• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

脂质 A 脂质体:一种有效、安全、通用的合成疫苗佐剂系统。

Liposomes containing lipid A: an effective, safe, generic adjuvant system for synthetic vaccines.

机构信息

Laboratory of Adjuvant and Antigen Research, US Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, USA.

出版信息

Expert Rev Vaccines. 2012 Jun;11(6):733-44. doi: 10.1586/erv.12.35.

DOI:10.1586/erv.12.35
PMID:22873129
Abstract

Liposomes containing monophosphoryl lipid A (MPLA) have previously exhibited considerable potency and safety in human trials with a variety of candidate vaccines, including vaccines to malaria, HIV-1 and several different types of cancer. The long history of research and development of MPLA and liposomal MPLA as vaccine adjuvants reveals that there are numerous opportunities for creation and development of generic (nonproprietary) adjuvant system formulations with these materials that are not only highly potent and safe, but also readily available as native materials or as synthetic compounds. They are easily manufactured as potentially inexpensive and easy to use adjuvant systems and might be effective even with synthetic peptides as antigens.

摘要

含有单磷酰脂质 A(MPLA)的脂质体在多种候选疫苗的人体试验中表现出相当大的效力和安全性,这些候选疫苗包括疟疾疫苗、HIV-1 疫苗和几种不同类型的癌症疫苗。MPLA 和脂质体 MPLA 作为疫苗佐剂的长期研发历史表明,有许多机会可以用这些材料创造和开发通用(非专利)佐剂系统配方,这些配方不仅效力高且安全,而且还可以作为天然材料或合成化合物随时获得。它们很容易制成潜在廉价且易于使用的佐剂系统,即使使用合成肽作为抗原,也可能有效。

相似文献

1
Liposomes containing lipid A: an effective, safe, generic adjuvant system for synthetic vaccines.脂质 A 脂质体:一种有效、安全、通用的合成疫苗佐剂系统。
Expert Rev Vaccines. 2012 Jun;11(6):733-44. doi: 10.1586/erv.12.35.
2
Lipopolysaccharide, lipid A, and liposomes containing lipid A as immunologic adjuvants.脂多糖、脂质A以及含有脂质A作为免疫佐剂的脂质体。
Immunobiology. 1993 Apr;187(3-5):430-46. doi: 10.1016/S0171-2985(11)80355-4.
3
Vaccine adjuvant systems containing monophosphoryl lipid A and QS21 induce strong and persistent humoral and T cell responses against hepatitis B surface antigen in healthy adult volunteers.含有单磷酰脂质A和QS21的疫苗佐剂系统在健康成年志愿者中诱导出针对乙肝表面抗原的强烈且持久的体液和T细胞应答。
Vaccine. 2008 Mar 4;26(10):1375-86. doi: 10.1016/j.vaccine.2007.12.038. Epub 2008 Jan 14.
4
Liposomal malaria vaccine in humans: a safe and potent adjuvant strategy.人用脂质体疟疾疫苗:一种安全有效的佐剂策略。
Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):358-62. doi: 10.1073/pnas.89.1.358.
5
Monophosphoryl lipid A as an adjuvant. Past experiences and new directions.单磷酰脂质A作为佐剂:既往经验与新方向
Pharm Biotechnol. 1995;6:495-524.
6
Liposomes containing monophosphoryl lipid A: a potent adjuvant system for inducing antibodies to heroin hapten analogs.脂质体中含有单磷酰脂质 A:一种用于诱导针对海洛因半抗原类似物的抗体的有效佐剂系统。
Vaccine. 2013 Jun 10;31(26):2804-10. doi: 10.1016/j.vaccine.2013.04.027. Epub 2013 Apr 23.
7
Comparison of liposome-polycation-DNA(LPD) and monophosphoryl lipid A(MPL) adjuvant formulations in BALB/c mice models.脂质体-聚阳离子-DNA(LPD)与单磷酰脂质 A(MPL)佐剂制剂在 BALB/c 小鼠模型中的比较。
Immunol Invest. 2012;41(4):356-66. doi: 10.3109/08820139.2011.606861. Epub 2011 Aug 24.
8
Monophosphoryl lipid A (MPL) formulations for the next generation of vaccines.用于下一代疫苗的单磷酰脂质A(MPL)制剂。
Methods. 1999 Sep;19(1):103-7. doi: 10.1006/meth.1999.0834.
9
Highly effective generic adjuvant systems for orphan or poverty-related vaccines.高效通用佐剂系统,适用于孤儿药或与贫困相关的疫苗。
Vaccine. 2011 Jan 29;29(5):873-7. doi: 10.1016/j.vaccine.2010.11.049. Epub 2010 Nov 27.
10
Liposomes containing lipid A: a potent nontoxic adjuvant for a human malaria sporozoite vaccine.含脂质A的脂质体:一种用于人类疟疾子孢子疫苗的高效无毒佐剂。
Immunol Lett. 1990 Aug;25(1-3):275-9. doi: 10.1016/0165-2478(90)90127-c.

引用本文的文献

1
A novel cationic liposome-formulated toll like receptor (TLR) 7/8 agonist enhances the efficacy of a vaccine against fentanyl toxicity.一种新型阳离子脂质体配方的Toll样受体(TLR)7/8激动剂可增强抗芬太尼毒性疫苗的效力。
J Control Release. 2025 Aug 10;384:113901. doi: 10.1016/j.jconrel.2025.113901. Epub 2025 May 27.
2
Assessment of the Anti-Inflammatory Effectiveness of Diclofenac Encapsulated in Chitosan-Coated Lipid Microvesicles in Rats.壳聚糖包被脂质微泡包裹双氯芬酸对大鼠抗炎效果的评估
Pharmaceutics. 2025 May 3;17(5):607. doi: 10.3390/pharmaceutics17050607.
3
SPA14 liposomes combining saponin with fully synthetic TLR4 agonist provide adjuvanticity to hCMV vaccine candidate.
将皂苷与全合成TLR4激动剂相结合的SPA14脂质体为候选人巨细胞病毒疫苗提供佐剂活性。
NPJ Vaccines. 2024 Dec 19;9(1):253. doi: 10.1038/s41541-024-01046-0.
4
Controlled production of lipopolysaccharides increases immune activation in Salmonella treatments of cancer.控制脂多糖的产生增加了癌症治疗中沙门氏菌的免疫激活。
Microb Biotechnol. 2024 May;17(5):e14461. doi: 10.1111/1751-7915.14461.
5
Vaccine approaches for antigen capture by liposomes.脂质体抗原捕获的疫苗方法。
Expert Rev Vaccines. 2023 Jan-Dec;22(1):1022-1040. doi: 10.1080/14760584.2023.2274479. Epub 2023 Nov 6.
6
Nanoadjuvants: Promising Bioinspired and Biomimetic Approaches in Vaccine Innovation.纳米佐剂:疫苗创新中具有前景的受生物启发和仿生方法
ACS Omega. 2023 Jul 24;8(31):27953-27968. doi: 10.1021/acsomega.3c02030. eCollection 2023 Aug 8.
7
Pan-cancer analysis of TASL: a novel immune infiltration-related biomarker for tumor prognosis and immunotherapy response prediction.泛癌症分析 TASL:一种新型免疫浸润相关的肿瘤预后和免疫治疗反应预测生物标志物。
BMC Cancer. 2023 Jun 9;23(1):528. doi: 10.1186/s12885-023-11015-w.
8
Effect of Glycosylation on Self-Assembly of Lipid A Lipopolysaccharides in Aqueous Solutions.糖基化对脂多糖脂酰化在水溶液中自组装的影响。
Langmuir. 2023 Jun 20;39(24):8516-8522. doi: 10.1021/acs.langmuir.3c00828. Epub 2023 Jun 8.
9
Similarities and differences of chemical compositions and physical and functional properties of adjuvant system 01 and army liposome formulation with QS21.佐剂系统 01 和 Army 脂质体制剂与 QS21 的化学成分、物理和功能特性的异同。
Front Immunol. 2023 Jan 25;14:1102524. doi: 10.3389/fimmu.2023.1102524. eCollection 2023.
10
Materials-based vaccines for infectious diseases.基于材料的传染病疫苗。
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2022 Sep;14(5):e1824. doi: 10.1002/wnan.1824. Epub 2022 Jun 16.