Abstract
The programmed death (PD)-1-PD-1 ligand (PD-L) pathway, which is part of the B7-CD28 family, consists of the PD-1 receptor and its two ligands PD-L1 and PD-L2. Engagement of PD-1 by its ligands inhibits immune responses, and recent work has shown that PD-1 is highly expressed on exhausted T cells during chronic lymphocytic choriomeningitis virus (LCMV) infection in mice. Blockade of this pathway reinvigorates the exhausted T cells, allowing them to expand and produce effector cytokines, raising the issue of whether this pathway has been exploited by a variety of viruses during chronic infection. New studies now extend these observations to HIV infection and human disease.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Animals
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Arenaviridae Infections / immunology*
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B7-1 Antigen / immunology
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B7-1 Antigen / metabolism*
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B7-H1 Antigen
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Gene Expression Regulation / immunology*
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HIV Infections / immunology*
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Ligands
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Lymphocytic choriomeningitis virus*
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Membrane Glycoproteins / immunology
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Membrane Glycoproteins / metabolism*
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Mice
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Models, Immunological
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Peptides / immunology
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Peptides / metabolism*
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Signal Transduction / immunology*
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T-Lymphocytes / immunology*
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T-Lymphocytes / metabolism
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T-Lymphocytes / virology
Substances
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B7-1 Antigen
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B7-H1 Antigen
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Cd274 protein, mouse
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Ligands
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Membrane Glycoproteins
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Peptides