Toms G L
Department of Virology, University of Newcastle-upon-Tyne Medical School, United Kingdom.
Lung. 1990;168 Suppl:388-95. doi: 10.1007/BF02718156.
Attempts to develop a respiratory syncytial virus vaccine have revealed the antigenic heterogeneity of the virus and have highlighted the difficulties of inducing protective responses in very young infants. Of the two subgroups of the virus, A and B, that cocirculate, A appears to be the most aggressive in infants, but protection against both will be required. Although a degree of protection is transferred from mother to the infant via the placenta and by breast feeding, the mechanisms of protection remain ill-understood and early hopes of exploiting this phenomenon have not been realized. The immune response to the virus in the very young is depressed but disease severity is not demonstrably linked to failure to control virus replication. Rather, immune mechanisms contribute directly to the development of bronchiolitis. The involvement of the immune response in the pathologic process increases the hazards of vaccination. Research is currently focused on the definition of viral epitopes necessary to induce only a protective immune response and their incorporation into a suitable vaccine vector.
研发呼吸道合胞病毒疫苗的尝试揭示了该病毒的抗原异质性,并凸显了在非常年幼的婴儿中诱导保护性反应的困难。在共同流行的病毒A和B两个亚组中,A在婴儿中似乎最具侵袭性,但需要对两者都提供保护。尽管一定程度的保护可通过胎盘和母乳喂养从母亲传递给婴儿,但保护机制仍未得到充分理解,而且利用这一现象的早期希望也尚未实现。非常年幼的婴儿对该病毒的免疫反应受到抑制,但疾病严重程度与未能控制病毒复制并无明显关联。相反,免疫机制直接导致细支气管炎的发展。免疫反应参与病理过程增加了疫苗接种的风险。目前的研究重点是确定仅诱导保护性免疫反应所需的病毒表位,并将其纳入合适的疫苗载体。