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来自旋毛虫的抗原可在小鼠体内诱导保护性反应。

Antigens from trichinella spiralis that induce a protective response in the mouse.

作者信息

Silberstein D S, Despommier D D

出版信息

J Immunol. 1984 Feb;132(2):898-904.

PMID:6690623
Abstract

A series of monoclonal antibodies was generated for the purpose of studying antigens of the infective L1 larva of Trichinella spiralis. Primary immunization of donor BALB/c mice was by oral infection with L1 larvae. Secondary immunization and screening procedures for hybridoma clones employed a pool of affinity-purified antigens recognized by pooled serum from infected rabbits. Three monoclonal antibodies, chosen for their high reactivity in screening assays and their unique specificities, were raised in quantity, purified, and attached to Sepharose 4B for affinity chromatography. The antigens selected by each affinity column were of different m.w. (37K, 48K, and 50/55K) and possessed different abilities to induce protection. The 48K antigen induced a high level of protection at biologically relevant doses (1.0 and 0.1 micrograms protein/mouse). The 50/55K antigen induced a lower level of protection than the 48K antigen, but was still effective at similar doses. The 37K antigen elicited protection only at a dose of 50 micrograms protein/mouse, and was not as effective as the unpurified antigen at any dose. Earlier studies indicated that many antigens involved in the immune response are secreted. Therefore, worm secretions and two subcellular fractions of homogenized worms (S2 = cytosol, S3 = soluble portion of the large particle fraction) were analyzed for content of the three purified antigens by a double antibody sandwich enzyme-linked assay. The 48K and 50/55K antigens represent significant components of the secretions (12% and 5%, respectively) but relatively minor components of the S2 and S3 fractions. The 37K antigen represents a major component of the S2 fraction, but is essentially absent from S3 and secretions. Immunocytolocalization studies employing immunoperoxidase methods on infected muscle tissue show that the 48K antigen is located in the beta-stichocytes, the lining of the gut, and the surface of the cuticle. The 50/55K antigen was detected in the alpha-stichocytes and was occasionally observed in the gut or on the cuticle. The 37K antigen was detected only in the pseudocoelom. The results from the quantitative ELISA and immunocytolocalization show that the two antigens that induce a protective response are secreted proteins. These data constitute the first account of antigens purified from a nematode that induce a strong protective response. One of these (48K) confers a level of protection comparable to that elicited by exposure of an entire infection.

摘要

为研究旋毛虫感染性L1幼虫的抗原,制备了一系列单克隆抗体。供体BALB/c小鼠通过口服感染L1幼虫进行初次免疫。杂交瘤克隆的二次免疫和筛选程序采用了一组经亲和纯化的抗原,这些抗原可被感染兔子的混合血清识别。选择了三种在筛选试验中具有高反应性且特异性独特的单克隆抗体进行大量制备、纯化,并偶联到琼脂糖4B上用于亲和层析。每个亲和柱选择的抗原分子量不同(37K、48K和50/55K),诱导保护的能力也不同。48K抗原在生物学相关剂量(1.0和0.1微克蛋白质/小鼠)下诱导高水平的保护。50/55K抗原诱导的保护水平低于48K抗原,但在相似剂量下仍有效。37K抗原仅在50微克蛋白质/小鼠的剂量下诱导保护,且在任何剂量下都不如未纯化的抗原有效。早期研究表明,许多参与免疫反应的抗原是分泌性的。因此,通过双抗体夹心酶联免疫吸附测定法分析了虫体分泌物以及匀浆虫体的两个亚细胞部分(S2 = 胞质溶胶,S3 = 大颗粒部分的可溶性部分)中三种纯化抗原的含量。48K和50/55K抗原分别占分泌物的12%和5%,但在S2和S3部分中相对较少。37K抗原是S2部分的主要成分,但在S3和分泌物中基本不存在。采用免疫过氧化物酶方法对感染肌肉组织进行免疫细胞定位研究表明,48K抗原位于β-杆状体细胞、肠道内衬和角质层表面。50/55K抗原在α-杆状体细胞中检测到,偶尔在肠道或角质层上观察到。37K抗原仅在假体腔中检测到。定量ELISA和免疫细胞定位的结果表明,两种诱导保护性反应的抗原是分泌蛋白。这些数据首次报道了从线虫中纯化出的能诱导强烈保护性反应的抗原。其中一种(48K)赋予的保护水平与整个感染所引发的保护水平相当。

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