Collins W E, Chin W, Skinner J C
Am J Trop Med Hyg. 1979 Nov;28(6):948-54. doi: 10.4269/ajtmh.1979.28.948.
Pladmodium fragile and the Macaca mulatta monkey are presented as a model system for the study of malarial vaccines. Four animals were immunized with culture-grown P. fragile merozoites and subsequently challenged with culture-produced parasites. One animal failed to develop a detectable parasitemia following primary challenge. Two other immunized animals had primary infections which were short-term. the parasitemias in these three monkeys following secondary challenge were short-term and the immunity was apparently sterilizing. The fourth immunized monkeys had recrudescences of the primary and secondary infection but differed markedly from the four control animals. Indirect fluorescent antibody titers increased as a result of the immunization and were indicative of the level of immunity. Because of the many similarities to the human-P. falciparum model system, the P. fragile-M. mulatta system appears to be particularly well suited for a number of malaria vaccine studies.
脆弱疟原虫和恒河猴被作为研究疟疾疫苗的模型系统。用培养生长的脆弱疟原虫子孢子免疫4只动物,随后用培养产生的寄生虫进行攻击。一只动物在初次攻击后未出现可检测到的寄生虫血症。另外两只免疫动物的初次感染为短期感染。这三只猴子在再次攻击后的寄生虫血症为短期感染,且免疫力显然具有杀菌作用。第四只免疫猴子出现了初次和再次感染的复发,但与四只对照动物有明显不同。免疫后间接荧光抗体滴度升高,表明了免疫水平。由于与人类恶性疟原虫模型系统有许多相似之处,脆弱疟原虫-恒河猴系统似乎特别适合进行多项疟疾疫苗研究。