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通过酶联免疫斑点分析和肠段培养评估小鼠轮状病毒特异性肠道免疫反应。

Rotavirus-specific intestinal immune response in mice assessed by enzyme-linked immunospot assay and intestinal fragment culture.

作者信息

Khoury C A, Brown K A, Kim J E, Offit P A

机构信息

Division of Gastroenterology and Nutrition, University of Pennsylvania School of Medicine, Philadelphia 19104, USA.

出版信息

Clin Diagn Lab Immunol. 1994 Nov;1(6):722-8. doi: 10.1128/cdli.1.6.722-728.1994.

Abstract

Primate rotavirus strain RRV and bovine strain WC3 or reassortants made between these animal viruses and human rotaviruses have been administered to infants as candidate vaccines. We compared RRV and WC3 in a murine model of oral infection. We determined the relative capacities of these viruses to induce a virus-specific humoral immune response by intestinal lymphocytes as tested by enzyme-linked immunospot assay, intestinal fragment culture, and enzyme-linked immunosorbent assay of intestinal contents. We found that inoculation of mice with RRV induced higher frequencies of virus-specific immunoglobulin A (IgA)-secreting cells in the lamina propria, greater quantities of virus-specific IgA in intestinal fragment cultures, and greater quantities of virus-specific IgA in intestinal secretions than did inoculation with WC3 or inactivated RRV (iRRV). The induction of an IgA response in serum was predictive of an IgA response among intestinal lymphocytes after inoculation with RRV but not WC3. In addition, large quantities of IgG, IgA, and IgM not specific for rotavirus were produced in fragment cultures from mice inoculated with RRV but not in cultures from mice inoculated with WC3 or iRRV. Possible mechanisms of RRV-induced polyclonal stimulation of intestinal B cells are discussed.

摘要

灵长类轮状病毒株RRV和牛轮状病毒株WC3,或由这些动物病毒与人类轮状病毒构建的重配病毒株,已作为候选疫苗接种于婴儿。我们在小鼠口腔感染模型中比较了RRV和WC3。我们通过酶联免疫斑点试验、肠段培养以及对肠内容物进行酶联免疫吸附试验,测定了这些病毒诱导肠道淋巴细胞产生病毒特异性体液免疫应答的相对能力。我们发现,与接种WC3或灭活RRV(iRRV)相比,给小鼠接种RRV能在固有层诱导出更高频率的病毒特异性分泌免疫球蛋白A(IgA)的细胞,在肠段培养物中产生更多量的病毒特异性IgA,以及在肠道分泌物中产生更多量的病毒特异性IgA。接种RRV后血清中IgA应答的诱导可预测肠道淋巴细胞中的IgA应答,但接种WC3后则不然。此外,接种RRV的小鼠的肠段培养物中产生了大量非轮状病毒特异性的IgG、IgA和IgM,而接种WC3或iRRV的小鼠的培养物中则未产生。本文讨论了RRV诱导肠道B细胞多克隆刺激的可能机制。

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