磷霉素的抗炎和免疫调节特性:一种众所周知的抗生素中被忽视的潜力。

IF 5.3 2区 医学 Q2 IMMUNOLOGY
Ali Darabniya
{"title":"磷霉素的抗炎和免疫调节特性:一种众所周知的抗生素中被忽视的潜力。","authors":"Ali Darabniya","doi":"10.1007/s10787-025-01968-8","DOIUrl":null,"url":null,"abstract":"<p><p>Fosfomycin, a broad-spectrum bactericidal antibiotic, has recently gained interest for its potential anti-inflammatory and immunomodulatory effects beyond its well-established antimicrobial activity. Emerging evidence from preclinical studies demonstrates that fosfomycin suppresses key pro-inflammatory cytokines, including TNF-α, IL-1β, and IL-6, while enhancing anti-inflammatory mediators such as IL-10. It modulates essential intracellular pathways by inhibiting NF-κB and MAPK signaling and reducing NLRP3 inflammasome activation. Fosfomycin also influences immune cell function by limiting neutrophil migration and activation, suppressing T-cell proliferation, and decreasing B-cell immunoglobulin production. In addition, it promotes tissue regeneration through enhanced collagen deposition, angiogenesis, and improved wound healing in experimental models. These combined effects suggest a dual therapeutic role for fosfomycin, both in controlling infection and modulating inflammatory responses. Despite promising preclinical results, clinical evidence on its immunomodulatory effects remains limited, with most human studies primarily addressing its antibacterial efficacy. This review summarizes current knowledge on fosfomycin's non-antibacterial properties, highlights its therapeutic potential in inflammatory and infectious diseases, and identifies research gaps that warrant further investigation. Overall, fosfomycin emerges as a promising adjunctive agent, particularly in conditions such as sepsis, chronic wounds, and sterile surgical inflammation, where excessive immune activation impairs recovery.</p>","PeriodicalId":13551,"journal":{"name":"Inflammopharmacology","volume":" ","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anti-inflammatory and immunomodulatory properties of fosfomycin: an overlooked potential in a well-known antibiotic.\",\"authors\":\"Ali Darabniya\",\"doi\":\"10.1007/s10787-025-01968-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Fosfomycin, a broad-spectrum bactericidal antibiotic, has recently gained interest for its potential anti-inflammatory and immunomodulatory effects beyond its well-established antimicrobial activity. Emerging evidence from preclinical studies demonstrates that fosfomycin suppresses key pro-inflammatory cytokines, including TNF-α, IL-1β, and IL-6, while enhancing anti-inflammatory mediators such as IL-10. It modulates essential intracellular pathways by inhibiting NF-κB and MAPK signaling and reducing NLRP3 inflammasome activation. Fosfomycin also influences immune cell function by limiting neutrophil migration and activation, suppressing T-cell proliferation, and decreasing B-cell immunoglobulin production. In addition, it promotes tissue regeneration through enhanced collagen deposition, angiogenesis, and improved wound healing in experimental models. These combined effects suggest a dual therapeutic role for fosfomycin, both in controlling infection and modulating inflammatory responses. Despite promising preclinical results, clinical evidence on its immunomodulatory effects remains limited, with most human studies primarily addressing its antibacterial efficacy. This review summarizes current knowledge on fosfomycin's non-antibacterial properties, highlights its therapeutic potential in inflammatory and infectious diseases, and identifies research gaps that warrant further investigation. Overall, fosfomycin emerges as a promising adjunctive agent, particularly in conditions such as sepsis, chronic wounds, and sterile surgical inflammation, where excessive immune activation impairs recovery.</p>\",\"PeriodicalId\":13551,\"journal\":{\"name\":\"Inflammopharmacology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2025-09-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inflammopharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10787-025-01968-8\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inflammopharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10787-025-01968-8","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

磷霉素是一种广谱杀菌抗生素,近年来由于其潜在的抗炎和免疫调节作用而引起了人们的兴趣。临床前研究的新证据表明,磷霉素抑制关键的促炎细胞因子,包括TNF-α、IL-1β和IL-6,同时增强IL-10等抗炎介质。它通过抑制NF-κB和MAPK信号传导和减少NLRP3炎性小体激活来调节细胞内必需通路。磷霉素还通过限制中性粒细胞的迁移和激活、抑制t细胞增殖和减少b细胞免疫球蛋白的产生来影响免疫细胞功能。此外,在实验模型中,它通过增强胶原沉积、血管生成和改善伤口愈合来促进组织再生。这些综合作用表明磷霉素在控制感染和调节炎症反应方面具有双重治疗作用。尽管有很好的临床前结果,但其免疫调节作用的临床证据仍然有限,大多数人体研究主要针对其抗菌功效。本文综述了目前关于磷霉素非抗菌特性的知识,强调了其在炎症和感染性疾病中的治疗潜力,并指出了值得进一步研究的研究空白。总的来说,磷霉素是一种很有前途的辅助剂,特别是在脓毒症、慢性伤口和无菌手术炎症等情况下,过度的免疫激活会损害恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-inflammatory and immunomodulatory properties of fosfomycin: an overlooked potential in a well-known antibiotic.

Fosfomycin, a broad-spectrum bactericidal antibiotic, has recently gained interest for its potential anti-inflammatory and immunomodulatory effects beyond its well-established antimicrobial activity. Emerging evidence from preclinical studies demonstrates that fosfomycin suppresses key pro-inflammatory cytokines, including TNF-α, IL-1β, and IL-6, while enhancing anti-inflammatory mediators such as IL-10. It modulates essential intracellular pathways by inhibiting NF-κB and MAPK signaling and reducing NLRP3 inflammasome activation. Fosfomycin also influences immune cell function by limiting neutrophil migration and activation, suppressing T-cell proliferation, and decreasing B-cell immunoglobulin production. In addition, it promotes tissue regeneration through enhanced collagen deposition, angiogenesis, and improved wound healing in experimental models. These combined effects suggest a dual therapeutic role for fosfomycin, both in controlling infection and modulating inflammatory responses. Despite promising preclinical results, clinical evidence on its immunomodulatory effects remains limited, with most human studies primarily addressing its antibacterial efficacy. This review summarizes current knowledge on fosfomycin's non-antibacterial properties, highlights its therapeutic potential in inflammatory and infectious diseases, and identifies research gaps that warrant further investigation. Overall, fosfomycin emerges as a promising adjunctive agent, particularly in conditions such as sepsis, chronic wounds, and sterile surgical inflammation, where excessive immune activation impairs recovery.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Inflammopharmacology
Inflammopharmacology IMMUNOLOGYTOXICOLOGY-TOXICOLOGY
CiteScore
8.00
自引率
3.40%
发文量
200
期刊介绍: Inflammopharmacology is the official publication of the Gastrointestinal Section of the International Union of Basic and Clinical Pharmacology (IUPHAR) and the Hungarian Experimental and Clinical Pharmacology Society (HECPS). Inflammopharmacology publishes papers on all aspects of inflammation and its pharmacological control emphasizing comparisons of (a) different inflammatory states, and (b) the actions, therapeutic efficacy and safety of drugs employed in the treatment of inflammatory conditions. The comparative aspects of the types of inflammatory conditions include gastrointestinal disease (e.g. ulcerative colitis, Crohn''s disease), parasitic diseases, toxicological manifestations of the effects of drugs and environmental agents, arthritic conditions, and inflammatory effects of injury or aging on skeletal muscle. The journal has seven main interest areas: -Drug-Disease Interactions - Conditional Pharmacology - i.e. where the condition (disease or stress state) influences the therapeutic response and side (adverse) effects from anti-inflammatory drugs. Mechanisms of drug-disease and drug disease interactions and the role of different stress states -Rheumatology - particular emphasis on methods of measurement of clinical response effects of new agents, adverse effects from anti-rheumatic drugs -Gastroenterology - with particular emphasis on animal and human models, mechanisms of mucosal inflammation and ulceration and effects of novel and established anti-ulcer, anti-inflammatory agents, or antiparasitic agents -Neuro-Inflammation and Pain - model systems, pharmacology of new analgesic agents and mechanisms of neuro-inflammation and pain -Novel drugs, natural products and nutraceuticals - and their effects on inflammatory processes, especially where there are indications of novel modes action compared with conventional drugs e.g. NSAIDs -Muscle-immune interactions during inflammation [...]
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信