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Immune Responses against Streptococcus pyogenes in Human Palatine Tonsils
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AbstractWe investigated cellular immunity against Streptococcus pyogenes in human tonsils by measuring antigen‐specific immunoglobulin‐secreting cells and the production of cytokines from CD4+ T cells in response to M proteins. The incidence of S pyogenes in tonsils was significantly higher in patients with recurrent tonsillitis (RT) than in patients with tonsillar hypertrophy (TH). M protein‐specific immunoglobulin A (IgA) and immunoglobulin G spot‐forming cells were increased in patients with RT compared with patients with TH. In RT the number of M protein‐specific IgA spot‐forming cells was significantly greater in the S pyogenes‐negative subjects than in the S pyogenes‐positive subjects. Proliferation of CD4+ T cells and production of interferon‐gamma (IFN‐γ) and interleukins−2,− 4, −5, and −6 (IL‐2, IL‐4, IL‐5, and IL‐6) from those T cells were observed in response to M protein. The concentrations of IFN‐γ and IL‐4 were higher in RT than in TH. These findings suggest thatS pyogenes is associated with the pathogenesis of RT and that immune responses against M protein may play an important role in preventing the colonization of this bacteria in tonsils.
Title: Immune Responses against Streptococcus pyogenes in Human Palatine Tonsils
Description:
AbstractWe investigated cellular immunity against Streptococcus pyogenes in human tonsils by measuring antigen‐specific immunoglobulin‐secreting cells and the production of cytokines from CD4+ T cells in response to M proteins.
The incidence of S pyogenes in tonsils was significantly higher in patients with recurrent tonsillitis (RT) than in patients with tonsillar hypertrophy (TH).
M protein‐specific immunoglobulin A (IgA) and immunoglobulin G spot‐forming cells were increased in patients with RT compared with patients with TH.
In RT the number of M protein‐specific IgA spot‐forming cells was significantly greater in the S pyogenes‐negative subjects than in the S pyogenes‐positive subjects.
Proliferation of CD4+ T cells and production of interferon‐gamma (IFN‐γ) and interleukins−2,− 4, −5, and −6 (IL‐2, IL‐4, IL‐5, and IL‐6) from those T cells were observed in response to M protein.
The concentrations of IFN‐γ and IL‐4 were higher in RT than in TH.
These findings suggest thatS pyogenes is associated with the pathogenesis of RT and that immune responses against M protein may play an important role in preventing the colonization of this bacteria in tonsils.
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