| Literature DB >> 29735365 |
Christopher A Pennell1, Jessie L Barnum2, Cameron S McDonald-Hyman2, Angela Panoskaltsis-Mortari2, Megan J Riddle3, Zhengming Xiong4, Michael Loschi2, Govindarajan Thangavelu2, Heather M Campbell5, Meghan D Storlie5, Yosef Refaeli6, Scott N Furlan7, Michael C Jensen7, Leslie S Kean7, Jeffrey S Miller8, Jakub Tolar9, Mark J Osborn2, Bruce R Blazar2.
Abstract
The clinical success of chimeric antigen receptor (CAR) T cell therapy for CD19+ B cell malignancies can be limited by acute toxicities and immunoglobulin replacement needs due to B cell aplasia from persistent CAR T cells. Life-threatening complications include cytokine release syndrome and neurologic adverse events, the exact etiologies of which are unclear. To elucidate the underlying toxicity mechanisms and test potentially safer CAR T cells, we developed a mouse model in which human CD19 (hCD19)-specific mouse CAR T cells were adoptively transferred into mice whose normal B cells express a hCD19 transgene at hemizygous levels. Compared to homozygous hCD19 transgenic mice that have ∼75% fewer circulating B cells, hemizygous mice had hCD19 frequencies and antigen density more closely simulating human B cells. Hemizygous mice given a lethal dose of hCD19 transgene-expressing lymphoma cells and treated with CAR T cells had undetectable tumor levels. Recipients experienced B cell aplasia and antigen- and dose-dependent acute toxicities mirroring patient complications. Interleukin-6 (IL-6), interferon γ (IFN-γ), and inflammatory pathway transcripts were enriched in affected tissues. As in patients, antibody-mediated neutralization of IL-6 (and IFN-γ) blunted toxicity. Apparent behavioral abnormalities associated with decreased microglial cells point to CAR-T-cell-induced neurotoxicity. This model will prove useful in testing strategies designed to improve hCD19-specific CAR T cell safety.Entities:
Keywords: B cell aplasia; CAR T cell; CD19; cytokine release syndrome; mouse model; neurologic adverse events; toxicity
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Year: 2018 PMID: 29735365 PMCID: PMC5986973 DOI: 10.1016/j.ymthe.2018.04.006
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454