Regenerative antibiotics: Mesenchymal stromal cells and their secretome as a dual-action platform for antimicrobial therapy and tissue repair

A BSTRACT The global antimicrobial resistance crisis demands innovative therapeutics, as pathogens such as methicillin-resistant Staphylococcus aureus and multidrug-resistant Pseudomonas aeruginosa continue to outpace drug development efforts, collectively driving approximately 1.27 million deaths annually. Beyond resistance, conventional antibiotics cause collateral damage to beneficial microbiota, immune effector cells, and tissue-resident progenitor populations, a fundamental limitation that demands a paradigm shift. This review introduces the concept of “regenerative antibiotics,” a therapeutic framework in which mesenchymal stem/stromal cells (MSCs) and their bioactive secretome serve not merely as tissue repair agents, but as active, programmable antimicrobial platforms. We trace this field’s evolution across six historical events from early immunomodulatory characterizations of MSCs (2000–2010) to the landmark discovery of LL-37-mediated bacterial killing in 2010, and through to the current era of regulatory engagement (2024–2026). The molecular mechanisms underlying MSC antimicrobial activity are examined in depth, including direct bactericidal peptide secretion (LL-37, β-defensins, and hepcidin), biofilm disruption, tryptophan deprivation via indoleamine 2,3-dioxygenase (IDO), and senotherapeutic remodeling of the infected tissue microenvironment. Five therapeutic delivery strategies are critically evaluated: antibiotic-MSC combination therapy, MSCs as targeted drug carriers, cell-free extracellular vesicle platforms, biomaterial-integrated delivery systems, and genetically engineered MSCs with amplified secretomes. Evidence from in- vitro , preclinical, and early veterinary studies demonstrates a tripartite action of bacterial clearance, biofilm disruption, and tissue regeneration, which is unachievable by any single antibiotic. Furthermore, the thematic understanding of MSC-based regenerative antibiotics is discussed from a practical neurological infection perspective. This review positions regenerative antibiotics as a compelling, clinically translatable paradigm for the postantibiotic era.

Authors

Publication Details

Journal
Tzu Chi Medical Journal
Published
2026-10-28
DOI
https://doi.org/10.4103/tcmj.tcmj-d-26-00165
Primary Topic
Mesenchymal stem cell research
Type
article
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article

Regenerative antibiotics: Mesenchymal stromal cells and their secretome as a dual-action platform for antimicrobial therapy and tissue repair

Sanjay Gottipamula, N. K. Venkataramana
Tzu Chi Medical Journal
Mesenchymal stem cell research
article

Regenerative antibiotics: Mesenchymal stromal cells and their secretome as a dual-action platform for antimicrobial therapy and tissue repair

Sanjay Gottipamula, N. K. Venkataramana
article en

Abstract

A BSTRACT The global antimicrobial resistance crisis demands innovative therapeutics, as pathogens such as methicillin-resistant Staphylococcus aureus and multidrug-resistant Pseudomonas aeruginosa continue to outpace drug development efforts, collectively driving approximately 1.27 million deaths annually. Beyond resistance, conventional antibiotics cause collateral damage to beneficial microbiota, immune effector cells, and tissue-resident progenitor populations, a fundamental limitation that demands a paradigm shift. This review introduces the concept of “regenerative antibiotics,” a therapeutic framework in which mesenchymal stem/stromal cells (MSCs) and their bioactive secretome serve not merely as tissue repair agents, but as active, programmable antimicrobial platforms. We trace this field’s evolution across six historical events from early immunomodulatory characterizations of MSCs (2000–2010) to the landmark discovery of LL-37-mediated bacterial killing in 2010, and through to the current era of regulatory engagement (2024–2026). The molecular mechanisms underlying MSC antimicrobial activity are examined in depth, including direct bactericidal peptide secretion (LL-37, β-defensins, and hepcidin), biofilm disruption, tryptophan deprivation via indoleamine 2,3-dioxygenase (IDO), and senotherapeutic remodeling of the infected tissue microenvironment. Five therapeutic delivery strategies are critically evaluated: antibiotic-MSC combination therapy, MSCs as targeted drug carriers, cell-free extracellular vesicle platforms, biomaterial-integrated delivery systems, and genetically engineered MSCs with amplified secretomes. Evidence from in- vitro , preclinical, and early veterinary studies demonstrates a tripartite action of bacterial clearance, biofilm disruption, and tissue regeneration, which is unachievable by any single antibiotic. Furthermore, the thematic understanding of MSC-based regenerative antibiotics is discussed from a practical neurological infection perspective. This review positions regenerative antibiotics as a compelling, clinically translatable paradigm for the postantibiotic era.

Tzu Chi Medical Journal
Good health and well-being
Openalex Percentile: Top 12%
Mesenchymal stem cell research
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Regenerative antibiotics: Mesenchymal stromal cells and their secretome as a dual-action platform for antimicrobial therapy and tissue repair — Sanjay Gottipamula, N. K. Venkataramana · Tzu Chi Medical Journal (2026) | TGRS Research Map | TGRS