Meuwissen J H
Institute of Medical Parasitology, Catholic University of Nijmegen, The Netherlands.
Trans R Soc Trop Med Hyg. 1989;83 Suppl:57-60. doi: 10.1016/0035-9203(89)90605-6.
Transmission-blocking malaria vaccines are expected to induce an immune response which, acting in the mosquito, will prevent its infection. It is generally considered that antigametocyte antibody is one factor in this effect, but there is also evidence that phagocytes and lymphocytes may contribute to blocking mosquito infection. Transmission-blocking immunity develops naturally. Antibody capable of interfering with infection of mosquitoes was shown to persist for 4 months after parasitaemia disappeared. Titres of antibody to a 230 kDa protein in developing Plasmodium falciparum oocysts correlated with the transmission-blocking capacity of serum. Monoclonal antibodies have been raised which are capable of blocking infection of mosquitoes by P. falciparum. Some of these interfere with fertilization. The antibodies react with protein expressed in freshly emerged gametes. It should be emphasized that despite progress in laboratory studies of transmission-blocking immunity, there remains a great need for specific epidemiological studies to determine the role of transmission-blocking immunity in endemic areas.
传播阻断型疟疾疫苗有望诱导一种免疫反应,这种反应在蚊子体内起作用,可防止其感染。一般认为抗配子体抗体是产生这种效应的一个因素,但也有证据表明吞噬细胞和淋巴细胞可能有助于阻断蚊子感染。传播阻断免疫力是自然产生的。在寄生虫血症消失后,能够干扰蚊子感染的抗体显示可持续4个月。恶性疟原虫发育中的卵囊中针对一种230 kDa蛋白的抗体滴度与血清的传播阻断能力相关。已经制备出能够阻断恶性疟原虫感染蚊子的单克隆抗体。其中一些抗体干扰受精过程。这些抗体与新出现的配子中表达的蛋白质发生反应。应该强调的是,尽管在传播阻断免疫力的实验室研究方面取得了进展,但仍然非常需要进行具体的流行病学研究,以确定传播阻断免疫力在流行地区所起的作用。