Plotkin Stanley
Emeritus Professor of Pediatrics, University of Pennsylvania, 4650 Wismer Road, Doylestown, PA, 18902, USA,
Med Microbiol Immunol. 2015 Jun;204(3):247-54. doi: 10.1007/s00430-015-0388-z. Epub 2015 Mar 20.
Cytomegalovirus vaccine development started in the 1970s with attenuated strains. In the 1980s, one of the strains was shown to be safe and effective in renal transplant patients. Then, attention switched to glycoprotein gB, which was shown to give moderate but transient protection against acquisition of the virus by women. The identification of the pp65 tegument protein as the principal target of cellular immune responses resulted in new approaches, particularly DNA, plasmids to protect hematogenous stem cell recipients. The subsequent discovery of the pentameric protein complex that generates most neutralizing antibodies led to efforts to incorporate that complex into vaccines. At this point, there are many candidate CMV vaccines, including live recombinants, replication-defective virus, DNA plasmids, soluble pentameric proteins, peptides, virus-like particles and vectored envelope proteins.
巨细胞病毒疫苗的研发始于20世纪70年代,最初使用的是减毒株。20世纪80年代,其中一种毒株在肾移植患者中显示出安全有效。随后,关注点转向糖蛋白gB,它对女性预防病毒感染有一定但短暂的保护作用。pp65被膜蛋白被确定为细胞免疫反应的主要靶点,这带来了新的方法,特别是DNA质粒,用于保护造血干细胞接受者。随后发现了产生大多数中和抗体的五聚体蛋白复合物,促使人们努力将该复合物纳入疫苗。目前,有许多候选的巨细胞病毒疫苗,包括活重组体、复制缺陷病毒、DNA质粒、可溶性五聚体蛋白、肽、病毒样颗粒和载体包膜蛋白。