CD229 CAR T cells eliminate multiple myeloma and tumor propagating cells without fratricide

Author:

Radhakrishnan Sabarinath V.,Luetkens TimORCID,Scherer Sandra D.,Davis Patricia,Vander Mause Erica R.,Olson Michael L.ORCID,Yousef Sara,Panse Jens,Abdiche Yasmina,Li K. David,Miles Rodney R.,Matsui William,Welm Alana L.,Atanackovic Djordje

Abstract

AbstractMultiple myeloma (MM) is a plasma cell malignancy and most patients eventually succumb to the disease. Chimeric antigen receptor (CAR) T cells targeting B-Cell Maturation Antigen (BCMA) on MM cells have shown high-response rates, but limited durability. CD229/LY9 is a cell surface receptor present on B and T lymphocytes that is universally and strongly expressed on MM plasma cells. Here, we develop CD229 CAR T cells that are highly active in vitro and in vivo against MM plasma cells, memory B cells, and MM-propagating cells. We do not observe fratricide during CD229 CAR T cell production, as CD229 is downregulated in T cells during activation. In addition, while CD229 CAR T cells target normal CD229high T cells, they spare functional CD229neg/low T cells. These findings indicate that CD229 CAR T cells may be an effective treatment for patients with MM.

Funder

American Association for Cancer Research

U.S. Department of Health & Human Services | NIH | National Cancer Institute

National Comprehensive Cancer Network (NCCN) Young Investigator Award

U.S. Department of Defense

U.S. Department of Health & Human Services | NIH | NCI | Division of Cancer Epidemiology and Genetics, National Cancer Institute

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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