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C3d融合口蹄疫疫苗平台通过诱导强大的适应性免疫克服母源抗体干扰。

The C3d-fused foot-and-mouth disease vaccine platform overcomes maternally-derived antibody interference by inducing a potent adaptive immunity.

作者信息

Lee Min Ja, Kim Hyun Mi, Shin Sehee, Jo Hyundong, Park So Hui, Kim Su-Mi, Park Jong-Hyeon

机构信息

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

出版信息

NPJ Vaccines. 2022 Jun 28;7(1):70. doi: 10.1038/s41541-022-00496-8.

Abstract

Vaccination prevents and controls foot-and-mouth disease (FMD). However, the current FMD vaccine remains disadvantageous since it cannot overcome maternally-derived antibody (MDA) interference in weeks-old animals, which suppress active immunity via vaccination. To address this, we developed the immune-enhancing O PA2-C3d and A22-C3d FMD vaccine strains that can stimulate receptors on the surface of B cells by inserting C3d (a B cell epitope) into the VP1 region of O PA2 (FMDV type O) and A22 (FMDV type A). We purified inactivated viral antigens from these vaccine strains and evaluated their immunogenicity and host defense against FMDV infection in mice. We also verified its efficacy in inducing an adaptive immune response and overcome MDA interference in MDA-positive (MDA(+), FMD-seropositive) and -negative (MDA(-), FMD-seronegative) pigs. These results suggest a key strategy for establishing novel FMD vaccine platform to overcome MDA interference and induce a robust adaptive immune response.

摘要

疫苗接种可预防和控制口蹄疫(FMD)。然而,目前的口蹄疫疫苗仍存在缺点,因为它无法克服幼龄动物母源抗体(MDA)的干扰,而这种抗体通过疫苗接种抑制主动免疫。为解决这一问题,我们开发了免疫增强型O PA2-C3d和A22-C3d口蹄疫疫苗株,通过将C3d(一种B细胞表位)插入O PA2(O型口蹄疫病毒)和A22(A型口蹄疫病毒)的VP1区域来刺激B细胞表面的受体。我们从这些疫苗株中纯化了灭活病毒抗原,并评估了它们在小鼠中的免疫原性以及宿主对口蹄疫病毒感染的防御能力。我们还验证了其在诱导适应性免疫反应以及克服MDA阳性(MDA(+),口蹄疫血清阳性)和MDA阴性(MDA(-),口蹄疫血清阴性)猪中MDA干扰方面的功效。这些结果提示了建立新型口蹄疫疫苗平台以克服MDA干扰并诱导强大适应性免疫反应的关键策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ae/9240001/1a07cbfb90e8/41541_2022_496_Fig1_HTML.jpg

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