表位疫苗诱导具有预定义ELNKWA表位特异性的单克隆抗体。

Hybridoma Pub Date : 2000-08-01 DOI:10.1089/027245700429918
Y Xiao, X N Dong, Y H Chen
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引用次数: 6

摘要

自杂交瘤技术产生单克隆抗体(mab)以来,已经产生了数千种具有预定蛋白特异性的单克隆抗体,而在传统的杂交瘤技术中,需要一种天然或重组蛋白作为抗原来诱导单克隆抗体。为了诱导表位特异性单克隆抗体,我们提出了一种表位疫苗作为一种新技术来诱导具有预定表位特异性的单克隆抗体。ELDKWA是HIV-1 gp41上一个重要的中和表位。识别ELNKWA表位的MAb 2F5已对许多HIV毒株(包括原代分离株)显示出广泛的中和活性,但ELNKWA表位突变导致逃逸2F5基中和。为了产生识别该突变表位的单克隆抗体,以考虑对携带ELNKWA表位的突变体进行被动免疫治疗,用合成的表位肽代替天然或重组的携带该表位的gp41诱导具有预定义ELNKWA表位特异性的单克隆抗体。在合成的ELNKWA表位肽上鉴定了3个单抗,并通过ELISA和免疫印迹分析发现它们可以将重组gp41与ELDKWA表位结合。
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Induction of monoclonal antibody with predefined ELNKWA epitope specificity by epitope vaccine.

Since the hybridoma technique to produce monoclonal antibodies (MAbs) was discovered, thousands of MAbs with predefined protein specificity have been produced, and a natural or recombinant protein as antigen is necessary for inducing MAbs in the conventional hybridoma technique. To induce epitope-specific MAbs, we suggest an epitope vaccine as a new technique to induce MAbs with predefined epitope specificity. ELDKWA was identified as an important neutralizing epitope on HIV-1 gp41. The MAb 2F5, recognizing ELDKWA epitope, has shown broad neutralizing activity to many HIV strains, including primary isolates, but the mutant in ELNKWA epitope results in escape 2F5-based neutralization. To produce MAbs recognizing this mutated epitope for consideration of passive immunotherapy against the mutant bearing the ELNKWA epitope, MAbs with predefined ELNKWA epitope specificity were induced by synthetic epitope-peptide instead of a natural or recombinant gp41 bearing this epitope. Three MAbs were identified to recognize ELNKWA epitope on the synthetic epitope-peptide, and interestingly could bind the recombinant gp41 with ELDKWA epitope in an ELISA assay and immunoblotting analysis.

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来源期刊
Hybridoma
Hybridoma 医学-免疫学
自引率
0.00%
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0
审稿时长
4-8 weeks
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