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Infection and Immunity, July 2005, p. 4427-4431, Vol. 73, No. 7
0019-9567/05/$08.00+0 doi:10.1128/IAI.73.7.4427-4431.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Department of Pathology, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, Maryland 20814
Received 16 November 2004/ Returned for modification 7 January 2005/ Accepted 4 March 2005
Immunoglobulin G (IgG) antiprotein and antipolysaccharide responses to intact Streptococcus pneumoniae are CD4+-T-cell dependent and therefore might be under the negative control of CD4+ CD25+ regulatory T cells. Injection of anti-interleukin 2 receptor
(anti-IL-2R
) MAb to deplete regulatory T cells, injection of agonistic MAb against glucocorticoid-induced tumor necrosis factor receptor family-related protein to inhibit regulatory-T-cell function, and adoptive transfer of regulatory-T-cell-depleted CD4+ T cells into athymic nude mice each had no effect on either the primary or secondary protein- or polysaccharide-specific IgG response to intact S. pneumoniae. Surprisingly, anti-IL-2R
MAb also had no effect on the IgG response to intact S. pneumoniae in MyD88/ mice or to a soluble protein-polysaccharide conjugate injected into wild-type mice in the absence of adjuvant. Collectively, these data are the first to suggest that, in contrast to their role in limiting chronic cell-mediated immunity, regulatory T cells may play no significant role in an acute humoral immune response to an intact extracellular bacterial pathogen.
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