Antitumor Responses of Invariant Natural Killer T Cells

被引:26
|
作者
Altman, Jennie B. [1 ]
Benavides, Adriana D. [1 ]
Das, Rupali [2 ]
Bassiri, Hamid [1 ]
机构
[1] Childrens Hosp Philadelphia, Div Infect Dis, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Div Oncol Res, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
ALPHA-GALACTOSYLCERAMIDE KRN7000; TRANSCRIPTION FACTOR PLZF; ANTIGEN-PRESENTING CELLS; V(ALPHA)14 NKT CELLS; RAPAMYCIN COMPLEX 1; PHASE-I; DENDRITIC CELLS; CUTTING EDGE; INTERFERON-GAMMA; INKT CELLS;
D O I
10.1155/2015/652875
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural killer T (NKT) cells are innate-like lymphocytes that were first described in the late 1980s. Since their initial description, numerous studies have collectively shed light on their development and effector function. These studies have highlighted the unique requirements for the activation of these lymphocytes and the functional responses that distinguish these cells from other effector lymphocyte populations such as conventional T cells and NK cells. This body of literature suggests that NKT cells play diverse nonredundant roles in a number of disease processes, including the initiation and propagation of airway hyperreactivity, protection against a variety of pathogens, development of autoimmunity, and mediation of allograft responses. In this review, however, we focus on the role of a specific lineage of NKT cells in antitumor immunity. Specifically, we describe the development of invariant NKT (iNKT) cells and the factors that are critical for their acquisition of effector function. Next, we delineate the mechanisms by which iNKT cells influence and modulate the activity of other immune cells to directly or indirectly affect tumor growth. Finally, we review the successes and failures of clinical trials employing iNKT cell-based immunotherapies and explore the future prospects for the use of such strategies.
引用
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页数:10
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