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鸡源树突状细胞靶向纳米抗体介导的同源序贯免疫研究中提高了对 H9N2 流感病毒攻击的保护作用。

Chicken dendritic cell-targeting nanobodies mediated improved protective effects against H9N2 influenza virus challenge in a homologous sequential immunization study.

机构信息

College of Animal Medicine, Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.

College of Animal Medicine, Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun 130118, China.

出版信息

Vet Microbiol. 2023 Oct;285:109875. doi: 10.1016/j.vetmic.2023.109875. Epub 2023 Sep 12.

Abstract

Global poultry production is still severely affected by H9N2 avian influenza virus (AIV), and the development of a novel universal AIV vaccine is still urgently needed. Neuraminidase (NA) has recently been shown to be an efficient conserved protective antigen. In this study, we fused the extracellular region of the NA gene with a ferritin cassette (pYL281), which resulted in self-assembled 24-mer nanoparticles with the NA protein displayed outside the nanoparticles. In addition, a chicken dendritic cell-targeting nanobody-phage74 was also inserted ahead of the NA protein to yield pYL294. Incubation with chicken bone marrow-derived dendritic cells (chBMDCs) showed that the DC-targeting nanoparticles purified from the pYL294 strain significantly increased the maturation of chBMDCs, as shown by increased levels of CCL5, CCR7, CD83 and CD86 compared with nontargeting proteins. Then, a chicken study was performed using Salmonella oral administration together with intranasal boost with purified proteins. Compared with the other groups, oral immunization with Salmonella harboring pYL294 followed by intranasal boost with purified DC-targeting nanoparticles dramatically increased the humoral IgY and mucosal IgA antibody response, as well as increased the cellular immune response, as shown by elevated splenic lymphocyte proliferation and intracellular mRNA levels of IL-4 and IFN-γ. Finally, sequential immunization with DC-targeting nanoparticles showed increased protection against G57 subtype H9N2 virus challenge compared with other groups, as shown by significantly decreased virus RNA copy numbers in oropharyngeal washes (Days 3, 5 and 7 post challenge) and cloacal washes (Day 7), significantly decreased lung virus titers on Day 5 post challenge and increased body weight gains during the challenge.

摘要

全球家禽生产仍严重受到 H9N2 禽流感病毒(AIV)的影响,因此仍然迫切需要开发新型通用 AIV 疫苗。神经氨酸酶(NA)最近已被证明是一种有效的保守保护性抗原。在这项研究中,我们将 NA 基因的细胞外区域与铁蛋白盒(pYL281)融合,导致 NA 蛋白在外层显示的 24 聚体自组装纳米颗粒。此外,还在 NA 蛋白前插入了一种鸡树突状细胞靶向纳米抗体噬菌体 74,从而产生了 pYL294。与鸡骨髓来源的树突状细胞(chBMDC)孵育表明,从 pYL294 株中纯化的靶向 DC 的纳米颗粒可显著增加 chBMDC 的成熟度,与非靶向蛋白相比,CCL5、CCR7、CD83 和 CD86 的水平增加。然后,使用沙门氏菌口服给药联合纯化蛋白鼻内加强进行了鸡研究。与其他组相比,用携带 pYL294 的沙门氏菌口服免疫,然后用纯化的靶向 DC 的纳米颗粒鼻内加强,可显著增加体液 IgY 和黏膜 IgA 抗体应答,并增强细胞免疫应答,表现为脾淋巴细胞增殖和 IFN-γ的细胞内 mRNA 水平升高。最后,与其他组相比,靶向 DC 的纳米颗粒的序贯免疫可显著提高针对 G57 亚型 H9N2 病毒的保护作用,表现为口咽冲洗液(攻毒后第 3、5 和 7 天)和泄殖腔冲洗液(攻毒后第 7 天)中的病毒 RNA 拷贝数显著降低,攻毒后第 5 天肺病毒滴度显著降低,攻毒期间体重增加。

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