CAR T-Cell Therapy: The Role of Physical Barriers and Immunosuppression in Lymphoma

被引:49
|
作者
Enblad, Gunilla [1 ]
Karlsson, Hannah [1 ]
Loskog, Angelica S. I. [1 ]
机构
[1] Uppsala Univ, Dept Immunol Genet & Pathol, Sci Life Lab, S-75185 Uppsala, Sweden
关键词
CHIMERIC ANTIGEN RECEPTOR; CHRONIC LYMPHOCYTIC-LEUKEMIA; TUMOR MICROENVIRONMENT; SUPPRESSOR-CELLS; REGULATORY CELLS; DENDRITIC CELLS; CANCER; MECHANISMS; CARCINOMA; EFFECTOR;
D O I
10.1089/hum.2015.054
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chimeric antigen receptor (CAR) T-cells have shown remarkable results in patients with B-cell leukemia and lymphoma. However, while CAR T-cells have shown complete responses in a majority of patients with acute lymphoblastic leukemia (ALL), lymphomas are more difficult to treat. Different CAR designs and conditioning protocols seem to affect the persistence of patient responses. However, factors that determine if patients receiving the same CARs will respond or not remain obscure. In Sweden, a phase I/IIa trial using third-generation CAR T-cells is ongoing in which we intend to compare tumor biology and immunology, in each patient, to treatment response. CAR T-cell therapy is a powerful tool to add to the treatment options for this patient group but we need to perform the necessary basic research on the multifactorial mechanisms of action to give patients the best possible option of survival. Such studies are also crucial to expand the success of CAR T-cells beyond CD19+ B-cell malignancy. This review will focus on possible barriers of treating lymphoma to define factors that need to be investigated to develop the next generation of CAR T-cell therapy.
引用
收藏
页码:498 / 505
页数:8
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