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Evidence for TLR4 and FcRγ-CARD9 activation by cholera toxin B subunit and its direct bindings to TREM2 and LMIR5 receptors.霍乱毒素B亚基激活TLR4和FcRγ-CARD9的证据及其与TREM2和LMIR5受体的直接结合。
Mol Immunol. 2015 Aug;66(2):463-71. doi: 10.1016/j.molimm.2015.05.008. Epub 2015 May 26.
2
Protection against multiple subtypes of influenza viruses by virus-like particle vaccines based on a hemagglutinin conserved epitope.基于血凝素保守表位的病毒样颗粒疫苗对多种流感病毒亚型的保护作用。
Biomed Res Int. 2015;2015:901817. doi: 10.1155/2015/901817. Epub 2015 Feb 12.
3
Induction of indoleamine 2, 3-dioxygenase in human dendritic cells by a cholera toxin B subunit-proinsulin vaccine.霍乱毒素B亚基-胰岛素原疫苗诱导人树突状细胞中吲哚胺2,3-双加氧酶的表达
PLoS One. 2015 Feb 25;10(2):e0118562. doi: 10.1371/journal.pone.0118562. eCollection 2015.
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Expression of recombinant T-cell epitopes of major Japanese cedar pollen allergens fused with cholera toxin B subunit in Escherichia coli.主要日本柳杉花粉过敏原的重组T细胞表位与霍乱毒素B亚基融合体在大肠杆菌中的表达
Protein Expr Purif. 2015 May;109:62-9. doi: 10.1016/j.pep.2015.02.001. Epub 2015 Feb 7.
5
N-glycosylation of cholera toxin B subunit in Nicotiana benthamiana: impacts on host stress response, production yield and vaccine potential.烟草中霍乱毒素B亚基的N-糖基化:对宿主应激反应、产量及疫苗潜力的影响
Sci Rep. 2015 Jan 23;5:8003. doi: 10.1038/srep08003.
6
Protective immunity against Naegleria fowleri infection on mice immunized with the rNfa1 protein using mucosal adjuvants.使用黏膜佐剂用rNfa1蛋白免疫的小鼠对福氏耐格里阿米巴感染的保护性免疫。
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A multi-epitope vaccine CTB-UE relieves Helicobacter pylori-induced gastric inflammatory reaction via up-regulating microRNA-155 to inhibit Th17 response in C57/BL6 mice model.一种多表位疫苗CTB-UE通过上调微小RNA-155抑制C57/BL6小鼠模型中的Th17反应,从而减轻幽门螺杆菌诱导的胃炎症反应。
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Oral administration of a fusion protein between the cholera toxin B subunit and the 42-amino acid isoform of amyloid-β peptide produced in silkworm pupae protects against Alzheimer's disease in mice.口服一种由霍乱毒素B亚基与家蚕蛹中产生的42个氨基酸的β淀粉样肽同种型组成的融合蛋白可预防小鼠患阿尔茨海默病。
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9
Novel mucosal DNA-MVA HIV vaccination in which DNA-IL-12 plus cholera toxin B subunit (CTB) cooperates to enhance cellular systemic and mucosal genital tract immunity.新型黏膜DNA-MVA HIV疫苗,其中DNA-IL-12与霍乱毒素B亚单位(CTB)协同作用,以增强细胞、全身和黏膜生殖道免疫力。
PLoS One. 2014 Sep 12;9(9):e107524. doi: 10.1371/journal.pone.0107524. eCollection 2014.
10
Production of a plant-derived immunogenic protein targeting ApoB100 and CETP: toward a plant-based atherosclerosis vaccine.一种靶向载脂蛋白B100和胆固醇酯转运蛋白的植物源免疫原性蛋白的制备:迈向基于植物的动脉粥样硬化疫苗
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霍乱毒素亚单位 B 作为佐剂——在保护性免疫中的加速器和自身免疫中的突破口。

Cholera Toxin Subunit B as Adjuvant--An Accelerator in Protective Immunity and a Break in Autoimmunity.

机构信息

Department of Physiology and Immunology, Faculty of Biology, University of Barcelona, Av. Diagonal 643, 3rd floor, Barcelona 08028, Spain.

出版信息

Vaccines (Basel). 2015 Jul 24;3(3):579-96. doi: 10.3390/vaccines3030579.

DOI:10.3390/vaccines3030579
PMID:26350596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4586468/
Abstract

Cholera toxin subunit B (CTB) is the nontoxic portion of cholera toxin. Its affinity to the monosialotetrahexosylganglioside (GM1) that is broadly distributed in a variety of cell types including epithelial cells of the gut and antigen presenting cells, macrophages, dendritic cells, and B cells, allows its optimal access to the immune system. CTB can easily be expressed on its own in a variety of organisms, and several approaches can be used to couple it to antigens, either by genetic fusion or by chemical manipulation, leading to strongly enhanced immune responses to the antigens. In autoimmune diseases, CTB has the capacity to evoke regulatory responses and to thereby dampen autoimmune responses, in several but not all animal models. It remains to be seen whether the latter approach translates to success in the clinic, however, the versatility of CTB to manipulate immune responses in either direction makes this protein a promising adjuvant for vaccine development.

摘要

霍乱毒素亚单位 B(CTB)是霍乱毒素的无毒部分。它与广泛分布于各种细胞类型(包括肠道上皮细胞和抗原呈递细胞、巨噬细胞、树突状细胞和 B 细胞)的单涎酸四己糖神经节苷脂(GM1)具有亲和力,使其能够最佳地进入免疫系统。CTB 可以很容易地在各种生物体中单独表达,并且可以使用多种方法将其与抗原偶联,无论是通过遗传融合还是通过化学修饰,从而导致对抗原的强烈增强的免疫反应。在自身免疫性疾病中,CTB 具有引发调节性反应的能力,从而在几种但不是所有动物模型中减弱自身免疫反应。然而,尚不清楚后者的方法是否会在临床上取得成功,但是,CTB 具有操纵免疫反应的多功能性使得这种蛋白质成为疫苗开发有前途的佐剂。