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SLAM Family Receptor Signaling in Viral Infections: HIV and Beyond

The signaling lymphocytic activation molecule (SLAM) family of receptors are expressed on the majority of immune cells. These receptors often serve as self-ligands, and play important roles in cellular communication and adhesion, thus modulating immune responses. SLAM family receptor signaling is di...

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Autores principales: O’Connell, Patrick, Amalfitano, Andrea, Aldhamen, Yasser A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963180/
https://www.ncbi.nlm.nih.gov/pubmed/31744090
http://dx.doi.org/10.3390/vaccines7040184
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author O’Connell, Patrick
Amalfitano, Andrea
Aldhamen, Yasser A.
author_facet O’Connell, Patrick
Amalfitano, Andrea
Aldhamen, Yasser A.
author_sort O’Connell, Patrick
collection PubMed
description The signaling lymphocytic activation molecule (SLAM) family of receptors are expressed on the majority of immune cells. These receptors often serve as self-ligands, and play important roles in cellular communication and adhesion, thus modulating immune responses. SLAM family receptor signaling is differentially regulated in various immune cell types, with responses generally being determined by the presence or absence of two SLAM family adaptor proteins—Ewing’s sarcoma-associated transcript 2 (EAT-2) and SLAM-associated adaptor protein (SAP). In addition to serving as direct regulators of the immune system, certain SLAM family members have also been identified as direct targets for specific microbes and viruses. Here, we will discuss the known roles for these receptors in the setting of viral infection, with special emphasis placed on HIV infection. Because HIV causes such complex dysregulation of the immune system, studies of the roles for SLAM family receptors in this context are particularly exciting.
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spelling pubmed-69631802020-01-27 SLAM Family Receptor Signaling in Viral Infections: HIV and Beyond O’Connell, Patrick Amalfitano, Andrea Aldhamen, Yasser A. Vaccines (Basel) Review The signaling lymphocytic activation molecule (SLAM) family of receptors are expressed on the majority of immune cells. These receptors often serve as self-ligands, and play important roles in cellular communication and adhesion, thus modulating immune responses. SLAM family receptor signaling is differentially regulated in various immune cell types, with responses generally being determined by the presence or absence of two SLAM family adaptor proteins—Ewing’s sarcoma-associated transcript 2 (EAT-2) and SLAM-associated adaptor protein (SAP). In addition to serving as direct regulators of the immune system, certain SLAM family members have also been identified as direct targets for specific microbes and viruses. Here, we will discuss the known roles for these receptors in the setting of viral infection, with special emphasis placed on HIV infection. Because HIV causes such complex dysregulation of the immune system, studies of the roles for SLAM family receptors in this context are particularly exciting. MDPI 2019-11-16 /pmc/articles/PMC6963180/ /pubmed/31744090 http://dx.doi.org/10.3390/vaccines7040184 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
O’Connell, Patrick
Amalfitano, Andrea
Aldhamen, Yasser A.
SLAM Family Receptor Signaling in Viral Infections: HIV and Beyond
title SLAM Family Receptor Signaling in Viral Infections: HIV and Beyond
title_full SLAM Family Receptor Signaling in Viral Infections: HIV and Beyond
title_fullStr SLAM Family Receptor Signaling in Viral Infections: HIV and Beyond
title_full_unstemmed SLAM Family Receptor Signaling in Viral Infections: HIV and Beyond
title_short SLAM Family Receptor Signaling in Viral Infections: HIV and Beyond
title_sort slam family receptor signaling in viral infections: hiv and beyond
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963180/
https://www.ncbi.nlm.nih.gov/pubmed/31744090
http://dx.doi.org/10.3390/vaccines7040184
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