Vesely Matthew D, Christensen Sean R
Department of Dermatology, and.
Department of Surgery, Division of Plastic and Reconstructive Surgery, Yale School of Medicine, New Haven, Connecticut, USA.
J Clin Invest. 2025 Jan 2;135(1):e188018. doi: 10.1172/JCI188018.
Cutaneous squamous cell carcinoma (cSCC) incidence and deaths continue to rise, underscoring the need for improved cSCC prevention. Elimination of actinic keratosis (AK) precursor lesions is a major strategy to prevent cSCC. Topical calcipotriol and 5-fluorouracil (5-FU) have been shown to eliminate AKs and reduce the risk of cSCC development, but the mechanism was undefined. In this issue of the JCI, Oka et al. demonstrate that type 2 immunity is necessary and sufficient for the elimination of premalignant keratinocytes and cSCC prevention. Paired biopsies from AK lesions and unaffected skin revealed that only keratinocytes from AKs produced thymic stromal lymphopoietin (TSLP) and damage-associated molecular patterns, resulting in selective recruitment of Th2 cells to the AK lesion. In mouse models of skin carcinogenesis, TSLP was necessary to recruit Th2 cells and trigger IL-24-mediated keratinocyte cell death. These findings suggest that the TSLP/Th2/IL-24 axis is a potential therapeutic target for SCC prevention.
皮肤鳞状细胞癌(cSCC)的发病率和死亡率持续上升,这凸显了改进cSCC预防措施的必要性。消除光化性角化病(AK)前驱病变是预防cSCC的一项主要策略。局部使用卡泊三醇和5-氟尿嘧啶(5-FU)已被证明可消除AK,并降低cSCC发生的风险,但其中的机制尚不清楚。在本期《临床研究杂志》(JCI)中,冈田等人证明2型免疫对于消除癌前角质形成细胞和预防cSCC是必要且充分的。对AK病变和未受影响皮肤进行的配对活检显示,只有来自AK的角质形成细胞产生胸腺基质淋巴细胞生成素(TSLP)和损伤相关分子模式,从而导致Th2细胞选择性募集至AK病变处。在皮肤癌发生的小鼠模型中,TSLP是募集Th2细胞并触发IL-24介导的角质形成细胞死亡所必需的。这些发现表明,TSLP/Th2/IL-24轴是预防SCC的一个潜在治疗靶点。