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用纯化的小配子抗原进行疫苗接种可预防啮齿动物疟疾的传播。

Vaccination with purified microgamete antigens prevents transmission of rodent malaria.

作者信息

Harte P G, Rogers N, Targett G A

出版信息

Nature. 1985;316(6025):258-9. doi: 10.1038/316258a0.

Abstract

Malaria vaccination with preparations of microgametes has been shown to inhibit transmission of Plasmodium spp. to the mosquito vectors of avian, rodent and simian parasites. This transmission-blocking immunity results from the induction of microgamete-agglutinating antibodies in the vaccinated host which, when ingested in a mosquito blood meal, react with exflagellating microgametes in the midgut to prevent fertilization and oocyst development. Here we have passively transferred the immunity with gamete-specific monoclonal antibodies raised against the rodent malaria parasite Plasmodium yoelii nigeriensis, and an IgG2a isotype monoclonal antibody from a hybridoma cell line, PYG-1, has been used to identify the target antigens on the gametes and to affinity-purify sufficient quantities of specific gamete antigen to facilitate vaccination studies. This transmission-blocking monoclonal antibody immunoprecipitated microgamete antigens of apparent relative molecular mass (Mr), 67K (67,000), 59K, 57K, 42K and 35K. Immunization of mice with these proteins before infection and mosquito feeding led to a 85-99.7% reduction in transmission to the mosquito vector; vaccination via intravenous or intramuscular routes was equally effective and did not require an adjuvant.

摘要

用微配子制剂进行疟疾疫苗接种已被证明可抑制疟原虫向禽类、啮齿动物和猿类寄生虫的蚊媒传播。这种传播阻断免疫是由于在接种疫苗的宿主体内诱导产生微配子凝集抗体,当这些抗体在蚊虫吸食血液时被摄入,会与中肠内逸出鞭毛的微配子发生反应,从而阻止受精和卵囊发育。在此,我们用针对啮齿动物疟原虫约氏疟原虫黑热亚种产生的配子特异性单克隆抗体被动转移了这种免疫力,并且来自杂交瘤细胞系PYG-1的IgG2a同种型单克隆抗体已被用于鉴定配子上的靶抗原,并亲和纯化足够量的特异性配子抗原来促进疫苗接种研究。这种传播阻断单克隆抗体免疫沉淀出相对分子质量(Mr)分别为67K(67,000)、59K、57K、42K和35K的微配子抗原。在感染和蚊虫叮咬前用这些蛋白质对小鼠进行免疫,可使向蚊媒的传播减少85%至99.7%;通过静脉或肌肉途径接种疫苗同样有效,且不需要佐剂。

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