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通过肽免疫可引发针对HIV-1 V3区的广泛中和单克隆抗体。

Broadly neutralizing monoclonal antibodies to the V3 region of HIV-1 can be elicited by peptide immunization.

作者信息

White-Scharf M E, Potts B J, Smith L M, Sokolowski K A, Rusche J R, Silver S

机构信息

Repligen Corporation, Cambridge, Massachusetts 02139.

出版信息

Virology. 1993 Jan;192(1):197-206. doi: 10.1006/viro.1993.1022.

DOI:10.1006/viro.1993.1022
PMID:7685962
Abstract

The third hypervariable region (V3) of the HIV-1 envelope gp120 protein contains the principal neutralizing domain. Most neutralizing antibodies directed toward this region are very type-specific. Conserved sequences do exist within this region, however, and may prove useful in developing vaccines and therapeutic monoclonal antibodies (MABs) capable of targeting diverse HIV-1 isolates. We have used synthetic peptides containing conserved V3 sequences as immunogens to produce a panel of neutralizing MABs. The characterization of these MABs is described here. In addition, a series of in vitro assays has been developed that may be useful in predicting the neutralization potential of individual antibodies.

摘要

HIV-1包膜糖蛋白gp120的第三个高变区(V3)包含主要的中和结构域。大多数针对该区域的中和抗体具有很强的型特异性。不过,该区域内确实存在保守序列,可能在开发能够靶向多种HIV-1分离株的疫苗和治疗性单克隆抗体(MAB)方面发挥作用。我们已将含有V3保守序列的合成肽用作免疫原,以制备一组中和性单克隆抗体。本文描述了这些单克隆抗体的特性。此外,还开发了一系列体外检测方法,可能有助于预测单个抗体的中和潜力。

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