免疫系统
医学
泌尿系统
免疫学
肾
肾炎
细胞毒性T细胞
癌症研究
生物
内科学
生物化学
体外
作者
Shailbala Singh,Letícia Campos Clemente,Edwin Roger Parra,Amanda S. Tchakarov,Chao Yang,Yisheng Li,James Patrick Long,Cassian Yee,Jamie S. Lin
出处
期刊:OncoImmunology
[Landes Bioscience]
日期:2022-09-22
卷期号:11 (1): 2124678-2124678
被引量:8
标识
DOI:10.1080/2162402x.2022.2124678
摘要
Acute kidney injury (AKI) occurs in ~20% of patients receiving immune checkpoint inhibitor (ICI) therapy; however, only 2-5% will develop ICI-mediated immune nephritis. Conventional tests are nonspecific in diagnosing disease pathology and invasive procedures (i.e. kidney biopsy) may not be feasible. In other autoimmune renal diseases, urinary immune cells correlated with the pathology or were predictive of disease activity. Corresponding evidence and analysis are absent for ICI-mediated immune nephritis. We report the first investigation analyzing immune cell profiles of matched kidney biopsies and urine of patients with ICI-AKI. We demonstrated the presence of urinary T cells in patients with immune nephritis by flow cytometry analysis. Clonotype analysis of T cell receptor (TCR) sequences confirmed enrichment of kidney TCRs in urine. As ICI therapies become standard of care for more cancers, noninvasively assessing urinary immune cells of ICI therapy recipients can facilitate clinical management and an opportunity to tailor ICI-nephritis treatment.
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