Leroux-Roels G, Van Hecke E, Michielsen W, Voet P, Hauser P, Pêtre J
Department of Clinical Chemistry, University of Gent, University Hospital, Belgium.
Vaccine. 1994 Jul;12(9):812-8. doi: 10.1016/0264-410x(94)90290-9.
To study the regulation of the human immune response to hepatitis B surface antigen (HBsAg) we have carefully monitored the in vivo humoral and in vitro cellular immune responses to HBsAg in 50 subjects receiving four doses of hepatitis B vaccine according to a 0, 1, 2, 12 month vaccination scheme. Twenty-three subjects were given a plasma-derived vaccine (Hevac B) and 27 received a recombinant HBsAg vaccine (yeast-derived; Engerix-B). The humoral and cellular immune responses were measured before vaccination (day 0); 6 days after the second dose (day 36); 6 days (day 66), 2 months (day 120) and 10 months (day 365) after the third dose and 1 month after the fourth dose (day 395). Based on the kinetics of the humoral immune responses, the vaccinees could be classified into fast, intermediate and slow/non-responders. Based on the magnitude of the immune response (anti-HBs titre) on day 395, the vaccinees could be divided into high (> or = 2000 U l-1) and low (< or = 2000 U l-1) responders. A close correlation between the kinetics and the magnitude of the humoral immune response was observed. The in vivo anti-HBs response was measured using commercially available immunoradiometric assays. The in vitro cellular immune response was measured using an HBsAg-specific lymphoproliferation assay. Because of interassay variability the results were considered as dichotomous variables (proliferation versus non-proliferation) for further data analysis. A statistically significant correlation was observed between the kinetics and magnitude of the humoral immune response on the one hand and the in vitro anti-HBs response on the other hand.(ABSTRACT TRUNCATED AT 250 WORDS)
为研究人体对乙型肝炎表面抗原(HBsAg)免疫反应的调节机制,我们对50名按照0、1、2、12月接种方案接种四剂乙肝疫苗的受试者,仔细监测了其对HBsAg的体内体液免疫反应和体外细胞免疫反应。23名受试者接种了血浆源性疫苗(Hevac B),27名接种了重组HBsAg疫苗(酵母源性;Engerix - B)。在接种前(第0天)、第二剂接种后6天(第36天)、第三剂接种后6天(第66天)、2个月(第120天)、10个月(第365天)以及第四剂接种后1个月(第395天)测量体液和细胞免疫反应。根据体液免疫反应的动力学,可将接种者分为快速、中等和缓慢/无反应者。根据第395天的免疫反应强度(抗HBs滴度),可将接种者分为高反应者(≥2000 U l-1)和低反应者(≤2000 U l-1)。观察到体液免疫反应的动力学与强度之间存在密切相关性。使用市售免疫放射分析测定体内抗HBs反应。使用HBsAg特异性淋巴细胞增殖试验测定体外细胞免疫反应。由于不同检测方法之间存在变异性,因此将结果视为二分变量(增殖与非增殖)用于进一步数据分析。一方面观察到体液免疫反应的动力学和强度与另一方面体外抗HBs反应之间存在统计学显著相关性。(摘要截短于250字)