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首页> 外文期刊>Clinical and vaccine immunology: CVI >A three-dose intramuscular injection schedule of anthrax vaccine adsorbed generates sustained humoral and cellular immune responses to protective antigen and provides long-term protection against inhalation anthrax in rhesus macaques
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A three-dose intramuscular injection schedule of anthrax vaccine adsorbed generates sustained humoral and cellular immune responses to protective antigen and provides long-term protection against inhalation anthrax in rhesus macaques

机译:肌内注射three-dose明细表炭疽疫苗吸附产生持续体液和细胞免疫反应保护性抗原,并提供长期的防止吸入炭疽在恒河短尾猿

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摘要

A 3-dose (0, 1, and 6 months) intramuscular (3-IM) priming series of a human dose (HuAVA) and dilutions of up to 1:10 of anthrax vaccine adsorbed (AVA) provided statistically significant levels of protection (60 to 100%) against inhalation anthrax for up to 4 years in rhesus macaques. Serum anti-protective antigen (anti-PA) IgG and lethal toxin neutralization activity (TNA) were detectable following a single injection of HuAVA or 1:5 AVA or following two injections of diluted vaccine (1:10, 1:20, or 1:40 AVA). Anti-PA and TNA were highly correlated (overall r 2=0.89 for log10-transformed data). Peak responses were seen at 6.5 months. In general, with the exception of animals receiving 1:40 AVA, serum anti-PA and TNA responses remained significantly above control levels at 28.5 months (the last time point measured for 1:20 AVA), and through 50.5 months for the HuAVA and 1:5 and 1:10 AVA groups (P0.05). PA-specific gamma interferon (IFN-γ) and interleukin-4 (IL-4) CD4 + cell frequencies and T cell stimulation indices were sustained through 50.5 months (the last time point measured). PA-specific memory B cell frequencies were highly variable but, in general, were detectable in peripheral blood mononuclear cells (PBMC) by 2 months, were significantly above control levels by 7 months, and remained detectable in the HuAVA and 1:5 and 1:20 AVA groups through 42 months (the last time point measured). HuAVA and diluted AVA elicited a combined Th1/Th2 response and robust immunological priming, with sustained production of high-avidity PA-specific functional antibody, long-term immune cell competence, and immunological memory (30 months for 1:20 AVA and 52 months for 1:10 AVA). Vaccinated animals surviving inhalation anthrax developed high-magnitude anamnestic anti-PA IgG and TNA responses.
机译:3-dose(0、1和6个月)肌内(我)启动一系列人类剂量(HuAVA)和稀释1:10的炭疽疫苗吸附(瓦)提供的统计学意义级别的保护(60 - 100%)吸入炭疽长达4年的恒河猕猴。免疫球蛋白和致命的毒素中和活动(TNA)检测单注入HuAVA 1:5艾娃或两个注射稀释疫苗(1:10,1:20,或40瓦)。(log10-transformed数据整体2 r = 0.89)。反应峰值出现在6.5个月。一般情况下,除了动物接收40瓦,血清anti-PA和TNA的响应仍显著高于控制水平28.5个月(最后一次点测量1:20艾娃),通过HuAVA 50.5个月和1:5和1:10艾娃组(术中,0.05)。paγ干扰素(IFN -γ)interleukin-4 (il - 4) CD4 + T细胞频率细胞刺激指数持续的通过50.5个月(最后一次点测量)。pa记忆B细胞频率高变量,但总的来说,被检测到外周血单核细胞(PBMC) 2个月,明显高于控制水平7个月,HuAVA仍可检测并通过42个月1:5和1:20艾娃团体(最后一次点测量)。艾娃引起了Th1 / Th2反应和相结合强大的免疫启动,持续生产high-avidity pa功能抗体,长期免疫细胞的能力,和免疫记忆(1:20艾娃和30个月1:10艾娃的52个月)。幸存的吸入炭疽发达高震级记忆的anti-PA免疫球蛋白和TNA响应。

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