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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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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