Cellular Immunotherapy Program, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts.
Blood Cancer Discov. 2022 Nov 2;3(6):478-480. doi: 10.1158/2643-3230.BCD-22-0126.
In this issue of Blood Cancer Discovery, Dhodapkar and colleagues find that myeloid, dendritic, and endogenous T-cell populations in the bone marrow microenvironment are associated with progression-free survival (PFS) in multiple myeloma patients responding to B-cell maturation antigen-targeted CAR T cells. Immunosuppressive myeloid cells are associated with short PFS, but a diverse T-cell receptor repertoire and more dendritic cells are associated with a longer PFS, suggesting a potential role for epitope spreading. See related article by Dhodapkar et al., p. 490 (6).
在本期《Blood Cancer Discovery》中,Dhodapkar 及其同事发现,骨髓微环境中的髓样细胞、树突状细胞和内源性 T 细胞群体与接受 B 细胞成熟抗原靶向嵌合抗原受体 T 细胞治疗后多发性骨髓瘤患者的无进展生存期(PFS)相关。抑制性髓样细胞与 PFS 较短相关,但多样性 T 细胞受体库和更多的树突状细胞与 PFS 较长相关,这表明表位扩展可能发挥作用。见 Dhodapkar 等人的相关文章,第 490 页(6)。