The Role of IL-10 in Malaria: A Double Edged Sword

IL-10 produced by CD4+ T cells suppresses inflammation by inhibiting T cell functions and the upstream activities of antigen presenting cells (APCs). IL-10 was first identified in Th2 cells, but has since been described in IFNγ-producing Tbet+ Th1, FoxP3+ CD4+ regulatory T (Treg) and IL-17-producing...

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Main Authors: Rajiv Kumar, Susanna Ng, Christian Engwerda
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-02-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2019.00229/full
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spelling doaj-e30266b384834fc681519dd4030baa952020-11-24T23:41:36ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-02-011010.3389/fimmu.2019.00229422104The Role of IL-10 in Malaria: A Double Edged SwordRajiv Kumar0Rajiv Kumar1Susanna Ng2Christian Engwerda3Department of Biochemistry, Institute of Science, Banaras Hindu University, Varanasi, IndiaCentre of Experimental Medicine and Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi, IndiaImmunology and Infection Lab, QIMR Berghofer Medical Research Institute, Brisbane, QLD, AustraliaImmunology and Infection Lab, QIMR Berghofer Medical Research Institute, Brisbane, QLD, AustraliaIL-10 produced by CD4+ T cells suppresses inflammation by inhibiting T cell functions and the upstream activities of antigen presenting cells (APCs). IL-10 was first identified in Th2 cells, but has since been described in IFNγ-producing Tbet+ Th1, FoxP3+ CD4+ regulatory T (Treg) and IL-17-producing CD4+ T (Th17) cells, as well as many innate and innate-like immune cell populations. IL-10 production by Th1 cells has emerged as an important mechanism to dampen inflammation in the face of intractable infection, including in African children with malaria. However, although these type I regulatory T (Tr1) cells protect tissue from inflammation, they may also promote disease by suppressing Th1 cell-mediated immunity, thereby allowing infection to persist. IL-10 produced by other immune cells during malaria can also influence disease outcome, but the full impact of this IL-10 production is still unclear. Together, the actions of this potent anti-inflammatory cytokine along with other immunoregulatory mechanisms that emerge following Plasmodium infection represent a potential hurdle for the development of immunity against malaria, whether naturally acquired or vaccine-induced. Recent advances in understanding how IL-10 production is initiated and regulated have revealed new opportunities for manipulating IL-10 for therapeutic advantage. In this review, we will summarize our current knowledge about IL-10 production during malaria and discuss its impact on disease outcome. We will highlight recent advances in our understanding about how IL-10 production by specific immune cell subsets is regulated and consider how this knowledge may be used in drug delivery and vaccination strategies to help eliminate malaria.https://www.frontiersin.org/article/10.3389/fimmu.2019.00229/fullIL-10malariaprotozoanT cellsInflammation
collection DOAJ
language English
format Article
sources DOAJ
author Rajiv Kumar
Rajiv Kumar
Susanna Ng
Christian Engwerda
spellingShingle Rajiv Kumar
Rajiv Kumar
Susanna Ng
Christian Engwerda
The Role of IL-10 in Malaria: A Double Edged Sword
Frontiers in Immunology
IL-10
malaria
protozoan
T cells
Inflammation
author_facet Rajiv Kumar
Rajiv Kumar
Susanna Ng
Christian Engwerda
author_sort Rajiv Kumar
title The Role of IL-10 in Malaria: A Double Edged Sword
title_short The Role of IL-10 in Malaria: A Double Edged Sword
title_full The Role of IL-10 in Malaria: A Double Edged Sword
title_fullStr The Role of IL-10 in Malaria: A Double Edged Sword
title_full_unstemmed The Role of IL-10 in Malaria: A Double Edged Sword
title_sort role of il-10 in malaria: a double edged sword
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2019-02-01
description IL-10 produced by CD4+ T cells suppresses inflammation by inhibiting T cell functions and the upstream activities of antigen presenting cells (APCs). IL-10 was first identified in Th2 cells, but has since been described in IFNγ-producing Tbet+ Th1, FoxP3+ CD4+ regulatory T (Treg) and IL-17-producing CD4+ T (Th17) cells, as well as many innate and innate-like immune cell populations. IL-10 production by Th1 cells has emerged as an important mechanism to dampen inflammation in the face of intractable infection, including in African children with malaria. However, although these type I regulatory T (Tr1) cells protect tissue from inflammation, they may also promote disease by suppressing Th1 cell-mediated immunity, thereby allowing infection to persist. IL-10 produced by other immune cells during malaria can also influence disease outcome, but the full impact of this IL-10 production is still unclear. Together, the actions of this potent anti-inflammatory cytokine along with other immunoregulatory mechanisms that emerge following Plasmodium infection represent a potential hurdle for the development of immunity against malaria, whether naturally acquired or vaccine-induced. Recent advances in understanding how IL-10 production is initiated and regulated have revealed new opportunities for manipulating IL-10 for therapeutic advantage. In this review, we will summarize our current knowledge about IL-10 production during malaria and discuss its impact on disease outcome. We will highlight recent advances in our understanding about how IL-10 production by specific immune cell subsets is regulated and consider how this knowledge may be used in drug delivery and vaccination strategies to help eliminate malaria.
topic IL-10
malaria
protozoan
T cells
Inflammation
url https://www.frontiersin.org/article/10.3389/fimmu.2019.00229/full
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