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首页> 外文期刊>Infection and immunity >Full-Length Plasmodium falciparum Circumsporozoite Protein Administered with Long-Chain Poly(I·C) or the Toll-Like Receptor 4 Agonist Glucopyranosyl Lipid Adjuvant-Stable Emulsion Elicits Potent Antibody and CD4+ T Cell Immunity and Protection in Mice
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Full-Length Plasmodium falciparum Circumsporozoite Protein Administered with Long-Chain Poly(I·C) or the Toll-Like Receptor 4 Agonist Glucopyranosyl Lipid Adjuvant-Stable Emulsion Elicits Potent Antibody and CD4+ T Cell Immunity and Protection in Mice

机译:长链聚(I·C)或Toll样受体4激动剂谷胱甘肽脂质佐剂稳定的乳剂可治疗全长恶性疟原虫环子孢子蛋白,具有有效的抗体和对小鼠的CD4 + T细胞免疫和保护作用

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The Plasmodium falciparum circumsporozoite (CS) protein (CSP) is a major vaccine target for preventing malaria infection. Thus, developing strong and durable antibody and T cell responses against CSP with novel immunogens and potent adjuvants may improve upon the success of current approaches. Here, we compare four distinct full-length P. falciparum CS proteins expressed in Escherichia coli or Pichia pastoris for their ability to induce immunity and protection in mice when administered with long-chain poly(I·C) [poly(I·C)LC] as an adjuvant. CS proteins expressed in E. coli induced high-titer antibody responses against the NANP repeat region and potent CSP-specific CD4+ T cell responses. Moreover, E. coli-derived CS proteins in combination with poly(I·C)LC induced potent multifunctional (interleukin 2-positive [IL-2+], tumor necrosis factor alpha-positive [TNF-α+], gamma interferon-positive [IFN-γ+]) CD4+ effector T cell responses in blood, in spleen, and particularly in liver. Using transgenic Plasmodium berghei expressing the repeat region of P. falciparum CSP [Pb-CS(Pf)], we showed that there was a 1- to 4-log decrease in malaria rRNA in the liver following a high-dose challenge and ~50% sterilizing protection with a low-dose challenge compared to control levels. Protection was directly correlated with high-level antibody titers but not CD4+ T cell responses. Finally, protective immunity was also induced using the Toll-like receptor 4 agonist glucopyranosyl lipid adjuvant-stable emulsion (GLA-SE) as the adjuvant, which also correlated with high antibody titers yet CD4+ T cell immunity that was significantly less potent than that with poly(I·C)LC. Overall, these data suggest that full-length CS proteins and poly(I·C)LC or GLA-SE offer a simple vaccine formulation to be used alone or in combination with other vaccines for preventing malaria infection.
机译:恶性疟原虫环子孢子(CS)蛋白(CSP)是预防疟疾感染的主要疫苗目标。因此,在新型方法成功的基础上,开发出具有新型免疫原和有效佐剂的针对CSP的强而持久的抗体和T细胞应答可能会有所改善。在这里,我们比较了在大肠杆菌或巴斯德毕赤酵母中表达的四种截然不同的全长恶性疟原虫CS蛋白在小鼠中与长链poly(I·C)[poly(I·C) LC]作为佐剂。在大肠杆菌中表达的CS蛋白诱导针对NANP重复区域的高滴度抗体应答和强效的CSP特异性CD4 + T细胞应答。此外,大肠杆菌衍生的CS蛋白与聚(I·C)LC组合可诱导有效的多功能(白介素2阳性[IL-2 + ],肿瘤坏死因子α阳性[TNF- α + ],γ干扰素阳性[IFN-γ + ])CD4 + 效应子,在血液,脾脏中特别是在细胞中在肝脏中。使用表达恶性疟原虫CSP [ Pb -CS( Pf )]重复区域的伯氏疟原虫,我们发现其减少了1至4个对数与对照水平相比,高剂量攻击后肝脏中的疟疾rRNA和低剂量攻击后〜50%的灭菌保护。保护作用与高水平的抗体滴度直接相关,而与CD4 + T细胞反应无关。最后,以Toll样受体4激动剂吡喃葡萄糖基脂质佐剂稳定乳剂(GLA-SE)为佐剂也诱导了保护性免疫,这与高抗体滴度和CD4 + T细胞免疫有关与聚(I·C)LC相比,其效力明显较低。总体而言,这些数据表明,全长CS蛋白和聚(I·C)LC或GLA-SE提供了一种简单的疫苗制剂,可以单独使用,也可以与其他疫苗一起用于预防疟疾感染。

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