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γδ T cells in cancer: a small population of lymphocytes with big implications
- Source :
- Clinical & Translational Immunology, Clinical & Translational Immunology, Vol 8, Iss 10, Pp n/a-n/a (2019)
- Publication Year :
- 2019
- Publisher :
- Wiley, 2019.
-
Abstract
- γδ T cells are a small population of mostly tissue‐resident lymphocytes, with both innate and adaptive properties. These unique features make them particularly attractive candidates for the development of new cellular therapy targeted against tumor development. Nevertheless, γδ T cells may play dual roles in cancer, promoting cancer development on the one hand, while participating in antitumor immunity on the other hand. In mice, γδ T‐cell subsets preferentially produce IL‐17 or IFN‐γ. While antitumor functions of murine γδ T cells can be attributed to IFN‐γ+ γδ T cells, recent studies have implicated IL‐17+ γδ T cells in tumor growth and metastasis. However, in humans, IL‐17‐producing γδ T cells are rare and most studies have attributed a protective role to γδ T cells against cancer. In this review, we will present the current knowledge and most recent findings on γδ T‐cell functions in mouse models of tumor development and human cancers. We will also discuss their potential as cellular immunotherapy against cancer.
- Subjects :
- lcsh:Immunologic diseases. Allergy
0301 basic medicine
Special Feature Reviews
antitumor immunity
medicine.medical_treatment
Immunology
Population
tumor progression
Biology
γδ T cells
Metastasis
Cell therapy
03 medical and health sciences
0302 clinical medicine
Special Feature Review
CAR T‐cells
DOT cells
medicine
Immunology and Allergy
education
General Nursing
education.field_of_study
Antitumor immunity
Cancer
Immunotherapy
medicine.disease
3. Good health
030104 developmental biology
Tumor progression
030220 oncology & carcinogenesis
immunotherapy
Cellular immunotherapy
lcsh:RC581-607
Subjects
Details
- ISSN :
- 20500068
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- Clinical & Translational Immunology
- Accession number :
- edsair.doi.dedup.....b50e63d908ae78fbc953058cf1a71c90