Payload-free protein nanoparticles target inflamed colons to restore intestinal barrier integrity for effectively treating inflammatory bowel diseases

IF 13.9 Q1 CHEMISTRY, MULTIDISCIPLINARY
Mei Yang, Honglan Shen, Suting Zhong, Zongpu Xu, Xiangyu Liu, Weicheng Wu, Chuanbin Mao, Mingying Yang
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Abstract

Anti-inflammatory compounds, delivered as a payload to the gastrointestinal tract (GIT) by carriers, still cannot treat inflammatory bowel diseases without avoiding side effects. Here, we developed payload-free protein nanoparticles (PNPs) that crossed GIT to retain in the colon and treat colitis by restoring intestinal barrier integrity by modulating gut microbiome and metabolome. Specifically, PNPs, orally administered to mice with acute colitis, reached the colon within three hours. Consequently, PNPs improve gut microbiota dysbiosis to reverse metabolism balance, suppressing the expression of tumor-necrosis factor α and toll-like receptor 4 that restores the intestinal barrier integrity. PNPs then ameliorated colon inflammation and attenuated gut microbiota dysbiosis by exerting probiotic effects on gut microbiota, treating colitis in a week more effectively than the clinically often used 5-aminosalicylic acid without causing undesired side effects. Such PNPs represent safe, sustainable, and cost-effective therapeutics for treating inflammatory and metabolic diseases by eliminating microbial and metabolomic imbalance.

Abstract Image

不含有效载荷的蛋白质纳米粒子可靶向发炎的结肠,恢复肠道屏障的完整性,从而有效治疗炎症性肠病
通过载体将抗炎化合物作为有效载荷输送到胃肠道(GIT),仍然无法在避免副作用的情况下治疗炎症性肠病。在这里,我们开发了不含载荷的蛋白纳米颗粒(PNPs),它能穿过胃肠道保留在结肠中,并通过调节肠道微生物组和代谢组来恢复肠道屏障的完整性,从而治疗结肠炎。具体来说,急性结肠炎小鼠口服 PNPs 后,可在三小时内到达结肠。因此,PNPs 可改善肠道微生物群失调,扭转代谢平衡,抑制肿瘤坏死因子 α 和收费样受体 4 的表达,从而恢复肠道屏障的完整性。然后,PNPs 通过对肠道微生物群发挥益生作用,改善结肠炎症并减轻肠道微生物群失调,在一周内治疗结肠炎的效果优于临床常用的 5- 氨基水杨酸,且不会产生不良副作用。这种 PNPs 是通过消除微生物和代谢组失衡来治疗炎症和代谢疾病的安全、可持续和具有成本效益的疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
17.40
自引率
0.00%
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审稿时长
7 weeks
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