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

Authors :
Radhakrishnan, Sabarinath V.
Luetkens, Tim
Scherer, Sandra D.
Davis, Patricia
Vander Mause, Erica R.
Olson, Michael L.
Yousef, Sara
Panse, Jens
Abdiche, Yasmina
Li, K. David
Miles, Rodney R.
Matsui, William
Welm, Alana L.
Atanackovic, Djordje
Source :
Nature Communications; 2/7/2020, Vol. 11 Issue 1, p1-9, 9p
Publication Year :
2020

Abstract

Multiple 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 CD229<superscript>high</superscript> T cells, they spare functional CD229<superscript>neg/low</superscript> T cells. These findings indicate that CD229 CAR T cells may be an effective treatment for patients with MM. CD229 is expressed on the surface of multiple myeloma cells, as well as B and T lymphocytes. Here, the authors engineer CD229-specific CAR T cells and, using patient samples and mouse models, show that treatment with these cells reduces tumour burden and results in limited targeting of T cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
11
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
141597019
Full Text :
https://doi.org/10.1038/s41467-020-14619-z