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Cytotoxic CD4+ T lymphocytes may induce endothelial cell apoptosis in systemic sclerosis
Takashi Maehara, … , Dinesh Khanna, Shiv Pillai
Takashi Maehara, … , Dinesh Khanna, Shiv Pillai
Published January 28, 2020
Citation Information: J Clin Invest. 2020;130(5):2451-2464. https://doi.org/10.1172/JCI131700.
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Research Article Autoimmunity Immunology

Cytotoxic CD4+ T lymphocytes may induce endothelial cell apoptosis in systemic sclerosis

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Abstract

Systemic sclerosis (SSc) is an autoimmune fibrotic disease whose pathogenesis is poorly understood and lacks effective therapies. We undertook quantitative analyses of T cell infiltrates in the skin of 35 untreated patients with early diffuse SSc and here show that CD4+ cytotoxic T cells and CD8+ T cells contribute prominently to these infiltrates. We also observed an accumulation of apoptotic cells in SSc tissues, suggesting that recurring cell death may contribute to tissue damage and remodeling in this fibrotic disease. HLA-DR–expressing endothelial cells were frequent targets of apoptosis in SSc, consistent with the prominent vasculopathy seen in patients with this disease. A circulating effector population of cytotoxic CD4+ T cells, which exhibited signatures of enhanced metabolic activity, was clonally expanded in patients with systemic sclerosis. These data suggest that cytotoxic T cells may induce the apoptotic death of endothelial and other cells in systemic sclerosis. Cell loss driven by immune cells may be followed by overly exuberant tissue repair processes that lead to fibrosis and tissue dysfunction.

Authors

Takashi Maehara, Naoki Kaneko, Cory A. Perugino, Hamid Mattoo, Jesper Kers,, Hugues Allard-Chamard, Vinay S. Mahajan, Hang Liu, Samuel J.H. Murphy, Musie Ghebremichael, David Fox, Aimee S. Payne, Robert Lafyatis, John H. Stone, Dinesh Khanna, Shiv Pillai

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Figure 7

CD28loCD57hiCD4+ CTLs from SSc patients have transcriptional signatures linked to cytotoxicity, fibrogenesis, and metabolic activity rather than senescence.

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CD28loCD57hiCD4+ CTLs from SSc patients have transcriptional signatures ...
Comparing CD28loCD57hiCD4+ CTLs to naive CD4+ T cells, we identified enrichment for many gene sets, including (A) alignment with previously reported CD4+ CTL transcriptomes and greater similarity with γδ T cell and CD8+ T cell transcriptomes rather than with conventional CD4+ T cells, and (B) those associated with fibrogenesis such as regulation of fibroblast apoptosis, regulation of endothelial cell migration and hemostasis. Size of dots represents number of genes within a given gene set. The x axes represent the percentages of genes within a gene set enriched for by the effector CD4+ CTL transcriptome. (C) CNETplot showing all genes upregulated by effector CD4+ CTLs from immune cell transcriptional gene sets showing a prominent cytotoxic profile with upregulation of GZMA, GZMB, GZMM, GZMH, PRF1, and SLAMF7. P values were calculated with the permutation method implemented in fgsea version 1.12.0.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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