Rollman E, Hinkula J, Arteaga J, Zuber B, Kjerrström A, Liu M, Wahren Britta, Ljungberg Karl
Department of Virology, Swedish Institute for Infectious Disease Control and Microbiology and Tumor Biology Center, Karolinska Institutet, Stockholm, Sweden.
Gene Ther. 2004 Jul;11(14):1146-54. doi: 10.1038/sj.gt.3302275.
A highly desirable feature for an human immunodeficiency virus type 1 (HIV-1) vaccine is the ability to induce broadly reactive anti-envelope antibodies that can neutralize primary HIV-1 isolates. Two immunizations with an HIV-1 envelope-encoding plasmid together with recombinant granulocyte-macrophage colony-stimulating factor (rGM-CSF) resulted in high antibody titers in mice. The antibody induction was further enhanced after immunization with genes encoding HIV-1 envelopes originating from subtypes A, B and C. The sera from these animals were able to neutralize A, B and C viral isolates, whereas the sera from animals immunized solely with subtype B DNA neutralized only subtype B virus. The combined DNA vaccine gave serum antibodies with broad recognition of HIV-1 envelope epitopes as determined by peptide mapping. Cell-mediated immunity was not compromised by the increased humoral immunity. This demonstrates the ability of multiple envelope genes to induce the desired antibody response against several subtypes. Moreover, it documents the ability of rGM-CSF to enhance the potency of such a vaccine when given simultaneously. The strategy may be useful for making an HIV vaccine more potent and broadly effective against strains of different clades.
一种非常理想的1型人类免疫缺陷病毒(HIV-1)疫苗特性是能够诱导产生可中和原发性HIV-1分离株的广泛反应性抗包膜抗体。用编码HIV-1包膜的质粒与重组粒细胞-巨噬细胞集落刺激因子(rGM-CSF)进行两次免疫接种后,小鼠体内产生了高抗体滴度。在用源自A、B和C亚型的HIV-1包膜编码基因免疫后,抗体诱导作用进一步增强。这些动物的血清能够中和A、B和C病毒分离株,而仅用B亚型DNA免疫的动物血清只能中和B亚型病毒。通过肽图谱分析确定,联合DNA疫苗产生的血清抗体对HIV-1包膜表位具有广泛识别能力。细胞介导的免疫并未因体液免疫增强而受到损害。这证明了多个包膜基因诱导针对多种亚型产生所需抗体反应的能力。此外,它还证明了rGM-CSF在同时给药时增强这种疫苗效力的能力。该策略可能有助于使HIV疫苗对不同进化枝的毒株更有效力且具有更广泛的效果。