implications for the diverse functions and roles of DP T cells. These findings demonstrate that peripheral DP T cells may have regulatory properties6, or follicular helper7 or innate and adaptive functions8. Thus, the abundance of DP T cells in the blood and/or target organs supports their involvement in pathological processes.
Like CD4+ or CD8+ single-positive T cells, the frequency of CD4+CD8+ DP T cells is readily observed in peripheral blood, but their composition, activation status, and immunological significance are poorly understood. Here, we used the scRNA-seq and trajectory platforms to analyze the characteristics of DP T cells from a rhesus monkey, and compare their transcriptomic profiles with those of cells from the cynomolgus monkey.
Results
scRNA-seq analysis of CD4+CD8+ DP T cells
To analyze circulating CD4+CD8+ DP T cells, we first separated peripheral DP T cells from a healthy adult rhesus monkey using MACS microbeads. Isolated DP T cells were labeled with CD4 and CD8α feature barcodes (FB), also known as an antibody-derived tag (ADT). We then ran the 10 × Genomics single-cell RNA sequencing. After filtering, 14,459 genes were detected and analyzed from 7601 cells. High expressions of CD3E, CD4 FB, and CD8 FB were identified in all clusters of sorted DP T cells. In contrast, the expression of NCAM1 (CD56), TRAV24 (TCRVα24-like), and TRAJ18 (TCRjα18) associated with NK or NKT was very low or absent (Fig. 1a). That is, the analyzed cells are all CD4+CD8+ DP T cells.
Heterogeneity within the CD4+CD8+ DP T cell population
The 11 clusters were identified using the nearest neighbor algorithm in the Seurat analysis platform (Fig. 1b). And then, ten cell types were classified based on differential expression and UMAP coordinates for specific marker genes (Fig. 1c and d, Supplementary Fig. S1a). We found that clusters (comprising parts of clusters 2, 3, and 4) of a substantial number of single cells shared naïve cell gene signatures such as SELL, LEF1, CD7, CCR7, PECAM1, and TCF7. To determine whether these cells differ from thymic immature DP T cells, we examined the expression of genes associated with stage markers. The immature DP stage markers AQP3 and SMPD39 were both absent (Supplementary Fig. S1b). We found that part of cluster 3 and cluster 4 can be defined as Treg-like cells based on high differential expression of regulatory T cell-associated gene signatures FOXP3, IL2RA, CTLA4, and IKZF210. We also identified a cluster that could be defined as circulating follicular helper T-like cells. This cluster, the majority of cluster 3, showed high differential expression of genes CXCR5, ICOS, PDCD1, and IL2111, along with homing receptors CCR7 and SELL12. In a part of cluster 2, we found a distinct subset showing high expression of CCR9 and ICAM2. We also identified genes (ITGA1, ABCB113, and ITGA4.) associated with blood CCR9+ Th cells. Thus, these cells were denoted as CCR9+ Th-like cells. Next, we identified differentially expressed genes by two clusters that showed gene signatures of helper T cell lineages. RORC, CCR6, IL23R, IL17A, and IL17RE10 were highly expressed in part of cluster 2. Part of cluster 1 exhibited high expression of Th2 cell-associated genes such as GATA3, CCR4, IL4R, and PTGDR210. Considering these gene signatures, we defined some cells in clusters 1 and 2 as Th2-like cells and Th17-like cells, respectively. Cluster 6 showed genes signatures of Eomes+ type 1 regulatory T (Tr1)-like cells such as EOMES, GZMK, CHI3L2, CST7, and NKG714, but the canonical Treg markers IL2RA and FOXP314 were not identified. Given these findings, the majority of cells in cluster 6 were defined as Eomes+ Tr1-like cells. Next, we identified a large cluster (clusters 0, 5, and 10) in which a large number of single-cells shared similar gene markers associated with cytotoxic function, such as GZMB, NKG7, CST7, CCL5, CX3CR1, KLRD1, PRF1, NKG2D, and ADGRG115,16,17,18. This cluster was defined as cytotoxic T lymphocyte (CTL)-like cells according to the differentially expressed gene signatures. Lastly, we found scRNA-seq data that could be divided into two distinct clusters (cluster 9 and part of cluster 6). Cluster 9 was characterized by exclusive and high expression of ZBTB16. In particular, this cluster also expressed high levels of KLRB1, MAP3K8, and TYROBP, which are known as innate-like markers19,20,21, along with KLRG1 and KLRD1. By contrast, part of cluster 6, a very small subset, exhibited high expression of EOMES, suggesting a potential difference in function. Within this cluster, the killer cell-like receptor (KLR) family (e.g., KLRC and KLRB1)22 and killer cell immunoglobulin-like receptor (KIR) family genes (e.g., KIRD2DL4 and KIR3DL12)23 were expressed exclusively. Additionally, IL2RB, NCR3, FCER1G, and TYROBP, all of which are associated with innate-like function23, were also highly expressed. Based on these gene signatures, we defined cluster 9 and the part of cluster 6 as PLZF+ innate- and Eomes+ innate-like cells, respectively.
Analysis of aggregated scRNA-seq data from the rhesus and a cynomolgus monkey
To investigate differences in DP T cell clustering by differentially expressed genes between the two monkeys, we integrated two scRNA-seq datasets from the rhesus monkey and a cynomolgus monkey using anchors and a canonical correlation analysis method. Single-cell data from the cynomolgus monkey were obtained from previously reported datasets4. After filtering, we analyzed 16,434 cells and identified 15,808 genes. Fourteen clusters were identified in the aggregated data using the nearest neighbor algorithm of Seurat analysis (Supplementary Fig. S2a). And then, ten cell subtypes were defined in the rhesus monkey (Fig. 2a) and eight cell subtypes in the cynomolgus monkey (Fig. 2b) based on UMAP coordinates and differential expression of specific marker genes between the identified clusters. Analysis of differentially expressed genes in each cluster revealed that eight cell subtypes were the same in both monkeys: naïve cells, Treg-, Tfh-, Th2-, Th17-, Eomes+ Tr1-, CTL-, and Eomes+ innate-like cells. A volcano plot (Fig. 2c) of the differentially expressed genes revealed that the rhesus monkey showed high expression of differentiation- or effector cell-associated genes such as GZMB, KLRG1, KLRD1, MKI67, ITGB1, PDCD1, and CCR9. By contrast, the cynomolgus monkey showed high expression of naïve- or regulatory T cell-associated genes such as LEF1, TCF7, CCR7, PECAM1, IKZF2, and FOXP3.
Most of the biomarker genes defining each cluster were similar in both monkeys; however, two cell subsets in the rhesus monkey differed from those in the cynomolgus monkey (Fig. 2d, e). First, a subset of CCR9+ Th-like cells that predominantly express CCR9 was characterized by high expression of ICAM2, which plays a role in lymphocyte homing and recirculation24. The CCR9+ Th-like cells are distinguishable from Tfh-like cells due to low expression of CXCR5 and ICOS (Fig. 2f), and also differ from Th17-like cells due to low expression of RORC and CCR6 (Fig. 2g). Second, the gene signatures of cluster 10 of the rhesus monkey, which expressed ZBTB16 exclusively, were distinct from those of the cynomolgus monkey. That is, we found that cluster 10 in the rhesus monkey expressed biomarker genes such as KLRB1, KLRG1, MAP3K8, TYROBP, and ZBTB16, which are known as innate-like markers19,20, along with high CD8A expression (Supplementary Fig. S2b). Furthermore, the gene signature of this cluster differs from that of Th17-like cells in that it shows high expression of IL2RB, NCR3, TBX21, PRF1, TYROBP, and GZMB (Fig. 2h). By contrast, the ZBTB16-expressing cell cluster (##cluster 10), which is a very small population in the cynomolgus monkey, showed the gene signature RORC, CCR6, IL23R, and IL17RE, with high expression of CD8A and CD8B (Fig. 2e,i). Thus, these cells are similar to a Th17-like cell subset rather than an innate-like cell subset in the cynomolgus monkey.
Cell state transitions of circulating DP T cells
The cell state transitions of DP T cells were expressed as a trajectory graph based on the changes in the analyzed gene signature of DP T cells. To better understand the differentiation of DP T cells, we constructed single-cell trajectories using Monocle 3 (version 0.1.2); all aggregated data from DP T cells were assessed using these trajectories based on changes in the transcriptomes. Most DP T cells from the rhesus monkey were allocated to the mid-to-late pseudotime (Fig. 3a), whereas those from the cynomolgus monkey were allocated to an early pseudotime corresponding to naïve T cells (Fig. 3b). Interestingly, we found that CCR9+ Th-like cluster in the rhesus monkey formed a distinct branch in the trajectory map, despite their close relationship with neighboring Tfh- and Th17-like clusters. This branch of the CCR9+ cluster was not observed in the cynomolgus monkey, suggesting that CCR9+ Th-like cells are a specific subtype of circulating DP T cells in the rhesus monkey. Next, genes related to T cell differentiation whose expression changed significantly over pseudotime were selected. Most genes exhibiting a large transition in the rhesus monkey were cytotoxic-related genes such as GZMB, GNLY17, CST725, NKG726, and CCL527 (Fig. 3c). A substantial number of single cells expressing these genes were allocated to the mid-to-late pseudotime; therefore, they differed from the transitions seen at a late pseudotime in the cynomolgus monkey (Fig. 3d). Given the expression patterns of these effector-related genes and their trajectory inferences, DP T cells from the rhesus monkey show a more diverse differentiation status than those from the cynomolgus monkey.
Characteristics of the cell populations expressing ZBTB16
To better understand the characteristics of the cell subsets we identified, we next focused on how the distinct cell subsets are related. The number of clusters detected by the Louvain algorithm was 38 in the rhesus monkey (Supplementary Fig. S3a) and 44 in the cynomolgus monkey (Supplementary Fig. S3b). We found that many clusters in the rhesus monkey comprised mainly helper and cytotoxic cell populations, in contrast to those in the cynomolgus monkey that mostly comprised naïve cell populations. This implies that we are able to identify more diverse cell subtypes of DP T cells in the rhesus monkey than in the cynomolgus monkey.
Interestingly, clusters expressing ZBTB16 showed sharply different characteristics between the two monkeys. That is, the cluster highly expressing ZBTB16 in rhesus DP T cells is a well-defined subset and characterized by high expression of innate-like gene signatures such as TYROBP, GZMB, GNLY, KLRD1, and MAP3K8 (Fig. 4a,c). In contrast, the ZBTB16+ cluster (##cluster 10) of cynomolgus DP T cells was a relatively small population, and exhibited high expression of Th17-associated gene signatures such as RORC, RORA, CCR6, and IL23R (Fig. 4b, c).
According to the co-regulated gene modules identified by Louvain community analysis, the ZBTB16-expressing cell population in the rhesus monkey clearly showed characteristics of innate-associated cells (Fig. 4d). That is, the cluster (23) expressing high ZBTB16 levels also had a high expression score for module 1, which contains innate-related gene signatures such as KLRB1, KIR2DL4, KIR3DL12, and TYROBP. Furthermore, we found that two clusters (23 and 37) corresponding to PLZF+ innate-like cells and Eomes+ innate-like cells, respectively, were not only closely related to each other, but also exhibited much higher expression scores in module 1 than the other clusters. This was not the case in the cynomolgus monkey. In this monkey, the ZBTB16+ cell cluster (44) was closely related to the Eomes+ innate-like cell cluster (42), but the ZBTB16+ cell cluster exhibited low expression of module 67 associated with innate-like gene signatures (e.g., KLRC, KLRD1, KIR2DL4, TYROBP, FCER1G, and NCR3). Rather, the ZBTB16+ cell cluster showed high expression of module 27, including ZBTB16, ICAM2, and ITGA3 (Fig. 4e), which is closely related to Th17-associated gene modules 6 and 49 (e.g., RORC, IL17A, and IL23R). Taken together, the data suggest that the PLZF+ innate-like cell subtype identified in the rhesus monkey showed gene signatures clearly distinct from those of other subsets with helper functions.
Discussion
The data presented here demonstrate that circulating DP T cells from a rhesus monkey comprise heterogeneous populations with various characteristics. Compared with conventional single-positive T cells, DP T cells exhibit diverse features, including helper-, regulatory-, cytotoxic-, and innate-like roles. In this study, scRNA aggregation analysis based on scRNA-seq data from one rhesus and one cynomolgus monkey showed that the composition of circulating DP T cells in rhesus monkey is distinctly different from that in cynomolgus monkeys4. That is, we identified CCR9+ Th-like and PLZF+ innate-like cells in the rhesus monkey, two distinct subsets that were not revealed by previous scRNA-seq analysis of DP T cells from cynomolgus monkey.
CCR9+ Th cells, which comprise only a small fraction of CD4+ T cells in the lymphoid tissues and circulation of healthy mice and humans28, are a subset of T cells that migrate selectively to the gastrointestinal tract (GIT) and predominately express CCR929,30. CCR9+ Th cells, which migrate to the GIT or pancreas via CCR9 and play an important role in inflammatory disease, show similar phenotypes to Tfh and Th17 cells and are often found at the site of inflammation as these cells31. That is, CCR9+ Th cells are similar to Tfh cells that produce IL-21, migrate to the GIT, and provide help to CD8+ T cells during the development of inflammatory diseases31. They also show characteristics similar to those of Th17 cells that secrete inflammatory cytokines such as IL-17, IL-21, and IL-22 and are involved in inflammatory diseases28. Thus, CCR9+ Th cells may contribute to the regional characteristics of organ-specific autoimmune diseases31. ICAM-2, which is highly expressed in this cluster, is readily detected on T and B cells from humans and rhesus monkeys32, and is implicated in lymphocyte homing and recirculation24. ICAM-2 may play a central role in the initial interaction between lymphocytes and antigen-presenting cells in that resting T lymphocytes express ICAM-2 but minimal levels of ICAM-133. Thus, the CCR9+ Th-like cells we identified seem to play a crucial role in adaptive immunity associated with intestinal inflammation.
Additionally, identification of PLZF+ innate-like cells based on expression of KLRG1, MAP3K8, and TYROBP may reveal another type of unconventional T cell because these cells also express high levels of KLRB1 and ZBTB16, both of which are hallmarks of innate lymphocytes19,20. A recent study reporting bulk scRNA-seq analysis of human thymus tissue showed that PLZF is highly expressed by a variety of unconventional T cells, including NKT-like cells and Th17-like cells9. However, the PLZF+ innate-like cell cluster we identified did not express the Th17-like cell-associated genes RORC, CD40LG, and CCR6, despite showing high expression of ZBTB16 and KLRB1. Rather, given that PLZF+ innate-like cells in the rhesus monkey express high IL2RB, IL15RA, and CD8αα, this population may be similar to unconventional PLZF+CD8αα+ cells, which depend on IL-15 signaling for development and survival in human peripheral blood34. Indeed, this subset exhibits an activated/memory phenotype and are capable of controlling effector T cell responses via a perforin-dependent mechanism typical of innate-like cytotoxic cells35, rather than secretion of immunosuppressive cytokines (e.g., IL-10 and TGF-β)34. Previously, we showed that PLZF was expressed at higher levels by DP T cells than by conventional T cells in the peripheral blood and liver of rhesus monkeys36. Although their origin cannot yet be definitively determined, it seems that this population is distinctly related to innate-like cells given the innate-associated gene signatures identified from the scRNA-seq data.
Another difference between the DP T cells from the two monkeys is that they exhibit different cellular differentiation trajectories over pseudotime. Although the number of analyzed subjects is limited, we found that a large number of single cells from the rhesus monkey were allocated to the mid-to-late pseudotime, suggesting that DP T cells were more likely to transit into multipotential cell fates. By contrast, most cell clusters in the cynomolgus monkey were allocated to an early pseudotime, implying that they have not yet progressed to effector or differentiated status and remained naïve.
Taken together, despite the limitation of the small cell population, we were able to demonstrate the heterogeneity of DP T cells using scRNA-seq and trajectory inference. Although comparative analysis of aggregated scRNA-seq datasets from different individuals has allowed us to identify the characteristics of small cell subsets, it can be difficult to view these data as representing interspecies differences. Therefore, further bulk data analysis may be necessary. However, we believe that these findings will provide useful information to advance our understanding of the relationship between circulating DP T cells and the pathological process of immune-related diseases.
Materials and methods
Subjects
One healthy male rhesus monkey (Macaca mulatta) aged 6 years was used for the study. Blood samples for single-cell RNA-seq were obtained from the femoral vein. Single-cell RNA-seq analysis was performed on a sample from the same monkey. The animal was cared for in strict accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals. The study was approved by the local Institutional Animal Care and Use Committee (IACUC) of Seoul National University Hospital (IACUC number:20–0004-S1A0). All experiments were performed in accordance with the relevant guidelines and regulations, and in accordance with the ARRIVE guidelines.
Cell preparation for single-cell RNA-seq
Cell preparation for scRNA-seq was performed in the same manner as in our previous study4. Peripheral blood mononuclear cells (PBMCs) in heparin-anticoagulated whole blood were separated using the Ficoll density gradient method (GE Healthcare, Uppsala, Sweden). CD4+ T cells were sorted from fresh PBMCs using the REAlease CD4 MicroBead Kit (Miltenyi Biotec). Next, CD4+CD8+ DP T cells were sorted from MACS isolated CD4+ T cells using the CD8 Microbeads Kit (Miltenyi Biotec). The isolated CD4+CD8+ DP T cells were then labeled with the following Totalseq-CD4 and Totalseq-CD8 antibodies: CD4, Clone SK3, Barcode sequence: GAGGTTAGTGATGGA (BioLegend); CD8, Clone SK1, Barcode sequence: GCGCAACTTGATGAT (BioLegend). Isolated DP T cells were used for single-cell RNA seq-analysis, including library construction, sequencing, preprocessing, and advanced analysis, following the method in our previous study4.
Library construction and sequencing
Libraries were prepared using the Chromium controller according to the 10 × Chromium Single-Cell V(D)J User Guide (10 × Genomics). Briefly, cell suspensions were diluted in nuclease-free water to achieve a targeted cell count of 10,000. The cell suspension was then mixed with master mix and loaded, along with Single-Cell 5′ Gel Beads and Partitioning Oil, into a Single-Cell A Chip. RNA transcripts from single cells were uniquely barcoded and reverse-transcribed within droplets. Next, cDNA molecules were pooled and enriched by PCR. For the 5′ Gene Expression Library, the cDNA pool went through an end repair process (i.e., addition of a single ‘A’ base), followed by ligation of the adapters. The products were then purified and enriched by PCR to create the 5′ Gene Expression Library. The purified libraries were quantified by qPCR according to the qPCR Quantification Protocol Guide (KAPA) and qualified using Agilent Technologies 4200 TapeStation (Agilent Technologies). Finally, the libraries were sequenced using the HiSeq platform (Illumina) according to the read length in the user guide.
Preprocessing and analysis of single-cell RNA-Seq data
The Cell Ranger v3.1.0 (10 × Genomics) pipeline was used to generate FASTQ files from raw sequencing data for gene expression analysis of 5′ Gene Expression Library data, and for cell surface protein expression analysis of the FB library. Illumina basecall files for each sample, generated by the Illumina sequencing instrument, were converted to the FASTQ format using the ‘mkfastq’ command. Gene expression libraries were analyzed using the ‘count’ command. Sequence reads were aligned to the Mmul_10 genome reference for Macaca mulatta using STAR (v2.5.1b) aligner. FB libraries were matched to the target FB reference. Next, gene and cell surface protein expression profiles for each cell were generated using information contained in the unique molecular identifier and 10 × cell barcode. Finally, cells were grouped into clusters according to gene expression.
Advanced analysis of scRNA-Seq data
The raw count matrices of 10 × genomics were imported into Seurat 3.1.3. Raw counts for all genes expressed in > = 3 cells, and of all cells with at least 200 detected genes, were used for downstream analysis. Since there may be a rare subset of cells with a clear outlier number of genes detected as potential multiplets, and there may be low-quality or dying cells, cells with over 4000 genes or mitochondrial counts over 20% were filtered out. After filtering, the count value of 14,459 genes across 7601 cells was normalized and scaled. Clustering and UMAP analysis were performed based on statistically significant principal components. Next, markers significant for each cluster compared with all remaining cells were identified using the minimum fraction of min.pct cells and the Wilcox rank sum test, reported only the positive ones. Gene-Enrichment and Functional Annotation analysis of the significant probe list was performed using the g:Profiler tool (https://biit.cs.ut.ee/gprofiler/). All data analysis using Seurat 3.1.3 was performed with standard settings.
Aggregation and trajectory analysis of scRNA-seq data
As with data from the rhesus monkey, published data for cynomolgus monkeys were preprocessed in the same way as in the previous study4. The resulting data were aggregated with data of the rhesus monkey into a single dataset to analyze samples using the Cell Ranger ‘aggr’ command. Raw count matrices aggregated by Cell Ranger ‘aggr’ were also processed as described above; after filtering, 15,808 genes across 16,434 cells were selected for analysis in the next step. Cell pairwise anchor correspondences between different single-cell data sets were identified with 15-dimensional spaces by canonical correlation analysis. Using these anchors, two datasets were integrated and transformed into a shared space. Gene expression values for each gene were scaled and normalized across all integrated cells. Clustering and UMAP analysis were performed as mentioned above. Additionally, rhesus monkey and cynomolgus monkey data within each cluster were compared using the Wilcox rank sum test (min.pct = 0.1; logfc.threshold = 0.4054651; min.cells.group = 3; min.cells.feature = 3; positive/negative ones were filtered) to identify differentially expressed genes. Gene-Enrichment and Functional Annotation analysis of significant gene lists from the two datasets was performed using g:Profiler tool (https://biit.cs.ut.ee/gprofiler/).
Trajectory reconstruction for each data set was performed by Monocle3 0.1.2, which defines a pseudotime measurement across a root cluster group through which the dynamics of gene expression can be examined.
Data availability
All scRNA-seq data are deposited in the Gene Expression Omnibus (GEO) accession number GSE199564.
References
Papalexi, E. & Satija, R. Single-cell RNA sequencing to explore immune cell heterogeneity. Nat. Rev. Immunol. 18, 35–45. https://doi.org/10.1038/nri.2017.76 (2018).
Griffiths, J. A., Scialdone, A. & Marioni, J. C. Using single cell genomics to understand developmental processes and cell fate decisions. Mol. Syst. Biol. https://doi.org/10.15252/msb.20178046 (2018).
Van den Berge, K. et al. Trajectory-based differential expression analysis for single-cell sequencing data. Nat. Commun. 11, 1201. https://doi.org/10.1038/s41467-020-14766-3 (2020).
Choi, S. M., Park, H. J., Choi, E. A., Jung, K. C. & Lee, J. I. Cellular heterogeneity of circulating CD4(+)CD8(+) double-positive T cells characterized by single-cell RNA sequencing. Sci. Rep. 11, 23607. https://doi.org/10.1038/s41598-021-03013-4 (2021).
Tanaskovic, S., Fernandez, S., Price, P., Lee, S. & French, M. A. CD31 (PECAM-1) is a marker of recent thymic emigrants among CD4+ T-cells, but not CD8+ T-cells or gammadelta T-cells, in HIV patients responding to ART. Immunol. Cell Biol. 88, 321–327. https://doi.org/10.1038/icb.2009.108 (2010).
Van Kaer, L., Rabacal, W. A., Scott Algood, H. M., Parekh, V. V. & Olivares-Villagomez, D. In vitro induction of regulatory CD4+CD8alpha+ T cells by TGF-beta, IL-7 and IFN-gamma. PLoS ONE 8, e67821. https://doi.org/10.1371/journal.pone.0067821 (2013).
Quandt, D., Rothe, K., Scholz, R., Baerwald, C. W. & Wagner, U. Peripheral CD4CD8 double positive T cells with a distinct helper cytokine profile are increased in rheumatoid arthritis. PLoS ONE 9, e93293. https://doi.org/10.1371/journal.pone.0093293 (2014).
Kerstein, A., Muller, A., Pitann, S., Riemekasten, G. & Lamprecht, P. Circulating CD4+CD8+ double-positive T-cells display features of innate and adaptive immune function in granulomatosis with polyangiitis. Clin. Exp. Rheumatol. 36(Suppl 111), 93–98 (2018).
Park, J. E. et al. A cell atlas of human thymic development defines T cell repertoire formation. Science https://doi.org/10.1126/science.aay3224 (2020).
Hollbacher, B. et al. Transcriptomic profiling of human effector and regulatory T cell subsets identifies predictive population signatures. Immunohorizons 4, 585–596. https://doi.org/10.4049/immunohorizons.2000037 (2020).
Schmitt, N., Bentebibel, S. E. & Ueno, H. Phenotype and functions of memory Tfh cells in human blood. Trends Immunol. 35, 436–442. https://doi.org/10.1016/j.it.2014.06.002 (2014).
Weber, J. P., Fuhrmann, F. & Hutloff, A. T-follicular helper cells survive as long-term memory cells. Eur. J. Immunol. 42, 1981–1988. https://doi.org/10.1002/eji.201242540 (2012).
Hinrichs, A. C. et al. Transcriptome analysis of CCR9+ T helper cells from primary sjogren’s syndrome patients identifies CCL5 as a novel effector molecule. Front. Immunol. 12, 702733. https://doi.org/10.3389/fimmu.2021.702733 (2021).
Bonnal, R. J. P. et al. Clonally expanded EOMES(+) Tr1-like cells in primary and metastatic tumors are associated with disease progression. Nat. Immunol. 22, 735–745. https://doi.org/10.1038/s41590-021-00930-4 (2021).
Hashimoto, K. et al. Single-cell transcriptomics reveals expansion of cytotoxic CD4 T cells in supercentenarians. Proc. Natl. Acad. Sci. U S A 116, 24242–24251. https://doi.org/10.1073/pnas.1907883116 (2019).
Patil, V. S. et al. Precursors of human CD4(+) cytotoxic T lymphocytes identified by single-cell transcriptome analysis. Sci. Immunol. https://doi.org/10.1126/sciimmunol.aan8664 (2018).
Szabo, P. A. et al. Single-cell transcriptomics of human T cells reveals tissue and activation signatures in health and disease. Nat. Commun. 10, 4706. https://doi.org/10.1038/s41467-019-12464-3 (2019).
Hidalgo, L. G. et al. The transcriptome of human cytotoxic T cells: measuring the burden of CTL-associated transcripts in human kidney transplants. Am. J. Transplant. 8, 637–646. https://doi.org/10.1111/j.1600-6143.2007.02129.x (2008).
Alonzo, E. S. & Sant’Angelo, D. B. Development of PLZF-expressing innate T cells. Curr. Opin. Immunol. 23, 220–227. https://doi.org/10.1016/j.coi.2010.12.016 (2011).
Fergusson, J. R., Fleming, V. M. & Klenerman, P. CD161-expressing human T cells. Front. Immunol. 2, 36. https://doi.org/10.3389/fimmu.2011.00036 (2011).
Watford, W. T. et al. Tpl2 kinase regulates T cell interferon-gamma production and host resistance to Toxoplasma gondii. J. Exp. Med. 205, 2803–2812. https://doi.org/10.1084/jem.20081461 (2008).
Mendez-Lagares, G. et al. Cytomegalovirus mediates expansion of IL-15-responsive innate-memory cells with SIV killing function. J. Clin. Invest. https://doi.org/10.1172/JCI148542 (2021).
Correia, M. P. et al. Distinct human circulating NKp30(+)FcepsilonRIgamma(+)CD8(+) T cell population exhibiting high natural killer-like antitumor potential. Proc. Natl. Acad. Sci. U S A 115, E5980–E5989. https://doi.org/10.1073/pnas.1720564115 (2018).
Halai, K., Whiteford, J., Ma, B., Nourshargh, S. & Woodfin, A. ICAM-2 facilitates luminal interactions between neutrophils and endothelial cells in vivo. J. Cell Sci. 127, 620–629. https://doi.org/10.1242/jcs.137463 (2014).
Nanut, M. P., Sabotic, J., Jewett, A. & Kos, J. Cysteine cathepsins as regulators of the cytotoxicity of NK and T cells. Front. Immunol. https://doi.org/10.3389/fimmu.2014.00616 (2014).
Ng, S. S. et al. The NK cell granule protein NKG7 regulates cytotoxic granule exocytosis and inflammation. Nat. Immunol. 21, 1205–1218. https://doi.org/10.1038/s41590-020-0758-6 (2020).
Kim, J. J. et al. CD8 positive T cells influence antigen-specific immune responses through the expression of chemokines. J. Clin. Invest. 102, 1112–1124. https://doi.org/10.1172/Jci3986 (1998).
Cosorich, I., McGuire, H. M., Warren, J., Danta, M. & King, C. CCR9 expressing T helper and T follicular helper cells exhibit site-specific identities during inflammatory disease. Front Immunol. 9, 2899. https://doi.org/10.3389/fimmu.2018.02899 (2018).
Papadakis, K. A. et al. CC chemokine receptor 9 expression defines a subset of peripheral blood lymphocytes with mucosal T cell phenotype and Th1 or T-regulatory 1 cytokine profile. J. Immunol. 171, 159–165. https://doi.org/10.4049/jimmunol.171.1.159 (2003).
Mora, J. R. et al. Selective imprinting of gut-homing T cells by Peyer’s patch dendritic cells. Nature 424, 88–93. https://doi.org/10.1038/nature01726 (2003).
McGuire, H. M. et al. A subset of interleukin-21+ chemokine receptor CCR9+ T helper cells target accessory organs of the digestive system in autoimmunity. Immunity 34, 602–615. https://doi.org/10.1016/j.immuni.2011.01.021 (2011).
Palesch, D. et al. Sooty mangabey genome sequence provides insight into AIDS resistance in a natural SIV host. Nature 553, 77–81. https://doi.org/10.1038/nature25140 (2018).
Zaretsky, I. et al. ICAMs support B cell interactions with T follicular helper cells and promote clonal selection. J. Exp. Med. 214, 3435–3448. https://doi.org/10.1084/jem.20171129 (2017).
Sheng, H. M. et al. Distinct PLZF(+)CD8 alpha alpha(+) unconventional T cells enriched in liver use a cytotoxic mechanism to limit autoimmunity. J. Immunol. 203, 2150–2162. https://doi.org/10.4049/jimmunol.1900832 (2019).
Beeston, T., Smith, T. R., Maricic, I., Tang, X. & Kumar, V. Involvement of IFN-gamma and perforin, but not Fas/FasL interactions in regulatory T cell-mediated suppression of experimental autoimmune encephalomyelitis. J. Neuroimmunol. 229, 91–97. https://doi.org/10.1016/j.jneuroim.2010.07.007 (2010).
Choi, Y. J., Park, H. J., Park, H. J., Jung, K. C. & Lee, J. I. CD4(hi)CD8(low) double-positive T cells are associated with graft rejection in a nonhuman primate model of islet transplantation. J. Immunol. Res. 2018, 3861079. https://doi.org/10.1155/2018/3861079 (2018).
Acknowledgements
This study was supported by a grant from the National Research Foundation of Korea (NRF), funded by the Korean Ministry of Science and ICT (grant number: NRF-2019R1F1A1061143).
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S.M.C. designed and performed the experiments and analyzed the data. H.J.P. and E.A.C. provided technical assistance and optimized the protocols. S.M.C. and J.I.L. optimized the scRNA-seq experiments and protocols, analyzed the data, and wrote the manuscript. K.C.J. and J.I.L. supervised the work and coordinated the study.
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Choi, S.M., Park, H.J., Choi, E.A. et al. Heterogeneity of circulating CD4+CD8+ double-positive T cells characterized by scRNA-seq analysis and trajectory inference. Sci Rep 12, 14111 (2022). https://doi.org/10.1038/s41598-022-18340-3
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DOI: https://doi.org/10.1038/s41598-022-18340-3
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