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Kinetics of the in vitro antibody response to transmissible gastroenteritis (TGE) virus from pig mesenteric lymph node cells using the ELISASPOT and ELISA tests

机译:使用ELISASPOT和ELISA测试对猪肠系膜淋巴结细胞对传染性胃肠炎(TGE)病毒的体外抗体反应的动力学

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摘要

A method is described for in vitro studies of viral humoral immune responses in the pig. After oral immunization with transmissible gastroenteritis (TGE) coronavirus, antibody production from primed mesenteric lymph node cells was revealed by an in vitro boost with viral antigen. For the latter the leukocytes were co-cultured with UV-inactivated virus using a variety of different methods of antigenic stimulation. Enumeration of specific antibody-secreting cells (ASC) and titration of secreted anti-virus antibodies were performed with ELISASPOT (using 3-amino 9-ethyl carbazole as the peroxidase chromogen) and ELISA tests respectively, according to the Ig isotype. The results showed a close relationship between ASC numbers and secreted antibody titres. The best in vitro antibody synthesis was observed when the sensitized cells were maintained in contact with virus during the whole culture period. Antibody responses were defined by a kinetic profile characterized by a narrow peak, with a maximum occuring after 4 and 6 days of culture and with the IgA response appearing earlier than the IgG. This methodology, which analyses specific antibody responses at the cellular level, may permit studies on the mechanisms of Ig isotype regulation. Extended to leukocytes from other organs of the immune system, it may also constitute an in vitro model to study antibody responses expressed in different lymphoid tissues of the pig.
机译:描述了一种用于体外研究猪中病毒体液免疫反应的方法。用可传播性胃肠炎(TGE)冠状病毒进行口服免疫后,通过体外用病毒抗原加强免疫,可以使初免的肠系膜淋巴结细胞产生抗体。对于后者,使用多种不同的抗原刺激方法将白细胞与紫外线灭活的病毒共培养。根据Ig同种型,分别使用ELISASPOT(使用3-氨基9-乙基咔唑作为过氧化物酶发色剂)和ELISA测试进行特异性抗体分泌细胞(ASC)的计数和滴定分泌的抗病毒抗体的滴定。结果表明,ASC数量与分泌的抗体滴度之间存在密切关系。当致敏细胞在整个培养过程中保持与病毒接触时,可以观察到最佳的体外抗体合成。抗体反应由动力学特征定义,该动力学特征以窄峰为特征,最大峰发生在培养4天和6天后,而IgA反应的出现要早于IgG。这种在细胞水平上分析特异性抗体应答的方法学可以允许研究Ig同种型调节的机制。它可以扩展到免疫系统其他器官的白细胞,也可以构成一个体外模型来研究在猪的不同淋巴组织中表达的抗体反应。

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