Journal Article Review Research Support, Non-U.S. Gov't Epublish 5 citations
PubMed: 36680187 DOI: 10.3390/v15010147
LAG-3 Contribution to T Cell Downmodulation during Acute Respiratory Viral Infections.
Viruses 15(1)
Authors: Linmar RodrÃguez-Guilarte, Mario A RamÃrez, Catalina A Andrade, Alexis M Kalergis
Affiliations
- Millennium Institute of Immunology and Immunotherapy, Departamento de Genética Molecular y MicrobiologÃa, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
- Departamento de EndocrinologÃa, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Abstract
LAG-3 is a type I transmembrane protein expressed on immune cells, such as activated T cells, and binds to MHC class II with high affinity. LAG-3 is an inhibitory receptor, and its multiple biological activities on T cell activation and effector functions play a regulatory role in the immune response. Immunotherapies directed at immune checkpoints, including LAG-3, have become a promising strategy for controlling malignant tumors and chronic viral diseases. Several studies have suggested an association between the expression of LAG-3 with an inadequate immune response during respiratory viral infections and the susceptibility to reinfections, which might be a consequence of the inhibition of T cell effector functions. However, important information relative to therapeutic potential during acute viral lower respiratory tract infections and the mechanism of action of the LAG-3 checkpoint remains to be characterized. In this article, we discuss the contribution of LAG-3 to the impairment of T cells during viral respiratory infections. Understanding the host immune response to respiratory infections is crucial for developing effective vaccines and therapies.
MeSH
Respiratory Tract Infections, Virus Diseases, Ligands, Virology, Cells, Therapeutics, T-Lymphocytes
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