Immune checkpoint inhibitor-induced severe epidermal necrolysis mediated by macrophage-derived CXCL10 and abated by TNF blockade

• Published in: Nature communications Vol. 15; no. 1; pp. 10733 - 19
• Main Authors: Chen, Chun-Bing, Hung, Shuen-Iu, Chang, John Wen-Cheng, Yang, Chan-Keng, Ma, David Hui-Kang, Teng, Yu-Chuan, Lu, Chun-Wei, Chen, Wei-Ti, Yang, Hsiao-Yin, Tsai, Cheng-Chang, Wang, Chih Liang, Chiang, Pin-Hsuan, Wu, Jennifer, Tsai, Ya-Wen, Lu, Lai-Ying, Lin, Yang Yu-Wei, Hui, Rosaline Chung-Yee, Hsieh, Fu-Mei, Hsu, Chao-Kai, Lee, Chaw-Ning, Chen, Yi-Ju, Chen, Chih-Chiang, Cui, Yilei, Hsu, Hung-Chih, Chang, Ya-Ching, Chang, Chih-Jung, Lin, Ho-Chen, Chang, Chee Jen, Lin, Yu-Jr, Ku, Cheng-Lung, Wang, Chuang-Wei, Chung, Wen-Hung
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 30.12.2024; Nature Publishing Group; Nature Portfolio
• Subjects: 13/106; 13/95; 38/39; 38/90; 38/91; 49/47; 631/250/249/1313; 631/250/2502; 631/250/580; 692/53/2423; 692/699/4033; 82/51; 96/21; 96/31; Aged; Antineoplastic drugs; Blistering; Cell activation; Cell differentiation; Chemokine CXCL10 - metabolism; Corticoids; Corticosteroids; CXCL10 protein; CXCR3 protein; Cytotoxicity; Female; Gene sequencing; Humanities and Social Sciences; Humans; Immune checkpoint inhibitors; Immune Checkpoint Inhibitors - adverse effects; Lesions; Lymphocytes; Lymphocytes T; Macrophages; Macrophages - drug effects; Macrophages - immunology; Macrophages - metabolism; Male; Middle Aged; Monocytes; multidisciplinary; Pathogenesis; Receptors, CXCR3 - metabolism; Science; Science (multidisciplinary); Side effects; Single-Cell Analysis; Skin - drug effects; Skin - immunology; Skin - pathology; Skin diseases; Skin lesions; Stevens-Johnson syndrome; Stevens-Johnson Syndrome - etiology; Stevens-Johnson Syndrome - immunology; Stevens-Johnson Syndrome - pathology; T-Lymphocytes, Cytotoxic - drug effects; T-Lymphocytes, Cytotoxic - immunology; Therapeutic targets; Therapy; Toxic epidermal necrolysis; Trajectory analysis; Transcriptomics; Tumor Necrosis Factor Inhibitors - adverse effects; Tumor Necrosis Factor-alpha - metabolism
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-024-54180-7

Immune checkpoint inhibitors (ICI) represent new anticancer agents and have been used worldwide. However, ICI can potentially induce life-threatening severe cutaneous adverse reaction (SCAR), such as Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN), hindering continuous ICI therapy. We examine 6 cohorts including 25 ICI-induced SJS/TEN patients and conduct single-cell RNA sequencing (scRNA-seq) analysis, which shows overexpression of macrophage-derived CXCL10 that recruits CXCR3 + cytotoxic T lymphocytes (CTL) in blister cells from ICI-SJS/TEN skin lesions. ScRNA expression profiles and ex vivo blocking studies further identify TNF signaling as a pathway responsible for macrophage-derived CXCL10 and CTL activation. Based on the trajectory analysis, ICI-activated T cells from whole blood are proposed to serve as the initial cells involved in inflammation, that lead to monocytes differentiating into macrophages and increasing their susceptibility to migrate to the lesion sites. Compared with systemic corticosteroids treatment, ICI-induced SJS/TEN patients treated with biologic TNF blockade showed a significantly rapid recovery and no recurrence of SCAR with continuous ICI therapy. Our findings identify that macrophage-eliciting CTL contribute to the pathogenesis of ICI-induced epidermal necrolysis and provide potential therapeutic targets for the management and prevention of SCAR induced by ICI therapy. As immune checkpoint therapy is more frequently used for cancer, side effects such as Stevens-Johson syndrome / toxic epidermal necrolysis (SJS/TEN) are becoming more common. Here the authors use single cell transcriptomics to implicate TNF and CXCL10 in recruitment of CXCR3 + cytotoxic T cell in SJS/TEN skin lesions.