Sitz K V, Ratto-Kim S, Hodgkins A S, Robb M L, Birx D L
Allergy/Immunology Section, Division of Pulmonary and Critical Care Medicine, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
J Infect Dis. 1999 Apr;179(4):817-24. doi: 10.1086/314685.
The proliferative responses to a series of peptides constituting the human immunodeficiency virus type 1 (HIV-1) gp120 sequence were evaluated in 19 HIV-1-infected rgp160 vaccine recipients, 17 HIV-1-infected rgp120 vaccine recipients, 15 HIV-1-infected placebo recipients, and 18 HIV-1-uninfected controls. Many regions of the gp120 molecule were found to contribute proliferative epitopes, although there were clearly regions of relative dominance and silence. Vaccine recipients tended to have broader, more robust, and more frequent peptide recognition than the placebo recipients. Despite the considerable variability in the pattern of peptide recognition among individuals, there was a striking similarity between the rgp160 and rgp120 vaccinee groups as a whole. Low-risk HIV-1-uninfected individuals may react to a few peptides within the gp120 sequence as well, despite a lack of significant response to the whole gp120 protein.
在19名感染人类免疫缺陷病毒1型(HIV-1)的rgp160疫苗接种者、17名感染HIV-1的rgp120疫苗接种者、15名感染HIV-1的安慰剂接受者和18名未感染HIV-1的对照者中,评估了对构成HIV-1 gp120序列的一系列肽的增殖反应。尽管gp120分子中明显存在相对优势和沉默区域,但发现该分子的许多区域都含有增殖表位。与安慰剂接受者相比,疫苗接种者往往具有更广泛、更强烈和更频繁的肽识别能力。尽管个体之间肽识别模式存在相当大的变异性,但rgp160和rgp120疫苗接种者群体总体上有惊人的相似性。低风险未感染HIV-1的个体尽管对整个gp120蛋白没有明显反应,但也可能对gp120序列中的少数肽产生反应。