Ragot Hélène, Gaucher Sonia, Bonnet des Claustres Mathilde, Basset Justine, Boudan Rose, Battistella Maxime, Bourrat Emmanuelle, Hovnanian Alain, Titeux Matthias
Laboratory of Genetic Skin Diseases, Imagine Institute, Université Paris Cité, INSERM UMR 1163, 75015 Paris, France.
Reference Center for Genodermatoses ("Maladies Génétiques à Expression Cutanée", MAGEC), Saint-Louis Hospital (Assistance Publique-Hôpitaux de Paris), 75010 Paris, France.
Cancers (Basel). 2024 Jul 6;16(13):2476. doi: 10.3390/cancers16132476.
Recessive dystrophic epidermolysis bullosa (RDEB) is a rare severe hereditary skin disease characterized by skin and mucosa fragility, resulting in blister formation. The most severe complication in RDEB patients is the development of cutaneous squamous cell carcinoma (SCC), leading to premature death. There is a great deal of evidence suggesting a permissive tumor microenvironment (TME) as a driver of SCC development in RDEB patients. In a cohort of RDEB patients, we characterized the immune profiles of RDEB-SCCs and compared them with clinical, histopathological, and prognostic features. RDEB-SCCs were subdivided into four groups based on their occurrence (first onset or recurrences) and grading according to clinical, histopathological parameters of aggressiveness. Thirty-eight SCCs from 20 RDEB patients were analyzed. Five RDEB patients experienced an unfavorable course after the diagnosis of the first SCC, with early recurrence or metastasis, whereas 15 patients developed multiple SCCs without metastasis. High-risk primary RDEB-SCCs showed a higher neutrophil-to-lymphocyte ratio in the tumor microenvironment and an increased proportion of neutrophil extracellular traps (NETs). Additionally, citrullinated histone H3, a marker of NETs, was increased in the serum of RDEB patients with high-risk primary SCC, suggesting that this modified form of histone H3 may serve as a potential blood marker of unfavorable prognosis in RDEB-SCCs.
隐性营养不良型大疱性表皮松解症(RDEB)是一种罕见的严重遗传性皮肤病,其特征为皮肤和黏膜脆弱,导致水疱形成。RDEB患者最严重的并发症是皮肤鳞状细胞癌(SCC)的发生,可导致过早死亡。有大量证据表明,在RDEB患者中,肿瘤微环境(TME)的宽松状态是SCC发生的驱动因素。在一组RDEB患者中,我们对RDEB-SCC的免疫特征进行了表征,并将其与临床、组织病理学和预后特征进行了比较。RDEB-SCC根据其发生情况(首次发病或复发)以及根据侵袭性的临床、组织病理学参数进行分级,分为四组。对来自20名RDEB患者的38例SCC进行了分析。5名RDEB患者在首次诊断SCC后病程不佳,出现早期复发或转移,而15名患者发生了多发性SCC但无转移。高危原发性RDEB-SCC在肿瘤微环境中显示出较高的中性粒细胞与淋巴细胞比值以及中性粒细胞胞外诱捕网(NETs)比例增加。此外,NETs的标志物瓜氨酸化组蛋白H3在高危原发性SCC的RDEB患者血清中升高,这表明这种组蛋白H3的修饰形式可能作为RDEB-SCC不良预后的潜在血液标志物。