首页> 外文期刊>Journal of Immunological Methods >The development of monoclonal human rabies virus-neutralizing antibodies as a substitute for pooled human immune globulin in the prophylactic treatment of rabies virus exposure.
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The development of monoclonal human rabies virus-neutralizing antibodies as a substitute for pooled human immune globulin in the prophylactic treatment of rabies virus exposure.

机译:预防人类狂犬病毒暴露的单克隆人类狂犬病毒中和抗体的开发,以替代合并的人类免疫球蛋白。

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摘要

To provide a more defined and safer replacement for the human rabies immune globulin (HRIG) from pooled serum which is currently used for treatment of exposure to rabies virus we have developed a series of human rabies virus-specific monoclonal antibodies. Mouse-human heterohybrid myeloma cells producing rabies virus-specific human monoclonal antibodies were prepared using B cells obtained from volunteers recently-immunized with a commercial rabies virus vaccine (HDCV). Cell lines producing antibody which neutralized the Evelyn-Rokitnicki-Abelseth (ERA) rabies virus strain in vitro were cloned and the resulting monoclonal antibodies characterized for isotype, specificity against a variety of rabies virus isolates, and neutralization capacity. The ability of the monoclonal antibodies to neutralize a variety of rabies virus strains in vitro correlated with their binding specificity for these viruses in an enzyme-linked immunoadsorbant assay (ELISA). A number of these antibodies have proven suitable for the formulation of a prophylactic human monoclonal antibody-based reagent which would provide significant advantages to the HRIG in having defined, reproducible specificity, lessened possibility of contamination with viral pathogens, and consistent availability.
机译:为了从目前用于治疗狂犬病病毒暴露的合并血清中更准确,更安全地替代人类狂犬病免疫球蛋白(HRIG),我们开发了一系列人类狂犬病病毒特异性单克隆抗体。使用从最近用商业狂犬病病毒疫苗(HDCV)免疫的志愿者获得的B细胞制备产生狂犬病病毒特异性人类单克隆抗体的小鼠-人类杂种骨髓瘤细胞。克隆产生在体外中和Evelyn-Rokitnicki-Abelseth(ERA)狂犬病病毒株的抗体的细胞系,并以单克隆抗体,同种型,针对多种狂犬病毒分离株的特异性和中和能力为特征的所得单克隆抗体。在酶联免疫吸附测定(ELISA)中,单克隆抗体在体外中和多种狂犬病毒株的能力与其对这些病毒的结合特异性相关。已证明许多这些抗体适用于预防性基于人单克隆抗体的试剂的配制,这将为HRIG提供显着的优势,因为它具有确定的,可再现的特异性,减少了病毒病原体污染的可能性以及稳定的可用性。

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