4.2 Article Proceedings Paper

Schistosoma mansoni antigen-driven interleukin-10 production in infected asthmatic individuals

期刊

MEMORIAS DO INSTITUTO OSWALDO CRUZ
卷 101, 期 -, 页码 339-343

出版社

FUNDACO OSWALDO CRUZ
DOI: 10.1590/S0074-02762006000900055

关键词

Schistosoma mansoni recombinant proteins; S. mansoni antigens; interleukin-10

资金

  1. FIC NIH HHS [D43 TW 00919, D43 TW 06216] Funding Source: Medline
  2. FOGARTY INTERNATIONAL CENTER [D43TW000919, R01TW006216] Funding Source: NIH RePORTER

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Asthmatics infected with Schistosoma mansoni have a less severe course of asthma and an inhibition of the Th2 inflammatory response that seems to be mediated by interleukin (IL-10). The objective of this study was to evaluate the capacity of some S. mansoni antigens to stimulate IL-10 production in vitro by cells of asthmatic infected individuals. Peripheral bloods mononuclear cells were stimulated with the S. mansoni recombinant antigens Sm22.6, Sm14, P24, and PIII antigen. IL-10 was measured in the supernatants of cultures. As the recombinant antigens were cloned in Escherichia coli, we blocked contaminant endotoxin with polymyxin B added to the cultures. We demonstrated that all antigens used drove high production of IL-10 in S. mansoni infected individuals (n = 13, 408 +/- 514 and 401 +/- 383 pg/ml, 484 +/- 245 pg/ml, 579 +/- 468 pg/ml, respectively). In asthmatics infected with S. mansoni (n = 21) rP24 induced higher levels of IL-10 (565 +/- 377 pg/ml) when compared to PIII, rSm14 and rSm22.6 (184 +/- 209 pg/ml; 292 +/- 243 pg/ml, 156 +/- 247 pg/ml, respectively). Conclusion: the S. mansoni antigens evaluated in this study stimulated IL-10 production by cells from infected individuals and therefore they have the potential to be used as a modulator of the inflammatory response in asthma.

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