author_facet Pillai, Shiv
Netravali, Ilka Arun
Cariappa, Annaiah
Mattoo, Hamid
Pillai, Shiv
Netravali, Ilka Arun
Cariappa, Annaiah
Mattoo, Hamid
author Pillai, Shiv
Netravali, Ilka Arun
Cariappa, Annaiah
Mattoo, Hamid
spellingShingle Pillai, Shiv
Netravali, Ilka Arun
Cariappa, Annaiah
Mattoo, Hamid
Annual Review of Immunology
Siglecs and Immune Regulation
Immunology
Immunology and Allergy
author_sort pillai, shiv
spelling Pillai, Shiv Netravali, Ilka Arun Cariappa, Annaiah Mattoo, Hamid 0732-0582 1545-3278 Annual Reviews Immunology Immunology and Allergy http://dx.doi.org/10.1146/annurev-immunol-020711-075018 <jats:p> Sialic acid–binding Ig-like lectins, or Siglecs, vary in their specificity for sialic acid–containing ligands and are mainly expressed by cells of the immune system. Many Siglecs are inhibitory receptors expressed in innate immune cells that regulate inflammation mediated by damage-associated and pathogen-associated molecular patterns (DAMPs and PAMPs). This family also includes molecules involved in adhesion and phagocytosis and receptors that can associate with the ITAM-containing DAP12 adaptor. Siglecs contribute to the inhibition of immune cells both by binding to cis ligands (expressed in the same cells) and by responding to pathogen-derived sialoglycoconjugates. They can help maintain tolerance in B lymphocytes, modulate the activation of conventional and plasmacytoid dendritic cells, and contribute to the regulation of T cell function both directly and indirectly. Siglecs modulate immune responses, influencing almost every cell in the immune system, and are of relevance both in health and disease. </jats:p> Siglecs and Immune Regulation Annual Review of Immunology
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title Siglecs and Immune Regulation
title_unstemmed Siglecs and Immune Regulation
title_full Siglecs and Immune Regulation
title_fullStr Siglecs and Immune Regulation
title_full_unstemmed Siglecs and Immune Regulation
title_short Siglecs and Immune Regulation
title_sort siglecs and immune regulation
topic Immunology
Immunology and Allergy
url http://dx.doi.org/10.1146/annurev-immunol-020711-075018
publishDate 2012
physical 357-392
description <jats:p> Sialic acid–binding Ig-like lectins, or Siglecs, vary in their specificity for sialic acid–containing ligands and are mainly expressed by cells of the immune system. Many Siglecs are inhibitory receptors expressed in innate immune cells that regulate inflammation mediated by damage-associated and pathogen-associated molecular patterns (DAMPs and PAMPs). This family also includes molecules involved in adhesion and phagocytosis and receptors that can associate with the ITAM-containing DAP12 adaptor. Siglecs contribute to the inhibition of immune cells both by binding to cis ligands (expressed in the same cells) and by responding to pathogen-derived sialoglycoconjugates. They can help maintain tolerance in B lymphocytes, modulate the activation of conventional and plasmacytoid dendritic cells, and contribute to the regulation of T cell function both directly and indirectly. Siglecs modulate immune responses, influencing almost every cell in the immune system, and are of relevance both in health and disease. </jats:p>
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author Pillai, Shiv, Netravali, Ilka Arun, Cariappa, Annaiah, Mattoo, Hamid
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description <jats:p> Sialic acid–binding Ig-like lectins, or Siglecs, vary in their specificity for sialic acid–containing ligands and are mainly expressed by cells of the immune system. Many Siglecs are inhibitory receptors expressed in innate immune cells that regulate inflammation mediated by damage-associated and pathogen-associated molecular patterns (DAMPs and PAMPs). This family also includes molecules involved in adhesion and phagocytosis and receptors that can associate with the ITAM-containing DAP12 adaptor. Siglecs contribute to the inhibition of immune cells both by binding to cis ligands (expressed in the same cells) and by responding to pathogen-derived sialoglycoconjugates. They can help maintain tolerance in B lymphocytes, modulate the activation of conventional and plasmacytoid dendritic cells, and contribute to the regulation of T cell function both directly and indirectly. Siglecs modulate immune responses, influencing almost every cell in the immune system, and are of relevance both in health and disease. </jats:p>
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spelling Pillai, Shiv Netravali, Ilka Arun Cariappa, Annaiah Mattoo, Hamid 0732-0582 1545-3278 Annual Reviews Immunology Immunology and Allergy http://dx.doi.org/10.1146/annurev-immunol-020711-075018 <jats:p> Sialic acid–binding Ig-like lectins, or Siglecs, vary in their specificity for sialic acid–containing ligands and are mainly expressed by cells of the immune system. Many Siglecs are inhibitory receptors expressed in innate immune cells that regulate inflammation mediated by damage-associated and pathogen-associated molecular patterns (DAMPs and PAMPs). This family also includes molecules involved in adhesion and phagocytosis and receptors that can associate with the ITAM-containing DAP12 adaptor. Siglecs contribute to the inhibition of immune cells both by binding to cis ligands (expressed in the same cells) and by responding to pathogen-derived sialoglycoconjugates. They can help maintain tolerance in B lymphocytes, modulate the activation of conventional and plasmacytoid dendritic cells, and contribute to the regulation of T cell function both directly and indirectly. Siglecs modulate immune responses, influencing almost every cell in the immune system, and are of relevance both in health and disease. </jats:p> Siglecs and Immune Regulation Annual Review of Immunology
spellingShingle Pillai, Shiv, Netravali, Ilka Arun, Cariappa, Annaiah, Mattoo, Hamid, Annual Review of Immunology, Siglecs and Immune Regulation, Immunology, Immunology and Allergy
title Siglecs and Immune Regulation
title_full Siglecs and Immune Regulation
title_fullStr Siglecs and Immune Regulation
title_full_unstemmed Siglecs and Immune Regulation
title_short Siglecs and Immune Regulation
title_sort siglecs and immune regulation
title_unstemmed Siglecs and Immune Regulation
topic Immunology, Immunology and Allergy
url http://dx.doi.org/10.1146/annurev-immunol-020711-075018