免疫球蛋白G, A和M对不同年龄组流感疫苗接种的反应:启动和增强的效果。

W E Beyer, J T Van der Logt, R van Beek, N Masurel
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引用次数: 19

摘要

50名志愿者接种了含有A/曼谷/1/79 (H3N2)、A/巴西/11/78 (H1N1)和B/新加坡/222/79病毒的灭活三价流感疫苗,根据他们一生中首次接触流感的估计时间(启动)和疫苗接种前血清中针对疫苗成分的抗体的存在,对他们进行了细分。采用抗体捕获血液吸附免疫吸附技术检测抗体的同型反应(IgG, IgA, IgM)。对于所有三种疫苗成分,以前血清阳性的受试者比以前血清阴性的人更频繁地产生IgG和iga类抗体。与未启动的受试者相比,启动甲型流感亚型之一的受试者表现出更多的IgG和IgA反应(启动效应)。相比之下,针对甲型H3N2和甲型H1N1, IgM抗体分别在引物组的19%和11%中出现,而在未引物组的59%和54%中分别出现。IgM滴度升高的发生率不受预防接种状态的影响。然而,抗甲型H1N1流感-IgM滴度的平均上升幅度在先前血清阴性的患者中更大。讨论了原发感染和再感染以及“原始抗原原罪”的概念,并建议在研究流感感染或疫苗接种后的同型抗体反应时,应考虑年龄和(如果可能的话)抗原暴露前的血清学状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunoglobulin G, A and M response to influenza vaccination in different age groups: effects of priming and boosting.

Fifty volunteers, treated with an inactivated trivalent influenza vaccine containing A/Bangkok/1/79 (H3N2), A/Brazil/11/78 (H1N1) and B/Singapore/222/79 virus, were subdivided according to the estimated first exposure to influenza in their lifetime (priming) and the presence of antibodies against the vaccine components in the pre-vaccination sera. The isotypic antibody response (IgG, IgA, IgM) was determined by means of an antibody capture haemadsorption immunosorbent technique. For all three vaccine components, previously seropositive subjects produced antibodies of the IgG- and IgA-class more frequently than previously seronegative persons. Subjects primed to one of the influenza A subtypes showed more IgG and IgA responses in comparison with those unprimed (prime-effect). In contrast, IgM antibodies occurred in only 19 and 11% of primed, but in 59 and 54% of unprimed subjects, for A (H3N2) and A (H1N1), respectively. The incidence of IgM titre rises was not influenced by the prevaccination state. However, the mean magnitude of anti-A (H1N1)-IgM titre rises was greater in those previously seronegative. The concepts of primary and reinfection and of 'original antigenic sin' are discussed, and it is suggested that age and, if possible, serological state prior to antigen-exposure should be taken into account when studying isotypic antibody responses after influenza infection or vaccination.

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