Folate Receptor-Alpha Targeted 7x19 CAR-γδT Suppressed Triple-Negative Breast Cancer Xenograft Model in Mice

Author:

Ye Xueshuai12,Deng Xinna2,Wen Junye2,Li Yang13,Zhang Mengya3,Cai Ziqi3,Liu Guan13,Wang Hezhi4,Cai Jianhui12ORCID

Affiliation:

1. Department of Surgery, Hebei Medical University, Shijiazhuang 050051, Hebei Province, China

2. Department of Oncology & Surgery, Hebei General Hospital, Shijiazhuang 050051, Hebei Province, China

3. Hebei Cell Therapy Technology Innovation Center, HOFOY Medicine Hebei Co., LTD, Shijiazhuang 050051, Hebei Province, China

4. Department of Liver Surgery & Transplantation, Liver Cancer Institute, Zhongshan Hospital of Fudan University, Shanghai City 200032, China

Abstract

Background. Triple-negative breast cancer (TNBC) is the worst prognosis subtype of breast cancer due to lack of specific targets. Recent studies have shown that immunotherapy may solve that problem by targeting folate receptor-alpha (FRα). Methods. Gene modified γδ T cells were manufactured to express FRa specific chimeric antigen receptor (FRa CAR) and secrete interleukin-7 (IL-7) and chemokine C–C motif ligand 19 (CCL19). CAR-γδT cells that secrete IL-7 and CCL19 (7 × 19 CAR-γδT) were evaluated for their antitumor activity both in vitro and in vivo. Results. 7 × 19 CAR-γδT showed remarkable antitumor activity in vitro. Combined with PBMC, 7 × 19 CAR-γδT inhibited TNBC xenograft model growth superiorly compared with single-application or conventional CAR-γδT cells. Histopathological analyses showed increased DC or T cells infiltration to tumor tissues. Conclusion. Taken together, our results showed that 7 × 19 CAR-γδT have remarkable anti-TNBC tumor activity and showed a broad application prospect in the treatment of incurable TNBC patients.

Funder

Hebei University of Science and Technology

Publisher

Hindawi Limited

Subject

Oncology

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