A Switch Protein Adapter for Anti‐LILRB4 CAR‐T Cells

Chimeric antigen receptor-T cell (CAR-T) immunotherapy has shown remarkable results for the treatment of certain hematologic malignancies. A redirection strategy that utilizes clinically relevant CAR-T cells in combination with adapter proteins may be an effective strategy to target other hematologic and solid cancers. We established a fusion antibody-based strategy with flexibility to target multiple tumor types in combination with a novel anti-leukocyte immunoglobulin-like receptor-B 4 (LILRB4) CAR-T cell. Specifically, we engineered switch protein (SwP) adapters containing the LILRB4 extracellular domain fused to either an anti-CD19 or anti-CD20 single-chain variable fragment (scFv). These SwPs were sufficient to stimulate anti-LILRB4 CAR-T cells against SwP-tagged LILRB4<sup>-</sup>CD19<sup>+</sup> and LILRB4<sup>-</sup>CD20<sup>+</sup> cancers in vitro and in vivo. This strategy may allow CAR-T cells to be redirected against a variety of tumor antigens and cancer types and become a valuable approach to expand the impact of cellular immunotherapy.

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Institutions

Publication Details

Journal
European Journal of Immunology
Published
2024-12-11
DOI
https://doi.org/10.1002/eji.202451172
Citations
1
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.28

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article

A Switch Protein Adapter for Anti‐LILRB4 CAR‐T Cells

Samuel John, Zhiqiang An, Heyu Chen, Ryan Huang et al.
1 citations
European Journal of Immunology
CAR-T cell therapy research
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article

A Switch Protein Adapter for Anti‐LILRB4 CAR‐T Cells

Samuel John, Zhiqiang An, Heyu Chen, Ryan Huang, Lingxiao Tan, Jingjing Xie, Qi Lou, Ningyan Zhang, Cheng Cheng Zhang
article en
1 citations

Abstract

Chimeric antigen receptor-T cell (CAR-T) immunotherapy has shown remarkable results for the treatment of certain hematologic malignancies. A redirection strategy that utilizes clinically relevant CAR-T cells in combination with adapter proteins may be an effective strategy to target other hematologic and solid cancers. We established a fusion antibody-based strategy with flexibility to target multiple tumor types in combination with a novel anti-leukocyte immunoglobulin-like receptor-B 4 (LILRB4) CAR-T cell. Specifically, we engineered switch protein (SwP) adapters containing the LILRB4 extracellular domain fused to either an anti-CD19 or anti-CD20 single-chain variable fragment (scFv). These SwPs were sufficient to stimulate anti-LILRB4 CAR-T cells against SwP-tagged LILRB4<sup>-</sup>CD19<sup>+</sup> and LILRB4<sup>-</sup>CD20<sup>+</sup> cancers in vitro and in vivo. This strategy may allow CAR-T cells to be redirected against a variety of tumor antigens and cancer types and become a valuable approach to expand the impact of cellular immunotherapy.

European Journal of ImmunologyVol. 55(2)
Brown Foundation (US), The University of Texas Southwestern Medical Center (US)
U.S. Department of Defense, Leukemia and Lymphoma Society, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 33%
CAR-T cell therapy research
0.28
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