CAR T cells targeting CD99 as an approach to eradicate T-cell acute lymphoblastic leukemia without normal blood cells toxicity

CAR T cell therapy has shown dramatic clinical success in relapsed or refractory B-ALL and other hematological malignancies. However, the loss of specific antigens, cell fratricide, T cell aplasia, and normal T cell separation are challenges in treating T cell leukemia/lymphoma with CAR T therapy. C...

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Veröffentlicht in:Journal of hematology and oncology 2021-10, Vol.14 (1), p.1-162, Article 162
Hauptverfasser: Shi, Jiangzhou, Zhang, Zijian, Cen, Hong, Wu, Han, Zhang, Shangkun, Liu, Jiaxing, Leng, Yingqi, Ren, Anqi, Liu, Xiyu, Zhang, Zhijie, Tong, Xiqin, Liang, Jinjue, Li, Zhe, Zhou, Fuling, Huang, Liang, Qin, You, Yang, Kunyu, Zhang, Tongcun, Zhu, Haichuan
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Sprache:eng
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Zusammenfassung:CAR T cell therapy has shown dramatic clinical success in relapsed or refractory B-ALL and other hematological malignancies. However, the loss of specific antigens, cell fratricide, T cell aplasia, and normal T cell separation are challenges in treating T cell leukemia/lymphoma with CAR T therapy. CD99 is a promising antigen to target T-ALL and AML as it is strongly expressed on the majority of T-ALL and AML. Here, we isolated a low-affinity CD99 (12E7) antibody, which specifically recognizes leukemia cells over normal blood cells. Moreover, T cells transduced with an anti-CD99-specific CAR that contained the 12E7 scFv expanded with minor fratricide and without normal blood cells toxicity. We observed that our anti-CD99 CAR T cells showed robust cytotoxicity specifically against CD99+ T-ALL cell lines and primary tumor cells in vitro and significantly prolonged cell line-derived xenografts (CDXs) or patient-derived xenografts (PDXs) models survival in vivo. Together, our results demonstrate that anti-CD99 CAR T cells could specifically recognize and efficiently eliminate CD99+ leukemia cells.
ISSN:1756-8722
1756-8722
DOI:10.1186/s13045-021-01178-z