The Jenner Institute, University of Oxford, Oxford, United Kingdom.
PLoS One. 2011;6(12):e29428. doi: 10.1371/journal.pone.0029428. Epub 2011 Dec 28.
The ookinete surface protein Pfs25 is a macrogamete-to-ookinete/ookinete stage antigen of Plasmodium falciparum, capable of exerting high-level anti-malarial transmission-blocking activity following immunization with recombinant protein-in-adjuvant formulations. Here, this antigen was expressed in recombinant chimpanzee adenovirus 63 (ChAd63), human adenovirus serotype 5 (AdHu5) and modified vaccinia virus Ankara (MVA) viral vectored vaccines. Two immunizations were administered to mice in a heterologous prime-boost regime. Immunization of mice with AdHu5 Pfs25 at week 0 and MVA Pfs25 at week 10 (Ad-MVA Pfs25) resulted in high anti-Pfs25 IgG titers, consisting of predominantly isotypes IgG1 and IgG2a. A single priming immunization with ChAd63 Pfs25 was as effective as AdHu5 Pfs25 with respect to ELISA titers at 8 weeks post-immunization. Sera from Ad-MVA Pfs25 immunized mice inhibited the transmission of P. falciparum to the mosquito both ex vivo and in vivo. In a standard membrane-feeding assay using NF54 strain P. falciparum, oocyst intensity in Anopheles stephensi mosquitoes was significantly reduced in an IgG concentration-dependent manner when compared to control feeds (96% reduction of intensity, 78% reduction in prevalence at a 1 in 5 dilution of sera). In addition, an in vivo transmission-blocking effect was also demonstrated by direct feeding of immunized mice infected with Pfs25DR3, a chimeric P. berghei line expressing Pfs25 in place of endogenous Pbs25. In this assay the density of Pfs25DR3 oocysts was significantly reduced when mosquitoes were fed on vaccinated as compared to control mice (67% reduction of intensity, 28% reduction in prevalence) and specific IgG titer correlated with efficacy. These data confirm the utility of the adenovirus-MVA vaccine platform for the induction of antibodies with transmission-blocking activity, and support the continued development of this alternative approach to transmission-blocking malaria subunit vaccines.
疟原虫合子表面蛋白 Pfs25 是恶性疟原虫配子体向合子/合子期的一种大配子抗原,用重组蛋白佐剂制剂免疫后能发挥高水平的抗疟传播阻断活性。在这里,该抗原在重组黑猩猩腺病毒 63(ChAd63)、人腺病毒 5 型(AdHu5)和改良痘苗病毒安卡拉(MVA)病毒载体疫苗中表达。在异源初免-加强免疫方案中,给小鼠进行了两次免疫接种。在第 0 周用 AdHu5 Pfs25 免疫小鼠,在第 10 周用 MVA Pfs25 免疫(Ad-MVA Pfs25),导致高水平的抗 Pfs25 IgG 滴度,主要由 IgG1 和 IgG2a 组成。用 ChAd63 Pfs25 进行单次初免与 AdHu5 Pfs25 相比,在免疫后 8 周时 ELISA 滴度相当。用 Ad-MVA Pfs25 免疫的小鼠血清在体外和体内均能抑制疟原虫向蚊子的传播。在使用 NF54 株疟原虫的标准膜喂养测定中,与对照饲料相比,在蚊子中,用 IgG 浓度依赖性方式显著降低了疟原虫孢子强度(强度降低 96%,血清稀释度为 1 比 5 时,流行率降低 78%)。此外,在用 Pf s25DR3 感染的免疫小鼠直接进行体内喂养时,也证明了具有阻断传播的作用,Pf s25DR3 是一种嵌合性伯氏疟原虫系,用 Pf s25 替代内源性 Pbs25 表达 Pf s25。在该测定中,与对照小鼠相比,当蚊子以接种疫苗的小鼠为食时,Pfs25DR3 合子囊泡的密度显著降低(强度降低 67%,流行率降低 28%),并且特异性 IgG 滴度与功效相关。这些数据证实了腺病毒-MVA 疫苗平台在诱导具有传播阻断活性的抗体方面的实用性,并支持继续开发这种替代的传播阻断疟疾亚单位疫苗的方法。