Lemckert Angelique A C, Goudsmit Jaap, Barouch Dan H
Crucell Holland BV, 2301 CA Leiden, The Netherlands.
Eur J Epidemiol. 2004;19(6):513-6. doi: 10.1023/b:ejep.0000032423.87658.68.
Considerable progress has been made over the past several years in the development of an HIV vaccine. As a result, a growing number of vaccine modalities are being investigated in pre-clinical and phase I/II clinical trials. However, a number of major scientific challenges still remain. It is widely believed that the ideal vaccine should elicit both neutralizing antibodies and cytotoxic T lymphocytes (CTL) against diverse isolates of HIV, but the precise correlates of immunity have not been defined. Recombinant live vector-based vaccines and plasmid DNA vaccines have been shown to induce CTL, either alone or in combination, and these CTL-based vaccines have shown partial protective efficacy in nonhuman primates challenge studies. An immunogen that elicits broadly reactive neutralizing antibodies, however, has yet to be developed.
在过去几年中,HIV疫苗的研发取得了相当大的进展。因此,越来越多的疫苗形式正在临床前和I/II期临床试验中进行研究。然而,仍存在一些重大的科学挑战。人们普遍认为,理想的疫苗应能引发针对多种HIV分离株的中和抗体和细胞毒性T淋巴细胞(CTL),但免疫的确切相关因素尚未明确。基于重组活载体的疫苗和质粒DNA疫苗已被证明可单独或联合诱导CTL,并且这些基于CTL的疫苗在非人灵长类动物攻毒研究中显示出部分保护效力。然而,一种能引发广泛反应性中和抗体的免疫原尚未研发出来。