Perera K L, Handunnetti S M, Holm I, Longacre S, Mendis K
Department of Parasitology, Faculty of Medicine, University of Colombo, Sri Lanka.
Infect Immun. 1998 Apr;66(4):1500-6. doi: 10.1128/IAI.66.4.1500-1506.1998.
A successful anti-blood stage malaria vaccine trial based on a leading vaccine candidate, the major merozoite surface antigen-1 (MSP1), is reported here. The trial was based on Plasmodium cynomolgi, which is a primate malaria parasite which is highly analogous to the human parasite Plasmodium vivax, in its natural host, the toque monkey, Macaca sinica. Two recombinant baculovirus-expressed P. cynomolgi MSP1 proteins, which are analogous to the 42- and 19-kDa C-terminal fragments of P. falciparum MSP1, were tested by immunizing three groups of three animals each with either p42, p19, or both together. The vaccines were delivered subcutaneously in three doses at 4-week intervals with complete and incomplete Freund's adjuvants. Very high antibody titers were obtained against both vaccinating antigens as measured by enzyme-linked immunosorbent assay (10[6] and above) and against whole parasites as measured by indirect immunofluorescence assay (>10[5]), achieving, in most animals, about a 10-fold increase from the first to the last immunization. A blood stage challenge with P. cynomolgi parasites led, in three adjuvant-treated and three naive control animals, to blood infections which were patent for at least 44 days, reaching peak densities of 0.6 and 3.8%, respectively. In contrast, all except one of the nine animals in the three vaccinated groups were highly protected, showing either no parasitemia at all or transient parasitemias which were patent for only 1 or 2 days. When the three p19-vaccinated monkeys were rechallenged 6 months later, the protective efficacy was unchanged. The success of this trial, and striking analogies of this natural host-parasite system with human P. vivax malaria, suggests that it could serve as a surrogate system for the development of a human P. vivax malaria vaccine based on similar recombinant analogs of the P. vivax MSP1 antigen.
本文报道了一项基于主要疫苗候选物——主要裂殖子表面抗原-1(MSP1)的成功的抗血液期疟疾疫苗试验。该试验以食蟹猴疟原虫为基础,它是一种灵长类疟原虫,在其天然宿主——斯里兰卡猕猴(Macaca sinica)中,与人类疟原虫间日疟原虫高度相似。通过用三种重组杆状病毒表达的食蟹猴疟原虫MSP1蛋白(分别类似于恶性疟原虫MSP1的42 kDa和19 kDa C末端片段)免疫三组动物(每组三只),对p42、p19或两者联合免疫进行了测试。疫苗通过皮下注射,分三次剂量,每隔4周一次,并使用完全和不完全弗氏佐剂。通过酶联免疫吸附测定(ELIS A)测量,针对两种疫苗接种抗原均获得了非常高的抗体滴度(10⁶及以上),通过间接免疫荧光测定针对完整寄生虫的抗体滴度也很高(>10⁵),在大多数动物中,从首次免疫到末次免疫抗体滴度增加了约10倍。用食蟹猴疟原虫进行血液期攻击后,在三只经佐剂处理的动物和三只未处理的对照动物中导致了血液感染,这些感染至少持续了44天,峰值密度分别达到0.6%和3.8%。相比之下,三个接种疫苗组的九只动物中,除一只外,其余均受到高度保护,要么完全没有寄生虫血症,要么仅有持续1或2天的短暂寄生虫血症。当三只接种p19疫苗的猴子在6个月后再次受到攻击时,保护效果不变。该试验的成功,以及这个天然宿主-寄生虫系统与人类间日疟原虫疟疾的显著相似性,表明它可以作为一个替代系统,用于基于间日疟原虫MSP1抗原的类似重组类似物开发人类间日疟原虫疟疾疫苗。