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非活性疫苗诱导针对曼氏血吸虫的保护性免疫。IV. 可溶性成虫免疫预防性活性的分级分离及抗原特性

Induction of protective immunity against Schistosoma mansoni by a nonliving vaccine. IV. Fractionation and antigenic properties of a soluble adult worm immunoprophylactic activity.

作者信息

Sher A, Pearce E, Hieny S, James S

出版信息

J Immunol. 1986 May 15;136(10):3878-83.

PMID:3084647
Abstract

An aqueous buffer-soluble, nonparticulate fraction of adult Schistosoma mansoni worms (SWAP) was separated by gel filtration on Ultragel AcA-34, and portions of the eluate were tested for their capacity to induce protective immunity against cercarial challenge when administered intradermally to mice in combination with the adjuvant BCG. All of the immunogenic activity was found in a single peak of protein excluded in the void volume of the column. This same fraction was determined by SDS-PAGE and Western immunoblotting to be unique in that it contained a component of Mr (X 10(-3) 97 (97,000) recognized monospecifically by antibodies from mice vaccinated with unseparated SWAP plus BCG. Similarly, the protective fraction was unique in possessing the capacity to elicit 24 hr delayed footpad swelling responses, as well as lymphokine production, in SWAP-BCG-immunized mice. These results suggest that the immunogenic activity of SWAP resides in a restricted population of molecules, and possibly in the 97,000 antigen detected with antibodies from vaccinated animals. Because both the protective capacity of unfractionated SWAP and the serologic reactivity of the 97,000 antigen are sensitive to digestion with protease, it is likely that the immunologic activity of these molecules is dependent on peptide-bonded structural elements.

摘要

曼氏血吸虫成虫的水缓冲液可溶性非颗粒部分(SWAP)通过在Ultragel AcA - 34上进行凝胶过滤分离,将部分洗脱液与佐剂卡介苗联合皮内注射给小鼠时,检测其诱导针对尾蚴攻击的保护性免疫的能力。所有免疫原性活性都在柱空体积中排除的单一蛋白质峰中发现。通过SDS - PAGE和Western免疫印迹确定该相同部分是独特的,因为它含有一种Mr(×10⁻³)97(97,000)的成分,该成分被接种未分离的SWAP加卡介苗的小鼠产生的抗体单特异性识别。同样,保护性部分的独特之处在于它能够在SWAP - 卡介苗免疫的小鼠中引发24小时延迟的足垫肿胀反应以及淋巴因子产生。这些结果表明,SWAP的免疫原性活性存在于有限的分子群体中,可能存在于用接种动物的抗体检测到的97,000抗原中。由于未分级的SWAP的保护能力和97,000抗原的血清学反应性对蛋白酶消化敏感,这些分子的免疫活性可能依赖于肽键连接的结构元件。

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