TIGIT-CD155 interactions in melanoma: a novel co-inhibitory pathway with potential for clinical intervention

Inozume et al. describe a novel immunosuppressive mechanism in melanoma that is triggered by the interaction between CD155 (expressed by melanomas) and T-cell Ig and ITIM domain (TIGIT) (expressed by tumor infiltrating lymphocytes). This pathway exists in addition to the "classical" co-inh...

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Bibliographic Details
Main Authors: Mahnke, Karsten (Author) , Enk, Alexander (Author)
Format: Article (Journal)
Language:English
Published: 4 January 2016
In: The journal of investigative dermatology
Year: 2016, Volume: 136, Issue: 1, Pages: 9-11
ISSN:1523-1747
DOI:10.1016/j.jid.2015.10.048
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.jid.2015.10.048
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Author Notes:Karsten Mahnke and Alexander H. Enk
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Summary:Inozume et al. describe a novel immunosuppressive mechanism in melanoma that is triggered by the interaction between CD155 (expressed by melanomas) and T-cell Ig and ITIM domain (TIGIT) (expressed by tumor infiltrating lymphocytes). This pathway exists in addition to the "classical" co-inhibitory PD-1-PD-L1 pathway. Hence, the combinatorial blockage of both pathways by specific antibodies resulted in the greatly enhanced effector function of melanoma-specific cytotoxic T cells. Given that CD155-TIGIT signaling exerts potent inhibitory action in different subsets of immune cells and that CD155 is expressed broadly in several tumor entities, this report points toward a novel and promising therapeutic strategy to combine different checkpoint blocking agents for greater success in antitumor therapy.
Item Description:Gesehen am 22.05.2020
Physical Description:Online Resource
ISSN:1523-1747
DOI:10.1016/j.jid.2015.10.048