Recent advances in T-cell immunotherapy for haematological malignancies

被引:21
作者
Rouce, Rayne H. [1 ,2 ,3 ,4 ]
Sharma, Sandhya [1 ,2 ]
Huynh, Mai [1 ,2 ]
Heslop, Helen E. [1 ,2 ]
机构
[1] Baylor Coll Med, Ctr Cell & Gene Therapy, Houston Methodist Hosp, 1102 Bates St,Suite 1640, Houston, TX 77030 USA
[2] Texas Childrens Hosp, 1102 Bates St,Suite 1640, Houston, TX 77030 USA
[3] Baylor Coll Med, Texas Childrens Canc Ctr, Houston, TX 77030 USA
[4] Baylor Coll Med, Hematol Ctr, Houston, TX 77030 USA
关键词
immunotherapy; T cells; lymphoma; CHIMERIC ANTIGEN RECEPTOR; ACUTE MYELOID-LEUKEMIA; B-CELL; ADOPTIVE IMMUNOTHERAPY; LYMPHOPROLIFERATIVE DISORDERS; MATURATION ANTIGEN; DONOR LYMPHOCYTES; VIRAL-INFECTIONS; THERAPY; TUMOR;
D O I
10.1111/bjh.14470
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In vitro discoveries have paved the way for bench-to-bedside translation in adoptive T cell immunotherapy, resulting in remarkable clinical responses in a variety of haematological malignancies. Adoptively transferred T cells genetically modified to express CD19 CARs have shown great promise, although many unanswered questions regarding how to optimize T-cell therapies for both safety and efficacy remain. Similarly, T cells that recognize viral or tumour antigens though their native receptors have produced encouraging clinical responses. Honing manufacturing processes will increase the availability of T-cell products, while combining T-cell therapies has the ability to increase complete response rates. Lastly, innovative mechanisms to control these therapies may improve safety profiles while genome editing offers the prospect of modulating T-cell function. This review will focus on recent advances in T-cell immunotherapy, highlighting both clinical and pre-clinical advances, as well as exploring what the future holds.
引用
收藏
页码:688 / 704
页数:17
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