首页> 外文期刊>The journal of immunology >Blockade of IL-10 Signaling during Bacillus Calmette-Guérin Vaccination Enhances and Sustains Th1, Th17, and Innate Lymphoid IFN-γ and IL-17 Responses and Increases Protection to Mycobacterium tuberculosis Infection
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Blockade of IL-10 Signaling during Bacillus Calmette-Guérin Vaccination Enhances and Sustains Th1, Th17, and Innate Lymphoid IFN-γ and IL-17 Responses and Increases Protection to Mycobacterium tuberculosis Infection

机译:卡介苗接种过程中IL-10信号的阻断增强并维持Th1,Th17和先天淋巴性IFN-γ和IL-17反应,并增强了对结核分枝杆菌感染的保护

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Vaccination with Mycobacterium bovis bacillus Calmette-Guérin (BCG) remains the only prophylactic vaccine against tuberculosis, caused by Mycobacterium tuberculosis , but gives variable protection against pulmonary disease. The generation of host Th1 responses following BCG vaccination is accepted as the major mechanism of protection against M. tuberculosis infection. Early production of IL-17 in the lungs following M. tuberculosis challenge of mice previously vaccinated with M. tuberculosis peptides in adjuvant has been shown to be required for efficient Th1 cell recruitment. IL-10 regulates various processes involved in generation of Th1 and Th17 responses. Previous studies have shown IL-10 as a negative regulator of the immune response to primary M. tuberculosis infection, with Il10 ?/? mice having reduced lung bacterial loads. In this study we show that inhibition of IL-10 signaling during BCG vaccination enhances host-generated Ag-specific IFN-γ and IL-17A responses, and that this regimen gives significantly greater protection against aerogenic M. tuberculosis challenge in both susceptible and relatively resistant strains of mice. In M. tuberculosis -susceptible CBA/J mice, Ab blockade of IL-10R specifically during BCG vaccination resulted in additional protection against M. tuberculosis challenge of 1-log10 compared with equivalent isotype-treated controls. The protection observed following BCG vaccination concurrent with anti–IL-10R mAb treatment was sustained through chronic M. tuberculosis infection and correlated with enhanced lung Th1 and Th17 responses and increased IFN-γ and IL-17A production by γδ T cells and an innate-like Thy1.2+CD3? lymphoid population. We show that IL-10 inhibits optimal BCG-elicited protection, therefore suggesting that antagonists of IL-10 may be of great benefit as adjuvants in preventive vaccination against tuberculosis.
机译:牛分枝杆菌卡介苗的接种(BCG)仍然是针对结核分枝杆菌引起的结核病的唯一预防性疫苗,但对肺部疾病具有多种保护作用。 BCG疫苗接种后宿主Th1应答的产生被认为是抵抗结核分枝杆菌感染的主要机制。业已证明,结核分枝杆菌攻击之前接种过结核分枝杆菌肽作为佐剂的小鼠,肺中IL-17的早期产生是有效招募Th1细胞所必需的。 IL-10调节涉及Th1和Th17反应产生的各种过程。先前的研究表明,IL-10是针对原发性结核分枝杆菌感染的免疫反应的负调节剂,Il10β/β可以作为免疫调节剂。肺细菌负荷降低的小鼠。在这项研究中,我们表明,在BCG疫苗接种过程中抑制IL-10信号传导可增强宿主产生的Ag特异性IFN-γ和IL-17A应答,并且该方案在易感性和相对性方面均提供了针对气源性结核分枝杆菌挑战的明显更大的保护抗性小鼠品系。在结核分枝杆菌易感的CBA / J小鼠中,IL-10R的Ab阻断(特别是在BCG疫苗接种期间)导致与等效同种型治疗的对照相比,对结核分枝杆菌挑战性的额外保护作用> 1-log10。卡介苗接种后与抗-IL-10R mAb治疗同时观察到的保护作用通过慢性结核分枝杆菌感染得以维持,并与增强的肺Th1和Th17反应以及γδT细胞和先天性IFN-γ和IL-17A产生增加有关。像Thy1.2 + CD3?淋巴样人群。我们显示IL-10抑制最佳BCG引起的保护,因此表明IL-10的拮抗剂作为佐剂在预防结核病的预防接种中可能会很有益处。

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