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单独使用菊粉或与CpG寡核苷酸联合使用可增强小鼠和非人灵长类新生动物体内抗体依赖性流感疫苗的保护作用。

Delta inulin alone or combined with CpG oligonucleotide enhances antibody-dependent influenza vaccine protection in mice and nonhuman primate newborns.

作者信息

Sakala Isaac G, Honda-Okubo Yoshikazu, Petrovsky Nikolai

机构信息

Vaxine Pty Ltd, Adelaide, SA, Australia.

Australian Respiratory and Sleep Medicine Institute, Adelaide, SA, Australia.

出版信息

Immunol Cell Biol. 2025 Jun 29. doi: 10.1111/imcb.70045.

Abstract

Newborns represent over half of hospitalized pediatric influenza infection cases, with current influenza vaccines not effective in the first months of life. Advax (delta inulin) is a polysaccharide particle that targets DC-SIGN, whereas CpG55.2 is a potent murine and human toll-like receptor (TLR)-9 agonist. This study asked whether Advax or CpG alone, or combined, could enhance the protection of an inactivated influenza virus vaccine (IIV) in newborns. One-day-old mouse pups were immunized subcutaneously with a single dose of IIV alone or with Advax or Advax-CpG55.2 adjuvants and then, at 28 days of age, challenged intranasally with a lethal dose of influenza virus. While IIV alone or with CpG adjuvant provided minimal protection, Advax alone or combined with CpG55.2 induced enhanced serum anti-influenza IgM and IgG responses to IIV and protected the newborns against clinical disease. Protection induced by a single vaccine dose was highly durable and was still evident 6-9 months after a single neonatal immunization. Protection was lost in B-cell-deficient μMT pups but preserved in β2m knockout pups and in CD4 and CD8 T-cell-depleted pups, indicating the importance of intact humoral immunity to the enhanced protection. The neonatal benefits of Advax and Advax-CpG55.2 adjuvant were confirmed in newborn macaques, where they similarly enhanced serum anti-influenza antibody responses to IIV. This raises the possibility that Advax adjuvant alone or in combination with CpG55.2 may have utility in improving influenza vaccine protection in human newborns.

摘要

住院儿童流感感染病例中,新生儿占比超过一半,而目前的流感疫苗在婴儿出生后的头几个月无效。Advax(δ-菊粉)是一种靶向树突状细胞特异性细胞间黏附分子-3抓取非整合素(DC-SIGN)的多糖颗粒,而CpG55.2是一种强效的鼠源和人源Toll样受体(TLR)-9激动剂。本研究探讨了单独使用Advax或CpG,或二者联合使用,是否能增强灭活流感病毒疫苗(IIV)对新生儿的保护作用。一日龄的幼鼠皮下注射单剂量的IIV,或与Advax或Advax-CpG55.2佐剂联合使用,然后在28日龄时经鼻内接种致死剂量的流感病毒。单独使用IIV或与CpG佐剂联合使用时提供的保护作用极小,而单独使用Advax或与CpG55.2联合使用则可诱导血清中针对IIV的抗流感IgM和IgG反应增强,并保护新生儿免受临床疾病侵害。单剂量疫苗诱导的保护作用具有高度持久性,在单次新生儿免疫后6至9个月仍很明显。在B细胞缺陷的μMT幼鼠中保护作用消失,但在β2微球蛋白(β2m)基因敲除幼鼠以及CD4和CD8 T细胞耗竭的幼鼠中保护作用得以保留,这表明完整的体液免疫对增强保护作用很重要。Advax和Advax-CpG55.2佐剂对新生儿的益处也在新生猕猴中得到证实,它们同样增强了血清中针对IIV的抗流感抗体反应。这增加了单独使用Advax佐剂或与CpG55.2联合使用可能有助于改善人类新生儿流感疫苗保护作用的可能性。

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