Gonzalez Ana María, Jaimes Maria C, Rojas Olga L, Angel Juana, Greenberg Harry B, A Franco Manuel
Instituto de Genetica Humana Pontificia Universidad Javeriana, Bogotá, Colombia.
Departments of Medicine, Microbiology and Immunology, Stanford University School of Medicine, 300 Pasteur Dr, CCSR Bldg Rm 3115, Stanford, CA 94305-5187, USA.
Perspect Med Virol. 2003;9:307-316. doi: 10.1016/S0168-7069(03)09018-9. Epub 2004 Sep 14.
This chapter discusses the human adaptive immune response to rotaviruses (RVs), placing the immune response to RVs in the context of the immune response to other mucosal viruses. The chapter discusses the studies of both RV-specific T and B cells. As children with T and/or B immunodeficiencies can develop chronic RV infection, prolonged symptoms, and extraintestinal infection, it is clear that both T and B cells are important for immunity to RV. The various reasons proposed to explain the absence of complete immunity to mucosal viruses such as RV, following primary infection, include a short incubation period after viral exposure, difficulty in maintaining a high level of protective antibody at respiratory and gastrointestinal mucosal surfaces, and a short-lived protective humoral mucosal immune response.
本章讨论了人类对轮状病毒(RVs)的适应性免疫反应,并将对RVs的免疫反应置于对其他黏膜病毒的免疫反应背景中。本章讨论了RV特异性T细胞和B细胞的研究。由于患有T和/或B免疫缺陷的儿童可能会发生慢性RV感染、症状迁延以及肠道外感染,显然T细胞和B细胞对RV免疫都很重要。对于初次感染后为何缺乏对RV等黏膜病毒的完全免疫力,人们提出了各种原因,包括病毒暴露后的潜伏期短、在呼吸道和胃肠道黏膜表面难以维持高水平的保护性抗体以及保护性体液黏膜免疫反应持续时间短。