炎症性肠病
颗粒酶A
化学发光
颗粒酶B
颗粒酶
炎症
医学
生物标志物
CXCL10型
免疫学
免疫系统
细胞毒性
溃疡性结肠炎
趋化因子
埃利斯波特
癌症研究
炎症性肠病
细胞毒性T细胞
疾病
分泌物
流式细胞术
白细胞介素
干扰素
克罗恩病
钙蛋白酶
促炎细胞因子
作者
Jamie I. Scott,Zhiming Cheng,Emily Thompson,Utsa Karmakar,Verity Cowell,Maya David,Doireann Gordon,Lorena Mendive-Tapia,Alexander Le Saint-Grant,Pia Volkmer,Cher S. Chuah,Phoebe Lau,Adriano G. Rossi,Wouter B. Nagengast,Doron Shabat,Gwo-Tzer Ho,Marc Vendrell
标识
DOI:10.1038/s41551-025-01588-1
摘要
The diagnosis and monitoring of inflammatory bowel disease (IBD) relies on histologic and endoscopic analysis, as well as measurements of generic markers of inflammation. However, there are no specific tests that report on T cell-mediated immune responses as a key driver of IBD pathogenesis. Here we detect increasing granzyme A (GzmA) in gut biopsies and confirm that CD8+ T cells secrete its active form to induce interleukin (IL)-8. We then rationally design a non-invasive chemiluminescence assay for measuring active GzmA in stool supernatants from patients with IBD. For our assay, we synthesize peptide-based GzmA-specific inhibitors and chemiluminescent reporters and use them to characterize biosamples from ~150 human patients with IBD and healthy controls. Our results demonstrate that GzmA activity is an indicator of gut inflammation that can enhance the identification of patients with IBD over existing tests and potentially act as a mechanistic biomarker for the dominance of T cell activity. We envision that the selectivity and sensitivity of our GzmA activity-based optical assay will accelerate the design of additional biomedical approaches to enhance precision medicine in IBD. A rationally designed assay detects granzyme A activity by integrating peptide-based GzmA-targeted inhibitors and probes with chemiluminescent reporters to monitor inflammatory bowel disease.
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