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猪蛔虫高分子量组分对 TLR2 和 TLR4 的免疫调节作用。

TLR2- and 4-independent immunomodulatory effect of high molecular weight components from Ascaris suum.

机构信息

Laboratory of Immunopathology, Butantan Institute, São Paulo, SP, Brazil.

Pasteur Institute, São Paulo, Brazil.

出版信息

Mol Immunol. 2014 Mar;58(1):17-26. doi: 10.1016/j.molimm.2013.10.011. Epub 2013 Nov 19.

Abstract

Components of high molecular-weight (PI) obtained from Ascaris suum extract down-regulate the Th1/Th2-related immune responses induced by ovalbumin (OVA)-immunization in mice. Furthermore, the PI down-modulates the ability of dendritic cells (DCs) to activate T lymphocytes by an IL-10-mediated mechanism. Here, we evaluated the role of toll like receptors 2 and 4 (TLR2 and 4) in the modulatory effect of PI on OVA-specific immune response and the PI interference on DC full activation. An inhibition of OVA-specific cellular and humoral responses were observed in wild type (WT) or in deficient in TLR2 (TLR2(-/-)) or 4 (TLR4(-/-)) mice immunized with OVA plus PI when compared with OVA-immunized mice. Low expression of class II MHC, CD40, CD80 and CD86 molecules was observed in lymph node (LN) cells from WT, TLR2(-/-) or TLR4(-/-) mice immunized with OVA plus PI compared with OVA-primed cells. We also verified that PI was able to modulate the activation of DCs derived from bone marrow of WT, TLR2(-/-) or TLR4(-/-) mice induced in vitro by agonists of TLRs, as observed by a decreased expression of class II MHC and costimulatory molecules and by low secretion of pro-inflammatory cytokines. Its effect was accompanied by IL-10 synthesis. In this sense, the modulatory effect of PI on specific-immune response and DC activation is independent of TLR2 or TLR4.

摘要

从猪蛔虫提取物中获得的高分子量(PI)成分可下调卵清蛋白(OVA)免疫诱导的 Th1/Th2 相关免疫反应。此外,PI 通过 IL-10 介导的机制下调树突状细胞(DC)激活 T 淋巴细胞的能力。在这里,我们评估了 Toll 样受体 2 和 4(TLR2 和 4)在 PI 对 OVA 特异性免疫反应的调节作用以及 PI 对 DC 完全激活的干扰中的作用。与 OVA 免疫小鼠相比,用 OVA 加 PI 免疫的野生型(WT)或 TLR2(TLR2(-/-))或 4(TLR4(-/-))缺陷小鼠观察到 OVA 特异性细胞和体液反应受到抑制。与 OVA 引发的细胞相比,用 OVA 加 PI 免疫的 WT、TLR2(-/-)或 TLR4(-/-)小鼠的淋巴结(LN)细胞中观察到 II 类 MHC、CD40、CD80 和 CD86 分子的低表达。我们还验证了 PI 能够调节 WT、TLR2(-/-)或 TLR4(-/-)小鼠骨髓来源的 DC 的激活,这是通过 TLR 激动剂诱导的,表现为 II 类 MHC 和共刺激分子的表达降低,以及促炎细胞因子的分泌减少。其作用伴随着 IL-10 的合成。在这种意义上,PI 对特异性免疫反应和 DC 激活的调节作用独立于 TLR2 或 TLR4。

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