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1
Immune response mediated by liposome-associated protein antigens. II. Comparison of the effectiveness of vesicle-entrapped and surface-associated antigen in immunopotentiation.脂质体相关蛋白抗原介导的免疫反应。II. 囊泡包裹抗原与表面结合抗原在免疫增强效果上的比较。
Immunology. 1982 Dec;47(4):627-32.
2
Comparison between multilamellar and unilamellar liposomes in enhancing antibody formation.多层脂质体与单层脂质体在增强抗体形成方面的比较。
Immunology. 1983 May;49(1):37-44.
3
Immune response mediated by liposome-associated protein antigens. I. Potentiation of the plaque-forming cell response.脂质体相关蛋白抗原介导的免疫反应。I. 对空斑形成细胞反应的增强作用。
Immunology. 1982 Feb;45(2):349-56.
4
Immune response mediated by liposome-associated protein antigens. III. Immunogenicity of bovine serum albumin covalently coupled to vesicle surface.脂质体相关蛋白抗原介导的免疫反应。III. 共价偶联至囊泡表面的牛血清白蛋白的免疫原性。
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Surgery. 1984 Aug;96(2):345-51.
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Immunomodulation with liposomes: the immune response elicited by liposomes with entrapped dichloromethylene-diphosphonate and surface-associated antigen or hapten.脂质体的免疫调节作用:包封二氯亚甲基二膦酸盐以及表面结合抗原或半抗原的脂质体引发的免疫反应。
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Immunopotentiation of the humoral response by liposomes: encapsulation versus covalent linkage.脂质体对体液免疫反应的免疫增强作用:包封与共价连接
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Immune response mediated by liposome-associated protein antigens. IV. Modulation of antibody formation by vesicle-encapsulated methotrexate.脂质体相关蛋白抗原介导的免疫反应。IV. 囊泡包裹的甲氨蝶呤对抗体形成的调节。
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Adjuvant effects of nonionic block polymer surfactants on liposome-induced humoral immune response.非离子嵌段聚合物表面活性剂对脂质体诱导的体液免疫反应的佐剂作用。
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The role of macrophages in the immunoadjuvant action of liposomes: effects of elimination of splenic macrophages on the immune response against intravenously injected liposome-associated albumin antigen.巨噬细胞在脂质体免疫佐剂作用中的角色:清除脾脏巨噬细胞对静脉注射脂质体相关白蛋白抗原免疫反应的影响。
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Small cationic DDA:TDB liposomes as protein vaccine adjuvants obviate the need for TLR agonists in inducing cellular and humoral responses.小阳离子 DDA:TDB 脂质体作为蛋白疫苗佐剂,在诱导细胞和体液应答方面不需要 TLR 激动剂。
PLoS One. 2012;7(3):e34255. doi: 10.1371/journal.pone.0034255. Epub 2012 Mar 28.
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Negatively charged liposomes show potent adjuvant activity when simply admixed with protein antigens.带负电荷的脂质体与蛋白抗原简单混合时表现出很强的佐剂活性。
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Immunopotentiation and delivery systems for antigens for single-step immunization: recent trends and progress.用于单步免疫的抗原免疫增强及递送系统:最新趋势与进展
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Immune response mediated by liposome-associated protein antigens. III. Immunogenicity of bovine serum albumin covalently coupled to vesicle surface.脂质体相关蛋白抗原介导的免疫反应。III. 共价偶联至囊泡表面的牛血清白蛋白的免疫原性。
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Liposomes as adjuvants with immunopurified tetanus toxoid: influence of liposomal characteristics.脂质体作为免疫纯化破伤风类毒素的佐剂:脂质体特性的影响
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7
Immune response mediated by liposome-associated protein antigens. IV. Modulation of antibody formation by vesicle-encapsulated methotrexate.脂质体相关蛋白抗原介导的免疫反应。IV. 囊泡包裹的甲氨蝶呤对抗体形成的调节。
Immunology. 1986 Jan;57(1):153-7.
8
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9
Immunopotentiation of the humoral response by liposomes: encapsulation versus covalent linkage.脂质体对体液免疫反应的免疫增强作用:包封与共价连接
Immunology. 1988 Oct;65(2):315-7.
10
Mannose-mediated targeted immunoadjuvant action of liposomes.甘露糖介导的脂质体靶向免疫佐剂作用。
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本文引用的文献

1
Immune response mediated by liposome-associated protein antigens. I. Potentiation of the plaque-forming cell response.脂质体相关蛋白抗原介导的免疫反应。I. 对空斑形成细胞反应的增强作用。
Immunology. 1982 Feb;45(2):349-56.
2
Liposomes in immunology: evidence that their adjuvant effect results from surface exposition of the antigens.
Cell Immunol. 1980 Feb;49(2):402-7. doi: 10.1016/0008-8749(80)90043-x.
3
Liposomes as immunological adjuvants.脂质体作为免疫佐剂。
Nature. 1974 Nov 15;252(5480):252. doi: 10.1038/252252a0.
4
Antibody-producing cells in rabbits injected with soluble BSA. II. Kinetica and dose response.注射可溶性牛血清白蛋白的兔子体内产生抗体的细胞。II. 动力学和剂量反应。
J Immunol. 1968 Dec;101(6):1230-5.
5
The adjuvant properties of liposomes.脂质体的佐剂特性。
Biochem Soc Trans. 1976;4(1):129-33. doi: 10.1042/bst0040129.
6
Liposomes in immunology: the immune response against antigen-containing liposomes.免疫学中的脂质体:针对含抗原脂质体的免疫反应。
Immunol Commun. 1977;6(5):489-98. doi: 10.3109/08820137709094148.
7
New aspects of liposomes.脂质体的新方面。
Biochim Biophys Acta. 1976 Dec 14;457(3-4):259-302. doi: 10.1016/0304-4157(76)90002-2.
8
Characterization of immunogenic properties of haptenated liposomal model membranes in mice. I. Thymus independence of the antigen.小鼠中半抗原化脂质体模型膜免疫原性特性的表征。I. 抗原的胸腺非依赖性
Immunology. 1979 Jun;37(2):505-14.
9
Immunogenic properties of liposomal model membranes in mice.小鼠中脂质体模型膜的免疫原性特性。
J Immunol. 1977 Dec;119(6):1863-7.
10
Primary in vitro immunogenicity of liposomal model membranes in mouse spleen cell cultures.脂质体模型膜在小鼠脾细胞培养中的原发性体外免疫原性
J Immunol. 1979 Oct;123(4):1535-9.

脂质体相关蛋白抗原介导的免疫反应。II. 囊泡包裹抗原与表面结合抗原在免疫增强效果上的比较。

Immune response mediated by liposome-associated protein antigens. II. Comparison of the effectiveness of vesicle-entrapped and surface-associated antigen in immunopotentiation.

作者信息

Shek P N, Sabiston B H

出版信息

Immunology. 1982 Dec;47(4):627-32.

PMID:6754583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1555561/
Abstract

The immunogenicity of different preparations of liposome-associated bovine serum albumin (LSM-BSA) was compared in order to examine the significance of the site of association between a protein antigen and the liposomal carrier. Animals immunized with liposomes containing both entrapped and surface-adsorbed BSA. (LSM-BSA) e + a, were found to give a BSA-specific plaque-forming cell (PFC) response comparable with that elicited by animals immunized with trypsinized (LSM-BSA) e + a which contained mainly entrapped BSA. In contrast, the PFC response elicited by animals immunized with liposomes containing BSA adsorbed on the membrane surface, (LSM-BSA)a, was significantly less than that of the above two groups. Finally, animals injected with trypsinized (LSM-BSA)a only elicited a marginally detectable PFC response. Results of this study demonstrate that liposomes can enhance the antibody response of a protein antigen regardless of whether the antigen is entrapped within the vesicle or absorbed on the outer surface. Entrapped antigen, however, proved to be more immunogenic than that which was surface-adsorbed.

摘要

为了研究蛋白质抗原与脂质体载体之间结合位点的重要性,对不同制剂的脂质体相关牛血清白蛋白(LSM-BSA)的免疫原性进行了比较。用同时含有包封型和表面吸附型牛血清白蛋白的脂质体(LSM-BSA)e + a免疫的动物,其牛血清白蛋白特异性空斑形成细胞(PFC)反应与用主要含有包封型牛血清白蛋白的胰蛋白酶处理的(LSM-BSA)e + a免疫的动物所引发的反应相当。相比之下,用含有吸附在膜表面的牛血清白蛋白的脂质体(LSM-BSA)a免疫的动物所引发的PFC反应明显低于上述两组。最后,仅注射胰蛋白酶处理的(LSM-BSA)a的动物仅引发了勉强可检测到的PFC反应。这项研究的结果表明,脂质体可以增强蛋白质抗原的抗体反应,无论抗原是包封在囊泡内还是吸附在外表面。然而,事实证明,包封型抗原比表面吸附型抗原具有更强的免疫原性。