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人乳头瘤病毒样颗粒作为抗原载体的药学及免疫学评价

Pharmaceutical and immunological evaluation of human papillomavirus viruslike particle as an antigen carrier.

作者信息

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

机构信息

Biologics and Vaccines PR&D, Merck Research Laboratories, Merck & Co., Inc., P.O Box 4, West Point, Pennsylvania 19486-0004, USA.

出版信息

J Pharm Sci. 2006 Jan;95(1):70-9. doi: 10.1002/jps.20493.

Abstract

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.

摘要

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。

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