Expansion of circulating Foxp3+CD25bright CD4+ T cells during specific venom immunotherapy-Reference-Cited by-同舟云学术

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Expansion of circulating Foxp3+CD25bright CD4+ T cells during specific venom immunotherapy

Published:2007-12-07 Issue:2 Volume:38 Page:291-297
ISSN:0954-7894
Container-title:Clinical & Experimental Allergy
language:en
Short-container-title:

Author:

Pereira-Santos M. C.,Baptista A. P.,Melo A.,Alves R. R.,Soares R. S.,Pedro E.,Pereira-Barbosa M.,Victorino R. M. M.,Sousa A. E.

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2222.2007.02887.x/fullpdf

Reference37 articles.

1. Are regulatory T cells the target of venom immunotherapy?;Jutel;Curr Opin Allergy Clin Immunol,2005

2. Insect sting allergy and venom immunotherapy;Golden;a model and a mystery,2005

3. Role of interleukin 10 in specific immunotherapy;Akdis;J Clin Invest,1998

4. Influence of bee venom immunotherapy on degranulation and leukotriene generation in human blood basophils;Jutel;Clin Exp Allergy,1996

5. Decreased release of histamine and sulfidoleukotrienes by human peripheral blood leukocytes after wasp venom immunotherapy is partially due to induction of IL-10 and IFN-gamma production of T cells;Pierkes;J Allergy Clin Immunol,1999

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