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重组狂犬病病毒表达的 MIP-1alpha(CCL3)通过诱导先天免疫和募集树突状细胞和 B 细胞增强其免疫原性。

Expression of MIP-1alpha (CCL3) by a recombinant rabies virus enhances its immunogenicity by inducing innate immunity and recruiting dendritic cells and B cells.

机构信息

Department of Pathology, University of Georgia, Athens, GA 30602, USA.

出版信息

J Virol. 2010 Sep;84(18):9642-8. doi: 10.1128/JVI.00326-10. Epub 2010 Jun 30.

Abstract

Previously, we showed that overexpression of MIP-1alpha in mouse brain further decreased rabies virus (RABV) pathogenicity (L. Zhao, H. Toriumi, Y. Kuang, H. Chen, and Z. F. Fu, J. Virol., 83:11808-11818, 2009). In the present study, the immunogenicity of recombinant RABV expressing MIP-1alpha (rHEP-MIP1alpha) was determined. It was found that intramuscular immunization of BALB/c mice with rHEP-MIP1alpha resulted in a higher level of expression of MIP-1alpha at the site of inoculation, increased recruitment of dendritic cells (DCs) and mature B cells into the draining lymph nodes and the peripheral blood, and higher virus-neutralizing antibody titers than immunization with the parent rHEP and recombinant RABVs expressing RANTES (CCL5) or IP-10 (CXCL10). Our data thus demonstrate that expression of MIP-1alpha not only reduces viral pathogenicity but also enhances immunogenicity by recruiting DCs and B cells to the site of immunization, the lymph nodes, and the blood.

摘要

先前,我们表明在小鼠大脑中过表达 MIP-1alpha 进一步降低了狂犬病病毒 (RABV) 的致病性 (L. Zhao, H. Toriumi, Y. Kuang, H. Chen, and Z. F. Fu, J. Virol., 83:11808-11818, 2009)。在本研究中,测定了表达 MIP-1alpha 的重组 RABV (rHEP-MIP1alpha) 的免疫原性。结果发现,肌肉内免疫 BALB/c 小鼠 rHEP-MIP1alpha 导致接种部位 MIP-1alpha 的表达水平更高,树突状细胞 (DCs) 和成熟 B 细胞募集到引流淋巴结和外周血中,以及更高的病毒中和抗体滴度比用亲本 rHEP 和表达 RANTES (CCL5) 或 IP-10 (CXCL10) 的重组 RABV 免疫。因此,我们的数据表明,MIP-1alpha 的表达不仅通过将 DCs 和 B 细胞募集到免疫部位、淋巴结和血液中来降低病毒的致病性,还增强了免疫原性。

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