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CD155/TIGIT, a novel immune checkpoint in human cancers (Review)

Authors: Lu, Liu; Xuewu, You; Sai, Han; Yu, Sun; Junhua, Zhang; Youzhong, Zhang;

CD155/TIGIT, a novel immune checkpoint in human cancers (Review)

Abstract

CD155/T cell immunoreceptor with Ig and ITIM domains (TIGIT) is a novel type of immune checkpoint. CD155 is an adhesion molecule that is upregulated during tumor progression and promotes the proliferative and migratory abilities of tumor cells via various pathways. TIGIT, an inhibitory receptor, is mainly expressed on natural killer (NK), CD8+ T, CD4+ T and T regulatory (Treg) cells. CD155 transmits immune signals via interacting with the inhibitory checkpoint receptor TIGIT, thereby inhibiting the function of T and NK cells. Several preclinical studies have supported the use of TIGIT blockade as a monotherapy or combined with other immune checkpoint inhibitors for the treatment of advanced solid malignant tumors. The present review summarized the current knowledge on CD155/TIGIT and the lymphocyte‑mediated inhibitory mechanism of CD155/TIGIT. An in‑depth understanding of the role of CD155/TIGIT in tumors may aid to improve the application of immune checkpoint inhibitors in tumor therapy.

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Keywords

CD4-Positive T-Lymphocytes, CD8-Positive T-Lymphocytes, Immune Checkpoint Proteins, Up-Regulation, Gene Expression Regulation, Neoplastic, Killer Cells, Natural, Neoplasms, Antineoplastic Combined Chemotherapy Protocols, Cell Adhesion, Disease Progression, Humans, Receptors, Immunologic, Immune Checkpoint Inhibitors

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Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
63
Top 1%
Top 10%
Top 1%
Related to Research communities
Cancer Research
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