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免疫抑制性PAS-1是猪蛔虫幼虫和成虫释放的一种排泄/分泌蛋白。

Immunosuppressive PAS-1 is an excretory/secretory protein released by larval and adult worms of the ascarid nematode Ascaris suum.

作者信息

Antunes M F P, Titz T O, Batista I F C, Marques-Porto R, Oliveira C F, Alves de Araujo C A, Macedo-Soares M F

机构信息

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

Peptide and Protein Sequencing Unit, Butantan Institute,São Paulo,Brazil.

出版信息

J Helminthol. 2015 May;89(3):367-74. doi: 10.1017/S0022149X14000200. Epub 2014 Apr 7.

Abstract

Helminths use several strategies to evade and/or modify the host immune response, including suppression or inactivation of the host antigen-specific response. Several helminth immunomodulatory molecules have been identified. Our studies have focused on immunosuppression induced by the roundworm Ascaris suum and an A. suum-derived protein named protein 1 from A. suum (PAS-1). Here we assessed whether PAS-1 is an excretory/secretory (E/S) protein and whether it can suppress lipopolysaccharide-induced inflammation. Larvae from infective eggs were cultured in unsupplemented Dulbecco's modified Eagle medium (DMEM) for 2 weeks. PAS-1 was then measured in the culture supernatants and in adult A. suum body fluid at different time points by enzyme-linked immunosorbent assay (ELISA) with the monoclonal antibody MAIP-1. Secreted PAS-1 was detected in both larval culture supernatant and adult body fluid. It suppressed lipopolysaccharide (LPS)-induced leucocyte migration and pro-inflammatory cytokine production, and stimulated interleukin (IL)-10 secretion, indicating that larval and adult secreted PAS-1 suppresses inflammation in this model. Moreover, the anti-inflammatory activity of PAS-1 was abolished by treatment with MAIP-1, a PAS-1-specific monoclonal antibody, confirming the crucial role of PAS-1 in suppressing LPS-induced inflammation. These findings demonstrate that PAS-1 is an E/S protein with anti-inflammatory properties likely to be attributable to IL-10 production.

摘要

蠕虫采用多种策略来逃避和/或改变宿主的免疫反应,包括抑制或使宿主抗原特异性反应失活。几种蠕虫免疫调节分子已被鉴定出来。我们的研究集中在由猪蛔虫以及一种来自猪蛔虫的名为猪蛔虫蛋白1(PAS-1)的蛋白质所诱导的免疫抑制作用上。在此,我们评估了PAS-1是否为一种排泄/分泌(E/S)蛋白,以及它是否能够抑制脂多糖诱导的炎症反应。将感染性虫卵中的幼虫在未添加其他成分的杜氏改良 Eagle 培养基(DMEM)中培养2周。然后,在不同时间点,通过使用单克隆抗体MAIP-1的酶联免疫吸附测定(ELISA)法,对培养上清液和成年猪蛔虫的体液中的PAS-1进行检测。在幼虫培养上清液和成虫体液中均检测到了分泌型PAS-1。它抑制了脂多糖(LPS)诱导的白细胞迁移和促炎细胞因子的产生,并刺激了白细胞介素(IL)-10的分泌,这表明幼虫和成虫分泌的PAS-1在该模型中可抑制炎症反应。此外,用PAS-1特异性单克隆抗体MAIP-1处理后,PAS-1的抗炎活性被消除,这证实了PAS-1在抑制LPS诱导的炎症反应中的关键作用。这些发现表明,PAS-1是一种具有抗炎特性的E/S蛋白,其抗炎特性可能归因于IL-10的产生。

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