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与Gal-KO小鼠脓毒症模型中天然抗αGal抗体选择性清除相关的细胞因子谱

Cytokine Profile Associated with Selective Removal of Natural Anti-αGal Antibodies in a Sepsis Model in Gal-KO Mice.

作者信息

Pérez-Cruz Magdiel, Bello-Gil Daniel, Costa Cristina, Mañez Rafael

机构信息

Bellvitge Biomedical Research Institute (IDIBELL), Hospitalet de Llobregat, 08908, Spain.

出版信息

Biochemistry (Mosc). 2017 Feb;82(2):205-212. doi: 10.1134/S0006297917020122.

Abstract

Selective depletion of natural anti-Galα1-3Galβ1-4GlcNAc (so-called anti-αGal) antibodies is achieved in α1,3-galactosyltransferase knockout (Gal-KO) mice by administration of the soluble glycoconjugate of αGal GAS914. This molecule removed up to 90% of natural circulating anti-αGal antibodies without causing unspecific production of cytokines in wild-type (CBA) and Gal-KO mice. However, the removal of anti-αGal antibodies in Gal-KO mice with GAS914 in the context of sepsis after cecal ligation and puncture (CLP) was associated with a significant increase in the production of leptin, CXLC1, CXLC13, and TIMP-1 cytokines compared to vehicle (PBS)-treated controls. Despite the current lack of understanding of the underlying mechanism, our data suggest a putative role of natural anti-αGal antibodies in the regulation of some cytokines during sepsis.

摘要

通过给予αGal GAS914的可溶性糖缀合物,在α1,3-半乳糖基转移酶基因敲除(Gal-KO)小鼠中实现了天然抗Galα1-3Galβ1-4GlcNAc(所谓的抗αGal)抗体的选择性消耗。该分子去除了高达90%的天然循环抗αGal抗体,而不会在野生型(CBA)和Gal-KO小鼠中引起细胞因子的非特异性产生。然而,在盲肠结扎和穿刺(CLP)后脓毒症的情况下,用GAS914去除Gal-KO小鼠中的抗αGal抗体与瘦素、CXLC1、CXLC13和TIMP-1细胞因子的产生显著增加有关,与用载体(PBS)处理的对照组相比(P < 0.05)。尽管目前对潜在机制尚不清楚,但我们的数据表明天然抗αGal抗体在脓毒症期间某些细胞因子的调节中可能具有作用。

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