首页> 外文OA文献 >Monoclonal Antibodies That Bind to Common Epitopes on the Dengue Virus Type 2 Nonstructural-1 and Envelope Glycoproteins Display Weak Neutralizing Activity and Differentiated Responses to Virulent Strains: Implications for Pathogenesis and Vaccines▿
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Monoclonal Antibodies That Bind to Common Epitopes on the Dengue Virus Type 2 Nonstructural-1 and Envelope Glycoproteins Display Weak Neutralizing Activity and Differentiated Responses to Virulent Strains: Implications for Pathogenesis and Vaccines▿

机译:与登革热病毒2型非结构性1和包膜糖蛋白常见抗原决定簇结合的单克隆抗体显示弱的中和活性和对强毒株的不同反应:对发病机理和疫苗的影响▿

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摘要

The abilities of monoclonal antibodies (MAbs) that bind to defined sequential epitopes on the dengue virus (DENV) nonstructural-1 (NS1) glycoproteins to cross-react with epitopes on the DENV envelope (E) glycoproteins were investigated. In this study, some of these MAbs cross-reacted with the DENV type 2 (DENV-2) E glycoprotein and with synthetic peptides representing X-ray crystallographically confirmed surface-exposed regions on this glycoprotein. MAb 1G5.3 cross-reacted with the flavivirus-conserved 101-WGNGCGLFG-109 fusion sequence, the 273-SSGNL-277 DENV-2 hinge region sequence, and the 156-GKHGKEIKIT-165 sequence of virulent DENV-2 strains. MAb 1G5.4-A1-C3 cross-reacted with the 67-NTTTESRCPT-76 and 156-GKHGKEIKIT-165 sequences of virulent DENV-2 strains, the 338-EIMDLDNRHV-347 sequence from a highly virulent DENV-2 (M2) strain, and two epitopes on a virulent DENV-3 strain (288-KMDKLELKG-296 and 323-RVEYRGEDAP-332), which all contained target ELK/KLE-type motifs (underlined). These MAbs showed reduced cross-reactions with the corresponding sequences from weakly pathogenic strains of all four DENV serotypes and had either no (MAb 1G5.4-A1-C3) or weak (MAb 1G5.3) neutralizing activity against them. MAb 1G5.3 more strongly neutralized DENV-2 strains with higher pathogenic capacities, while MAb 1G5.4-A1-C3 showed increasing neutralizing titers against the virulent DENV-3 strain and the moderately virulent and highly virulent (M2) DENV-2 strains. These cross-reactions with the E glycoprotein accord with the observation that MAb 1G5.3 caused dramatic and lethal antibody-enhanced replication (AER) of a DENV-2 strain in vivo. Together with in vivo AER studies of these DENV strains using MAb 1G5.4-A1-C3, these results may account for the increased pathogenic capacities of such strains, which is likely to have important implications for pathogenesis and vaccines.
机译:研究了与登革热病毒(DENV)非结构性1(NS1)糖蛋白上定义的顺序表位结合的单克隆抗体(MAb)与DENV包膜(E)糖蛋白上的表位交叉反应的能力。在这项研究中,其中一些单克隆抗体与DENV 2型(DENV-2)E糖蛋白以及代表该糖蛋白X射线晶体学确认的表面暴露区域的合成肽发生了交叉反应。 MAb 1G5.3与黄病毒保留的101-WGNGCGLFG-109融合序列,273-SSGNL-277 DENV-2铰链区序列以及强毒DENV-2菌株的156-GKHGKEIKIT-165序列交叉反应。 MAb 1G5.4-A1-C3与高毒DENV-2(M2)菌株的67-NTTTESRCPT-76和156-GKHGKEIKIT-165序列和强DENV-2菌株,338-EIMDLDNRHVHV-347序列发生交叉反应,以及在具有毒性的DENV-3株上的两个表位(288-KMDKLELKG-296和323-RVEYRGEDAP-332),均包含目标ELK / KLE型基序(带下划线)。这些单克隆抗体显示与来自所有四种DENV血清型的弱致病菌株的相应序列的交叉反应减少,并且没有针对它们的中和活性(MAb 1G5.4-A1-C3)或弱(MAb 1G5.3)中和活性。 MAb 1G5.3更强地中和了具有更高致病能力的DENV-2菌株,而MAb 1G5.4-A1-C3显示了对有毒力的DENV-3菌株以及中毒和高毒力(M2)DENV-2菌株的中和效价增加。这些与E糖蛋白的交叉反应符合以下观察结果:MAb 1G5.3在体内引起了DENV-2株的急剧而致命的抗体增强复制(AER)。结合使用MAb 1G5.4-A1-C3对这些DENV菌株进行的体内AER研究,这些结果可能说明了此类菌株的致病能力增强,这可能对发病机理和疫苗产生重要影响。

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    Falconar, Andrew K. I.;

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  • 年度 2007
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