Author:
Altan Mehmet,Li Quan-Zhen,Wang Qi,Vokes Natalie I.,Sheshadri Ajay,Gao Jianjun,Zhu Chengsong,Tran Hai T.,Gandhi Saumil,Antonoff Mara B.,Swisher Stephen,Wang Jing,Byers Lauren A.,Abdel-Wahab Noha,Franco-Vega Maria C.,Wang Yinghong,Lee J. Jack,Zhang Jianjun,Heymach John V.
Abstract
The roles of preexisting auto-reactive antibodies in immune-related adverse events (irAEs) associated with immune checkpoint inhibitor therapy are not well defined. Here, we analyzed plasma samples longitudinally collected at predefined time points and at the time of irAEs from 58 patients with immunotherapy naïve metastatic non-small cell lung cancer treated on clinical protocol with ipilimumab and nivolumab. We used a proteomic microarray system capable of assaying antibody reactivity for IgG and IgM fractions against 120 antigens for systemically evaluating the correlations between auto-reactive antibodies and certain organ-specific irAEs. We found that distinct patterns of auto-reactive antibodies at baseline were associated with the subsequent development of organ-specific irAEs. Notably, ACHRG IgM was associated with pneumonitis, anti-cytokeratin 19 IgM with dermatitis, and anti-thyroglobulin IgG with hepatitis. These antibodies merit further investigation as potential biomarkers for identifying high-risk populations for irAEs and/or monitoring irAEs during immunotherapy treatment.Trial registrationClinicalTrials.gov identifier: NCT03391869.
Subject
Immunology,Immunology and Allergy
Cited by
1 articles.
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