Bacteriophages as Potential Clinical Immune Modulators
Open accessAbstract
Bacteriophages (phages for short) are bacteria-specific viruses that have been drawing attention when it comes to countering the ever-growing antibiotic bacterial resistance, and are being seen as one of the most promising technologies against multi-antibiotic-resistant bacteria. Although bacteriophages are commonly regarded only as anti-bacterial objects unable to directly interact with eukaryotic cell metabolism, an increasing quantity of evidence has indicated that bacteriophages can directly affect cells bacteria in both in vitro and in vivo applications, influencing the behavior of tissues and immune systems. In sight of this new range of applications, several authors have expressed enthusiasm in phage therapy as direct modulators of eukaryotic cells for clinical usage, highlighting the need for further investigations covering the pharmacology of these new “eukaryotic-viruses”, as even harmful interactions with eukaryotic cells were detected after phage therapy. The present review aims to cover and highlight mechanisms through which bacteriophages may interact with immune cells, analyzing potential clinical applications and obstacles presented in the use of bacteriophages as anti-inflammatory tools.
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Phage DNA and structural proteins engage pattern recognition receptors within innate immune pathways, thereby enhancing antitumor immune responses.
“Additionally, phage DNA and structural proteins engage pattern recognition receptors within innate immune pathways, thereby enhancing antitumor immune responses [21,23–26]”
From Phage therapy in oncology: opportunities for cancer prevention and treatment (2026) · cites this paper as [25]
Sections 6 and 7 describe phage genetic material and proteins affecting Toll-like receptor pathways and immune signals, including IFN-γ induction after phage DNA was introduced to dendritic cells. They do not establish that these interactions enhance antitumor immune responses; the tumor-destruction study appears only in the References. Page numbers are unavailable in our copy. (LLM, conf=0.84)
Experimental — accuracy not yet measuredPhages can enhance antitumor immunity.
“Phages can eliminate cancer-associated bacteria, remodel the tumor microenvironment, enhance antitumor immunity, and deliver targeted therapeutic payloads.”
From Phage therapy in oncology: opportunities for cancer prevention and treatment (2026) · cites this paper as [25]
Phage particles and phage-derived nucleic acids can influence antigen-presenting cell function.
“Once present in tissues or circulation, phage particles and phage-derived nucleic acids can be sensed by innate immune receptors, influence antigen-presenting cell function, and modulate adaptive immune responses [23,25]”
From Phage therapy in oncology: opportunities for cancer prevention and treatment (2026) · cites this paper as [25]
Phage particles and phage-derived nucleic acids can be sensed by innate immune receptors.
“Once present in tissues or circulation, phage particles and phage-derived nucleic acids can be sensed by innate immune receptors, influence antigen-presenting cell function, and modulate adaptive immune responses [23,25]”
From Phage therapy in oncology: opportunities for cancer prevention and treatment (2026) · cites this paper as [25]
Studies have begun uncovering direct and indirect immunomodulatory properties of phages beyond their antimicrobial effects.
“Studies have begun uncovering direct and indirect immunomodulatory properties of phages beyond their antimicrobial effects [21,25,74]”
From Phage therapy in oncology: opportunities for cancer prevention and treatment (2026) · cites this paper as [25]
Phage particles and phage-derived nucleic acids can modulate adaptive immune responses.
“Once present in tissues or circulation, phage particles and phage-derived nucleic acids can be sensed by innate immune receptors, influence antigen-presenting cell function, and modulate adaptive immune responses [23,25]”
From Phage therapy in oncology: opportunities for cancer prevention and treatment (2026) · cites this paper as [25]
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Integrin Beta 3 Regulates Cellular Senescence by Activating the TGF-β Pathway
Rapisarda, V., Borghesan, M., Miguela, V., Encheva, V., Snijders, A. P., Lujambio, A., & O’Loghlen, A. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.02.012 · Cited by 190 · see citing works
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- [1]Golkar Z. Bagasra O. Pace D.G. Bacteriophage therapy: A potential solution for the antibiotic resistance crisis J. Infect. Dev. Ctries. 2014 8 129 136 10.3855/jidc.3573 24518621 · DOI
- [2]Hatfull G.F. Dedrick R.M. Schooley R.T. Phage Therapy for Antibiotic-Resistant Bacterial Infections Annu. Rev. Med. 2022 73 197 211 10.1146/annurev-med-080219-122208 34428079 · DOI
- [3]Furfaro L.L. Payne M.S. Chang B.J. Bacteriophage Therapy: Clinical trials and regulatory hurdles Front. Cell. Infect. Microbiol. 2018 8 376 10.3389/fcimb.2018.00376 30406049 PMC6205996 · DOI
- [4]Abedon S.T. Phage therapy of pulmonary infections Bacteriophage 2015 5 e1020260 10.1080/21597081.2015.1020260 26442188 PMC4422798 · DOI
- [5]Górski A. Kniotek M. Perkowska-Ptasińska A. Mróz A. Przerwa A. Gorczyca W. Dąbrowska K. Weber-Dąbrowska B. Nowaczyk M. Bacteriophages and Transplantation Tolerance Transplant. Proc. 2006 38 331 333 10.1016/j.transproceed.2005.12.073 16504739 · DOI
- [6]Międzybrodzki R. Borysowski J. Kłak M. Jończyk-Matysiak E. Obmińska-Mrukowicz B. Suszko-Pawłowska A. Bubak B. Weber-Dąbrowska B. Górski A. In Vivo Studies on the Influence of Bacteriophage Preparations on the Autoimmune Inflammatory Process BioMed Res. Int. 2017 2017 3612015 10.1155/2017/3612015 29201902 PMC5671675 · DOI
- [7]Kaur S. Harjai K. Chhibber S. Bacteriophage-aided intracellular killing of engulfed methicillin-resistant Staphylococcus aureus (MRSA) by murine macrophages Appl. Microbiol. Biotechnol. 2014 98 4653 4661 10.1007/s00253-014-5643-5 24633444 · DOI
- [8]Jończyk-Matysiak E. Łusiak-Szelachowska M. Kłak M. Bubak B. Międzybrodzki R. Weber-Dąbrowska B. Żaczek M. Fortuna W. Rogóż P. Letkiewicz S. The Effect of Bacteriophage Preparations on Intracellular Killing of Bacteria by Phagocytes J. Immunol. Res. 2015 2015 482863 10.1155/2015/482863 26783541 PMC4689956 · DOI
- [9]Gogokhia L. Buhrke K. Bell R. Hoffman B. Brown D.G. Hanke-Gogokhia C. Ajami N.J. Wong M.C. Ghazaryan A. Valentine J.F. Expansion of Bacteriophages Is Linked to Aggravated Intestinal Inflammation and Colitis Cell Host Microbe 2019 25 285 299 10.1016/j.chom.2019.01.008 30763538 PMC6885004 · DOI
- [10]Gorski A. Dabrowska K. Switala-Jeleń K. Nowaczyk M. Weber-Dabrowska B. Boratynski J. Wietrzyk J. Opolski A. New insights into the possible role of bacteriophages in host defense and disease Med. Immunol. 2003 2 2 10.1186/1476-9433-2-2 12625836 PMC151275 · DOI
- [11]Górski A. Międzybrodzki R. Borysowski J. Dąbrowska K. Wierzbicki P. Ohams M. Korczak-Kowalska G. Olszowska-Zaremba N. Łusiak-Szelachowska M. Kłak M. Phage as a Modulator of Immune Responses Adv. Virus Res. 2012 83 41 71 10.1016/b978-0-12-394438-2.00002-5 22748808 · DOI
- [12]Wahida A. Tang F. Barr J.J. Rethinking phage-bacteria-eukaryotic relationships and their influence on human health Cell Host Microbe 2021 29 681 688 10.1016/j.chom.2021.02.007 33735620 · DOI
- [13]Van Belleghem J.D. Dąbrowska K. Vaneechoutte M. Barr J.J. Bollyky P.L. Interactions between Bacteriophage, Bacteria, and the Mammalian Immune System Viruses 2018 11 10 10.3390/v11010010 30585199 PMC6356784 · DOI · Paper page
- [14]Duerkop B. Hooper L.V. Resident viruses and their interactions with the immune system Nat. Immunol. 2013 14 654 659 10.1038/ni.2614 23778792 PMC3760236 · DOI
- [15]Huh H. Wong S. Jean J.S. Slavcev R. Bacteriophage interactions with mammalian tissue: Therapeutic applications Adv. Drug Deliv. Rev. 2019 145 4 17 10.1016/j.addr.2019.01.003 30659855 · DOI
- [16]Gibb B. Hyman P. Schneider C.L. The Many Applications of Engineered Bacteriophages—An Overview Pharmaceuticals 2021 14 634 10.3390/ph14070634 34208847 PMC8308837 · DOI
- [17]Sunderland K.S. Yang M. Mao C. Phage-Enabled Nanomedicine: From probes to therapeutics in precision medicine Angew. Chem. Int. Ed. 2017 56 1964 1992 10.1002/anie.201606181 PMC5311110 27491926 · DOI
- [18]Farr R. Choi D.S. Lee S.-W. Phage-based nanomaterials for biomedical applications Acta Biomater. 2014 10 1741 1750 10.1016/j.actbio.2013.06.037 23823252 · DOI
- [19]Dąbrowska K. Abedon S.T. Pharmacologically Aware Phage Therapy: Pharmacodynamic and pharmacokinetic obstacles to phage antibacterial action in animal and human bodies Microbiol. Mol. Biol. Rev. 2019 83 e00012-19 10.1128/mmbr.00012-19 31666296 PMC6822990 · DOI
- [20]Dąbrowska K. Phage therapy: What factors shape phage pharmacokinetics and bioavailability? systematic and critical review Med. Res. Rev. 2019 39 2000 2025 10.1002/med.21572 30887551 PMC6767042 · DOI
- [21]Tetz G. Brown S.M. Hao Y. Tetz V. Type 1 Diabetes: An association between autoimmunity, the dynamics of gut amyloid-producing e. coli and their phages Sci. Rep. 2019 9 22 10.1038/s41598-019-46087-x 31273267 PMC6609616 · DOI
- [22]Zimecki M. Artym J. Kocięba M. Weber-Dąbrowska B. Borysowski J. Górski A. Effects of prophylactic administration of bacteriophages to immunosuppressed mice infected with Staphylococcus aureus BMC Microbiol. 2009 9 169 10.1186/1471-2180-9-169 19686585 PMC2741470 · DOI
- [23]Kumar S. Harja K. Chhibber S. Evidence to Support the Therapeutic Potential of Bacteriophage Kpn5 in Burn Wound Infection Caused by Klebsiella pneumoniae in BALB/c Mice J. Microbiol. Biotechnol. 2010 20 935 941 10.4014/jmb.0909.09010 20519918 · DOI
- [24]Hung C.-H. Kuo C.-F. Wang C.-H. Wu C.-M. Tsao N. Experimental Phage Therapy in Treating Klebsiella pneumoniae -Mediated Liver Abscesses and Bacteremia in Mice Antimicrob. Agents Chemother. 2011 55 1358 1365 10.1128/aac.01123-10 21245450 PMC3067190 · DOI
- [25]Secor P.R. Michaels L.A. Smigiel K.S. Rohani M.G. Jennings L.K. Hisert K.B. Arrigoni A. Braun K.R. Birkland T.P. Lai Y. Filamentous Bacteriophage Produced by Pseudomonas aeruginosa Alters the Inflammatory Response and Promotes Noninvasive Infection In Vivo Infect. Immun. 2017 85 e00648-16 10.1128/IAI.00648-16 27795361 PMC5203648 · DOI
- [26]Van Belleghem J.D. Clement F. Merabishvili M. Lavigne R. Vaneechoutte M. Pro- and anti-inflammatory responses of peripheral blood mononuclear cells induced by Staphylococcus aureus and Pseudomonas aeruginosa phages Sci. Rep. 2017 7 22 40 10.1038/s41598-017-08336-9 28808331 PMC5556114 · DOI
- [27]Przerwa A. Zimecki M. Świtała-Jeleń K. Dąbrowska K. Krawczyk E. Łuczak M. Weber-Dąbrowska B. Syper D. Międzybrodzki R. Górski A. Effects of bacteriophages on free radical production and phagocytic functions Med. Microbiol. Immunol. 2006 195 143 150 10.1007/s00430-006-0011-4 16447074 · DOI
- [28]Cafora M. Brix A. Forti F. Loberto N. Aureli M. Briani F. Pistocchi A. Phages as immunomodulators and their promising use as anti-inflammatory agents in a cftr loss-of-function zebrafish model J. Cyst. Fibros. 2021 20 1046 1052 10.1016/j.jcf.2020.11.017 33298374 · DOI
- [29]Spooren A. Kolmus K. Laureys G. Clinckers R. De Keyser J. Haegeman G. Gerlo S. Interleukin-6, a mental cytokine Brain Res. Rev. 2011 67 157 183 10.1016/j.brainresrev.2011.01.002 21238488 · DOI · Paper page
- [30]Tothova L. Celec P. Babickova J. Gajdosova J. Al-Alami H. Kamodyova N. Drahovska H. Liptakova A. Turna J. Hodosy J. Phage therapy of Cronobacter-induced urinary tract infection in mice Med. Sci. Monit. 2011 17 173 178 10.12659/msm.881844 PMC3539570 21709627 · DOI
- [31]Cao F. Wang X. Wang L. Li Z. Che J. Wang L. Li X. Cao Z. Zhang J. Jin L. Evaluation of the Efficacy of a Bacteriophage in the Treatment of Pneumonia Induced by Multidrug Resistance Klebsiella pneumoniae in Mice BioMed Res. Int. 2015 2015 752930 10.1155/2015/752930 25879036 PMC4387947 · DOI
- [32]Sweere J.M. Van Belleghem J.D. Ishak H. Bach M.S. Popescu M. Sunkari V. Kaber G. Manasherob R. Suh G.A. Cao X. Bacteriophage trigger antiviral immunity and prevent clearance of bacterial infection Science 2019 363 6434 10.1126/science.aat9691 PMC6656896 30923196 · DOI
- [33]Popescu M.C. Pennetzdorfer N. Hargil A. Kaber G. Bollyky P.L. Pf Bacteriophage Inhibits Neutrophil Migration in the Lung bioRxiv 2022 10.1101/2022.10.12.511980 · DOI
- [34]Møller-Olsen C. Ross T. Leppard K.N. Foisor V. Smith C. Grammatopoulos D.K. Sagona A.P. Bacteriophage K1F targets Escherichia coli K1 in cerebral endothelial cells and influences the barrier function Sci. Rep. 2020 10 10 10.1038/s41598-020-65867-4 32483257 PMC7264188 · DOI
- [35]Wang Z. Zheng P. Ji W. Fu Q. Wang H. Yan Y. Sun J. SLPW: A virulent bacteriophage targeting methicillin-resistant staphylococcus aureus in vitro and in vivo Front. Microbiol. 2016 7 15 10.3389/fmicb.2016.00934 27379064 PMC4908117 · DOI
- [36]Miernikiewicz P. Kłopot A. Soluch R. Szkuta P. Kęska W. Hodyra-Stefaniak K. Konopka A. Nowak M. Lecion D. Kaźmierczak Z. T4 Phage Tail Adhesin Gp12 Counteracts LPS-Induced Inflammation In Vivo Front. Microbiol. 2016 7 4 10.3389/fmicb.2016.01112 27471503 PMC4943950 · DOI
- [37]Szermer-Olearnik B. Boratyński J. Removal of Endotoxins from Bacteriophage Preparations by Extraction with Organic Solvents PLoS ONE 2015 10 122672 10.1371/journal.pone.0122672 PMC4374689 25811193 · DOI
- [38]Suda T. Hanawa T. Tanaka M. Tanji Y. Miyanaga K. Hasegawa-Ishii S. Shirato K. Kizaki T. Matsuda T. Modification of the immune response by bacteriophages alters methicillin-resistant Staphylococcus aureus infection Sci. Rep. 2022 12 15656 10.1038/s41598-022-19922-x 36123529 PMC9483902 · DOI
- [39]Miedzybrodzki R. Switala-Jelen K. Fortuna W. Weber-Dabrowska B. Przerwa A. Lusiak-Szelachowska M. Dabrowska K. Kurzepa A. Boratynski J. Syper D. Bacteriophage preparation inhibition of reactive oxygen species generation by endotoxin-stimulated polymorphonuclear leukocytes Virus Res. 2008 131 233 242 10.1016/j.virusres.2007.09.013 17996972 · DOI
- [40]Kobayashi S.D. Voyich J.M. DeLeo F.R. Regulation of the neutrophil-mediated inflammatory response to infection Microbes Infect. 2003 5 1337 1344 10.1016/j.micinf.2003.09.013 14613777 · DOI
- [41]Betten Å. Dahlgren C. Mellqvist U.-H. Hermodsson S. Hellstrand K. Oxygen radical-induced natural killer cell dysfunction: Role of myeloperoxidase and regulation by serotonin J. Leukoc. Biol. 2004 75 1111 1115 10.1189/jlb.1103595 15039463 · DOI
- [42]Petrovič D. Effects of Environmental, Genetic, and Epigenetic Factors on Platelet Glycoproteins and the Development of Diabetic Retinopathy Handbook of Nutrition, Diet and the Eye Elsevier Amsterdam, The Netherlands 2014 535 542 10.1016/b978-0-12-401717-7.00054-x · DOI
- [43]Brilha S. Wysoczanski R. Whittington A.M. Friedland J.S. Porter J.C. Monocyte Adhesion, Migration, and Extracellular Matrix Breakdown Are Regulated by Integrin αVβ3 in Mycobacterium tuberculosis Infection J. Immunol. 2017 199 982 991 10.4049/jimmunol.1700128 28646039 PMC5523580 · DOI
- [44]Neto E.H. Coelho A.L.J. Sampaio A.L.F. Henriques M.d.G.M. Marcinkiewicz C. De Freitas M.S. Barja-Fidalgo C. Activation of human T lymphocytes via integrin signaling induced by RGD-disintegrins Biochim. Et Biophys. Acta (BBA)—Mol. Cell Res. 2007 1773 176 184 10.1016/j.bbamcr.2006.09.026 17081636 · DOI
- [45]Pan B. Guo J. Liao Q. Zhao Y. β1 and β3 integrins in breast, prostate and pancreatic cancer: A novel implication (review) Oncol. Lett. 2018 15 5412 5416 10.3892/ol.2018.8076 29556293 PMC5844128 · DOI
- [46]Vonlaufen A. Wiedle G. Borisch B. Birrer S. Luder P. Imhof B. Integrin αvβ3 Expression in Colon Carcinoma Correlates with Survival Mod. Pathol. 2001 14 1126 1132 10.1038/modpathol.3880447 11706074 · DOI
- [48]Huo Y. Schober A. Forlow S.B. Smith D.F. Hyman M.C. Jung S. Littman D.R. Weber C. Ley K. Circulating activated platelets exacerbate atherosclerosis in mice deficient in apolipoprotein E Nat. Med. 2002 9 61 67 10.1038/nm810 12483207 · DOI
- [49]Gros A. Ollivier V. Ho-Tin-Noã B. Platelets in inflammation: Regulation of leukocyte activities and vascular repair Front. Immunol. 2014 5 678 10.3389/fimmu.2014.00678 25610439 PMC4285099 · DOI
- [50]Smyth S.S. Mcever R.P. Weyrich A.S. Morrell C.N. Hoffman M.R. Arepally G.M. French P.A. Dauerman H.L. Becker R.C. Platelet functions beyond hemostasis J. Thromb. Haemost. 2009 7 1759 1766 10.1111/j.1538-7836.2009.03586.x 19691483 · DOI
- [51]Morrell C.N. Immunomodulatory Mediators in Platelet Transfusion Reactions Hematology 2011 2011 470 474 10.1182/asheducation-2011.1.470 22160076 · DOI
- [52]André P. Prasad K.S. Denis C.V. He M. Papalia J.M. Hynes R.O. Phillips D.R. Wagner D.D. CD40L stabilizes arterial thrombi by a β3 integrin–dependent mechanism Nat. Med. 2002 8 247 252 10.1038/nm0302-247 11875495 · DOI
- [53]Karnell J.L. Albulescu M. Drabic S. Wang L. Moate R. Baca M. Oganesyan V. Gunsior M. Thisted T. Yan L. A CD40L-targeting protein reduces autoantibodies and improves disease activity in patients with autoimmunity Sci. Transl. Med. 2019 11 22 10.1126/scitranslmed.aar6584 31019027 · DOI
- [54]Dufour N. Delattre R. Chevallereau A. Ricard J.-D. Debarbieux L. Phage Therapy of Pneumonia Is Not Associated with an Overstimulation of the Inflammatory Response Compared to Antibiotic Treatment in Mice Antimicrob. Agents Chemother. 2019 63 e00379-19 10.1128/AAC.00379-19 31182526 PMC6658787 · DOI
- [55]Fore F. Indriputri C. Mamutse J. Nugraha J. TLR10 and Its Unique Anti-Inflammatory Properties and Potential Use as a Target in Therapeutics Immune Netw. 2020 20 e21 10.4110/in.2020.20.e21 32655969 PMC7327153 · DOI
- [56]Eriksson F. Tsagozis P. Lundberg K. Parsa R. Mangsbo S.M. Persson M.A.A. Harris R.A. Pisa P. Tumor-Specific Bacteriophages Induce Tumor Destruction through Activation of Tumor-Associated Macrophages J. Immunol. 2009 182 3105 3111 10.4049/jimmunol.0800224 19234207 · DOI · Paper page
- [57]Park K. Cha K. Myung H. Observation of inflammatory responses in mice orally fed with bacteriophage T7 J. Appl. Microbiol. 2014 117 627 633 10.1111/jam.12565 24916438 · DOI
- [58]Mirzaei M.K. Haileselassie Y. Navis M. Cooper C. Sverremark-Ekström E. Nilsson A.S. Morphologically Distinct Escherichia coli Bacteriophages Differ in Their Efficacy and Ability to Stimulate Cytokine Release In Vitro Front. Microbiol. 2016 7 437 10.3389/fmicb.2016.00437 27065990 PMC4814447 · DOI
- [59]Shiley J.R. Comfort K.K. Robinson J.B. Immunogenicity and antimicrobial effectiveness of Pseudomonas aeruginosa specific bacteriophage in a human lung in vitro model Appl. Microbiol. Biotechnol. 2017 101 7977 7985 10.1007/s00253-017-8504-1 28914348 · DOI
- [60]Chechushkov A. Kozlova Y. Baykov I. Morozova V. Kravchuk B. Ushakova T. Bardasheva A. Zelentsova E. Al Allaf L. Tikunov A. Influence of Caudovirales Phages on Humoral Immunity in Mice Viruses 2021 13 1241 10.3390/v13071241 34206836 PMC8310086 · DOI
- [61]Łusiak-Szelachowska M. Międzybrodzki R. Fortuna W. Borysowski J. Górski A. Anti-phage serum antibody responses and the outcome of phage therapy Folia Microbiol. 2020 66 127 131 10.1007/s12223-020-00835-z 33126265 PMC7854414 · DOI
- [62]Majewska J. Kaźmierczak Z. Lahutta K. Lecion D. Szymczak A. Miernikiewicz P. Drapała J. Harhala M. Marek-Bukowiec K. Jędruchniewicz N. Induction of Phage-Specific Antibodies by Two Therapeutic Staphylococcal Bacteriophages Administered per os Front. Immunol. 2019 10 45 10.3389/fimmu.2019.02607 31803179 PMC6871536 · DOI
- [63]Hodyra-Stefaniak K. Miernikiewicz P. Drapała J. Drab M. Jończyk-Matysiak E. Lecion D. Kaźmierczak Z. Beta W. Majewska J. Harhala M. Mammalian Host-Versus-Phage immune response determines phage fate in vivo Sci. Rep. 2015 5 14802 10.1038/srep14802 26440922 PMC4594097 · DOI · Paper page
- [64]Dąbrowska K. Miernikiewicz P. Piotrowicz A. Hodyra K. Owczarek B. Lecion D. Kaźmierczak Z. Letarov A. Górski A. Immunogenicity Studies of Proteins Forming the T4 Phage Head Surface J. Virol. 2014 88 12551 12557 10.1128/JVI.02043-14 25142581 PMC4248953 · DOI
- [65]Łusiak-Szelachowska M. Żaczek M. Weber-Dąbrowska B. Międzybrodzki R. Kłak M. Fortuna W. Letkiewicz S. Rogóż P. Szufnarowski K. Jończyk-Matysiak E. Phage Neutralization by Sera of Patients Receiving Phage Therapy Viral Immunol. 2014 27 295 304 10.1089/vim.2013.0128 24893003 PMC4076984 · DOI
- [66]Majewska J. Beta W. Lecion D. Hodyra-Stefaniak K. Kłopot A. Kaźmierczak Z. Miernikiewicz P. Piotrowicz A. Ciekot J. Owczarek B. Oral Application of T4 Phage Induces Weak Antibody Production in the Gut and in the Blood Viruses 2015 7 4783 4799 10.3390/v7082845 26308042 PMC4576206 · DOI
- [67]Łusiak-Szelachowska M. Żaczek M. Weber-Dąbrowska B. Międzybrodzki R. Letkiewicz S. Fortuna W. Rogóż P. Szufnarowski K. Jończyk-Matysiak E. Olchawa E. Antiphage activity of sera during phage therapy in relation to its outcome Future Microbiol. 2017 12 109 117 10.2217/fmb-2016-0156 27643529 · DOI
- [68]Sun Y. Li Y. Wu B. Wang J. Lu X. Qu S. Weng J. Feng B. Biological responses to M13 bacteriophage modified titanium surfaces in vitro Acta Biomater. 2017 58 527 538 10.1016/j.actbio.2017.06.019 28624655 · DOI
- [69]Zhang L. Hou X. Sun L. He T. Wei R. Pang M. Wang R. Staphylococcus aureus Bacteriophage Suppresses LPS-Induced Inflammation in MAC-T Bovine Mammary Epithelial Cells Front. Microbiol. 2018 9 1614 10.3389/fmicb.2018.01614 30083140 PMC6064726 · DOI
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Phage therapy in oncology: opportunities for cancer prevention and treatment
Mutalik, V. K., Inman, J. L., Chang, H., Arkin, A., & Mao, J.-H. (2026) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2026.02.001 · Cited by 5 · see citing works
- Authors
- Souza, E. B. D., Pinto, A. R., & Fongaro, G.
- Affiliations
- Universidade Federal de Santa Catarina (BR)
- Corresponding author
- Souza, Estêvão Brasiliense de
- Fongaro, Gislaine
- Venue
- Microorganisms
- Publisher
- MDPI AG
- Published
- 2023-09-01
- Volume
- 11
- Issue
- 9
- Pages
- 2222
- ISSN
- 2076-2607 (ISSN-L)
- PMC
- PMC10535580
- OpenAlex
- W4386373325
- Cited by
- 42
- References
- 1
- Citations by year
- 2026: 18 · 2025: 17 · 2024: 7
- FWCI
- 1.25
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Microorganisms (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Federal University of Santa Catarina—PROAP/Postgraduate Program in Biotechnology and Biosciences (304463/2021-3)
- CNPq (304463/2021-3)
- Topics
- Physical Sciences › Environmental Science › Ecology › Bacteriophages and microbial interactions
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › Invertebrate Immune Response Mechanisms
- Keywords
- bacteriophages, phage therapy, immunomodulation, anti-inflammatory activity, immune cells, antibiotic resistance
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