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Prenatal Exposure of Staphylococcal Enterotoxin B Attenuates the Development and Function of Blood Regulatory T Cells to Repeated Staphylococcal Enterotoxin B Exposure in Adult Offspring Rats

Overview
Journal J Med Microbiol
Specialty Microbiology
Date 2020 Feb 12
PMID 32043953
Citations 2
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Abstract

Staphylococcal enterotoxin B (SEB) is an extensively studied super-antigen. A previous study by us suggested that SEB exposure during pregnancy could alter the percentage of CD4 and CD8 T cells in the peripheral blood of neonatal offspring rats. It is unknown whether SEB exposure during pregnancy can influence the development of regulatory T cells (Tregs) in the peripheral blood of neonatal offspring rats. Pregnant rats at gestational day 16 were intravenously injected with 15 µg SEB. Peripheral blood was acquired from neonatal offspring rats on days 1, 3 and 5 after delivery and from adult offspring rats for determination of Treg number by cytometry, cytokines by ELISA, and FoxP3 expression by real-time PCR and western blot. SEB given to pregnant rats significantly increased the absolute number of Tregs and the expression levels of FoxP3, IL-10 and TGF-β (<0.05, <0.01) in the peripheral blood of not only neonatal but also adult offspring rats. Furthermore, repeated SEB exposure in adult offspring rats significantly decreased the absolute number of Tregs (<0.01), and the expression levels of FoxP3, IL-10 and TGF-β (<0.05, <0.01) in their peripheral blood. Prenatal SEB exposure attenuates the development and function of Tregs to repeated SEB exposure in the peripheral blood of adult offspring rats.

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References
1.
Shevach E . From vanilla to 28 flavors: multiple varieties of T regulatory cells. Immunity. 2006; 25(2):195-201. DOI: 10.1016/j.immuni.2006.08.003. View

2.
Miller C, Ragheb J, Schwartz R . Anergy and cytokine-mediated suppression as distinct superantigen-induced tolerance mechanisms in vivo. J Exp Med. 1999; 190(1):53-64. PMC: 2195559. DOI: 10.1084/jem.190.1.53. View

3.
Osborne B, Caulfield J, Solomotis S, Schwarz J . Neonatal infection produces significant changes in immune function with no associated learning deficits in juvenile rats. Dev Neurobiol. 2017; 77(10):1221-1236. PMC: 5777507. DOI: 10.1002/dneu.22512. View

4.
Kawabe Y, Ochi A . Programmed cell death and extrathymic reduction of Vbeta8+ CD4+ T cells in mice tolerant to Staphylococcus aureus enterotoxin B. Nature. 1991; 349(6306):245-8. DOI: 10.1038/349245a0. View

5.
Hassoun A, Linden P, Friedman B . Incidence, prevalence, and management of MRSA bacteremia across patient populations-a review of recent developments in MRSA management and treatment. Crit Care. 2017; 21(1):211. PMC: 5557425. DOI: 10.1186/s13054-017-1801-3. View