结直肠免疫相关不良事件:抗 CTLA-4 和抗 PD-1 阻断诱导不同的免疫病理实体。

Colon Immune-Related Adverse Events: Anti-CTLA-4 and Anti-PD-1 Blockade Induce Distinct Immunopathological Entities.

机构信息

Gustave Roussy, Laboratory d'Immunomonitoring en Oncologie, CNRS-UMS 3655 and INSERM-US23, Villejuif F-94805, France.

University Paris-Sud, Faculté de Médecine, Le Kremlin Bicêtre, F-94276, France.

出版信息

J Crohns Colitis. 2017 Oct 1;11(10):1238-1246. doi: 10.1093/ecco-jcc/jjx081.

Abstract

BACKGROUND AND AIM

Immune checkpoint inhibitors targeting CTLA-4 and PD-1 improve survival in cancer patients but may induce immune-related adverse events, including colitis. The immunological characteristics of anti-CTLA-4 [αCTLA-4]- and anti-PD-1 [αPD-1]-related colitis have been poorly described. The aim of the present study was to compare the immunological and histological characteristics of αCTLA-4-induced colitis and αPD-1-induced colitis.

METHODS

Colonic biopsies from patients with αCTLA-4-induced colitis, αPD-1-induced colitis, and inflammatory bowel disease [IBD] were analysed by immunohistochemistry and flow cytometry. Tumour necrosis factor alpha [TNFα] concentration was assessed in biopsy supernatants.

RESULTS

CD8+ T cells were found in the lamina propria and epithelium in αPD-1-induced colitis, whereas CD4+ T cells were found in the lamina propria in αCTLA-4-induced colitis. No or low intraepithelial lymphocytes were observed in αCTLA-4-induced colitis. No difference in numbers of mucosal regulatory T cells was observed between αCTLA-4- or αPD-1-induced colitis and IBD patients. Higher numbers of activated ICOS+ conventional CD4+ T cells were observed in αCTLA-4-induced colitis compared with patients with IBD. Among ICOS+CD4+ T cells, conventional CD4+ T cells were the main T cell population in patents with αCTLA-4-induced colitis, whereas Treg cells were predominant in IBD or αPD-1-induced colitis. High mucosal TNFα concentrations were observed in αCTLA-4-induced colitis. Low mucosal TNFα concentrations were associated with steroid sensitivity.

CONCLUSIONS

These observations show that αCTLA-4- and αPD-1-induced colitis have distinct immunological characteristics. Mucosal TNFα concentration might detect patients at risk of developing corticosteroid resistance after CTLA-4 blockade.

摘要

背景与目的

针对 CTLA-4 和 PD-1 的免疫检查点抑制剂可改善癌症患者的生存率,但可能引发包括结肠炎在内的免疫相关不良反应。抗 CTLA-4(αCTLA-4)和抗 PD-1(αPD-1)相关结肠炎的免疫学特征尚未得到充分描述。本研究旨在比较 αCTLA-4 诱导的结肠炎和 αPD-1 诱导的结肠炎的免疫学和组织学特征。

方法

通过免疫组织化学和流式细胞术分析 αCTLA-4 诱导的结肠炎、αPD-1 诱导的结肠炎和炎症性肠病(IBD)患者的结肠活检组织。评估活检上清液中肿瘤坏死因子α(TNFα)的浓度。

结果

αPD-1 诱导的结肠炎中可见 CD8+T 细胞存在于固有层和上皮内,而 αCTLA-4 诱导的结肠炎中可见 CD4+T 细胞存在于固有层内。αCTLA-4 诱导的结肠炎中未见或仅有少量上皮内淋巴细胞。αCTLA-4 或 αPD-1 诱导的结肠炎与 IBD 患者之间黏膜调节性 T 细胞的数量无差异。与 IBD 患者相比,αCTLA-4 诱导的结肠炎中观察到更多的活化 ICOS+常规 CD4+T 细胞。在 ICOS+CD4+T 细胞中,常规 CD4+T 细胞是 αCTLA-4 诱导的结肠炎患者中的主要 T 细胞群,而 Treg 细胞在 IBD 或 αPD-1 诱导的结肠炎中占主导地位。αCTLA-4 诱导的结肠炎中观察到高黏膜 TNFα浓度。低黏膜 TNFα浓度与皮质类固醇敏感性相关。

结论

这些观察结果表明,αCTLA-4 和 αPD-1 诱导的结肠炎具有不同的免疫学特征。黏膜 TNFα浓度可能有助于检测接受 CTLA-4 阻断治疗后发生皮质类固醇耐药的风险患者。

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