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超抗原金黄色葡萄球菌肠毒素 C2 的连续口服给药可激活肠道免疫并调节小鼠肠道微生物群。

Continuous Oral Administration of the Superantigen Staphylococcal Enterotoxin C2 Activates Intestinal Immunity and Modulates the Gut Microbiota in Mice.

机构信息

Institute of Applied Ecology, Chinese Academy of Sciences, 72 WenHua Road, Shenyang, 110016, P. R. China.

University of Chinese Academy of Sciences, No.1 Yanqihu East Rd, Huairou District, Beijing, 101408, P. R. China.

出版信息

Adv Sci (Weinh). 2024 Nov;11(41):e2405039. doi: 10.1002/advs.202405039. Epub 2024 Sep 9.

DOI:10.1002/advs.202405039
PMID:39248343
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11538665/
Abstract

Staphylococcal Enterotoxin C2 (SEC2), a classical superantigen, is an antitumor immunotherapy agent. However, the injectable formulation of SEC2 limits its clinical application. Here, it is reported that oral administration of SEC2 activates the intestinal immune system and benefits intestinal health in a mouse model. These results indicate that intact SEC2 is detected in the stomach, intestine, and serum after oral administration. Continuous oral administration of SEC2 activates immune cells in gut-associated lymphoid tissues, promoting extensive differentiation and proliferation of CD4 and CD8 T cells and CD19 B cells, leading to increased production of cytokines and secretory immunoglobulin A. SEC2 also enhances intestinal barrier function, as demonstrated by an increased villus length/crypt depth ratio and elevated expression of mucins and tight junction proteins. Additionally, SEC2 indirectly influenced gut microbiota, reinforcing potential probiotics and short-chain fatty acid synthesis. Enhanced differentiation of T and B cells in the spleen, coupled with elevated serum interleukin-2 levels, suggests systemic immune enhancement following oral administration of SEC2. These findings provide a scientific basis for the development of SEC2 as an oral immunostimulant for immune enhancement and anti-tumor immunotherapy.

摘要

葡萄球菌肠毒素 C2(SEC2)是一种经典的超抗原,可用作抗肿瘤免疫治疗药物。然而,SEC2 的注射剂型限制了其临床应用。本研究报道 SEC2 的口服给药能够激活肠道免疫系统,有益于小鼠模型的肠道健康。结果表明 SEC2 口服给药后可在胃、肠道和血清中检测到完整的 SEC2。连续口服 SEC2 能够激活肠道相关淋巴组织中的免疫细胞,促进 CD4 和 CD8 T 细胞及 CD19 B 细胞的广泛分化和增殖,导致细胞因子和分泌型免疫球蛋白 A 的产生增加。SEC2 还增强了肠道屏障功能,表现为绒毛长度/隐窝深度比值增加,黏蛋白和紧密连接蛋白的表达水平升高。此外,SEC2 还间接影响肠道微生物群,增强潜在的益生菌和短链脂肪酸的合成。口服 SEC2 后,脾脏中 T 和 B 细胞的分化增强,血清中白细胞介素-2 水平升高,提示全身免疫增强。这些发现为 SEC2 作为口服免疫刺激剂用于增强免疫和抗肿瘤免疫治疗提供了科学依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/cd88d50acc25/ADVS-11-2405039-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/8554264fdf6a/ADVS-11-2405039-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/1d3e8babfe82/ADVS-11-2405039-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/f06331718079/ADVS-11-2405039-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/73590e89aff3/ADVS-11-2405039-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/d62c3a315e61/ADVS-11-2405039-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/cd88d50acc25/ADVS-11-2405039-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/8554264fdf6a/ADVS-11-2405039-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/5dfed286de32/ADVS-11-2405039-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/c2d05e308dcf/ADVS-11-2405039-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/1d3e8babfe82/ADVS-11-2405039-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/f06331718079/ADVS-11-2405039-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/73590e89aff3/ADVS-11-2405039-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/d62c3a315e61/ADVS-11-2405039-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/11538665/cd88d50acc25/ADVS-11-2405039-g005.jpg

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Low-Dose Staphylococcal Enterotoxin C2 Mutant Maintains Bone Homeostasis via Regulating Crosstalk between Bone Formation and Host T-Cell Effector Immunity.低剂量葡萄球菌肠毒素C2突变体通过调节骨形成与宿主T细胞效应免疫之间的相互作用维持骨稳态。
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Adverse effect of oxidized cholesterol exposure on colitis is mediated by modulation of gut microbiota.
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