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Immune Responses against Major Outer Membrane Antigens of Neisseria meningitidis in Vaccinees and Controls Who Contracted Meningococcal Disease during the Norwegian Serogroup B Protection Trial

机译:在挪威B血清群保护试验中,对患有脑膜炎球菌疾病的疫苗和对照中脑膜炎奈瑟氏球菌主要外膜抗原的免疫反应。

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Sera from vaccinees and controls who contracted serogroup B meningococcal disease during the blinded and open parts of a two-dose protection trial in Norway were compared for antigen-specific and bactericidal antibodies against vaccine strain 44/76 (B:15:P1.7,16). From 16 of 20 (80%) vaccinees and 26 of 35 (74%) controls, one or more serum samples (n = 104) were collected during the acute phase (1 to 4 days), early convalescent phase (5 to 79 days), and late convalescent phase (8 to 31 months) after onset of disease. Binding of immunoglobulin G (IgG) to the major outer membrane antigens (80- and 70-kDa proteins, class 1, 3, and 5 proteins, and lipopolysaccharide [LPS]) on immunoblots was measured by digital image analysis. Specific IgG levels in vaccinees increased from acute to early convalescent phases, followed by a decline, while controls showed a small increase over time. Vaccinees had significantly higher levels than controls against class 1 and 3 porins and LPS in acute sera, against all antigens during early convalescence, and against class 1 and 3 porins in the later sera. Vaccinees who were infected with strains expressing subtype P1.7,16 proteins demonstrated a level of IgG binding to protein P1.7,16 with early-convalescent-phase sera that was fourfold higher than that of those infected with other strains. Bactericidal titers in serum against the vaccine strain were 192-fold higher for vaccinees than those for controls during early convalescence, but similarly low levels were found during late convalescence. A vaccine-induced anamnestic response of specific and functional antibody activities was thus shown, but the decrease in protection over time after vaccination indicated that two vaccine doses did not induce sufficient levels of long-term protective antibodies.
机译:在挪威进行的两剂保护试验的盲法和开放试验中,患有乙型脑膜炎双球菌血清的疫苗和对照血清比较了针对疫苗株44/76的抗原特异性和杀菌抗体(B:15:P1.7, 16)。在急性期(1-4天)早期,从20种疫苗(80%)中的16种和35种疫苗(74%)中的26种( n = 104)中采集了一个或多个血清样本疾病发作后的恢复期(5至79天)和晚期恢复期(8至31个月)。通过数字图像分析测量免疫球蛋白G(IgG)与免疫印迹上主要的外膜抗原(80-kDa和70-kDa蛋白质,1、3和5类蛋白质以及脂多糖[LPS])的结合。疫苗中特定IgG的水平从急性期恢复到早期恢复期,然后下降,而对照显示随着时间的推移略有增加。与急性血清中针对1和3类孔蛋白和LPS,早期恢复期针对所有抗原的对照以及后期血清中针对1和3类孔蛋白的对照相比,疫苗的水平明显高于对照。感染表达P1.7,16亚型蛋白的菌株的疫苗在早期恢复期血清中与蛋白P1.7,16结合的IgG水平比感染其他菌株的IgG高四倍。疫苗的血清对疫苗菌株的杀菌效价在早期恢复期比对照组高192倍,但在后期恢复期也发现相似的低水平。因此显示了疫苗诱导的特异性和功能性抗体活性的记忆消除反应,但是疫苗接种后随时间的保护作用降低表明两种疫苗剂量不能诱导足够水平的长期保护性抗体。

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