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Regulatory T Cells Contribute to Resistance against Lyme Arthritis. Infect Immun 2020 Oct 19;88(11)

Date

08/12/2020

Pubmed ID

32778610

Pubmed Central ID

PMC7573436

DOI

10.1128/IAI.00160-20

Scopus ID

2-s2.0-85093883170 (requires institutional sign-in at Scopus site)   6 Citations

Abstract

The symptoms of Lyme disease are caused by inflammation induced by species of the Borrelia burgdorferisensu lato complex. The various presentations of Lyme disease in the population suggest that differences exist in the intensity and regulation of the host response to the spirochete. Previous work has described correlations between the presence of regulatory T cells and recovery from Lyme arthritis. However, the effects of Foxp3-expressing CD4+ T cells existing prior to, and during, B. burgdorferi infection have not been well characterized. Here, we used C57BL/6 "depletion of regulatory T cell" mice to assess the effects these cells have on the arthritis-resistant phenotype characteristic of this mouse strain. We showed that depletion of regulatory T cells prior to infection with B. burgdorferi resulted in sustained swelling, as well as histopathological changes, of the tibiotarsal joints that were not observed in infected control mice. Additionally, in vitro stimulation of splenocytes from these regulatory T cell-depleted mice resulted in increases in gamma interferon and interleukin-17 production and decreases in interleukin-10 production that were not evident among splenocytes of infected mice in which Treg cells were not depleted. Depletion of regulatory T cells at various times after infection also induced rapid joint swelling. Collectively, these findings provide evidence that regulatory T cells existing at the time of, and possibly after, B. burgdorferi infection may play an important role in limiting the development of arthritis.

Author List

Siebers EM, Liedhegner ES, Lawlor MW, Schell RF, Nardelli DT

Author

Michael W. Lawlor MD, PhD Adjunct Professor in the Pathology department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Animals
Borrelia burgdorferi
Female
Lyme Disease
Male
Mice
Mice, Inbred C57BL
T-Lymphocytes, Regulatory