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针对毒性分泌型磷脂酶A2和出血毒素的特异性抗体在抗极北蝰毒液抗血清中和潜力中的作用。

The role of antibodies specific for toxic sPLA2s and haemorrhagins in neutralizing potential of antisera raised against Vipera ammodytes ammodytes venom.

作者信息

Halassy Beata, Habjanec Lidija, Brgles Marija, Balija Maja Lang, Leonardi Adrijana, Kovacic Lidija, Prijatelj Petra, Tomasić Jelka, Krizaj Igor

机构信息

Research and Development Department, Institute of Immunology, Inc., Rockefellerova 10, HR-10 000 Zagreb, Croatia.

出版信息

Comp Biochem Physiol C Toxicol Pharmacol. 2008 Aug;148(2):178-83. doi: 10.1016/j.cbpc.2008.05.005. Epub 2008 May 17.

Abstract

The contribution of antibodies directed against the two main toxic groups of proteins in the Vipera ammodytes ammodytes venom, haemorrhagic metalloproteinases (H) and neurotoxic sPLA2s (Atxs), to the overall protective efficacy of the whole venom antisera was investigated. Using ELISA assays we established a high correlation between the protective efficacy of the whole venom antisera in mice and their anti-Atxs antibody content. As the haemorrhage is the prevailing toxic effect of the venom in human, the lack of correlation also with anti-H IgG content exposed that the mouse model might not be optimal to evaluate the neutralizing potential of the venom-specific antisera for human therapy. We further revealed that Atxs and structurally very similar but non-toxic AtnI2 from the venom are not immuno cross-reactive.

摘要

研究了针对极北蝰毒液中两种主要毒性蛋白组,即出血性金属蛋白酶(H)和神经毒性分泌型磷脂酶A2(Atxs)的抗体对全毒液抗血清总体保护效力的贡献。通过酶联免疫吸附测定(ELISA),我们确定了全毒液抗血清在小鼠体内的保护效力与其抗Atxs抗体含量之间存在高度相关性。由于出血是该毒液对人类的主要毒性作用,且与抗H IgG含量也缺乏相关性,这表明小鼠模型可能并非评估毒液特异性抗血清用于人类治疗的中和潜力的最佳模型。我们进一步发现,毒液中的Atxs与结构非常相似但无毒的AtnI2不存在免疫交叉反应。

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