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TIGIT as an emerging immune checkpoint
1Molecular and Integrative Biosciences, Faculty of Biological and Environmental Sciences, The University of Helsinki, Helsinki, Finland.
Clinical and Experimental Immunology
|December 13, 2019
Summary
T cell immunoglobulin and ITIM domain (TIGIT) is a key target in cancer immunotherapy. Blocking TIGIT shows promise for treating various cancers by enhancing anti-tumour immune responses.
Area of Science:
- Immunology
- Oncology
- Cancer Immunotherapy
Background:
- T cell immunoglobulin and ITIM domain (TIGIT) is an inhibitory receptor on lymphocytes.
- TIGIT negatively regulates T cell and natural killer (NK) cell functions by interacting with CD155.
- TIGIT is a significant barrier to effective anti-tumour immune responses in the cancer immunity cycle.
Purpose of the Study:
- To review the current understanding of TIGIT.
- To highlight TIGIT as a promising target in cancer immunotherapy.
- To discuss the clinical development of TIGIT-blocking agents.
Main Methods:
- Literature review of TIGIT research from discovery to clinical trials.
- Analysis of pre-clinical data on TIGIT blockade efficacy.
- Overview of ongoing clinical trials for TIGIT-targeted therapies.
Main Results:
- TIGIT blockade has demonstrated potential in pre-clinical models against solid and hematological cancers.
- Monoclonal antibodies targeting human TIGIT have been developed.
- Clinical trials are evaluating TIGIT blockade, alone or with PD-1/PD-L1 inhibitors, in advanced solid tumors.
Conclusions:
- TIGIT is a critical inhibitory checkpoint in cancer immunity.
- TIGIT-blocking therapies represent a novel and advancing strategy in cancer immunotherapy.
- Further clinical investigation is warranted to establish the efficacy of TIGIT-targeted treatments.
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