首页> 外文OA文献 >Tissue distribution of mucosal antibody-producing cells specific for respiratory syncytial virus in severe combined immune deficiency (SCID) mice engrafted with human tonsils.
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Tissue distribution of mucosal antibody-producing cells specific for respiratory syncytial virus in severe combined immune deficiency (SCID) mice engrafted with human tonsils.

机译:在植入人扁桃体的严重联合免疫缺陷(SCID)小鼠中,对呼吸道合胞病毒具有特异性的粘膜抗体产生细胞的组织分布。

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摘要

Groups of C.B-17 SCID mice were reconstituted intraperitoneally with human tonsillar mononuclear cells (hu-TMC) from children seropositive for antibody to respiratory syncytial virus (RSV) and subsequently challenged intraperitoneally with inactivated RSV or sham-immunized. The synthesis and the distribution characteristics of human antibody to RSV in various murine tissues were studied using an enzyme-linked immunospot assay (ELISPOT). No specific antibody was observed in sham-immunized animals. In contrast, mice engrafted with hu-TMC exhibited the appearance of specific human antibody secreting cells (hu-ASC) after i.p. immunization with inactivated RSV. RSV-specific hu-ASC were detected only in animals engrafted with cells from donors seropositive for antibodies to Epstein-Barr virus. Hu-TMC engrafted mice showed RSV-specific IgM and, in lower numbers, IgG hu-ASC in several tissues including the lungs. Numbers of RSV-specific IgA hu-ASC were low, however, and detected only in the lung. No RSV-specific hu-ASC were detected in the intestine. These data demonstrate for the first time that hu-TMC-SCID chimeras respond to immunization with viral antigen. Furthermore, the results suggest that hu-TMC engraft in lungs but not in the intestinal tissue.
机译:用对呼吸道合胞病毒(RSV)抗体呈血清反应阳性的儿童的人扁桃体单核细胞(hu-TMC)腹膜内重构成组的C.B-17 SCID小鼠,随后用灭活的RSV进行腹膜内攻击或进行假免疫。使用酶联免疫斑点法(ELISPOT)研究了抗鼠源病毒的人源抗体在鼠类组织中的合成及其分布特征。在假免疫动物中未观察到特异性抗体。相反,植入hu-TMC的小鼠在腹腔镜手术后表现出特异性人抗体分泌细胞(hu-ASC)的外观。用灭活的RSV进行免疫。仅在移植了来自对爱泼斯坦-巴尔病毒抗体呈血清反应阳性的供体细胞的动物中检测到RSV特异性hu-ASC。植入Hu-TMC的小鼠在包括肺在内的多种组织中显示出RSV特异性IgM和IgG hu-ASC较少。但是,RSV特异性IgA hu-ASC的数量很低,仅在肺中检测到。在肠道中未检测到RSV特异性的hu-ASC。这些数据首次证明hu-TMC-SCID嵌合体对病毒抗原的免疫应答。此外,结果表明,hu-TMC移入肺部,但未移入肠组织。

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