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减毒nef DNA疫苗构建体诱导细胞免疫反应:在HIV-1多蛋白疫苗中的作用。

Attenuated nef DNA vaccine construct induces cellular immune response: role in HIV-1 multiprotein vaccine.

作者信息

Majumder Biswanath, Gray Benjamin, McBurney Sean, Schaefer Todd M, Dentchev Tzvete, Mahalingam Sundarasamy, Reinhart Todd A, Ayyavoo Velpandi

机构信息

Department of Infectious Diseases and Microbiology, University of Pittsburgh/GSPH, 130 DeSoto Street, Pittsburgh, PA 15261, USA.

出版信息

Immunol Lett. 2003 Oct 31;89(2-3):207-14. doi: 10.1016/s0165-2478(03)00141-x.

Abstract

HIV-1 positive patients generate Nef-specific CTL response, indicating that Nef is a potent immunogen. However, Nef is also known to down regulate the expression of CD4 and MHC-I molecules, thereby protecting virally infected target cells. We compared the immunogenicity of non-functional nef vaccine constructs to wild type functional nef as potential immunogen. Mice were immunized with different nef constructs and assessed for their ability to induce cellular immune responses. Evaluation of T cell immune responses in mice showed that non-functional nef vaccine constructs are capable of inducing a significant T cell immune response measured by IFN-gamma ELISPOT. Further epitope mapping studies indicate that one of our attenuated constructs, Nef R-38, has multiple CTL epitopes spanning throughout the gene. Our results indicate that functionally attenuated Nef antigen might be a better candidate for future multiprotein HIV-1 vaccine.

摘要

HIV-1阳性患者会产生针对Nef的细胞毒性T淋巴细胞(CTL)应答,这表明Nef是一种有效的免疫原。然而,已知Nef还会下调CD4和MHC-I分子的表达,从而保护病毒感染的靶细胞。我们将无功能的nef疫苗构建体与野生型功能性nef作为潜在免疫原的免疫原性进行了比较。用不同的nef构建体免疫小鼠,并评估它们诱导细胞免疫应答的能力。对小鼠T细胞免疫应答的评估表明,无功能的nef疫苗构建体能够诱导出通过γ干扰素酶联免疫斑点法(IFN-γ ELISPOT)测定的显著T细胞免疫应答。进一步的表位作图研究表明,我们的一种减毒构建体Nef R-38在整个基因中具有多个CTL表位。我们的结果表明,功能减毒的Nef抗原可能是未来多蛋白HIV-1疫苗的更好候选物。

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