Brandt E R, Good M F
Molecular Immunology Laboratory, The Co-operative Centre for Vaccine Technology, Queensland Institute of Medical Research.
Immunol Res. 1999;19(1):89-103. doi: 10.1007/BF02786478.
Group A streptococci (GAS) are responsible for numerous human illnesses, ranging from pharyngitis to severe invasive infections, such as necrotizing fascitis and toxic shock syndrome to the postinfectious sequelae, acute rheumatic fever (ARF), and glomerulonephritis. To date, to develop a vaccine, studies have focused on the M protein. However, designing a vaccine to prevent GAS infection based on this molecule has been hampered by the vast number of M protein serotypes and the possibility that it may induce potentially harmful autoimmune reactions. In this article, the authors discuss recent approaches to overcoming the problems of an M protein-based vaccine. In addition, recent studies identifying the protective properties of other streptococcal antigens and their potential as vaccine candidates are discussed.
A组链球菌(GAS)可引发多种人类疾病,从咽炎到严重的侵袭性感染,如坏死性筋膜炎和中毒性休克综合征,再到感染后后遗症、急性风湿热(ARF)和肾小球肾炎。迄今为止,为研发疫苗,研究主要集中在M蛋白上。然而,基于该分子设计预防GAS感染的疫苗一直受到大量M蛋白血清型的阻碍,以及它可能诱导潜在有害自身免疫反应的可能性。在本文中,作者讨论了克服基于M蛋白疫苗问题的最新方法。此外,还讨论了最近确定其他链球菌抗原的保护特性及其作为候选疫苗潜力的研究。