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使用包含来自病毒蛋白R免疫显性T辅助细胞决定簇的合成肽构建体诱导针对1型人类免疫缺陷病毒的中和抗体。

Induction of neutralizing antibodies against human immunodeficiency virus type 1 using synthetic peptide constructs containing an immunodominant T-helper cell determinant from vpr.

作者信息

Sarobe P, Lasarte J J, Golvano J J, Prieto I, Gullón A, Soto M J, Labarga P, Prieto J, Borrás-Cuesta F

机构信息

Departamento de Medicina Interna, Universidad de Navarra, Pamplona, Spain.

出版信息

J Acquir Immune Defic Syndr (1988). 1994 Jul;7(7):635-40.

PMID:8207641
Abstract

Identification of immunodominant T-helper-cell determinants after natural infection is an important step in the design of immunogens for potential use in vaccination. Using cells from human immunodeficiency virus type 1 (HIV-1)-infected individuals and a panel of peptides encompassing the sequence of the regulatory protein vpr from HIV-1, we identified the T-helper determinant QLLFIHFRIGCRHSR, which is active in 37.5% of these individuals. To gain insight on the efficacy of this peptide in helping induce neutralizing antibodies against a B-cell determinant (BD), we synthesized constructs containing B- and T-cell determinants and tested them in BALB/c mice, the highest responders to the T-cell determinant moiety among several strains tested. These immunogens induced antibodies against two chosen B-cell determinants from HIV-1IIIB gp160 (amino acids 310-322 from the V3 loop of gp120 and 736-751 from gp41) that were able to neutralize HIV-1 infection in vitro. The highest neutralization titer against HIV-1IIIB was obtained by immunization with the homopolymer of the construct containing the T-cell epitope from vpr and the B-cell epitope from the V3 loop. We believe that the immunodominant T-cell determinant from vpr is a promising epitope to consider in the design of future peptide vaccines.

摘要

鉴定自然感染后的免疫显性T辅助细胞决定簇是设计可能用于疫苗接种的免疫原的重要一步。利用来自1型人类免疫缺陷病毒(HIV-1)感染者的细胞以及一组涵盖HIV-1调节蛋白vpr序列的肽段,我们鉴定出了T辅助决定簇QLLFIHFRIGCRHSR,在这些个体中有37.5%的个体该决定簇具有活性。为深入了解该肽段在帮助诱导针对B细胞决定簇(BD)的中和抗体方面的功效,我们合成了包含B细胞和T细胞决定簇的构建体,并在BALB/c小鼠中进行测试,BALB/c小鼠是所测试的几个品系中对T细胞决定簇部分反应最强的。这些免疫原诱导产生了针对HIV-1IIIB gp160的两个选定B细胞决定簇(gp120 V3环的氨基酸310 - 322以及gp41的736 - 751)的抗体,这些抗体能够在体外中和HIV-1感染。通过用包含来自vpr的T细胞表位和来自V3环的B细胞表位的构建体的同聚物进行免疫,获得了针对HIV-1IIIB的最高中和效价。我们认为,来自vpr的免疫显性T细胞决定簇是未来肽疫苗设计中值得考虑的一个有前景的表位。

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