首页> 外文期刊>Veterinary Microbiology >Carbopol improves the early cellular immune responses induced by the modified-life vaccine Ingelvac PRRS (R) MLV
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Carbopol improves the early cellular immune responses induced by the modified-life vaccine Ingelvac PRRS (R) MLV

机译:卡波姆改善了改良寿命的疫苗Ingelvac PRRS(R)MLV诱导的早期细胞免疫应答

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Adjuvants enhance both the magnitude and duration of immune responses, therefore representing a central component of vaccines. The nature of the adjuvant can determine the particular type of immune response, which may be skewed toward cytotoxic T cell (CTL) responses, antibody responses, or particular classes of T helper (Th) responses and antibody isotypes. Traditionally, adjuvants have been added to intrinsically poor immunogenic vaccines, such as those using whole killed organisms or subunit vaccines. Here, we have compared cellular immune responses induced by the immunogenic modified life-attenuated vaccine Ingelvac PRRS (R) MLV when administered alone or in combination with carbopol, a widely used adjuvant in veterinary medicine. Using functional readouts (IFN-gamma ELISpot and cell proliferation) and analyzing phenotypical hallmarks of CD4T cell differentiation, we show that carbopol improves cellular immunity by inducing early IFN-gamma-producing cells and by preferentially driving T cell differentiation to effector phenotypes. Our data suggest that adjuvants may enhance and modulate life-attenuated - not only subunit/inactivated - vaccines. (C) 2015 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
机译:佐剂增强了免疫反应的强度和持续时间,因此代表了疫苗的重要组成部分。佐剂的性质可以确定特定的免疫应答类型,其可能偏向细胞毒性T细胞(CTL)应答,抗体应答或特定类型的T辅助(Th)应答和抗体同种型。传统上,佐剂已被添加到本质上免疫原性较差的疫苗中,例如使用完整杀灭生物或亚单位疫苗的佐剂。在这里,我们比较了单独或与兽药中广泛使用的佐剂卡波普(Carbopol)联合使用时,经免疫原性修饰的减毒疫苗Ingelvac PRRS(R)MLV诱导的细胞免疫应答。使用功能性读数(IFN-γELISpot和细胞增殖)并分析CD4T细胞分化的表型特征,我们显示卡波普通过诱导早期产生IFN-γ的细胞和优先驱动T细胞分化为效应子表型来提高细胞免疫力。我们的数据表明佐剂可以增强和调节减毒的疫苗-不仅限于亚单位/灭活的疫苗。 (C)2015作者。由Elsevier B.V.发布。这是CC BY-NC-ND许可(http://creativecommons.org/licenses/by-nc-nd/4.0/)上的开放获取文章。

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