Cancer immunotherapy by γδ T cells

被引:5
|
作者
Hayday, Adrian [1 ,2 ,3 ]
Dechanet-Merville, Julie [4 ]
Rossjohn, Jamie [5 ,6 ,7 ]
Silva-Santos, Bruno [8 ]
机构
[1] Francis Crick Inst, London, England
[2] Kings Coll London, Peter Gorer Dept Immunobiol, London, England
[3] CRUK City London Canc Ctr, London, England
[4] Univ Bordeaux, Ctr Natl Rech Sci, Unitn Mixte Rech 5164, ImmunoConcEpT, Bordeaux, France
[5] Monash Univ, Biomed Discovery Inst, Infect & Immun Program, Clayton, Vic, Australia
[6] Monash Univ, Biomed Discovery Inst, Dept Biochem & Mol Biol, Clayton, Vic, Australia
[7] Cardiff Univ, Inst Infect & Immun, Sch Med, Heath Pk, Cardiff, Wales
[8] Univ Lisbon, Fac Med, Inst Med Mol Joao Lobo Antunes, Lisbon, Portugal
基金
英国惠康基金; 英国医学研究理事会;
关键词
BUTYROPHILIN BTN; ANTIGEN RECEPTOR; IMMUNE-RESPONSE; TCR; RECOGNITION; ACTIVATION; GENERATION; MOLECULES; INFECTION; EXPANSION;
D O I
10.1126/science.abq7248
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The premise of cancer immunotherapy is that cancers are specifically visible to an immune system tolerized to healthy self. The promise of cancer immunotherapy is that immune effector mechanisms and immunological memory can jointly eradicate cancers and inoperable metastases and de facto vaccinate against recurrence. For some patients with hitherto incurable diseases, including metastatic melanoma, this promise is being realized by game-changing immunotherapies based on alpha beta T cells. Today's challenges are to bring benefit to greater numbers of patients of diverse ethnicities, target more cancer types, and achieve a cure while incurring fewer adverse events. In meeting those challenges, specific benefits may be offered by gamma delta T cells, which compose a second T cell lineage with distinct recognition capabilities and functional traits that bridge innate and adaptive immunity. gamma delta T cell-based clinical trials, including off-the-shelf adoptive cell therapy and agonist antibodies, are yielding promising results, although identifiable problems remain. In addressing those problems, we advocate that immunotherapies be guided by the distinctive biology of gamma delta T cells, as elucidated by ongoing research.
引用
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页数:11
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