Department of Infectious, Parasitic, and Immunomediated Diseases, Istituto Superiore di Sanita`, Rome, Italy.
mBio. 2010 May 18;1(1):e00042-10. doi: 10.1128/mBio.00042-10.
Human vaccines, with their exquisite antigenic specificity, have greatly helped to eliminate or dramatically abate the incidence of a number of historical and current plagues, from smallpox to bacterial meningitis. Nonetheless, as new infectious agents emerge and the number of vaccine-preventable diseases increases, the practice and benefits of single-pathogen- or disease-targeted vaccination may be put at risk by constraints of timely production, formulation complexity, and regulatory hurdles. During the last influenza pandemic, extraordinary efforts by vaccine producers and health authorities have had little or no influence on disease prevention or mitigation. Recent research demonstrating the possibility of protecting against all influenza A virus types or even phylogenetically distant pathogens with vaccines based on highly conserved peptide or saccharide sequences is changing our paradigm. "Universal vaccine" strategies could be particularly advantageous to address protection from antibiotic-resistant bacteria and fungi for which no vaccine is currently available.
人类疫苗具有高度精确的抗原特异性,极大地帮助消除或显著减少了一些历史和当前瘟疫的发病率,从小天花到细菌性脑膜炎。尽管如此,随着新的传染病原体的出现和可预防疫苗疾病的数量增加,单一病原体或疾病靶向疫苗接种的实践和益处可能会受到及时生产、配方复杂性和监管障碍的限制。在过去的流感大流行期间,疫苗生产商和卫生当局的非凡努力对疾病的预防或缓解几乎没有影响。最近的研究表明,使用基于高度保守的肽或糖序列的疫苗来预防甚至是来自亲缘关系较远的病原体的所有甲型流感病毒类型是可能的,这正在改变我们的观念。“通用疫苗”策略对于解决对抗生素耐药细菌和真菌的保护可能特别有利,因为目前还没有针对这些细菌和真菌的疫苗。