American tegumentary leishmaniasis: mRNA expression for Th1 and Treg mediators are predominant in patients with recent active disease

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• 作者：Marina A. Souza^a ; ^{marinaasouza@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Thays M. Almeida^a ; ^{thaysmdealmeida@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Maria Carolina A.B. Castro^a ; ^{carolina.brelaz@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Andresa P. Oliveira-Mendes^a ; ^{andresadeolinda@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Amanda F. Almeida^a ; ^{amanda.ferreira@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Beatriz C. Oliveira^a ; ^{oliveira.cbeatriz@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Lucas F. Rocha^a ; ^{lf.rocha7@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Angela C.R. Medeiros^b ; ^{rapelaac@yahoo.com.br" class="auth_mail" title="E-mail the corresponding author} ; Maria E.F. Brito^a ; ^{britomef@cpqam.fiocruz.br" class="auth_mail" title="E-mail the corresponding author} ; Alain J.J. Dessein^c ; ^{alain.dessein@univ-amu.fr" class="auth_mail" title="E-mail the corresponding author} ; Valé ; ria R.A. Pereira^a ; ^{valeriaph@gmail.com" class="auth_mail" title="E-mail the corresponding author}
• 关键词：AgSol ; soluble antigen ; AgIns ; insoluble antigen
• 刊名：Immunobiology
• 出版年：2016
• 出版时间：February 2016
• 年：2016
• 卷：221
• 期：2
• 页码：253-259
• 全文大小：936 K

文摘

Besides the Th1 × Th2 paradigm, Treg and Th17 cytokines may play a role in the response to American tegumentary leishmaniasis. Considering the sensitivity and accuracy of qPCR and the lack of studies using this approach, we evaluated mRNA expression for IFN-γ, TNF-α, IL-4, IL-10, IL-6, IL-17A, IL-22, TGF-β, Foxp3 and RORC in peripheral blood mononuclear cells (PBMC) from patients with active disease, after stimulation with L. (V.) braziliensis soluble or insoluble fractions. Our results show that the antigens promoted specific mRNA expression related to the immune response in patients with ATL, and the insoluble fraction seems to stimulate the immune response in a higher intensity. The pro-inflammatory response was also fueled by IFN-γ and TNF-α, probably due to the active disease. IL-4, in certain way, seems to regulate this response along with IL-10 that may be produced by Treg cells, which are supposedly present in the patients’ samples due the evidenced expression of Foxp3, in the presence of AgIns. In contrast, down-regulated RORC suggests that the significant levels of IL-6 expressed in response to AgSol were not able to induce an expressive Th17 profile along with TGF-β, which might have predominantly contributed to the development of a regulatory profile in the active disease.