Affiliation:
1. Division of Biomedical Sciences, School of Medicine, University of California—Riverside, Riverside, California, USA
2. Cardiovascular Research Institute, University of California—San Francisco, San Francisco, California, USA
Abstract
ABSTRACT
Resistin-like molecules (RELMs) are highly expressed following helminth infection, where they impact both the host and helminth. While RELMα (
Retnla
) impairs helminth expulsion by inhibiting protective Th2 immunity, RELMβ (
Retnlb
) can promote its expulsion. We employed
Retnla
−/−
and
Retnlb
−/−
mice to delineate the function of both proteins following infection with
Nippostrongylus brasiliensis
, a hookworm that infects the lung and intestine. Whereas wild-type (WT) and
Retnlb
−/−
mice exhibited equivalent infection-induced inflammation,
Retnla
−/−
mice suffered a heightened inflammatory response, including increased mortality, weight loss, and lung inflammation. In the intestine,
Retnla
−/−
mice had low parasite egg burdens compared to those of WT mice, while
Retnlb
−/−
mice exhibited high egg burdens, suggesting that RELMα and RELMβ have functionally distinct effects on immunity and inflammation to
N. brasiliensis
. To test the importance of both proteins, we generated
Retnla
−/−
Retnlb
−/−
mice. Infected
Retnla
−/−
Retnlb
−/−
mice exhibited similar responses to
Retnla
−/−
mice, including increased mortality and lung inflammation. This inflammatory response in
Retnla
−/−
Retnlb
−/−
mice negatively impacted
N. brasiliensis
fitness, as demonstrated by significantly lower worm ATP levels and decreased intestinal worm burden and fecundity. Lung cytokine analysis revealed that
Retnla
−/−
and
Retnla
−/−
Retnlb
−/−
mice expressed significantly increased levels of interleukin-4 (IL-4). Finally, we generated
Retnla
−/−
mice on the
Rag
−/−
background and observed that the effects of RELMα were abrogated in the absence of adaptive immunity. Together, these data demonstrate that RELMα but not RELMβ significantly impacts the immune response to
N. brasiliensis
infection by downregulating the Th2 adaptive immune response in the lung, which protects the host but allows improved parasite fitness.
Funder
Office of Extramural Research, National Institutes of Health
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
36 articles.
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