Brown T A, Murphy B R, Radl J, Haaijman J J, Mestecky J
J Clin Microbiol. 1985 Aug;22(2):259-64. doi: 10.1128/jcm.22.2.259-264.1985.
Serum and nasal wash specimens from 13 human volunteers undergoing experimental secondary infection with influenza A/Peking/2/79 (H3N2) wild-type virus were examined for the molecular form and subclass distribution of immunoglobulin A (IgA) antibodies to the viral hemagglutinin (HA). Nasal IgA antibodies were polymeric and did not bind radiolabeled secretory component, indicating that they were secretory IgA antibodies. Both IgA1 and IgA2 antibodies were detected; however, IgA1 accounted for most of the rise in IgA anti-HA levels seen after infection. In serum virtually all of the IgA HA antibodies were of the IgA1 subclass. Furthermore, the serum antibodies were predominantly polymeric and were capable of binding radiolabeled secretory component. These results suggested that the serum IgA antibodies to HA were of mucosal origin and that influenza A virus HA preferentially stimulates an IgA1 response.
对13名接受甲型/北京/2/79(H3N2)野生型病毒实验性继发感染的人类志愿者的血清和鼻洗液样本进行检测,以分析针对病毒血凝素(HA)的免疫球蛋白A(IgA)抗体的分子形式和亚类分布。鼻内IgA抗体呈多聚体形式,且不与放射性标记的分泌成分结合,表明它们是分泌型IgA抗体。同时检测到了IgA1和IgA2抗体;然而,感染后IgA抗HA水平的升高主要是由IgA1引起的。在血清中,几乎所有的IgA HA抗体都属于IgA1亚类。此外,血清抗体主要为多聚体,并且能够与放射性标记的分泌成分结合。这些结果表明,针对HA的血清IgA抗体起源于黏膜,并且甲型流感病毒HA优先刺激IgA1反应。