Review: Impact of Helminth Infection on Antimycobacterial Immunity—A Focus on the Macrophage

Successful immune control of (MTB) requires robust CD4 T cell responses, with IFNγs as the key cytokine promoting killing of intracellular mycobacteria by macrophages. By contrast, helminth infections typically direct the immune system toward a type 2 response, characterized by high levels of the cy...

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Bibliographic Details
Published inFrontiers in immunology Vol. 8; p. 1864
Main Authors Lang, Roland, Schick, Judith
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 22.12.2017
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ISSN1664-3224
1664-3224
DOI10.3389/fimmu.2017.01864

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Summary:Successful immune control of (MTB) requires robust CD4 T cell responses, with IFNγs as the key cytokine promoting killing of intracellular mycobacteria by macrophages. By contrast, helminth infections typically direct the immune system toward a type 2 response, characterized by high levels of the cytokines IL-4 and IL-10, which can antagonize IFNγ production and its biological effects. In many countries with high burden of tuberculosis, helminth infections are endemic and have been associated with increased risk to develop tuberculosis or to inhibit vaccination-induced immunity. Mechanistically, regulation of the antimycobacterial immune response by helminths has been mostly been attributed to the T cell compartment. Here, we review the current status of the literature on the impact of helminths on vaccine-induced and natural immunity to MTB with a focus on the alterations enforced on the capacity of macrophages to function as sensors of mycobacteria and effector cells to control their replication.
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Edited by: Ulrich Emil Schaible, Forschungszentrum Borstel (LG), Germany
Reviewed by: Subash Babu, International Centers for Excellence in Research (NIH), India; Thomas Jacobs, Bernhard-Nocht-Institut für Tropenmedizin, Germany
Specialty section: This article was submitted to Microbial Immunology, a section of the journal Frontiers in Immunology
ORCID ID: orcid.org/0000-0003-0502-3677
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2017.01864