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恶性疟原虫:人源单克隆抗体33G2及与抗原Pf332反应的抗体的细胞黏附抑制分析

Plasmodium falciparum: analysis of the cytoadherence inhibition of the human monoclonal antibody 33G2 and of antibodies reactive with antigen Pf332.

作者信息

Iqbal J, Perlmann P, Berzins K

机构信息

Department of Immunology, Stockholm University, Sweden.

出版信息

Exp Parasitol. 1993 Aug;77(1):79-87. doi: 10.1006/expr.1993.1063.

Abstract

The capacity of a human monoclonal antibody (MAb 33G2) to interfere in vitro both with Plasmodium falciparum merozoite invasion and cytoadherence of infected erythrocytes to melanoma cells has been reported. MAb 33G2 cross-reacts with several P. falciparum antigens but shows highest reactivity with repeated sequences in the asexual blood stage antigen Pf332. This study was conducted in order to further analyze the cytoadherence inhibition mediated by MAb 33G2 and to evaluate the relative contribution of antibodies to Pf332 in the inhibitory activity of immunoglobulins from P. falciparum immune donors. We show here that MAb 33G2 inhibits cytoadherence of infected erythrocytes (PRBCs) with similar efficiency independently of the strain of parasite, while the inhibitory capacity of immunoglobulin fractions from Liberian immune donors was restricted to some strains only. There appears to be no correlation between the reactivity with Pf332 of immunoglobulin preparations from different donors and their capacity to inhibit cytoadherence of PRBCs to melanoma cells. In contrast to MAb 33G2, polyclonal antibodies affinity purified on the Pf332 peptide containing the epitope seen by the MAb showed little or no inhibition of cytoadherence of infected erythrocytes.

摘要

据报道,一种人源单克隆抗体(MAb 33G2)在体外既能干扰恶性疟原虫裂殖子的入侵,又能抑制感染红细胞与黑色素瘤细胞的细胞黏附。MAb 33G2能与几种恶性疟原虫抗原发生交叉反应,但与无性血液期抗原Pf332中的重复序列反应性最高。进行本研究是为了进一步分析MAb 33G2介导的细胞黏附抑制作用,并评估抗体对Pf332在恶性疟原虫免疫供体免疫球蛋白抑制活性中的相对贡献。我们在此表明,MAb 33G2能以相似的效率抑制感染红细胞(PRBCs)的细胞黏附,而与寄生虫菌株无关,而利比里亚免疫供体的免疫球蛋白组分的抑制能力仅局限于某些菌株。不同供体的免疫球蛋白制剂与Pf332的反应性与其抑制PRBCs与黑色素瘤细胞细胞黏附的能力之间似乎没有相关性。与MAb 33G2不同,在含有该单克隆抗体所识别表位的Pf332肽上亲和纯化的多克隆抗体对感染红细胞的细胞黏附几乎没有抑制作用。

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