Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Haidian, Beijing 100850, China.
Virol J. 2011 Nov 4;8:507. doi: 10.1186/1743-422X-8-507.
To investigate the enhancement of humoral immunity when CpG ODN (cytidine phosphate guanosine oligodeoxynucleotides) and aluminium adjuvants are complexed with the HCV (Hepatitis C virus) recombinant immunogen in mice.
After immunizing Balb/c mice with the recombination HCV antigen adjuvanted with pUCpGs10 and/or aluminium(antigen+CpG+alum, antigen+CpG, antigen+alum, antigen+PBS), enzyme-linked immunosorbent assay (ELISA) was used to measure the specific serum antibody titers of IgG, to determine the neutralization response to various peptide genotypes, and to determine the concentration of IL-6 and IL-10 in supernatants of in vitro cultured splenic lymphocytes. Enzyme-linked immunospot assay (ELISPOT) was used to quantify the non-specific and specific splenic antibody-secreting cells (ASCs), and flow cytometry (FCM) determined the ratio of different splenic lymphocytes. The serum of rabbits immunized with the recombinant pBVGST/HVR1 antigen immunoprecipitated the HCV isolated from 12 patients' serum.
The sera antibody titers were 1:51200, 1:9051, 1:18102, 1:6400 respectively after the final immunization and demonstrated good neutralization responses to the six gene peptide containing 1a, 1b, 2a, 3a, 4a and 6a. The aluminum adjuvant increased the population of both specific ASCs (P < 0.01) and total ASCs(P < 0.05), with a proportional rise in concentrations of CD19+CD27+ (P < 0.05), as well as levels of IL-6, IL-10 (P < 0.05) in splenic lymphocytes. The results clearly indicated a significantly higher number of CD19+CD38+ splenic lymphocytes with the aluminum and pUCpGs10 adjuvant present compared to the control group(P < 0.05). Anti-HVR1 antibody in induced mice can cross-reactively capture HCV particles (10/12).
研究 CpG ODN(胞嘧啶磷酸鸟嘌呤寡脱氧核苷酸)和铝佐剂与 HCV(丙型肝炎病毒)重组免疫原复合后在小鼠体内体液免疫增强的情况。
用 pUCpGs10 和/或铝佐剂(抗原+CpG+铝、抗原+CpG、抗原+铝、抗原+PBS)佐剂免疫 Balb/c 小鼠,酶联免疫吸附试验(ELISA)检测 IgG 特异性血清抗体滴度,测定对各种肽基因型的中和反应,以及测定体外培养脾淋巴细胞上清液中 IL-6 和 IL-10 的浓度。酶联免疫斑点法(ELISPOT)用于定量非特异性和特异性脾抗体分泌细胞(ASCs),流式细胞术(FCM)测定不同脾淋巴细胞的比例。用重组 pBVGST/HVR1 抗原免疫的兔血清免疫沉淀来自 12 名患者血清的 HCV。
末次免疫后血清抗体滴度分别为 1:51200、1:9051、1:18102、1:6400,对包含 1a、1b、2a、3a、4a 和 6a 的 6 种基因肽均有良好的中和反应。铝佐剂增加了特异性 ASCs 的数量(P < 0.01)和总 ASCs 的数量(P < 0.05),CD19+CD27+的比例也呈上升趋势(P < 0.05),脾淋巴细胞中 IL-6、IL-10 的水平也升高(P < 0.05)。结果表明,与对照组相比,铝佐剂和 pUCpGs10 佐剂组的 CD19+CD38+脾淋巴细胞数量明显增加(P < 0.05)。诱导的小鼠中的抗 HVR1 抗体可交叉反应性捕获 HCV 颗粒(10/12)。