Regulatory B cell repertoire defects predispose lung cancer patients to immune-related toxicity following checkpoint blockade

Nat Commun. 2022 Jun 7;13(1):3148. doi: 10.1038/s41467-022-30863-x.

Abstract

Checkpoint blockade with Pembrolizumab, has demonstrated durable clinical responses in advanced non-small cell lung cancer, however, treatment is offset by the development of high-grade immune related adverse events (irAEs) in some patients. Here, we show that in these patients a deficient Breg checkpoint fails to limit self-reactive T cell enhanced activity and auto-antibody formation enabled by PD-1/PD-L1 blockade, leading to severe auto-inflammatory sequelae. Principally a failure of IL-10 producing regulatory B cells as demonstrated through functional ex vivo assays and deep phenotyping mass cytometric analysis, is a major and significant finding in patients who develop high-grade irAEs when undergoing treatment with anti-PD1/PD-L1 checkpoint blockade. There is currently a lack of biomarkers to identify a priori those patients at greatest risk of developing severe auto-inflammatory syndrome. Pre-therapy B cell profiling could provide an important tool to identify lung cancer patients at high risk of developing severe irAEs on checkpoint blockade.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocytes, Regulatory*
  • B7-H1 Antigen / genetics
  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • Carcinoma, Non-Small-Cell Lung* / genetics
  • Humans
  • Lung Neoplasms* / drug therapy
  • Lung Neoplasms* / genetics
  • Programmed Cell Death 1 Receptor / genetics

Substances

  • B7-H1 Antigen
  • Programmed Cell Death 1 Receptor