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三价流感疫苗与阳离子脂质体佐剂联合免疫后增强体液和细胞介导的免疫应答。

Enhanced humoral and cell-mediated immune responses after immunization with trivalent influenza vaccine adjuvanted with cationic liposomes.

机构信息

Department of Infectious Disease Immunology, Statens Serum Institut, 5 Orestads Boulevard, DK-2300 Copenhagen, Denmark.

出版信息

Vaccine. 2011 Aug 26;29(37):6283-91. doi: 10.1016/j.vaccine.2011.06.040. Epub 2011 Jun 29.

Abstract

The recent pandemic caused by new influenza A (H1N1) has emphasized the need for improved influenza vaccines with enhanced immune responses that ideally include longlived humoral and CMI responses and mediate a broad protection. This study demonstrates that administration of trivalent influenza vaccine (TIV) with the cationic liposome adjuvant system CAF01 enhances the humoral immune response as measured by hemagglutinin inhibition titers and influenza-specific serum antibody titers, and promote a strong Th1 response with augmented levels of IL-1β, IL-2, IL-12, IFN-γ and TNF-α. Furthermore, high levels of IL-17 are detected in agreement with CAF01's ability to promote TH17 responses. Importantly, the Th1/Th17 cytokine profile is still maintained 20 weeks after the last vaccination. The CAF01 adjuvanted influenza vaccine reduces weight loss and temperature decrease and results in complete survival of mice challenged with the drifted H1N1 influenza strain A/PR/8/34. Overall, the results suggest that CAF01 is a potent adjuvant system for future, improved influenza vaccines.

摘要

最近由新型甲型流感(H1N1)引起的大流行强调了需要改进流感疫苗,以增强免疫反应,理想情况下包括具有持久体液和细胞介导免疫反应的免疫反应,并介导广泛的保护。本研究表明,三价流感疫苗(TIV)与阳离子脂质体佐剂系统 CAF01 联合使用可增强体液免疫反应,如通过血凝素抑制滴度和流感特异性血清抗体滴度测量,促进强烈的 Th1 反应,增加 IL-1β、IL-2、IL-12、IFN-γ 和 TNF-α 的水平。此外,高水平的 IL-17 与 CAF01 促进 TH17 反应的能力一致。重要的是,Th1/Th17 细胞因子谱在最后一次接种后 20 周仍保持不变。CAF01 佐剂流感疫苗可减少体重减轻和体温下降,并导致用漂移的 H1N1 流感株 A/PR/8/34 挑战的小鼠完全存活。总体而言,结果表明 CAF01 是未来改进流感疫苗的有效佐剂系统。

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