Campbell Connor, Kandalgaonkar Mrunmayee R, Golonka Rachel M, Yeoh Beng San, Vijay-Kumar Matam, Saha Piu
Department of Physiology & Pharmacology, University of Toledo College of Medicine, Toledo, OH 43614, USA.
Department of Physiology & Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.
Biomedicines. 2023 Jan 20;11(2):294. doi: 10.3390/biomedicines11020294.
Gut microbes and their metabolites are actively involved in the development and regulation of host immunity, which can influence disease susceptibility. Herein, we review the most recent research advancements in the gut microbiota-immune axis. We discuss in detail how the gut microbiota is a tipping point for neonatal immune development as indicated by newly uncovered phenomenon, such as maternal imprinting, in utero intestinal metabolome, and weaning reaction. We describe how the gut microbiota shapes both innate and adaptive immunity with emphasis on the metabolites short-chain fatty acids and secondary bile acids. We also comprehensively delineate how disruption in the microbiota-immune axis results in immune-mediated diseases, such as gastrointestinal infections, inflammatory bowel diseases, cardiometabolic disorders (e.g., cardiovascular diseases, diabetes, and hypertension), autoimmunity (e.g., rheumatoid arthritis), hypersensitivity (e.g., asthma and allergies), psychological disorders (e.g., anxiety), and cancer (e.g., colorectal and hepatic). We further encompass the role of fecal microbiota transplantation, probiotics, prebiotics, and dietary polyphenols in reshaping the gut microbiota and their therapeutic potential. Continuing, we examine how the gut microbiota modulates immune therapies, including immune checkpoint inhibitors, JAK inhibitors, and anti-TNF therapies. We lastly mention the current challenges in metagenomics, germ-free models, and microbiota recapitulation to a achieve fundamental understanding for how gut microbiota regulates immunity. Altogether, this review proposes improving immunotherapy efficacy from the perspective of microbiome-targeted interventions.
肠道微生物及其代谢产物积极参与宿主免疫的发育和调节,这会影响疾病易感性。在此,我们综述了肠道微生物群-免疫轴的最新研究进展。我们详细讨论了肠道微生物群如何成为新生儿免疫发育的一个关键点,这体现在新发现的现象中,如母体印记、子宫内肠道代谢组和断奶反应。我们描述了肠道微生物群如何塑造先天性免疫和适应性免疫,重点是代谢产物短链脂肪酸和次级胆汁酸。我们还全面阐述了微生物群-免疫轴的破坏如何导致免疫介导的疾病,如胃肠道感染、炎症性肠病、心脏代谢紊乱(如心血管疾病、糖尿病和高血压)、自身免疫(如类风湿性关节炎)、超敏反应(如哮喘和过敏)、心理障碍(如焦虑)和癌症(如结直肠癌和肝癌)。我们进一步探讨了粪便微生物群移植、益生菌、益生元以及膳食多酚在重塑肠道微生物群方面的作用及其治疗潜力。接着,我们研究肠道微生物群如何调节免疫疗法,包括免疫检查点抑制剂、JAK抑制剂和抗TNF疗法。我们最后提到了宏基因组学、无菌模型和微生物群重现方面目前存在的挑战,以实现对肠道微生物群如何调节免疫的基本理解。总之,本综述建议从针对微生物群的干预措施角度提高免疫治疗效果。
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