| Literature DB >> 31920059 |
Al Caraffa1, C E Gallenga2, S K Kritas3, G Ronconi4, P Di Emidio5, P Conti6.
Abstract
Chimeric antigen receptor (CAR) T cells are genetically modified T cells that act against cancer. When CAR-T cells are administered they can trigger inflammatory cytokines and increase toxicity. Interleukin (IL)-1 is the classic cytokine that mediates inflammatory reactions including those that occur in CAR-T-cell therapy. IL-1 also induces IL-33 in mast cells (MCs), amplifying the allergic reaction. IL- 37 (ILF7) is an IL-1 family member which binds IL-18 receptor alpha (IL-18Rα) chain and suppresses innate and acquired immunity. IL-37 is an anti-inflammatory cytokine which inhibits pro-inflammatory cytokines including IL-1 and IL-33. Here, we hypothesize that inflammation and toxicity generated in tumor CAR-T therapy could be inhibited by IL-37, contributing to an improvement in the treatment of tumors with CAR-T therapy. Copyright 2019 Biolife Sas. www.biolifesas.org full article.Entities:
Keywords: CAR-T therapy; chimeric antigen receptor ; cytokines; mast cells
Year: 2019 PMID: 31920059 DOI: 10.23812/EditorialCaraffa
Source DB: PubMed Journal: J Biol Regul Homeost Agents ISSN: 0393-974X Impact factor: 1.711