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小鼠中针对乙型肝炎表面抗原的DNA介导免疫:体液免疫反应的某些方面模拟人类的乙型肝炎病毒感染。

DNA-mediated immunization to the hepatitis B surface antigen in mice: aspects of the humoral response mimic hepatitis B viral infection in humans.

作者信息

Michel M L, Davis H L, Schleef M, Mancini M, Tiollais P, Whalen R G

机构信息

Unité de Recombinaison et Expression Génétique, Institut Pasteur, France.

出版信息

Proc Natl Acad Sci U S A. 1995 Jun 6;92(12):5307-11. doi: 10.1073/pnas.92.12.5307.

Abstract

Intramuscular injection of plasmid DNA expression vectors encoding the three envelope proteins of the hepatitis B virus (HBV) induced humoral responses in C57BL/6 mice specific to several antigenic determinants of the viral envelope. The first antibodies appeared within 1-2 weeks after injection of DNA and included antibodies of the IgM isotype. Over the next few weeks, an IgM to IgG class switch occurred, indicating helper T-lymphocyte activity. Peak IgG titers were reached by 4-8 weeks after a single DNA injection and were maintained for at least 6 months without further DNA injections. The antibodies to the envelope proteins reacted with group- and subtype-specific antigenic determinants of the HBV surface antigen (HBsAg). Expression vectors encoding the major (S) and middle (preS2 plus S) envelope proteins induced antibodies specific to the S protein and preS2 domain, and preS2 antibodies were prominent at early time points. In general, the expression vectors induced humoral responses in mice that mimic those observed in humans during the course of natural HBV infection.

摘要

肌肉注射编码乙肝病毒(HBV)三种包膜蛋白的质粒DNA表达载体,可在C57BL/6小鼠中诱导出针对病毒包膜多个抗原决定簇的体液免疫反应。首次注射DNA后1 - 2周内出现抗体,其中包括IgM同种型抗体。在接下来的几周内,发生了从IgM到IgG的类别转换,表明存在辅助性T淋巴细胞活性。单次注射DNA后4 - 8周达到IgG滴度峰值,且在不再进行DNA注射的情况下至少维持6个月。针对包膜蛋白的抗体与HBV表面抗原(HBsAg)的组特异性和亚型特异性抗原决定簇发生反应。编码主要(S)和中间(前S2加S)包膜蛋白的表达载体诱导出针对S蛋白和前S2结构域的特异性抗体,且在前S2抗体在早期时间点较为突出。总体而言,这些表达载体在小鼠中诱导出的体液免疫反应类似于人类在自然HBV感染过程中观察到的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5080/41683/9de07ef868a0/pnas01488-0068-a.jpg

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