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恶性疟原虫有性阶段抗原的顺序表达,这些抗原可被蚊子体内的传播阻断抗体识别。

Sequential expression of antigens on sexual stages of Plasmodium falciparum accessible to transmission-blocking antibodies in the mosquito.

作者信息

Vermeulen A N, Ponnudurai T, Beckers P J, Verhave J P, Smits M A, Meuwissen J H

出版信息

J Exp Med. 1985 Nov 1;162(5):1460-76. doi: 10.1084/jem.162.5.1460.

Abstract

Plasmodium falciparum gametocytes contain specific antigens, some of which (Mr 230,000, 48,000, 45,000) are expressed on the surface of the newly emerged macrogamete. A different antigen (Mr 25,000) surrounds the surface of the ookinete and, although present to some extent in the developing gametocyte, is synthesized in high quantities by the macrogamete/zygote and expressed progressively on the transforming zygote surface. These antigens are targets of transmission blocking antibodies that are effective at two distinct points after gametogenesis: fertilization of the macrogamete and ookinete to oocyst development. The antigens involved in the fertilization blockade are the Mr 48 and 45 proteins, which are expressed on the macrogamete surface. The Mr 230 K coprecipitating protein probably plays no part in transmission block. mAb directed against the Mr 25 K ookinete surface protein blocked transmission without inhibiting ookinete formation, indicating that this protein has an important role in the transformation of ookinete into oocyst. A combination of mAb recognizing different epitopes on the same protein molecule acted synergistically in inhibiting oocyst formation. Using a mixture of two blocking mAb reacting against the Mr 48/45 and 25 K proteins, respectively, an additive blocking effect could be demonstrated.

摘要

恶性疟原虫配子体含有特定抗原,其中一些抗原(分子量230,000、48,000、45,000)在新出现的大配子表面表达。另一种抗原(分子量25,000)围绕动合子表面,尽管在发育中的配子体中也有一定程度的存在,但由大配子/合子大量合成,并在转化中的合子表面逐渐表达。这些抗原是传播阻断抗体的靶标,这些抗体在配子发生后的两个不同阶段有效:大配子受精以及动合子发育为卵囊。参与受精阻断的抗原是分子量48和45的蛋白质,它们在大配子表面表达。分子量230K的共沉淀蛋白可能在传播阻断中不起作用。针对分子量25K动合子表面蛋白的单克隆抗体可阻断传播,而不抑制动合子形成,这表明该蛋白在动合子转化为卵囊过程中起重要作用。识别同一蛋白分子上不同表位的单克隆抗体组合在抑制卵囊形成方面具有协同作用。分别使用针对分子量48/45和25K蛋白的两种阻断单克隆抗体的混合物,可证明具有累加阻断效应。

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