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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Requirement of MyD88 and Fas pathways for the efficacy of allergen-free immunotherapy

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Author(s):
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Fonseca, D. M. [1] ; Wowk, P. F. [1, 2] ; Paula, M. O. [1] ; Gembre, A. F. [1] ; Baruffi, M. D. [3] ; Fermino, M. L. [3] ; Turato, W. M. [1] ; Campos, L. W. [1] ; Silva, C. L. [1] ; Ramos, S. G. [4] ; Horn, C. [5] ; Marchal, G. [6] ; Arruda, L. K. [7] ; Russo, M. [8] ; Bonato, V. L. D. [1]
Total Authors: 15
Affiliation:
[1] Univ Sao Paulo, Dept Biochem & Immunol, Ribeirao Preto Med Sch, BR-14049 Ribeirao Preto - Brazil
[2] Fundacao Oswaldo Cruz, Carlos Chagas Inst, Curitiba, Parana - Brazil
[3] Univ Sao Paulo, Fac Pharmaceut Sci Ribeirao Preto, Dept Clin Anal Toxicol & Food Sci, BR-14049 Ribeirao Preto - Brazil
[4] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Pathol, BR-14049 Ribeirao Preto - Brazil
[5] Fundacao Oswaldo Cruz, Evandro Chagas Clin Res Inst, Lab Immunol & Immunogenet, Rio De Janeiro - Brazil
[6] Inst Pasteur, Paris - France
[7] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Med, BR-14049 Ribeirao Preto - Brazil
[8] Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, BR-14049900 Sao Paulo - Brazil
Total Affiliations: 8
Document type: Journal article
Source: ALLERGY; v. 70, n. 3, p. 275-284, MAR 2015.
Web of Science Citations: 8
Abstract

BackgroundWe have shown that mycobacterial antigens and CpG oligodeoxynucleotides downmodulate airway allergic inflammation by mechanisms dependent on T-cell activation. Here, we investigated the participation of the innate response, particularly the role of MyD88 adaptor, and Fas molecules in the effectiveness of DNA-HSP65 or CpG/culture filtrated proteins (CFP) immunotherapy. MethodsMice sensitized and challenged with Der p 1 allergen were treated with DNA-HSP65, CpG/CFP, or with adoptively transferred cells from immunized mice. The treatment efficacy was assessed by evaluating eosinophil recruitment, antibody, and cytokine production. ResultsIn addition to downregulating the Th2 response, DNA-HSP65 and CpG/CFP promoted IL-10 and IFN- production. Adoptive transfer of cells from mice immunized with DNA-HSP65 or CpG/CFP to allergic recipients downmodulated the allergic response. Notably, transfer of cells from DNA-HSP65- or CpG/CFP-immunized MyD88(-/-) mice failed to reduce allergy. Additionally, for effective reduction of allergy by cells from CpG/CFP-immunized mice, Fas molecules were required. Although DNA-HSP65 or CpG/CFP immunization stimulated antigen-specific production of IFN- and IL-10, the effect of DNA-HSP65 was associated with IL-10 while CpG/CFP was associated with IFN-. Moreover, after stimulation with mycobacterial antigens plus Der p 1 allergen, cells from mite-allergic patients with asthma exhibited similar patterns of cytokine production as those found in the lung of treated mice. ConclusionsThis study provides new insights on the mechanisms of allergen-free immunotherapy by showing that both DNA-HSP65 and CpG/CFP downregulated house dust mite-induced allergic airway inflammation via distinct pathways that involve not only induction of mycobacterial-specific adaptive responses but also signaling via MyD88 and Fas molecules. (AU)

FAPESP's process: 05/01995-0 - Role of T regulatory cells (CD4+ CD25+) in Mycobacterium tuberculosis infected mice
Grantee:Vânia Luiza Deperon Bonato
Support Opportunities: Regular Research Grants