首页> 外文OA文献 >Expression of MIP-1α (CCL3) by a Recombinant Rabies Virus Enhances Its Immunogenicity by Inducing Innate Immunity and Recruiting Dendritic Cells and B Cells▿
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Expression of MIP-1α (CCL3) by a Recombinant Rabies Virus Enhances Its Immunogenicity by Inducing Innate Immunity and Recruiting Dendritic Cells and B Cells▿

机译:重组狂犬病病毒表达MIP-1α(CCL3)通过诱导先天免疫并招募树突状细胞和B细胞增强其免疫原性。

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摘要

Previously, we showed that overexpression of MIP-1α 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-1α (rHEP-MIP1α) was determined. It was found that intramuscular immunization of BALB/c mice with rHEP-MIP1α resulted in a higher level of expression of MIP-1α 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-1α 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.
机译:以前,我们证明了MIP-1α在小鼠脑中的过度表达进一步降低了狂犬病毒(RABV)的致病性(L. Zhao,H。Toriumi,Y。Kuang,H。Chen和ZF Fu,J。Virol。,83:11808)。 -11818,2009)。在本研究中,确定了表达MIP-1α的重组RABV(rHEP-MIP1α)的免疫原性。已发现,用rHEP-MIP1α肌肉注射免疫BALB / c小鼠可导致接种部位MIP-1α表达水平升高,树突状细胞(DC)和成熟B细胞募集到引流淋巴结中。与使用RANTES(CCL5)或IP-10(CXCL10)的亲本rHEP和重组RABV免疫相比,外周血的病毒中和抗体效价更高。因此,我们的数据表明,MIP-1α的表达不仅可以减少病毒的致病性,而且还可以通过将DC和B细胞募集到免疫部位,淋巴结和血液来增强免疫原性。

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