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辅助性T细胞2型定向免疫疗法可消除癌前皮肤病变。

T helper 2 cell-directed immunotherapy eliminates precancerous skin lesions.

作者信息

Oka Tomonori, Smith Sabrina S, Son Heehwa G, Lee Truelian, Oliver-Garcia Valeria S, Mortaja Mahsa, Trerice Kathryn E, Isakoff Lily S, Conrad Danielle N, Azin Marjan, Raval Neel S, Tabacchi Mary, Emdad Luni, Das Swadesh K, Fisher Paul B, Cornelius Lynn A, Demehri Shadmehr

机构信息

Center for Cancer Immunology and Cutaneous Biology Research Center, Krantz Family Center for Cancer Research and Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts, USA.

Division of Dermatology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.

出版信息

J Clin Invest. 2025 Jan 2;135(1):e183274. doi: 10.1172/JCI183274.

Abstract

The continuous rise in skin cancer incidence highlights an imperative for improved skin cancer prevention. Topical calcipotriol-plus-5-fluorouracil (calcipotriol-plus-5-FU) immunotherapy effectively eliminates precancerous skin lesions and prevents squamous cell carcinoma (SCC) in patients. However, its mechanism of action remains unclear. Herein, we demonstrate that calcipotriol-plus-5-FU immunotherapy induces T helper type 2 (Th2) immunity, eliminating premalignant keratinocytes in humans. CD4+ Th2 cells were required and were sufficient downstream of thymic stromal lymphopoietin cytokine induction by calcipotriol to suppress skin cancer development. Th2-associated cytokines induced IL-24 expression in cancer cells, resulting in toxic autophagy and anoikis followed by apoptosis. Calcipotriol-plus-5-FU immunotherapy was dependent on IL-24 to suppress skin carcinogenesis in vivo. Collectively, our findings establish a critical role for Th2 immunity in cancer immunoprevention and highlight the Th2/IL-24 axis as an innovative target for skin cancer prevention and therapy.

摘要

皮肤癌发病率的持续上升凸显了改善皮肤癌预防措施的紧迫性。外用卡泊三醇联合5-氟尿嘧啶(卡泊三醇联合5-FU)免疫疗法能有效消除癌前皮肤病变,并预防患者发生鳞状细胞癌(SCC)。然而,其作用机制尚不清楚。在此,我们证明卡泊三醇联合5-FU免疫疗法可诱导2型辅助性T细胞(Th2)免疫,消除人体中的癌前角质形成细胞。CD4+ Th2细胞是必需的,并且在卡泊三醇诱导胸腺基质淋巴细胞生成素细胞因子下游足以抑制皮肤癌发展。Th2相关细胞因子诱导癌细胞中IL-24表达,导致毒性自噬和失巢凋亡,随后发生细胞凋亡。卡泊三醇联合5-FU免疫疗法在体内依赖IL-24来抑制皮肤癌发生。总体而言,我们的研究结果确立了Th2免疫在癌症免疫预防中的关键作用,并突出了Th2/IL-24轴作为皮肤癌预防和治疗的创新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8354/11684800/4f1056c9ef5c/jci-135-183274-g124.jpg

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