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一种 Advax-CpG 佐剂的重组 H5 血凝素疫苗可保护小鼠免受致死性流感感染。

An Advax-CpG adjuvanted recombinant H5 hemagglutinin vaccine protects mice against lethal influenza infection.

机构信息

Vaxine Pty Ltd, Warradale, Adelaide, SA 5046, Australia; Flinders University, Bedford Park, Adelaide, SA 5042, Australia.

Institute for Antiviral Research, Department of Animal, Dairy, and Veterinary Sciences, 5600 Old Main Hill, Utah State University, Logan, UT 84322, USA.

出版信息

Vaccine. 2023 Sep 7;41(39):5730-5741. doi: 10.1016/j.vaccine.2023.08.009. Epub 2023 Aug 9.

Abstract

There is a major unmet need for strategies to improve the immunogenicity of vaccines to protect against highly pathogenic avian influenza strains with pandemic potential. This study tested the ability of adjuvants based on delta inulin (Advax™) alone or combined with a TLR9 agonist (Advax-CpG™) to enhance the immunogenicity of recombinant H5 hemagglutinin antigen expressed in insect cells (rH5HA) to protect mice against lethal influenza infection. The Advax-adjuvanted rH5HA induced high serum hemagglutination inhibition activity, as well as Th1 and Th2 cytokine secreting CD4 and CD8 T cells. Immunization protected mice against a lethal heterosubtypic H5N1 virus challenge. Mice immunized with an Advax-adjuvanted rHA2 stem antigen prepared by enzymatic cleavage of rH5HA produced serum antibodies devoid of hemagglutination inhibition activity, but these anti-HA2 antibodies were nevertheless able to transfer protection against lethal H1N1 or H3N2 infections to naïve mice. We hypothesize that the enhanced protection afforded by Advax-adjuvanted rH5HA may be mediated by the combination of neutralizing antibodies directed at the HA head, anti-HA2 stem antibodies plus memory CD4 + and CD8 + T cells. This outcome supports further development of the Advax-adjuvanted rH5 pandemic influenza vaccine platform.

摘要

目前,人们迫切需要开发新策略,以提高疫苗的免疫原性,从而预防具有大流行潜力的高致病性禽流感病毒株。本研究检测了基于德尔塔菊粉(Advax™)的佐剂单独或与 TLR9 激动剂(Advax-CpG™)联合应用,增强昆虫细胞表达的重组 H5 血凝素抗原(rH5HA)免疫原性,以保护小鼠免受致死性流感感染的能力。Advax 佐剂的 rH5HA 诱导了高血清血凝抑制活性,以及 Th1 和 Th2 细胞因子分泌的 CD4 和 CD8 T 细胞。免疫接种可保护小鼠免受致死性异源 H5N1 病毒攻击。用 rH5HA 的酶切 rHA2 茎抗原免疫接种的小鼠产生的血清抗体缺乏血凝抑制活性,但这些抗 HA2 抗体仍然能够将对致死性 H1N1 或 H3N2 感染的保护转移给无经验的小鼠。我们假设 Advax 佐剂的 rH5HA 提供的增强保护作用可能是由针对 HA 头部的中和抗体、抗 HA2 茎抗体以及记忆性 CD4+和 CD8+T 细胞的组合介导的。这一结果支持进一步开发 Advax 佐剂的 rH5 大流行性流感疫苗平台。

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