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与肺结核患者相比,分枝杆菌热休克蛋白65抗原上调健康个体的细胞免疫反应。

Mycobacterial Hsp65 antigen upregulates the cellular immune response of healthy individuals compared with tuberculosis patients.

作者信息

Wowk Pryscilla Fanini, Franco Luís Henrique, Fonseca Denise Morais da, Paula Marina Oliveira, Vianna Élcio Dos Santos Oliveira, Wendling Ana Paula, Augusto Valéria Maria, Elói-Santos Silvana Maria, Teixeira-Carvalho Andréa, Silva Flávia Dias Coelho, Vinhas Solange Alves, Martins-Filho Olindo Assis, Palaci Moisés, Silva Célio Lopes, Bonato Vânia Luiza Deperon

机构信息

a Department of Biochemistry and Immunology , Ribeirão Preto Medical School, University of São Paulo , Ribeirão Preto , Brazil.

b Respiratory Division, School of Medicine of Ribeirão Preto, University of São Paulo , São Paulo , Ribeirão Preto , Brazil.

出版信息

Hum Vaccin Immunother. 2017 May 4;13(5):1040-1050. doi: 10.1080/21645515.2016.1264547. Epub 2017 Jan 6.

Abstract

Previously we showed that 65-kDa Mycobacterium leprae heat shock protein (Hsp65) is a target for the development of a tuberculosis vaccine. Here we evaluated peripheral blood mononuclear cells (PBMC) from healthy individuals or tuberculosis patients stimulated with two forms of Hsp65 antigen, recombinant DNA that encodes Hsp65 (DNA-HSP65) or recombinant Hsp65 protein (rHsp65) in attempting to mimic a prophylactic or therapeutic study in vitro, respectively. Proliferation and cytokine-producing CD4 or CD8 cell were assessed by flow cytometry. The CD4 cell proliferation from healthy individuals was stimulated by DNA-HSP65 and rHsp65, while CD8 cell proliferation from healthy individuals or tuberculosis patients was stimulated by rHSP65. DNA-HSP65 did not improve the frequency of IFN-gamma cells from healthy individuals or tuberculosis patients. Furthermore, we found an increase in the frequency of IL-10-producing cells in both groups. These findings show that Hsp65 antigen activates human lymphocytes and plays an immune regulatory role that should be addressed as an additional antigen for the development of antigen-combined therapies.

摘要

此前我们表明,65 kDa麻风分枝杆菌热休克蛋白(Hsp65)是结核病疫苗研发的一个靶点。在此,我们评估了来自健康个体或结核病患者的外周血单核细胞(PBMC),分别用两种形式的Hsp65抗原进行刺激,即编码Hsp65的重组DNA(DNA-HSP65)或重组Hsp65蛋白(rHsp65),试图在体外模拟预防性或治疗性研究。通过流式细胞术评估增殖情况以及产生细胞因子的CD4或CD8细胞。健康个体的CD4细胞增殖受到DNA-HSP65和rHsp65的刺激,而健康个体或结核病患者的CD8细胞增殖受到rHSP65的刺激。DNA-HSP65并未提高健康个体或结核病患者中IFN-γ细胞的频率。此外,我们发现两组中产生IL-10的细胞频率均增加。这些发现表明,Hsp65抗原激活人淋巴细胞并发挥免疫调节作用,在开发抗原联合疗法时应将其作为一种额外的抗原加以考虑。

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