Yano Akira, Onozuka Atsuko, Matin Khairul, Imai Susumu, Hanada Nobuhiro, Nisizawa Tosiki
Department of Oral Health, National Institute of Public Health, Toyama 1-23-1, Shinjuku-ku, 163-8640, Tokyo, Japan.
Vaccine. 2003 Dec 12;22(2):237-43. doi: 10.1016/s0264-410x(03)00561-9.
The use of peptides for various aspects of medical science has been a significant advance. Peptide-based vaccines are promising, but weak immunogenic potency is impeding the clinical application. We have remarkably enhanced the immunogenicity of peptide antigens by addition of motifs that bind to cell attachment proteins, such as arginine-glysine-aspartate (RGD), to the amino acid sequence. The modified peptides induced antigen-specific serum antibodies by intranasal immunization without adjuvants. RGD, an integrin-binding motif was the strongest, among several molecules tested in this experiment, giving an average of 10 times enhancement of antibody titers when incorporated into several peptide antigens. The peptides also acted as an efficient adjuvant following the intranasal immunization with protein antigens. Our data support the feasibility of developing peptide vaccines and peptide adjuvants for intranasal vaccination.
肽在医学科学各个方面的应用是一项重大进展。基于肽的疫苗前景广阔,但免疫原性较弱阻碍了其临床应用。我们通过在氨基酸序列中添加与细胞附着蛋白结合的基序,如精氨酸-甘氨酸-天冬氨酸(RGD),显著增强了肽抗原的免疫原性。经鼻内免疫无佐剂的情况下,修饰后的肽诱导产生了抗原特异性血清抗体。在本实验测试的几种分子中,整合素结合基序RGD的作用最强,当它被掺入几种肽抗原时,抗体滴度平均提高了10倍。这些肽在用蛋白抗原经鼻内免疫后还可作为一种有效的佐剂。我们的数据支持开发用于鼻内接种的肽疫苗和肽佐剂的可行性。