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热休克蛋白70融合口蹄疫表位可引发细胞免疫和体液免疫,并产生广谱保护效力。

The HSP70-fused foot-and-mouth disease epitope elicits cellular and humoral immunity and drives broad-spectrum protective efficacy.

作者信息

Jo Hyundong, Kim Bong Yoon, Park So Hui, Kim Hyun Mi, Shin Sung Ho, Hwang Seong Yun, Kim Su-Mi, Kim Byounghan, Park Jong-Hyeon, Lee Min Ja

机构信息

Animal and Plant Quarantine Agency, 177, Hyeoksin 8-ro, Gimcheon City, 39660, Gyeongsangbuk-do, Republic of Korea.

Watson RnD Sharing Co. Ltd., 19, Sanmaru-ro, Guri-si, 11901, Gyeonggi-do, Republic of Korea.

出版信息

NPJ Vaccines. 2021 Mar 26;6(1):42. doi: 10.1038/s41541-021-00304-9.

Abstract

Current foot-and-mouth disease (FMD) vaccines have significant limitations, including side effects due to oil emulsions at the vaccination site, a narrow spectrum of protective efficacy, and incomplete host defenses mediated by humoral immunity alone. To overcome these limitations, new FMD vaccines must ensure improved safety with non-oil-based adjuvants, a broad spectrum of host defenses within/between serotypes, and the simultaneous induction of cellular and humoral immunity. We designed a novel, immune-potent, recombinant protein rpHSP70-AD that induces robust cellular immunity and elicits a broad spectrum of host defenses against FMD virus (FMDV) infections. We demonstrated that an oil emulsion-free vaccine containing rpHSP70-AD mediates early, mid-term, and long-term immunity and drives potent host protection against FMDV type O and A, suggesting its potential as an FMD vaccine adjuvant in mice and pigs. These results suggest a key strategy for establishing next-generation FMD vaccines, including novel adjuvants.

摘要

目前的口蹄疫(FMD)疫苗存在显著局限性,包括接种部位因油乳剂产生的副作用、保护效力谱狭窄以及仅由体液免疫介导的宿主防御不完整。为克服这些局限性,新型FMD疫苗必须确保使用非油基佐剂提高安全性、在血清型内/血清型间具备广泛的宿主防御能力,并同时诱导细胞免疫和体液免疫。我们设计了一种新型、具有免疫活性的重组蛋白rpHSP70-AD,它能诱导强大的细胞免疫,并引发针对口蹄疫病毒(FMDV)感染的广泛宿主防御。我们证明,含有rpHSP70-AD的无油乳剂疫苗介导早期、中期和长期免疫,并对O型和A型FMDV提供强大的宿主保护,表明其在小鼠和猪中作为FMD疫苗佐剂的潜力。这些结果提示了建立下一代FMD疫苗(包括新型佐剂)的关键策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2df/7998017/a24be0cfcb97/41541_2021_304_Fig1_HTML.jpg

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