Outer membrane vesicles (OMVs) from Gram-negative bacteria are dynamic nanoparticles that shape host–pathogen interactions, acting as both immunostimulatory and immunosuppressive agents critical for microbial pathogenesis and therapeutic innovation.
This scoping review aimed to synthesize recent advancements (2020–2025) in understanding OMVs' roles in immune modulation, pathogenesis, and microbiota-immune crosstalk, as well as their potential as vaccine platforms and drug delivery systems.
Relevant literature was identified through searches in PubMed, Google Scholar, and Web of Science, targeting peer-reviewed studies from 2020 to 2025. Approximately 80 were selected based on their relevance to OMV biogenesis, immune interactions, and applications in infectious diseases and cancer.
OMVs activate proinflammatory pathways via pathogen-associated molecular patterns, contributing to diseases like inflammatory bowel disease and sepsis, while commensal OMVs (e.g., from Bacteroides fragilis) promote tolerogenic immunity and gut homeostasis. Diverse uptake mechanisms enable targeted delivery of virulence or regulatory factors. OMVs enhance microbiota-immune crosstalk, strengthening epithelial barriers and modulating immunity. Therapeutically, bioengineered OMVs show promise in vaccines and personalized medicine, though scalability, heterogeneity, and toxicity pose challenges.
OMVs are versatile tools bridging microbiology and immunology, with significant therapeutic potential. This review's novelty lies in its exclusive focus on Gram-negative OMVs, integrating 2020–2025 advances to address gaps in microbiota-driven immunity and bioengineered therapeutics, guiding future research in vaccine development and clinical translation.
Citation: Mohammad Karimbakhsh, Rouzbeh Sojoudi Masuleh, Mehrnaz Eramian, Hamid Reza Goli, Mehrdad Gholami. Bacterial outer membrane vesicles: A scoping review on their dual roles in immunity and disease (2020–2025)[J]. AIMS Allergy and Immunology, 2026, 10(1): 1-15. doi: 10.3934/Allergy.2026001
Outer membrane vesicles (OMVs) from Gram-negative bacteria are dynamic nanoparticles that shape host–pathogen interactions, acting as both immunostimulatory and immunosuppressive agents critical for microbial pathogenesis and therapeutic innovation.
This scoping review aimed to synthesize recent advancements (2020–2025) in understanding OMVs' roles in immune modulation, pathogenesis, and microbiota-immune crosstalk, as well as their potential as vaccine platforms and drug delivery systems.
Relevant literature was identified through searches in PubMed, Google Scholar, and Web of Science, targeting peer-reviewed studies from 2020 to 2025. Approximately 80 were selected based on their relevance to OMV biogenesis, immune interactions, and applications in infectious diseases and cancer.
OMVs activate proinflammatory pathways via pathogen-associated molecular patterns, contributing to diseases like inflammatory bowel disease and sepsis, while commensal OMVs (e.g., from Bacteroides fragilis) promote tolerogenic immunity and gut homeostasis. Diverse uptake mechanisms enable targeted delivery of virulence or regulatory factors. OMVs enhance microbiota-immune crosstalk, strengthening epithelial barriers and modulating immunity. Therapeutically, bioengineered OMVs show promise in vaccines and personalized medicine, though scalability, heterogeneity, and toxicity pose challenges.
OMVs are versatile tools bridging microbiology and immunology, with significant therapeutic potential. This review's novelty lies in its exclusive focus on Gram-negative OMVs, integrating 2020–2025 advances to address gaps in microbiota-driven immunity and bioengineered therapeutics, guiding future research in vaccine development and clinical translation.
| [1] |
Ho MY, Liu S, Xing B (2024) Bacteria extracellular vesicle as nanopharmaceuticals for versatile biomedical potential. Nano Converg 11: 28. https://doi.org/10.1186/s40580-024-00434-5
|
| [2] |
Juodeikis R, Carding SR (2022) Outer membrane vesicles: Biogenesis, functions, and issues. Microbiol Mol Biol Rev 86: e0003222. https://doi.org/10.1128/mmbr.00032-22
|
| [3] |
Zhao X, Wei Y, Bu Y, et al. (2025) Review on bacterial outer membrane vesicles: Structure, vesicle formation, separation and biotechnological applications. Microb Cell Fact 24: 27. https://doi.org/10.1186/s12934-025-02653-9
|
| [4] |
Chen S, Lei Q, Zou X, et al. (2023) The role and mechanisms of gram-negative bacterial outer membrane vesicles in inflammatory diseases. Front Immunol 14: 1157813. https://doi.org/10.3389/fimmu.2023.1157813
|
| [5] |
Sharif E, Mobasheri T, Mohit E (2025) Bioengineered ClearColi™-derived outer membrane vesicles displaying CT26 neoepitopes as potent vaccine adjuvants against colon carcinoma in a preventive mouse model. Vaccine 53: 127088. https://doi.org/10.1016/j.vaccine.2025.127088
|
| [6] |
Meng R, Zeng M, Ji Y, et al. (2023) The potential role of gut microbiota outer membrane vesicles in colorectal cancer. Front Microbiol 14: 1270158. https://doi.org/10.3389/fmicb.2023.1270158
|
| [7] |
Li M, Zhou H, Yang C, et al. (2020) Bacterial outer membrane vesicles as a platform for biomedical applications: An update. J Control Release 323: 253-268. https://doi.org/10.1016/j.jconrel.2020.04.031
|
| [8] | Huang C, Cao W, Zhou S, et al. (2025) Biogenesis mechanisms, regulatory strategies, and applications of bacterial extracellular vesicles. Crit Rev Biotechnol : 1-17. https://doi.org/10.1080/07388551.2025.2496300 |
| [9] |
Avila-Calderón ED, Ruiz-Palma MDS, Aguilera-Arreola MG, et al. (2021) Outer membrane vesicles of gram-negative bacteria: An outlook on biogenesis. Front Microbiol 12: 557902. https://doi.org/10.3389/fmicb.2021.557902
|
| [10] |
Magaña G, Harvey C, Taggart CC, et al. (2023) Bacterial outer membrane vesicles: Role in pathogenesis and host-cell interactions. Antibiotics (Basel) 13: 32. https://doi.org/10.3390/antibiotics13010032
|
| [11] | Castro-Vargas P, Barloy-Hubler F, Acuña-Amador L (2023) Outer membrane vesicles from commensal and pathogenic anaerobic bacteria: A systematic review of literature reviews. bioRxiv . https://doi.org/10.1101/2023.11.21.568143 |
| [12] |
Zavan L, Fang H, Johnston EL, et al. (2023) The mechanism of Pseudomonas aeruginosa outer membrane vesicle biogenesis determines their protein composition. Proteomics 23: e2200464. https://doi.org/10.1002/pmic.202200464
|
| [13] |
Mandal PK, Ballerin G, Nolan LM, et al. (2021) Bacteriophage infection of Escherichia coli leads to the formation of membrane vesicles via both explosive cell lysis and membrane blebbing. Microbiology (Reading) 167: 001021. https://doi.org/10.1099/mic.0.001021
|
| [14] |
Baeza N, Delgado L, Comas J, et al. (2021) Phage-mediated explosive cell lysis induces the formation of a different type of O-IMV in Shewanella vesiculosa M7(T). Front Microbiol 12: 713669. https://doi.org/10.3389/fmicb.2021.713669
|
| [15] |
Furuyama N, Sircili MP (2021) Outer membrane vesicles (OMVs) produced by gram-negative bacteria: Structure, functions, biogenesis, and vaccine application. Biomed Res Int 2021: 1490732. https://doi.org/10.1155/2021/1490732
|
| [16] | Castro-Vargas P, Barloy-Hubler F, Acuña-Amador L (2024) Unveiling oral anaerobic bacteria outer membrane vesicles: A comprehensive systematic review. Odovtos Int J Dent Sci 26: 41-61. https://doi.org/10.15517/ijds.2024.59287 |
| [17] |
Zingl FG, Thapa HB, Scharf M, et al. (2021) Outer membrane vesicles of Vibrio cholerae protect and deliver active cholera toxin to host cells via porin-dependent uptake. mBio 12: e0053421. https://doi.org/10.1128/mBio.00534-21
|
| [18] |
Khan A, Sardar A, Tarafdar PK, et al. (2023) Heterogeneity and compositional diversities of Campylobacter jejuni outer membrane vesicles (OMVs) drive multiple cellular uptake processes. ACS Infect Dis 9: 2325-2339. https://doi.org/10.1021/acsinfecdis.3c00422
|
| [19] | Taieb F, David L, Pin C, et al. (2025) Outer membrane vesicles from bacteria expressing the HlyF/CprA family of enzymes are more efficient at delivering their cargo into host cells. bioRxiv 27: 2025. https://doi.org/10.1101/2025.03.27.645671 |
| [20] |
Sirisaengtaksin N, O'Donoghue EJ, Jabbari S, et al. (2023) Bacterial outer membrane vesicles provide an alternative pathway for trafficking of Escherichia coli O157 type III secreted effectors to epithelial cells. mSphere 8: e0052023. https://doi.org/10.1128/msphere.00520-23
|
| [21] |
Giordano NP, Cian MB, Dalebroux ZD (2020) Outer membrane lipid secretion and the innate immune response to gram-negative bacteria. Infect Immun 88: e00920. https://doi.org/10.1128/IAI.00920-19
|
| [22] |
George E, Goswami A, Lodhiya T, et al. (2022) Immunomodulatory effect of mycobacterial outer membrane vesicles coated nanoparticles. Biomater Adv 139: 213003. https://doi.org/10.1016/j.bioadv.2022.213003
|
| [23] |
Johnston EL, Heras B, Kufer TA, et al. (2021) Detection of bacterial membrane vesicles by NOD-like receptors. Int J Mol Sci 22. https://doi.org/10.3390/ijms22031005
|
| [24] |
Zhang X, Zhang K, Yan L, et al. (2023) The role of toll-like receptors in immune tolerance induced by Helicobacter pylori infection. Helicobacter 28: e13020. https://doi.org/10.1111/hel.13020
|
| [25] |
Gilmore WJ, Johnston EL, Bitto NJ, et al. (2022) Bacteroides fragilis outer membrane vesicles preferentially activate innate immune receptors compared to their parent bacteria. Front Immunol 13: 970725. https://doi.org/10.3389/fimmu.2022.970725
|
| [26] |
Yang J, Hwang I, Lee E, et al. (2020) Bacterial outer membrane vesicle-mediated cytosolic delivery of flagellin triggers host NLRC4 canonical inflammasome signaling. Front Immunol 11: 581165. https://doi.org/10.3389/fimmu.2020.581165
|
| [27] |
Engevik MA, Danhof HA, Ruan W, et al. (2021) Fusobacterium nucleatum secretes outer membrane vesicles and promotes intestinal inflammation. mBio 12: e02706. https://doi.org/10.1128/mBio.02706-20
|
| [28] |
Sheikh A, Scano C, Xu J, et al. (2024) Abstract C003: Outer membrane vesicles from Bacteroides fragilis contain coding and non-coding small RNA species that modulate inflammatory signaling in intestinal epithelial cells. J Extracell Biol 4: e70086. https://doi.org/10.1002/jex2.70086
|
| [29] |
Wang X, Ye C, Xun T, et al. (2021) Bacteroides Fragilis polysaccharide a ameliorates abnormal voriconazole metabolism accompanied with the inhibition of TLR4/NF-κB pathway. Front Pharmacol 12: 663325. https://doi.org/10.3389/fphar.2021.663325
|
| [30] |
Zhou P, Chen C, Patil S, et al. (2024) Unveiling the therapeutic symphony of probiotics, prebiotics, and postbiotics in gut-immune harmony. Front Nutr 11: 1355542. https://doi.org/10.3389/fnut.2024.1355542
|
| [31] |
Prame Kumar K, Ooi JD, Goldberg R (2023) The interplay between the microbiota, diet and T regulatory cells in the preservation of the gut barrier in inflammatory bowel disease. Front Microbiol 14: 1291724. https://doi.org/10.3389/fmicb.2023.1291724
|
| [32] |
Sun D, Chen P, Xi Y, et al. (2023) From trash to treasure: The role of bacterial extracellular vesicles in gut health and disease. Front Immunol 14: 1274295. https://doi.org/10.3389/fimmu.2023.1274295
|
| [33] |
Domínguez Rubio AP, D'Antoni CL, Piuri M, et al. (2022) Probiotics, their extracellular vesicles and infectious diseases. Front Microbiol 13: 864720. https://doi.org/10.3389/fmicb.2022.864720
|
| [34] | Zhou J, Zou S, Dai D, et al. (2025) Bacterial outer membrane vesicles: From physics to clinical. J Biomater Appl 2: e70013. https://doi.org/10.1002/mba2.70013 |
| [35] |
Charpentier LA, Dolben EF, Hendricks MR, et al. (2023) Bacterial outer membrane vesicles and immune modulation of the host. Membranes (Basel) 13: 752. https://doi.org/10.3390/membranes13090752
|
| [36] |
Abolhasani FS, Vaghefinanekaran N, Yarahmadi A, et al. (2025) Outer membrane vesicles in gram-negative bacteria and its correlation with pathogenesis. Front Immunol 16: 154. https://doi.org/10.3389/fimmu.2025.1541636
|
| [37] |
Liu Q, Shang Y, Shen L, et al. (2024) Outer membrane vesicles from genetically engineered Salmonella enterica serovar Typhimurium presenting Helicobacter pylori antigens UreB and CagA induce protection against Helicobacter pylori infection in mice. Virulence 15: 2367783. https://doi.org/10.1080/21505594.2024.2367783
|
| [38] |
Meng D, Lai Y, Zhang L, et al. (2024) Helicobacter pylori outer membrane vesicles directly promote Aβ aggregation and enhance Aβ toxicity in APP/PS1 mice. Commun Biol 7: 1474. https://doi.org/10.1038/s42003-024-07125-1
|
| [39] | Chen X, Lin Z, Wang N, et al. (2025) Helicobacter pylori-derived outer membrane vesicles: Pathogenic roles, microbiota interactions, and biomedical applications. J Adv Res 30: S2090. https://doi.org/10.1016/j.jare.2025.09.055 |
| [40] |
Song Z, Li B, Zhang Y, et al. (2020) Outer membrane vesicles of Helicobacter pylori 7.13 as adjuvants promote protective efficacy against Helicobacter pylori infection. Front Microbiol 11: 1340. https://doi.org/10.3389/fmicb.2020.01340
|
| [41] |
Yang Y, Wu Y (2025) Potential of bacterial outer membrane vesicles in tumor vaccine: Characteristics, advancements, and future directions. Essays Biochem 69: EBC20253004. https://doi.org/10.1042/EBC20253004
|
| [42] |
Shanmugaraja M, Suvetha R, Ramadevi S (2025) Escherichia coli nissle 1917 efficiently expresses the RBD domain of SARS-CoV-2 spike protein without codon optimization. Sci Rep 15: 15670. https://doi.org/10.1038/s41598-025-99902-z
|
| [43] |
Qin S, Xiao W, Zhou C, et al. (2022) Pseudomonas aeruginosa: Pathogenesis, virulence factors, antibiotic resistance, interaction with host, technology advances and emerging therapeutics. Signal Transduct Target Ther 7: 199. https://doi.org/10.1038/s41392-022-01056-1
|
| [44] |
Liu Q, Li B, Ma J, et al. (2025) Development of a recombinant outer membrane vesicles (OMVs)-based vaccine against Helicobacter pylori infection in mice. J Extracell Vesicles 14: e70085. https://doi.org/10.1002/jev2.70085
|
| [45] |
Nadalian B, Nadalian B, Zali MR, et al. (2024) Outer membrane vesicles derived from adherent-invasive Escherichia coli induce inflammatory response and alter the gene expression of junction-associated proteins in human intestinal epithelial cells. Can J Infect Dis Med Microbiol 2024: 2701675. https://doi.org/10.1155/2024/2701675
|
| [46] |
Guangzhang C, Fangfang F, Siqian D, et al. (2023) Outer membrane vesicles from Escherichia coli are efficiently internalized by macrophage cells and alter their inflammatory response. Microb Pathog 175: 105965. https://doi.org/10.1016/j.micpath.2022.105965
|
| [47] |
Imamiya R, Shinohara A, Yakura D, et al. (2023) Escherichia coli-derived outer membrane vesicles relay inflammatory responses to macrophage-derived exosomes. mBio 14: e0305122. https://doi.org/10.1128/mbio.03051-22
|
| [48] |
Li N, Wu M, Wang L, et al. (2024) Efficient isolation of outer membrane vesicles (OMVs) secreted by gram-negative bacteria via a novel gradient filtration method. Membranes (Basel) 14: 135. https://doi.org/10.3390/membranes14060135
|
| [49] |
Wang X, Lin S, Wang L, et al. (2023) Versatility of bacterial outer membrane vesicles in regulating intestinal homeostasis. Sci Adv 9: eade5079. https://doi.org/10.1126/sciadv.ade5079
|
| [50] |
Adejumo SA, Oli AN, Rowaiye AB, et al. (2023) Immunomodulatory benefits of probiotic bacteria: A review of evidence. OBM Genetics 7: 206. https://doi.org/10.21926/obm.genet.2304206
|
| [51] |
Zheng D, Liwinski T, Elinav E (2020) Interaction between microbiota and immunity in health and disease. Cell Res 30: 492-506. https://doi.org/10.1038/s41422-020-0332-7
|
| [52] |
Chen Y, Cui W, Li X, et al. (2021) Interaction between commensal bacteria, immune response and the intestinal barrier in inflammatory bowel disease. Front Immunol 12: 761981. https://doi.org/10.3389/fimmu.2021.761981
|
| [53] |
Mazziotta C, Tognon M, Martini F, et al. (2023) Probiotics mechanism of action on immune cells and beneficial effects on human health. Cells 12: 184. https://doi.org/10.3390/cells12010184
|
| [54] |
Zitvogel L, Kroemer G (2021) Commensals shape the immune system. Nat Rev Immunol 21: 615. https://doi.org/10.1038/s41577-021-00606-y
|
| [55] | Jari V, Frank RMS (2025) Probiotic membrane vesicles: Emerging tools for disease treatment. Microbiome Res Rep 4: 25. https://doi.org/10.20517/mrr.2025.20 |
| [56] |
Kurata A, Uegaki K (2025) Recent advances in understanding the role of extracellular vesicles from probiotics in intestinal immunity signaling. Biochem Soc Trans 53: 419-429. https://doi.org/10.1042/BST20240150
|
| [57] |
Nie X, Li Q, Ji H, et al. (2025) Bifidobacterium longum NSP001-derived extracellular vesicles ameliorate ulcerative colitis by modulating T cell responses in gut microbiota-(in)dependent manners. NPJ Biofilms Microbiomes 11: 27. https://doi.org/10.1038/s41522-025-00663-4
|
| [58] |
Zhang X, Wang Y, E QY, et al. (2025) The biological activity and potential of probiotics-derived extracellular vesicles as postbiotics in modulating microbiota-host communication. J Nanobiotechnology 23: 349. https://doi.org/10.1186/s12951-025-03435-6
|
| [59] |
Ma D, Zhang Y, Zhang J, et al. (2025) Outer membrane vesicles derived from probiotic Escherichia coli Nissle 1917 promote metabolic remodeling and M1 polarization of RAW264.7 macrophages. Front Immunol 16: 1501174. https://doi.org/10.3389/fimmu.2025.1501174
|
| [60] |
Balhuizen MD, Veldhuizen EJA, Haagsman HP (2021) Outer membrane vesicle induction and isolation for vaccine development. Front Microbiol 12: 629090. https://doi.org/10.3389/fmicb.2021.629090
|
| [61] |
Prior JT, Davitt C, Kurtz J, et al. (2021) Bacterial-derived outer membrane vesicles are potent adjuvants that drive humoral and cellular immune responses. Pharmaceutics 13: 131. https://doi.org/10.3390/pharmaceutics13020131
|
| [62] |
Lu L, Zhai L, Ou Q, et al. (2025) Engineered outer membrane vesicles for antigen delivery: exploratory study on adjuvant activity and systemic reactogenicity. Vaccines (Basel) 13: 552. https://doi.org/10.3390/vaccines13060552
|
| [63] |
Aytar Çelik P, Erdogan-Gover K, Barut D, et al. (2023) Bacterial membrane vesicles as smart drug delivery and carrier systems: A new nanosystems tool for current anticancer and antimicrobial therapy. Pharmaceutics 15: 1052. https://doi.org/10.3390/pharmaceutics15041052
|
| [64] |
Sun C, Qin Y, Zhuang H, et al. (2023) Membrane vesicles as drug delivery systems: Source, preparation, modification, drug loading, In vivo administration and biodistribution, and application in various diseases. Pharmaceutics 15: 1903. https://doi.org/10.3390/pharmaceutics15071903
|
| [65] |
Zhu Z, Antenucci F, Villumsen KR, et al. (2021) Bacterial outer membrane vesicles as a versatile tool in vaccine research and the fight against antimicrobial resistance. mBio 12: e0170721. https://doi.org/10.1128/mBio.01707-21
|
| [66] |
Pschunder B, Locati L, López O, et al. (2024) Outer membrane vesicles derived from Bordetella pertussis are potent adjuvant that drive Th1-biased response. Front Immunol 15: 1387534. https://doi.org/10.3389/fimmu.2024.1387534
|
| [67] |
Galeas-Pena M, Hirsch A, Kuang E, et al. (2024) A novel outer membrane vesicle adjuvant improves vaccine protection against Bordetella pertussis. NPJ Vaccines 9: 190. https://doi.org/10.1038/s41541-024-00990-1
|
| [68] | Harrell JE, Kurtz JR, Bauer DL, et al. (2021) An outer membrane vesicle-adjuvanted oral vaccine protects against lethal, oral Salmonella infection. Pathogens 10. https://doi.org/10.3390/pathogens10050616 |
| [69] |
Zhang H, Liu Z, Li Y, et al. (2024) Adjuvants for Helicobacter pylori vaccines: Outer membrane vesicles provide an alternative strategy. Virulence 15: 2425773. https://doi.org/10.1080/21505594.2024.2425773
|
| [70] |
Zhu W, Waltmann A, Little MB, et al. (2025) Protection against N. gonorrhoeae induced by OMV-based meningococcal vaccines are associated with cross-species directed humoral and cellular immune responses. Front Immunol 16: 1539795. https://doi.org/10.3389/fimmu.2025.1539795
|
| [71] |
Qasim M, Wrage M, Nüse B, et al. (2022) Shigella outer membrane vesicles as promising targets for vaccination. Int J Mol Sci 23: 994. https://doi.org/10.3390/ijms23020994
|
| [72] |
Banerjee S, Halder P, Das S, et al. (2024) Trivalent outer membrane vesicles-based combination vaccine candidate induces protective immunity against Campylobacter and invasive non-typhoidal Salmonella in adult mice. Med Microbiol Immunol 213: 21. https://doi.org/10.1007/s00430-024-00805-z
|
| [73] |
Lu Y, Ma N, Cheng K, et al. (2025) An OMV-based nanovaccine as antigen presentation signal enhancer for cancer immunotherapy. Adv Mater 37: e2413392. https://doi.org/10.1002/adma.202413392
|
| [74] |
Torres-Vanegas JD, Rincon-Tellez N, Guzmán-Sastoque P, et al. (2024) Production and purification of outer membrane vesicles encapsulating green fluorescent protein from Escherichia coli: A step towards scalable OMV technologies. Front Bioeng Biotechnol 12: 1436352. https://doi.org/10.3389/fbioe.2024.1436352
|
| [75] |
Xiang S, Yao Q, Khan A, et al. (2024) Recent advances in bacterial outer membrane vesicles: Effects on the immune system, mechanisms and their usage for tumor treatment. J Pharm Anal 14: 101049. https://doi.org/10.1016/j.jpha.2024.101049
|
| [76] | Pamulaparthyvenkata S, Reddy SG, Singh S (2023) Leveraging technological advancements to optimize healthcare delivery: A comprehensive analysis of value-based care, patient-centered engagement, and personalized medicine strategies. JAASD 3: 371-378. |
| [77] |
Jiang Y, Zhou Z, Liu C, et al. (2023) Bacterial outer membrane vesicles as drug delivery carrier for photodynamic anticancer therapy. Front Chem 11: 1284292. https://doi.org/10.3389/fchem.2023.1284292
|
| [78] |
Cheng K, Zhao R, Li Y, et al. (2021) Bioengineered bacteria-derived outer membrane vesicles as a versatile antigen display platform for tumor vaccination via Plug-and-Display technology. Nat Commun 12: 2041. https://doi.org/10.1038/s41467-021-22308-8
|
| [79] |
Rezaei Adriani R, Mousavi Gargari SL, Bakherad H, et al. (2023) Anti-EGFR bioengineered bacterial outer membrane vesicles as targeted immunotherapy candidate in triple-negative breast tumor murine model. Sci Rep 13: 16403. https://doi.org/10.1038/s41598-023-43762-y
|
| [80] | Moghaddam ZS, Dehghan A, Halimi S, et al. (2025) Bacterial extracellular vesicles: Bridging pathogen biology and therapeutic innovation. Acta Biomater 15: 200. https://doi.org/10.1016/j.actbio.2025.05.028 |