Immunotherapy for acute myeloid leukemia: from allogeneic stem cell transplant to novel therapeutics

被引:2
|
作者
Knorr, David A. [1 ,2 ]
Goldberg, Aaron D. [1 ]
Stein, Eytan M. [1 ]
Tallman, Martin S. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Leukemia Serv, 1275 York Ave, New York, NY 10021 USA
[2] Rockefeller Univ, Lab Mol Genet & Immunol, 1230 York Ave, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
Immunotherapy; AML; antibodies; vaccines; T cells; neoantigen; checkpoint blockade; MINIMAL RESIDUAL DISEASE; REGULATORY T-CELLS; IMMUNE CHECKPOINT BLOCKADE; ACUTE MYELOGENOUS LEUKEMIA; WT1 PEPTIDE VACCINATION; CANCER TESTIS ANTIGEN; NATURAL-KILLER-CELLS; PD-1; BLOCKADE; CTLA-4; NK CELLS;
D O I
10.1080/10428194.2019.1639167
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunotherapy in the form of allogeneic stem cell transplantation (SCT) plays an instrumental role in the treatment of acute myeloid leukemia (AML), with non-transplant modalities of immunotherapy including checkpoint blockade now being actively explored. Here, we provide an overview of the graft versus leukemia (GVL) effect in AML as a window into understanding the prospects of AML immunotherapy. We explore the roles of various cell types in orchestrating anti-leukemic immunity, as well as those contributing to the unique immune suppressive state of myeloid diseases. We discuss specific approaches to engage the immune system, while noting the challenges of the AML antigen landscape and the barriers to immune modulation. We review the potential for immunomodulatory agents in combination with cellular therapies, donor lymphocyte infusion, and following SCT. Finally, to address the challenge of minimal residual disease (MRD) following chemotherapy, we propose combination epigenetic and immunotherapy for the eradication of MRD.
引用
收藏
页码:3350 / 3362
页数:13
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