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聚(丙交酯-乙交酯)微粒释放杀鱼菌素肽和重组甘油醛-3-磷酸脱氢酶单次疫苗接种诱导石斑鱼的保护性免疫

Protective Immunity against in Grouper Induced by Single Vaccination with Poly (Lactide-co-glycolide) Microparticles Releasing Pleurocidin Peptide and Recombinant Glyceraldehyde-3-phosphate Dehydrogenase.

作者信息

Liu Shang-Pin, Chuang Shu-Chun, Yang Chung-Da

机构信息

Department of Biological Science and Technology, College of Health and Nursing, Meiho University, 23 Pingguang Road, Neipu, Pingtung 912, Taiwan.

Orthopaedic Research Center, Kaohsiung Medical University, No. 100, Shih-Chuan 1st Road, Kaohsiung 807, Taiwan.

出版信息

Vaccines (Basel). 2020 Jan 19;8(1):33. doi: 10.3390/vaccines8010033.

Abstract

The peptide adjuvant, pleurocidin (PLE), and the i antigen, recombinant glyceraldehyde-3-phosphate dehydrogenase (rGAPDH) protein, were encapsulated with poly (lactide-co-glycolide) (PLG) polymers in our previous study to produce PLG-encapsulated PLE plus rGAPDH microparticles (PLG-PLE/rGAPDH MPs) that sustained stable release of both PLE and rGAPDH as well as, after two-time vaccination with MPs, generated long-term protective immunity against in grouper. Stable controlled-release of PLE plus rGAPDH from PLG-PLE/rGAPDH MPs is an attractive feature for developing an effective single-dose vaccine. In the present study, therefore, we aim to evaluate whether single administration with PLG-PLE/rGAPDH MPs in grouper would result in protective immunity against . Peritoneal vaccination of grouper with one dose of PLG-PLE/rGAPDH MPs raised serum titers over a long 12-week period. Moreover, twelve weeks after vaccination, significant lymphocyte proliferation and maximum TNF-α production were found in grouper immunized with a single dose of PLG-PLE/rGAPDH MPs. More importantly, immune responses elicited by single vaccination with PLG-PLE/rGAPDH MPs protected 80% of fish against a lethal peritoneal challenge of the highly virulent (Vh MML-1). In conclusion, our data truly reveal the feasibility of the development of a single-dose vaccine against based on PLG-PLE/rGAPDH MPs.

摘要

在我们之前的研究中,肽佐剂杀鲇素(PLE)和i抗原重组甘油醛-3-磷酸脱氢酶(rGAPDH)蛋白被包裹于聚(丙交酯-共-乙交酯)(PLG)聚合物中,制成了包裹PLG的PLE加rGAPDH微粒(PLG-PLE/rGAPDH MPs),该微粒能持续稳定释放PLE和rGAPDH,并且在用微粒进行两次疫苗接种后,能对石斑鱼产生针对[病原体名称未给出]的长期保护性免疫。PLG-PLE/rGAPDH MPs对PLE加rGAPDH的稳定控释是开发有效单剂量疫苗的一个吸引人的特性。因此,在本研究中,我们旨在评估在石斑鱼中单次施用PLG-PLE/rGAPDH MPs是否会产生针对[病原体名称未给出]的保护性免疫。用一剂PLG-PLE/rGAPDH MPs对石斑鱼进行腹腔疫苗接种后,血清效价在长达12周的时间内持续升高。此外,在接种疫苗12周后,在用单剂量PLG-PLE/rGAPDH MPs免疫的石斑鱼中发现了显著的淋巴细胞增殖和最大程度的TNF-α产生。更重要的是,用PLG-PLE/rGAPDH MPs单次接种引发的免疫反应保护了80%的鱼免受高毒力[病原体名称未给出](Vh MML-1)的致死性腹腔攻击。总之,我们的数据真实地揭示了基于PLG-PLE/rGAPDH MPs开发针对[病原体名称未给出]的单剂量疫苗的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a3/7157564/25380a3b51fe/vaccines-08-00033-g001.jpg

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