Ionescu Roxana M, Przysiecki Craig T, Liang Xiaoping, Garsky Victor M, Fan Jiang, Wang Bei, Troutman Robert, Rippeon Yvette, Flanagan Elizabeth, Shiver John, Shi Li
Biologics and Vaccines PR&D, Merck Research Laboratories, Merck & Co., Inc., P.O Box 4, West Point, Pennsylvania 19486-0004, USA.
J Pharm Sci. 2006 Jan;95(1):70-9. doi: 10.1002/jps.20493.
We report the preparation and the immunogenicity of a conjugate vaccine obtained by chemically conjugating a variant of the extracellular peptide fragment of influenza type A M2 protein to the human papillomavirus (HPV) viruslike particle (VLP). Conjugates comprised of approximately 4,000 copies of the antigenic peptide per VLP are obtained as the result of the reaction between a C-terminal cysteine residue on the peptide and the maleimide-activated HPV VLP. The resulting conjugates have an average particle size slightly larger than the carrier and present enhanced overall stability against chemical and thermal-induced denaturation. The M2-HPV VLP conjugates lost the binding affinity for anti-HPV conformational antibodies but retained reactivity to a M2-specific monoclonal antibody. The conjugate vaccine formulated with aluminum adjuvant and delivered in two doses of 30-ng peptide was found to be highly immunogenic and conferred good protection against lethal challenge of influenza virus in mice. These results suggest that HPV VLP can be used as a carrier for synthetic or small antigens for the development of subunit vaccines.
我们报告了一种结合疫苗的制备及其免疫原性,该疫苗通过将甲型流感病毒M2蛋白细胞外肽片段的变体与人类乳头瘤病毒(HPV)病毒样颗粒(VLP)进行化学偶联而获得。肽段C末端的半胱氨酸残基与马来酰亚胺活化的HPV VLP反应,结果是每个VLP获得由约4000个抗原肽拷贝组成的偶联物。所得偶联物的平均粒径略大于载体,并且对化学和热诱导的变性具有增强的整体稳定性。M2-HPV VLP偶联物失去了与抗HPV构象抗体的结合亲和力,但保留了对M2特异性单克隆抗体的反应性。发现用铝佐剂配制并以两剂30 ng肽给药的偶联疫苗具有高度免疫原性,并在小鼠中对流感病毒的致死性攻击提供了良好的保护。这些结果表明,HPV VLP可用作合成或小抗原的载体,用于开发亚单位疫苗。