Sedegah M, Weiss W W, Hoffman S L
Malaria Program, Naval Medical Research Center, Silver Spring, MD, USA.
Parasite Immunol. 2007 Nov;29(11):559-65. doi: 10.1111/j.1365-3024.2007.00976.x.
An attenuated Plasmodium falciparum sporozoite (PfSPZ) vaccine is under development, in part, based on studies in mice with P. berghei. We used P. berghei and P. yoelii to study vaccine-induced protection against challenge with a species of parasite different from the immunizing parasite in BALB/c mice. One-hundred percent of mice were protected against homologous challenge. Seventy-nine percent immunized with attenuated P. berghei sporozoite (PbSPZ) (six experiments) were protected against challenge with P. yoelii sporozoite (PySPZ), and 63% immunized with attenuated PySPZ (three experiments) were protected against challenge with PbSPZ. Antibodies in sera of immunized mice only recognized homologous sporozoites and could not have mediated protection against heterologous challenge. Immunization with attenuated PySPZ or PbSPZ induced CD8+ T cell-dependent protection against heterologous challenge. Immunization with attenuated PySPZ induced CD8+ T cell-dependent protection against homologous challenge. However, homologous protection induced by attenuated PbSPZ was not dependent on CD8+ or CD4+ T cells, and depletion of both populations only reduced protection by 36%. Immunization of C57BL/10 mice with PbSPZ induced CD8+ T cell-dependent protection against P. berghei, but no protection against P. yoelii. The cross-protection data in BALB/c mice support testing a human vaccine based on attenuated PfSPZ for its efficacy against P. vivax.
一种减毒恶性疟原虫子孢子(PfSPZ)疫苗正在研发中,部分是基于对感染伯氏疟原虫小鼠的研究。我们使用伯氏疟原虫和约氏疟原虫来研究疫苗诱导的针对与免疫所用寄生虫不同种类寄生虫攻击的保护作用,在BALB/c小鼠中进行试验。100%的小鼠对同源攻击具有保护作用。用减毒伯氏疟原虫子孢子(PbSPZ)免疫的小鼠中有79%(六个实验)对约氏疟原虫子孢子(PySPZ)攻击具有保护作用,用减毒PySPZ免疫的小鼠中有63%(三个实验)对PbSPZ攻击具有保护作用。免疫小鼠血清中的抗体仅识别同源子孢子,不能介导针对异源攻击的保护作用。用减毒PySPZ或PbSPZ免疫可诱导CD8 + T细胞依赖性的针对异源攻击的保护作用。用减毒PySPZ免疫可诱导CD8 + T细胞依赖性的针对同源攻击的保护作用。然而,减毒PbSPZ诱导的同源保护不依赖于CD8 +或CD4 + T细胞,去除这两种细胞群体仅使保护作用降低36%。用PbSPZ免疫C57BL/10小鼠可诱导针对伯氏疟原虫的CD8 + T细胞依赖性保护作用,但对约氏疟原虫无保护作用。BALB/c小鼠中的交叉保护数据支持对基于减毒PfSPZ的人类疫苗针对间日疟原虫的疗效进行测试。