Integrating inflammasome signaling in sexually transmitted infections
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Accepted version
Published version
Author(s)
Lupfer, C
Anand, PK
Type
Journal Article
Abstract
Inflammasomes are cytosolic multiprotein platforms with pivotal roles in infectious diseases. Activation of inflammasomes results in pro-inflammatory cytokine signaling and pyroptosis.
Sexually transmitted infections are a major health problem worldwide, yet few studies have probed the impact of inflammasome signaling during these infections. Due to the dearth of appropriate infection models, our current understanding of inflammasomes in sexually
transmitted infections is mostly drawn from results obtained
in vitro, from distant infection sites, or from related microbial strains that are not sexually transmitted. Understanding how
inflammasomes influence the outcome of sexually transmitted infections may lead to the development of novel and effective strategies to control disease and prevent transmission.
Here, we discuss and highlight the recent progress in this field.
Sexually transmitted infections are a major health problem worldwide, yet few studies have probed the impact of inflammasome signaling during these infections. Due to the dearth of appropriate infection models, our current understanding of inflammasomes in sexually
transmitted infections is mostly drawn from results obtained
in vitro, from distant infection sites, or from related microbial strains that are not sexually transmitted. Understanding how
inflammasomes influence the outcome of sexually transmitted infections may lead to the development of novel and effective strategies to control disease and prevent transmission.
Here, we discuss and highlight the recent progress in this field.
Date Issued
2016-08-31
Date Acceptance
2016-08-05
Citation
Trends in Immunology, 2016, 37 (10), pp.703-714
ISSN
1471-4981
Publisher
Elsevier (Cell Press)
Start Page
703
End Page
714
Journal / Book Title
Trends in Immunology
Volume
37
Issue
10
Copyright Statement
© 2016 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Sponsor
The Royal Society
Wellcome Trust
Grant Number
N/A
N/A
Subjects
Immunology
1107 Immunology
Publication Status
Published