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疫苗佐剂 U-Omp19 的稳定性研究。

Stability Studies of the Vaccine Adjuvant U-Omp19.

机构信息

Instituto de Investigaciones Biotecnológicas (UNSAM-CONICET), Universidad Nacional de San Martín, Buenos Aires, Argentina.

Fundación Instituto Leloir, IIBBA-CONICET, Buenos Aires, Argentina.

出版信息

J Pharm Sci. 2021 Feb;110(2):707-718. doi: 10.1016/j.xphs.2020.10.011. Epub 2020 Oct 12.

DOI:10.1016/j.xphs.2020.10.011
PMID:33058898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7815325/
Abstract

Unlipidated outer membrane protein 19 (U-Omp19) is a novel mucosal adjuvant in preclinical development to be used in vaccine formulations. U-Omp19 holds two main properties, it is capable of inhibiting gastrointestinal and lysosomal peptidases, increasing the amount of co-administered antigen that reaches the immune inductive sites and its half-life inside cells, and it is able to stimulate antigen presenting cells in vivo. These activities enable U-Omp19 to enhance the adaptive immune response to co-administrated antigens. To characterize the stability of U-Omp19 we have performed an extensive analysis of its physicochemical and biological properties in a 3-year long-term stability study, and under potentially damaging freeze-thawing and lyophilization stress processes. Results revealed that U-Omp19 retains its full protease inhibitor activity, its monomeric state and its secondary structure even when stored in solution for 36 months or after multiple freeze-thawing cycles. Non-enzymatic hydrolysis resulted the major degradation pathway for storage in solution at 4 °C or room temperature which can be abrogated by lyophilization yet increasing protein tendency to form aggregates. This information will play a key role in the development of a stable formulation of U-Omp19, allowing an extended shelf-life during manufacturing, storage, and shipping of a future vaccine containing this pioneering adjuvant.

摘要

未脂化的外膜蛋白 19(U-Omp19)是一种新型黏膜佐剂,正在临床前开发阶段,将用于疫苗制剂。U-Omp19 具有两个主要特性,它能够抑制胃肠道和溶酶体肽酶,增加到达免疫诱导部位的共给药抗原的量及其在细胞内的半衰期,并且能够在体内刺激抗原呈递细胞。这些活性使 U-Omp19 能够增强对共给药抗原的适应性免疫反应。为了表征 U-Omp19 的稳定性,我们在长达 3 年的长期稳定性研究中以及在潜在的破坏性冻融和冷冻干燥应激过程中对其物理化学和生物学特性进行了广泛分析。结果表明,即使在溶液中储存 36 个月或经过多次冻融循环后,U-Omp19 仍保留其完整的蛋白酶抑制剂活性、单体状态和二级结构。非酶水解是在 4°C 或室温下溶液储存时的主要降解途径,但通过冷冻干燥可以阻止这种途径,从而增加蛋白质形成聚集体的趋势。这些信息将在 U-Omp19 稳定制剂的开发中发挥关键作用,允许在含有这种开创性佐剂的未来疫苗的制造、储存和运输过程中延长保质期。

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1
Stability Studies of the Vaccine Adjuvant U-Omp19.疫苗佐剂 U-Omp19 的稳定性研究。
J Pharm Sci. 2021 Feb;110(2):707-718. doi: 10.1016/j.xphs.2020.10.011. Epub 2020 Oct 12.
2
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4
A disordered region retains the full protease inhibitor activity and the capacity to induce CD8 T cells of the oral vaccine adjuvant U-Omp19.一个无序区域保留了口服疫苗佐剂U-Omp19的全部蛋白酶抑制剂活性以及诱导CD8 T细胞的能力。
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A Brucella spp. Protease Inhibitor Limits Antigen Lysosomal Proteolysis, Increases Cross-Presentation, and Enhances CD8+ T Cell Responses.一种布鲁氏菌属蛋白酶抑制剂可限制抗原的溶酶体蛋白水解、增强交叉提呈并增强CD8+ T细胞反应。
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Brucella abortus Omp19 recombinant protein subcutaneously co-delivered with an antigen enhances antigen-specific T helper 1 memory responses and induces protection against parasite challenge.流产布鲁氏菌Omp19重组蛋白与一种抗原皮下共同递送可增强抗原特异性辅助性T细胞1记忆反应并诱导对寄生虫攻击的保护作用。
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The Trypanosoma cruzi TcTASV-C protein subfamily administrated with U-Omp19 promotes a protective response against a lethal challenge in mice.克氏锥虫 TcTASV-C 蛋白亚家族与 U-Omp19 联合给药可促进小鼠对致死性攻击产生保护反应。
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Survey of Omp19 immunogenicity against Brucella abortus and Brucella melitensis: influence of nanoparticulation versus traditional immunization.针对流产布鲁氏菌和羊种布鲁氏菌的Omp19免疫原性研究:纳米颗粒化与传统免疫的影响
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U-Omp19 from Is a Useful Adjuvant for Vaccine Formulations against Infection in Mice.来自[具体来源]的U - Omp19是针对小鼠感染的疫苗制剂的一种有用佐剂。 (注:原文中“Is a Useful Adjuvant for Vaccine Formulations against Infection in Mice.”前面缺少具体主语,这里按照推测补充了“来自[具体来源]的”,以便更完整地表达句子意思)
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A bacterial protease inhibitor protects antigens delivered in oral vaccines from digestion while triggering specific mucosal immune responses.一种细菌蛋白酶抑制剂在触发特定黏膜免疫应答的同时,保护口服疫苗中递呈的抗原不被消化。
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A disordered region retains the full protease inhibitor activity and the capacity to induce CD8 T cells of the oral vaccine adjuvant U-Omp19.

本文引用的文献

1
Freezing of Biologicals Revisited: Scale, Stability, Excipients, and Degradation Stresses.重新审视生物制品的冷冻:规模、稳定性、赋形剂和降解压力。
J Pharm Sci. 2020 Jan;109(1):44-61. doi: 10.1016/j.xphs.2019.10.062. Epub 2019 Nov 6.
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Science and art of protein formulation development.蛋白质制剂开发的科学与艺术。
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Selection of adjuvants for vaccines targeting specific pathogens.针对特定病原体的疫苗佐剂的选择。
一个无序区域保留了口服疫苗佐剂U-Omp19的全部蛋白酶抑制剂活性以及诱导CD8 T细胞的能力。
Comput Struct Biotechnol J. 2022 Sep 6;20:5098-5114. doi: 10.1016/j.csbj.2022.08.054. eCollection 2022.
Expert Rev Vaccines. 2019 May;18(5):505-521. doi: 10.1080/14760584.2019.1604231. Epub 2019 Apr 22.
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Chemical and physical instabilities in manufacturing and storage of therapeutic proteins.治疗性蛋白质生产和储存中的化学和物理不稳定性。
Curr Opin Biotechnol. 2019 Dec;60:159-167. doi: 10.1016/j.copbio.2019.01.014. Epub 2019 Mar 9.
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Oral co-administration of a bacterial protease inhibitor in the vaccine formulation increases antigen delivery at the intestinal epithelial barrier.疫苗配方中口服给予细菌蛋白酶抑制剂可增加抗原在肠道上皮屏障中的递送。
J Control Release. 2019 Jan 10;293:158-171. doi: 10.1016/j.jconrel.2018.11.025. Epub 2018 Nov 27.
6
Analysis of phase behavior and morphology during freeze-thaw applications of lysozyme.溶菌酶在冻融过程中的相行为和形态分析。
Int J Pharm. 2019 Jan 30;555:153-164. doi: 10.1016/j.ijpharm.2018.11.047. Epub 2018 Nov 17.
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Applications of Freezing and Freeze-Drying in Pharmaceutical Formulations.冷冻和冷冻干燥在药物制剂中的应用。
Adv Exp Med Biol. 2018;1081:371-383. doi: 10.1007/978-981-13-1244-1_20.
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The Mucosal Vaccine Adjuvant LT(R192G/L211A) or dmLT.黏膜疫苗佐剂 LT(R192G/L211A)或 dmLT。
mSphere. 2018 Jul 25;3(4):e00215-18. doi: 10.1128/mSphere.00215-18.
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Factors affecting the physical stability (aggregation) of peptide therapeutics.影响肽类治疗药物物理稳定性(聚集)的因素。
Interface Focus. 2017 Dec 6;7(6):20170030. doi: 10.1098/rsfs.2017.0030. Epub 2017 Oct 20.
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Forced degradation of recombinant monoclonal antibodies: A practical guide.重组单克隆抗体的强制降解:实用指南。
MAbs. 2017 Nov/Dec;9(8):1217-1230. doi: 10.1080/19420862.2017.1368602. Epub 2017 Aug 30.