Weiss Robin A, Verrips C Theo
Division of Infection & Immunity, University College London, 90 Gower Street, London WC1E 6BT, UK.
QVQ Holding bv, Padualaan 8, 3584 CL Utrecht, The Netherlands.
Vaccines (Basel). 2019 Jul 31;7(3):77. doi: 10.3390/vaccines7030077.
Nanobodies or VHH (variable domains of heavy-chain only antibodies) are derived from camelid species such as llamas and camels. Nanobodies isolated and selected through phage display can neutralize a broad range of human immunodeficiency virus type 1 (HIV-1) strains. Nanobodies fit into canyons on the HIV envelope that may not be accessible to IgG (immunoglobulin G) containing both heavy and light chains, and they tend to have long CDR3 (complementarity-determining region 3) loops that further enhance recognition of otherwise cryptic epitopes. Nanobodies are readily expressed at high levels in bacteria and yeast, as well as by viral vectors, and they form relatively stable, heat-resistant molecules. Nanobodies can be linked to human Fc chains to gain immune effector functions. Bivalent and trivalent nanobodies recognizing the same or distinct epitopes on the envelope glycoproteins, gp120 and gp41, greatly increase the potency of HIV-1 neutralization. Nanobodies have potential applications for HIV-1 diagnostics, vaccine design, microbicides, immunoprophylaxis, and immunotherapy.
纳米抗体或VHH(仅重链抗体的可变结构域)源自骆驼科动物,如美洲驼和骆驼。通过噬菌体展示分离和筛选出的纳米抗体能够中和多种1型人类免疫缺陷病毒(HIV-1)毒株。纳米抗体可嵌入HIV包膜上的峡谷区域,而含有重链和轻链的免疫球蛋白G(IgG)可能无法触及这些区域,并且它们往往具有较长的互补决定区3(CDR3)环,这进一步增强了对原本隐蔽表位的识别。纳米抗体易于在细菌、酵母以及病毒载体中高水平表达,并且它们能形成相对稳定、耐热的分子。纳米抗体可与人Fc链连接以获得免疫效应功能。识别包膜糖蛋白gp120和gp41上相同或不同表位的二价和三价纳米抗体,可大大增强HIV-1中和效力。纳米抗体在HIV-1诊断、疫苗设计、杀微生物剂、免疫预防和免疫治疗方面具有潜在应用价值。