The Dichotomous Responses Driven by β-Defensins

Defensins are short, rapidly evolving, cationic antimicrobial host defence peptides with a repertoire of functions, still incompletely realised, that extends beyond direct microbial killing. They are released or secreted at epithelial surfaces, and in some cases, from immune cells in response to inf...

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Main Authors: Jennifer R. Shelley, Donald J. Davidson, Julia R. Dorin
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-06-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2020.01176/full
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author Jennifer R. Shelley
Donald J. Davidson
Julia R. Dorin
author_facet Jennifer R. Shelley
Donald J. Davidson
Julia R. Dorin
author_sort Jennifer R. Shelley
collection DOAJ
description Defensins are short, rapidly evolving, cationic antimicrobial host defence peptides with a repertoire of functions, still incompletely realised, that extends beyond direct microbial killing. They are released or secreted at epithelial surfaces, and in some cases, from immune cells in response to infection and inflammation. Defensins have been described as endogenous alarmins, alerting the body to danger and responding to inflammatory signals by promoting both local innate and adaptive systemic immune responses. However, there is now increasing evidence that they exert variable control on the response to danger; creating a dichotomous response that can suppress inflammation in some circumstances but exacerbate the response to danger and damage in others and, at higher levels, lead to a cytotoxic effect. Focussing in this review on human β-defensins, we discuss the evidence for their functions as proinflammatory, immune activators amplifying the response to infection or damage signals and/or as mediators of resolution of damage, contributing to a return to homeostasis. Finally, we consider their involvement in the development of autoimmune diseases.
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spelling doaj.art-c46953f7446b4265bf20c50baccf682a2022-12-21T18:25:07ZengFrontiers Media S.A.Frontiers in Immunology1664-32242020-06-011110.3389/fimmu.2020.01176542721The Dichotomous Responses Driven by β-DefensinsJennifer R. ShelleyDonald J. DavidsonJulia R. DorinDefensins are short, rapidly evolving, cationic antimicrobial host defence peptides with a repertoire of functions, still incompletely realised, that extends beyond direct microbial killing. They are released or secreted at epithelial surfaces, and in some cases, from immune cells in response to infection and inflammation. Defensins have been described as endogenous alarmins, alerting the body to danger and responding to inflammatory signals by promoting both local innate and adaptive systemic immune responses. However, there is now increasing evidence that they exert variable control on the response to danger; creating a dichotomous response that can suppress inflammation in some circumstances but exacerbate the response to danger and damage in others and, at higher levels, lead to a cytotoxic effect. Focussing in this review on human β-defensins, we discuss the evidence for their functions as proinflammatory, immune activators amplifying the response to infection or damage signals and/or as mediators of resolution of damage, contributing to a return to homeostasis. Finally, we consider their involvement in the development of autoimmune diseases.https://www.frontiersin.org/article/10.3389/fimmu.2020.01176/fullbeta defensinpsoriasisatopic dermatitisautoimmunityimmunomodulationAMP
spellingShingle Jennifer R. Shelley
Donald J. Davidson
Julia R. Dorin
The Dichotomous Responses Driven by β-Defensins
Frontiers in Immunology
beta defensin
psoriasis
atopic dermatitis
autoimmunity
immunomodulation
AMP
title The Dichotomous Responses Driven by β-Defensins
title_full The Dichotomous Responses Driven by β-Defensins
title_fullStr The Dichotomous Responses Driven by β-Defensins
title_full_unstemmed The Dichotomous Responses Driven by β-Defensins
title_short The Dichotomous Responses Driven by β-Defensins
title_sort dichotomous responses driven by β defensins
topic beta defensin
psoriasis
atopic dermatitis
autoimmunity
immunomodulation
AMP
url https://www.frontiersin.org/article/10.3389/fimmu.2020.01176/full
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