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Use of Fusion Proteins and Procaryotic Display Systems for Delivery of HIV-1 Antigens: Development of Novel Vaccines for HIV-1 Infection

机译:使用融合蛋白和原核展示系统传递HIV-1抗原:针对HIV-1感染的新型疫苗的开发

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摘要

Two non-pathogenic scaffolds (represented by the filamentous bacteriophage fd and the dihydrolipoyl acetyltransferase E2 protein of the Bacillus stearothermophilus pyruvate dehydrogenase (PDH) complex) able to deliver human immunodeficiency virus (HIV)-1 antigenic determinants, were designed in our laboratories and investigated in controlled assay conditions.nnBased on a modification of the phage display technology, we developed an innovative concept for a safe and inexpensive vaccine in which conserved antigenic determinants of HIV-1 reverse transcriptase (RTase) were inserted into the N-terminal region of the major pVIII coat protein of bacteriophage fd virions. Analogously, we developed another antigen delivery system based on the E2 component from the PDH complex and capable of displaying large intact proteins on the surface of an icosahedral lattice. Our data show that both of these systems can deliver B and T epitopes to their respective presentation compartments in target cells and trigger a humoral response as well as a potent helper and cytolytic response in vitro and in vivo.
机译:在我们的实验室中设计了两个非致病性支架(以丝状噬菌体fd和嗜热脂肪芽孢杆菌丙酮酸脱氢酶(PDH)复合物的二氢脂酰乙酰基转移酶E2蛋白代表),可以在我们的实验室中进行设计和研究。在对噬菌体展示技术的改进的基础上,我们开发了一种安全,廉价的疫苗的创新概念,其中将HIV-1逆转录酶(RTase)的保守抗原决定簇插入了该疫苗的N端区域。噬菌体fd病毒体的主要pVIII外壳蛋白。类似地,我们开发了另一种基于PDH复合物中E2成分的抗原递送系统,该系统能够在二十面体晶格的表面上展示完整的蛋白质。我们的数据表明,这两种系统均可将B和T表位传递至靶细胞中各自的呈递区室,并在体外和体内触发体液反应以及有效的辅助和细胞溶解反应。

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