Silvie O, Semblat J P, Franetich J F, Hannoun L, Eling W, Mazier D
INSERM U511 Immunobiologie Cellulaire et Moléculaire des Infections Parasitaires, CHU Pitié-Salpêtrière, Université Pierre et Marie Curie, Paris, France.
Parasite Immunol. 2002 Apr;24(4):221-3. doi: 10.1046/j.1365-3024.2002.00450.x.
Immunization with irradiation-attenuated Plasmodium sporozoites confer protection against live sporozoite challenge. Protection relies primarily on cytotoxic lymphocyte activity against infected hepatocytes, and is suppressed when sporozoites are over-irradiated. Here, we demonstrate that over-irradiated (25-30 krad) Plasmodium falciparum sporozoites invade human hepatocytes and transform into uninucleate liver-trophozoites with the same efficiency as non-irradiated and irradiation-attenuated (12-15 krad) sporozoites. Since hepatocytes infected with over-irradiated non-protective sporozoites are likely to express sporozoite-derived peptide/major histocompatibility complex class I molecules on their surface, our results strongly suggest that sporozoite proteins are not the main immunogens involved in protection, and thus may not per se constitute proper malaria vaccine candidates.
用经辐射减毒的疟原虫子孢子进行免疫可提供针对活子孢子攻击的保护作用。这种保护主要依赖于细胞毒性淋巴细胞对受感染肝细胞的活性,当子孢子过度辐射时,这种保护作用会受到抑制。在此,我们证明,过度辐射(25 - 30千拉德)的恶性疟原虫子孢子侵入人肝细胞并转化为单核肝滋养体的效率与未辐射和经辐射减毒(12 - 15千拉德)的子孢子相同。由于感染了过度辐射的无保护作用子孢子的肝细胞可能在其表面表达源自子孢子的肽/主要组织相容性复合体I类分子,我们的结果强烈表明,子孢子蛋白不是参与保护作用的主要免疫原,因此其本身可能不构成合适的疟疾疫苗候选物。