Perlaza B L, Arévalo-Herrera M, Brahimi K, Quintero G, Palomino J C, Gras-Masse H, Tartar A, Druilhe P, Herrera S
Instituto de Inmunologia, Universidad del Valle, AA 2188 Cali, Colombia.
Infect Immun. 1998 Jul;66(7):3423-8. doi: 10.1128/IAI.66.7.3423-3428.1998.
Aotus lemurinus monkeys were immunized with pools of either lipid-tailed peptides injected in PBS or peptides in Montanide ISA-51, all derived from four Plasmodium falciparum pre-erythrocytic antigens, namely, LSA1, LSA3, SALSA, and STARP. These formulations were well tolerated. Their immunogenicity was demonstrated by the induction of both B- and T-cell responses to most of the peptides studied (of the 12, 10 induced antibody production, 9 induced T-cell proliferative responses, and all 12 induced gamma interferon secretion). Immune responses proved to be long lasting, since some were still detectable 210 days after immunization. Of particular importance is the fact that B- and T-cell responses elicited in this way by synthetic peptides were specific for native parasite proteins on P. falciparum sporozoites and liver stage parasites.
夜猴用注射于PBS中的脂尾肽池或Montanide ISA - 51中的肽进行免疫,所有这些肽均源自四种恶性疟原虫红细胞前期抗原,即LSA1、LSA3、SALSA和STARP。这些制剂耐受性良好。通过对大多数研究肽诱导B细胞和T细胞反应证明了它们的免疫原性(在12种肽中,10种诱导抗体产生,9种诱导T细胞增殖反应,所有12种均诱导γ干扰素分泌)。免疫反应被证明是持久的,因为在免疫后210天仍可检测到一些反应。特别重要的是,合成肽以这种方式引发的B细胞和T细胞反应对恶性疟原虫子孢子和肝期寄生虫上的天然寄生虫蛋白具有特异性。