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单克隆抗配子体抗体可识别恶性疟原虫所有血液阶段中存在的一种抗原。

Monoclonal anti-gametocyte antibodies identify an antigen present in all blood stages of Plasmodium falciparum.

作者信息

Masuda A, Zavala F, Nussenzweig V, Nussenzweig R S

出版信息

Mol Biochem Parasitol. 1986 Jun;19(3):213-22. doi: 10.1016/0166-6851(86)90003-4.

Abstract

Two polypeptides of 150 and 130 kDa present in all asexual and sexual blood stages of Plasmodium falciparum have been identified with anti-gametocyte monoclonal antibodies. The apparent molecular mass of these antigens is identical in different developmental stages of the parasite and in different isolates. These antigens are released in the culture supernatant during the process of schizogony and are also detected in the sera of patients undergoing a primary P. falciparum infection. Antibodies against these antigens occur in sera of a large percentage of children and most adults living in malaria-endemic areas, suggesting that they are highly immunogenic. The anti-gametocyte monoclonal antibodies react with a synthetic peptide (Glu-Glu-Asn-Val)4, present in antigen Pf155 [Perlmann, H. et al. (1984) J. Exp. Med. 159, 1686-1704] and in the ring-infected erythrocyte surface antigen [Coppel, R.L. et al. (1984) Nature 310, 789-792], indicating that these polypeptides are closely related. In contrast, two glycophorin-binding proteins of similar molecular mass [Perkins, M.E. (1984) J. Exp. Med. 160, 788-798] appear to be entirely distinct from the presently described antigens. We failed to observe any in vitro inhibitory activity of the monoclonal antibodies on merozoite invasion and on gametocyte infectivity.

摘要

用抗配子体单克隆抗体已鉴定出存在于恶性疟原虫所有无性和有性血液阶段的两种分子量分别为150 kDa和130 kDa的多肽。这些抗原的表观分子量在寄生虫的不同发育阶段以及不同分离株中是相同的。这些抗原在裂殖生殖过程中释放到培养上清液中,并且在初次感染恶性疟原虫的患者血清中也可检测到。生活在疟疾流行地区的大部分儿童和大多数成年人的血清中存在针对这些抗原的抗体,这表明它们具有高度免疫原性。抗配子体单克隆抗体与存在于抗原Pf155 [佩尔曼,H.等人(1984年)《实验医学杂志》159卷,第1686 - 1704页]和环状感染红细胞表面抗原[科佩尔,R.L.等人(1984年)《自然》310卷,第789 - 792页]中的合成肽(Glu - Glu - Asn - Val)4发生反应,表明这些多肽密切相关。相比之下,两种分子量相似的血型糖蛋白结合蛋白[珀金斯,M.E.(1984年)《实验医学杂志》160卷,第788 - 798页]似乎与目前描述的抗原完全不同。我们未观察到单克隆抗体对裂殖子入侵和配子体感染性的任何体外抑制活性。

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