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用针对恶性疟原虫抗原Pf155/RESA的人抗体对夜猴进行被动免疫。

Passive immunization of Aotus monkeys with human antibodies to the Plasmodium falciparum antigen Pf155/RESA.

作者信息

Berzins K, Perlmann H, Wåhlin B, Ekre H P, Högh B, Petersen E, Wellde B, Schoenbechler M, Williams J, Chulay J

机构信息

Department of Immunology, Stockholm University, Sweden.

出版信息

Infect Immun. 1991 Apr;59(4):1500-6. doi: 10.1128/iai.59.4.1500-1506.1991.

Abstract

In order to assess the protective effects of anti-Pf155/RESA antibodies of different specificities in vivo, passive immunizations of Aotus monkeys were performed. Antibodies reactive with the Pf155/RESA repeat sequences (EENV)2 and EENVEHDA were isolated from the immunoglobulin G (IgG) fraction of a pool of plasmas from Liberia by affinity chromatography on synthetic peptides. The two fractions of antibodies differed in specificity but displayed similar capacities to inhibit merozoite invasion in Plasmodium falciparum in vitro cultures. Four groups of monkeys (named groups I to IV) were injected with (i) 160 mg of total control IgG, (ii) 2 mg of IgG affinity purified on (EENV)2, (iii) 2 mg of IgG affinity purified on EENVEHDA, and (iv) 160 mg of total immune IgG, respectively. The monkeys were then challenged with P. falciparum-infected erythrocytes, and the levels of parasitemia and hematocrits as well as other serological parameters were determined daily. Although all groups developed parasitemia, groups II and IV tended to show lower mean daily levels. Three monkeys of group II and two monkeys (each) of groups III and IV self cured the infections, but so did one monkey from the group treated with control IgG (group I). The serum levels of transfused antibodies were low at the peak of parasitemia, suggesting that clearance of parasites was mediated by immune responses mounted by the monkeys. The results indicate that antibodies to epitopes formed by repeats of Pf155/RESA may depress P. falciparum parasitemias and thus that immunogens based on such repeats should be suitable components in a subunit vaccine against asexual stages of P. falciparum.

摘要

为了评估体内不同特异性的抗Pf155/RESA抗体的保护作用,对夜猴进行了被动免疫。通过在合成肽上进行亲和层析,从利比里亚血浆池中分离出与Pf155/RESA重复序列(EENV)2和EENVEHDA反应的抗体,这些抗体来自免疫球蛋白G(IgG)部分。这两组抗体特异性不同,但在体外培养中对恶性疟原虫裂殖子入侵的抑制能力相似。四组猴子(命名为I至IV组)分别注射:(i)160mg总对照IgG,(ii)2mg在(EENV)2上亲和纯化的IgG,(iii)2mg在EENVEHDA上亲和纯化的IgG,以及(iv)160mg总免疫IgG。然后用感染恶性疟原虫的红细胞对猴子进行攻击,并每天测定疟原虫血症水平、血细胞比容以及其他血清学参数。虽然所有组都出现了疟原虫血症,但II组和IV组的平均每日水平往往较低。II组的三只猴子以及III组和IV组的各两只猴子自愈了感染,但用对照IgG治疗的组(I组)中的一只猴子也自愈了。在疟原虫血症高峰期,输注抗体的血清水平较低,这表明寄生虫的清除是由猴子产生的免疫反应介导的。结果表明,针对Pf155/RESA重复序列形成的表位的抗体可能会降低恶性疟原虫的疟原虫血症,因此基于此类重复序列的免疫原应该是抗恶性疟原虫无性阶段亚单位疫苗的合适成分。

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