Modulation of Alloimmunity by Heat Shock Proteins

The immunological mechanisms that evolved for host defense against pathogens and injury are also responsible for transplant rejection. Host rejection of foreign tissue was originally thought to be mediated mainly by T cell recognition of foreign MHC alleles. Management of solid organ transplant reje...

Full description

Bibliographic Details
Main Authors: Borges, Thiago J., Lang, Benjamin J., Lopes, Rafael L., Bonorino, Cristina
Format: Online
Language:English
Published: Frontiers Media S.A. 2016
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977877/
id pubmed-4977877
recordtype oai_dc
spelling pubmed-49778772016-08-23 Modulation of Alloimmunity by Heat Shock Proteins Borges, Thiago J. Lang, Benjamin J. Lopes, Rafael L. Bonorino, Cristina Immunology The immunological mechanisms that evolved for host defense against pathogens and injury are also responsible for transplant rejection. Host rejection of foreign tissue was originally thought to be mediated mainly by T cell recognition of foreign MHC alleles. Management of solid organ transplant rejection has thus focused mainly on inhibition of T cell function and matching MHC alleles between donor and host. Recently, however, it has been demonstrated that the magnitude of the initial innate immune responses upon transplantation has a decisive impact on rejection. The exact mechanisms underlying this phenomenon have yet to be characterized. Ischemic cell death and inflammation that occur upon transplantation are synonymous with extracellular release of various heat shock proteins (Hsps), many of which have been shown to have immune-modulatory properties. Here, we review the impact of Hsps upon alloimmunity and discuss the potential use of Hsps as accessory agents to improve solid organ transplant outcomes. Frontiers Media S.A. 2016-08-09 /pmc/articles/PMC4977877/ /pubmed/27555846 http://dx.doi.org/10.3389/fimmu.2016.00303 Text en Copyright © 2016 Borges, Lang, Lopes and Bonorino. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Borges, Thiago J.
Lang, Benjamin J.
Lopes, Rafael L.
Bonorino, Cristina
spellingShingle Borges, Thiago J.
Lang, Benjamin J.
Lopes, Rafael L.
Bonorino, Cristina
Modulation of Alloimmunity by Heat Shock Proteins
author_facet Borges, Thiago J.
Lang, Benjamin J.
Lopes, Rafael L.
Bonorino, Cristina
author_sort Borges, Thiago J.
title Modulation of Alloimmunity by Heat Shock Proteins
title_short Modulation of Alloimmunity by Heat Shock Proteins
title_full Modulation of Alloimmunity by Heat Shock Proteins
title_fullStr Modulation of Alloimmunity by Heat Shock Proteins
title_full_unstemmed Modulation of Alloimmunity by Heat Shock Proteins
title_sort modulation of alloimmunity by heat shock proteins
description The immunological mechanisms that evolved for host defense against pathogens and injury are also responsible for transplant rejection. Host rejection of foreign tissue was originally thought to be mediated mainly by T cell recognition of foreign MHC alleles. Management of solid organ transplant rejection has thus focused mainly on inhibition of T cell function and matching MHC alleles between donor and host. Recently, however, it has been demonstrated that the magnitude of the initial innate immune responses upon transplantation has a decisive impact on rejection. The exact mechanisms underlying this phenomenon have yet to be characterized. Ischemic cell death and inflammation that occur upon transplantation are synonymous with extracellular release of various heat shock proteins (Hsps), many of which have been shown to have immune-modulatory properties. Here, we review the impact of Hsps upon alloimmunity and discuss the potential use of Hsps as accessory agents to improve solid organ transplant outcomes.
publisher Frontiers Media S.A.
publishDate 2016
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977877/
_version_ 1613624034663071744