Su Zhong, Tam Mi-Fong, Jankovic Dragana, Stevenson Mary M
Centre for the Study of Host Resistance, McGill University Health Centre Research Institute, McGill University, Montreal, Quebec, Canada.
Infect Immun. 2003 Sep;71(9):5178-87. doi: 10.1128/IAI.71.9.5178-5187.2003.
An important aspect of malaria vaccine development is the identification of an appropriate adjuvant which is both capable of stimulating a protective immune response and safe for use by humans. Here, we investigated the feasibility of using novel immunostimulatory molecules as adjuvants combined with a crude antigen preparation and coadsorbed to aluminum hydroxide (alum) as a vaccine against blood-stage Plasmodium chabaudi AS malaria. Prior to challenge infection, immunization of genetically susceptible A/J mice with the combination of malaria antigen plus recombinant interleukin-12 (IL-12) in alum induced a Th1 immune response with production of high levels of gamma interferon (IFN-gamma) and diminished IL-4 levels by spleen cells stimulated in vitro with parasite antigen compared to mice immunized with antigen alone, antigen in alum, or antigen plus IL-12. Mice immunized with malaria antigen plus recombinant IL-12 in alum had high levels of total malaria-specific antibody and immunoglobulin G2a. Compared to unimmunized mice, immunization with antigen plus IL-12 in alum induced the highest level of protective immunity against challenge infection with P. chabaudi AS, which was evident as a significantly decreased peak parasitemia level and 100% survival. Protective immunity was dependent on CD4(+) T cells, IFN-gamma, and B cells and was long-lasting. Replacement of IL-12 as an adjuvant by synthetic oligodeoxynucleotides (ODN) containing CpG motifs induced a similar level of vaccine-induced protection against challenge infection with P. chabaudi AS. These results illustrate that it is possible to enhance the potency of a crude malaria antigen preparation delivered in alum by inclusion of immunostimulatory molecules, such as IL-12 or CpG-ODN.
疟疾疫苗研发的一个重要方面是确定一种合适的佐剂,该佐剂既要能够刺激产生保护性免疫反应,又要对人类使用安全。在此,我们研究了使用新型免疫刺激分子作为佐剂与粗抗原制剂联合,并共吸附于氢氧化铝(明矾)上作为针对血液期查巴迪疟原虫AS株疟疾疫苗的可行性。在进行攻击感染之前,用疟疾抗原加重组白细胞介素-12(IL-12)与明矾的组合对基因易感的A/J小鼠进行免疫,与单独用抗原、抗原加明矾或抗原加IL-12免疫的小鼠相比,体外经寄生虫抗原刺激的脾细胞产生高水平的γ干扰素(IFN-γ)并降低IL-4水平,从而诱导了Th1免疫反应。用疟疾抗原加重组IL-12与明矾免疫的小鼠具有高水平的总疟疾特异性抗体和免疫球蛋白G₂a。与未免疫的小鼠相比,用抗原加IL-12与明矾免疫诱导了针对查巴迪疟原虫AS攻击感染的最高水平的保护性免疫,这表现为明显降低的峰值寄生虫血症水平和100%的存活率。保护性免疫依赖于CD4⁺T细胞、IFN-γ和B细胞,并且是持久的。用含CpG基序的合成寡脱氧核苷酸(ODN)替代IL-12作为佐剂,诱导了类似水平的疫苗诱导的针对查巴迪疟原虫AS攻击感染的保护作用。这些结果表明,通过加入免疫刺激分子,如IL-12或CpG-ODN,可以提高明矾中递送的粗疟疾抗原制剂的效力。