Gray J J, Cunliffe C, Ball J, Graham D Y, Desselberger U, Estes M K
Clinical Microbiology and Public Health Laboratory, Addenbrooke's Hospital, Cambridge, United Kingdom.
J Clin Microbiol. 1994 Dec;32(12):3059-63. doi: 10.1128/jcm.32.12.3059-3063.1994.
Pre- and postexposure sera collected from 17 adult volunteers challenged with Norwalk virus as described previously (D. Y. Graham, X. Jiang, T. Tanaka, A. Opekun, P. Madore, and M. K. Estes, J. Infect. Dis. 170:34-43, 1994) were examined for Norwalk virus-specific immunoglobulin M (IgM), IgA, and IgG by indirect enzyme-linked immunosorbent assays with recombinant Norwalk virus antigen bound to the solid phase. Sixteen of the 17 volunteers had evidence of past infection, all presenting with preexisting IgG antibody of high avidity; only one volunteer had no evidence of previous infection. Virus infection was detected in 14 of the 16 volunteers with evidence of past infection, and 9 of the infected volunteers had symptomatic illness. A significant rise in both virus-specific IgA and IgG titers was detected after challenge in all of the volunteers who became ill. Five of the asymptomatic volunteers who were infected had rising titers of virus-specific IgG, but only two of the five had a concomitant rise in their virus-specific IgA antibody titers. Antibody rises were detectable in eight of nine ill volunteers 8 to 11 days after challenge but in the asymptomatic volunteers only after more than 15 days had elapsed. Virus-specific IgM was detected after challenge in all 14 infected volunteers. Between symptomatic and asymptomatic volunteers there were no significant differences in titers of virus-specific IgG and IgA in serum before challenge; however, there were significantly higher titers in symptomatic volunteers between 8 and > 90 days after challenge for virus-specific IgG and 8 and 24 days after challenge for virus-specific IgA.
如先前所述(D.Y.格雷厄姆、蒋新、田中、A.奥佩昆、P.马多尔和M.K.埃斯蒂斯,《传染病杂志》170:34 - 43,1994年),从17名接受诺如病毒攻击的成年志愿者身上采集了暴露前和暴露后的血清,通过间接酶联免疫吸附测定法检测诺如病毒特异性免疫球蛋白M(IgM)、IgA和IgG,固相结合重组诺如病毒抗原。17名志愿者中有16名有既往感染证据,均表现为预先存在高亲和力的IgG抗体;只有1名志愿者没有既往感染证据。在16名有既往感染证据的志愿者中,有14名检测到病毒感染,其中9名受感染志愿者出现了症状性疾病。在所有患病的志愿者中,攻击后均检测到病毒特异性IgA和IgG滴度显著升高。5名无症状但受感染的志愿者病毒特异性IgG滴度升高,但其中只有2名志愿者的病毒特异性IgA抗体滴度同时升高。9名患病志愿者中有8名在攻击后8至11天可检测到抗体升高,但无症状志愿者仅在15天以上才出现抗体升高。在所有14名受感染志愿者中,攻击后均检测到病毒特异性IgM。在有症状和无症状志愿者之间,攻击前血清中病毒特异性IgG和IgA滴度无显著差异;然而,在攻击后8至>90天,有症状志愿者的病毒特异性IgG滴度以及攻击后8至24天的病毒特异性IgA滴度显著更高。