The beneficial role of probiotics and gut microbiota in signaling pathways, immunity, apoptosis, autophagy, and intestinal barrier for effective wound healing post-burn injury.

IF 3.3 3区 医学 Q3 IMMUNOLOGY
Microbial pathogenesis Pub Date : 2025-09-01 Epub Date: 2025-06-18 DOI:10.1016/j.micpath.2025.107816
Roya Hajialibabaei, Fatemeh Ghaffarian Sayeli, Esmat Aghadavood, Mohsen Poudineh, Azad Khaledi, Khadijeh Bamneshin
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引用次数: 0

Abstract

Severe burn injuries are associated with complex systemic disturbances, including profound immune dysregulation, compromised intestinal barrier function, and alterations in gut microbiota composition-factors that collectively contribute to impair wound healing and increased mortality. While broad-spectrum antibiotics are routinely employed to combat infection, their use may inadvertently aggravate mucosal barrier dysfunction and facilitate bacterial translocation. Emerging evidence underscores the potential of probiotics in restoring intestinal homeostasis and enhancing immune responses in critically ill populations; however, their application within the context of burn care remains insufficiently studied. This review seeks to address this knowledge gap by evaluating the therapeutic utility of probiotic supplementation in supporting gastrointestinal barrier integrity, attenuating inflammatory responses, and facilitating post-burn recovery. A comprehensive narrative review of relevant literature was performed via PubMed and Google Scholar, targeting studies involving microbiota, probiotics, and burn trauma. Probiotic strains, particularly Lactobacillus and Bifidobacterium, have been shown to modulate cytokine profiles, boost secretory IgA production, enhance epithelial regeneration, and influence key signaling pathways such as PI3K/Akt/mTOR, which are integral to regulating apoptosis and autophagy. Experimental models indicate that probiotics can decrease bacterial translocation and systemic inflammation, reinforce tight junction architecture, and elevate short-chain fatty acid concentrations. Notably, probiotic administration in burn models has resulted in up to a 75 % reduction in infection-related mortality and enhanced anti-inflammatory responses via IL-10 and Th1 pathway activation. Moreover, adjunctive use of probiotics in topical formulations has shown efficacy in promoting wound healing in both diabetic and surgical settings. Collectively, these findings highlight the promise of probiotics as a complementary therapeutic approach in burn management, offering multifaceted benefits in reducing infection, supporting tissue regeneration, and improving clinical outcomes.

益生菌和肠道菌群在信号通路、免疫、细胞凋亡、自噬和肠道屏障中对烧伤后有效伤口愈合的有益作用。
严重烧伤与复杂的全身紊乱有关,包括严重的免疫失调、肠屏障功能受损和肠道微生物群组成的改变——这些因素共同导致伤口愈合受损和死亡率增加。虽然广谱抗生素通常用于对抗感染,但它们的使用可能会无意中加重粘膜屏障功能障碍并促进细菌易位。新出现的证据强调了益生菌在恢复肠道稳态和增强危重患者免疫反应方面的潜力;然而,它们在烧伤护理中的应用仍然没有得到充分的研究。本综述旨在通过评估益生菌补充剂在支持胃肠道屏障完整性、减轻炎症反应和促进烧伤后恢复方面的治疗效用来解决这一知识差距。通过PubMed和谷歌Scholar对相关文献进行了全面的叙述性回顾,针对涉及微生物群,益生菌和烧伤创伤的研究。益生菌菌株,特别是乳杆菌和双歧杆菌,已被证明可以调节细胞因子谱,促进分泌IgA的产生,促进上皮再生,并影响关键的信号通路,如PI3K/Akt/mTOR,这些信号通路是调节细胞凋亡和自噬的组成部分。实验模型表明,益生菌可以减少细菌易位和全身炎症,增强紧密连接结构,提高短链脂肪酸浓度。值得注意的是,在烧伤模型中给予益生菌可使感染相关死亡率降低75%,并通过激活IL-10和Th1途径增强抗炎反应。此外,在局部配方中辅助使用益生菌已显示出促进糖尿病和外科环境伤口愈合的功效。总的来说,这些发现突出了益生菌作为烧伤管理补充治疗方法的前景,在减少感染,支持组织再生和改善临床结果方面提供多方面的益处。
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
Microbial pathogenesis
Microbial pathogenesis 医学-免疫学
CiteScore
7.40
自引率
2.60%
发文量
472
审稿时长
56 days
期刊介绍: Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports. Research Areas Include: -Pathogenesis -Virulence factors -Host susceptibility or resistance -Immune mechanisms -Identification, cloning and sequencing of relevant genes -Genetic studies -Viruses, prokaryotic organisms and protozoa -Microbiota -Systems biology related to infectious diseases -Targets for vaccine design (pre-clinical studies)
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