Cited by 42Gut microbiota and healthSARS-CoV-2 and COVID-19 ResearchNutritional Studies and Diet

The microbiota-mediated dietary and nutritional interventions for COVID-19

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Gasmi, Amin, Tippairote, Torsak, Mujawdiya, Pavan Kumar, Peana, Massimiliano, Menzel, Alain, Dadar, Maryam, Gasmi Benahmed, Asma, Bjørklund, Geir·2021·Clinical Immunology

Abstract

Worldwide, scientists are looking for specific treatment for COVID-19. Apart from the antiviral approach, the interventions to support healthy immune responses to the virus are feasible through diet, nutrition, and lifestyle approaches. This narrative review explores the recent studies on dietary, nutritional, and lifestyle interventions that influence the microbiota-mediated immunomodulatory effects against viral infections. Cumulative studies reported that the airway microbiota and SARS-CoV-2 leverage each other and determine the pathogen-microbiota-host responses. Cigarette smoking can disrupt microbiota abundance. The composition and diversification of intestinal microbiota influence the airway microbiota and the innate and adaptive immunity, which require supports from the balance of macro- and micronutrients from the diet. Colorful vegetables supplied fermentable prebiotics and anti-inflammatory, antioxidant phytonutrients. Fermented foods and beverages support intestinal microbiota. In sensitive individuals, the avoidance of the high immunoreactive food antigens contributes to antiviral immunity. This review suggests associations between airway and intestinal microbiota, antiviral host immunity, and the influences of dietary, nutritional, and lifestyle interventions to prevent the clinical course toward severe COVID-19.

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  • Probiotics and synbiotics can mediate the balance and diversity of the gut microbiota, which plays a significant role in the host's response to many viral infections.

    “Probiotics and synbiotics can mediate the balance and diversity of the gut microbiota, which plays a significant role in the host's response to many viral infections, either by promoting the attachment of viruses to host cells or by supporting antiviral immunity (such as interferons and innate immune activation).”

    From Comparative effectiveness of oral nutritional supplements in preventing respiratory tract infections among adults: a systematic review and network meta-analysis (2025) · cites this paper as [6]

    The Probiotics section says probiotics may mediate intestinal microbiome balance and diversification and augment antiviral immunity. The section on microbiota and SARS-CoV-2 infections says microbiota can affect responses to many viruses through viral attachment or antiviral immunity. The paper does not make the same balance-and-diversity claim for synbiotics; no page numbers are available in our copy. (LLM, conf=0.86)

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  • Supplementing with micronutrients (including vitamins A, C, D, E, zinc, selenium, iron) and plant-based antioxidants (such as flavonoids and polyphenols) can reduce the risk of RTI by activating the immune system, reducing oxidative stress, providing anti-inflammatory effects, and maintaining respiratory tract barrier function.

    “Supplementing with micronutrients (including vitamins A, C, D, E, zinc, selenium, iron, etc.) and plant-based antioxidants (such as flavonoids and polyphenols) can reduce the risk of RTI by activating the immune system, reducing oxidative stress, providing anti-inflammatory effects, and maintaining respiratory tract barrier function.”

    From Comparative effectiveness of oral nutritional supplements in preventing respiratory tract infections among adults: a systematic review and network meta-analysis (2025) · cites this paper as [6]

    The General aspects section says vitamin D, zinc and selenium deficiencies can compromise antiviral responses and that supplementation may benefit people with those deficiencies. It also says antioxidant, anti-inflammatory phytonutrients may support responses to SARS-CoV-2. It does not establish that the full listed set of supplements reduces respiratory tract infection risk, or that maintaining respiratory tract barrier function is a mechanism. Page numbers are unavailable in our copy. (LLM, conf=0.87)

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References 123 · Cited by 42

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  1. [1]Wang L. Wang Y. Ye D. Liu Q. Review of the 2019 novel coronavirus (SARS-CoV-2) based on current evidence Int. J. Antimicrob. Agents 55 2020 105948 10.1016/j.ijantimicag.2020.105948 32201353 PMC7156162 · DOI
  2. [2]Singhal T. A review of coronavirus Disease-2019 (COVID-19) Indian J. Pediatr. 87 2020 281 286 10.1007/s12098-020-03263-6 32166607 PMC7090728 · DOI
  3. [3]Yang Y. Shang W. Rao X. Facing the COVID-19 outbreak: what should we know and what could we do? J. Med. Virol. 92 2020 536 537 10.1002/jmv.25720 32091134 PMC7228352 · DOI
  4. [4]Day M. Covid-19: four fifths of cases are asymptomatic, China figures indicate BMJ 369 2020 m1375 10.1136/bmj.m1375 32241884 · DOI
  5. [6]Wu Z. McGoogan J.M. Characteristics of and important lessons from the coronavirus disease 2019 (COVID-19) outbreak in China: summary of a report of 72 314 cases from the Chinese center for disease control and prevention JAMA 323 2020 1239 1242 10.1001/jama.2020.2648 32091533 · DOI · Paper page
  6. [7]Gasmi A. Noor S. Tippairote T. Dadar M. Menzel A. Bjørklund G. Individual risk management strategy and potential therapeutic options for the COVID-19 pandemic Clin. Immunol. 108409 2020 10.1016/j.clim.2020.108409 PMC7139252 32276137 · DOI
  7. [8]Gasmi A. Peana M. Pivina L. Srinath S. Gasmi Benahmed A. Semenova Y. Menzel A. Dadar M. Bjorklund G. Interrelations between COVID-19 and other disorders Clin. Immunol. 224 2021 108651 10.1016/j.clim.2020.108651 33333255 PMC7833539 · DOI
  8. [9]Tippairote T. Peana M. Chirumbolo S. Bjørklund G. Individual risk management strategy for SARS-CoV2 infection: a step toward personalized healthcare Int. Immunopharmacol. 107629 2021 10.1016/j.intimp.2021.107629 PMC8015431 33862554 · DOI
  9. [10]Gasmi A. Chirumbolo S. Peana M. Noor S. Menzel A. Dadar M. Bjorklund G. The role of diet and supplementation of natural products in COVID-19 prevention Biol. Trace Elem. Res. 2021 10.1007/s12011-021-02623-3 PMC7905195 33630276 · DOI
  10. [11]Dhama K. Sharun K. Tiwari R. Dadar M. Malik Y.S. Singh K.P. Chaicumpa W. COVID-19, an emerging coronavirus infection: advances and prospects in designing and developing vaccines, immunotherapeutics, and therapeutics Hum. Vaccin Immunother. 2020 1 7 10.1080/21645515.2020.1735227 32186952 PMC7103671 · DOI
  11. [12]Wang Y. Hooper L.V. Immune control of the microbiota prevents obesity Science 365 2019 316 317 10.1126/science.aay2057 31346050 · DOI
  12. [13]Levy M. Thaiss C.A. Elinav E. Metabolites: messengers between the microbiota and the immune system Genes Dev. 30 2016 1589 1597 10.1101/gad.284091.116 27474437 PMC4973288 · DOI
  13. [15]Mathieu E. Escribano-Vazquez U. Descamps D. Cherbuy C. Langella P. Riffault S. Remot A. Thomas M. Paradigms of lung microbiota functions in health and disease, particularly, in asthma Front. Physiol. 9 2018 1168 10.3389/fphys.2018.01168 30246806 PMC6110890 · DOI
  14. [17]Gao L. Xu T. Huang G. Jiang S. Gu Y. Chen F. Oral microbiomes: more and more importance in oral cavity and whole body Protein Cell 9 2018 488 500 10.1007/s13238-018-0548-1 29736705 PMC5960472 · DOI · Paper page
  15. [19]Wypych T.P. Wickramasinghe L.C. Marsland B.J. The influence of the microbiome on respiratory health Nat. Immunol. 2019 10.1038/s41590-019-0451-9 31501577 · DOI · Paper page
  16. [20]Domínguez-Díaz C. García-Orozco A. Riera-Leal A. Padilla-Arellano J.R. Fafutis-Morris M. Microbiota and its role on viral evasion: is it with us or against us? Front. Cell. Infect. Microbiol. 9 2019 256 10.3389/fcimb.2019.00256 31380299 PMC6657001 · DOI
  17. [21]Dang A.T. Marsland B.J. Microbes, metabolites, and the gut–lung axis Mucosal Immunol. 12 2019 843 850 10.1038/s41385-019-0160-6 30976087 · DOI · Paper page
  18. [22]Haiminen N. Utro F. Seabolt E. Parida L. Functional profiling of COVID-19 respiratory tract microbiomes Sci. Rep. 11 2021 6433 10.1038/s41598-021-85750-0 33742096 PMC7979704 · DOI
  19. [23]Stavropoulou E. Kantartzi K. Tsigalou C. Konstantinidis T. Voidarou C. Bezirtzoglou E. Unraveling the interconnection patterns across lung microbiome, respiratory diseases, and COVID-19 Front. Cell. Infect. Microbiol. 10 2020 619075 10.3389/fcimb.2020.619075 33585285 PMC7876344 · DOI
  20. [24]Xu R. Lu R. Zhang T. Wu Q. Cai W. Han X. Wan Z. Jin X. Zhang Z. Zhang C. Temporal association between human upper respiratory and gut bacterial microbiomes during the course of COVID-19 in adults Commun. Biol. 4 2021 240 10.1038/s42003-021-01796-w 33603076 PMC7893062 · DOI
  21. [25]Villapol S. Gastrointestinal symptoms associated with COVID-19: impact on the gut microbiome Transl. Res. 226 2020 57 69 10.1016/j.trsl.2020.08.004 32827705 PMC7438210 · DOI
  22. [26]Rinninella E. Cintoni M. Raoul P. Lopetuso L.R. Scaldaferri F. Pulcini G. Miggiano G.A.D. Gasbarrini A. Mele M.C. Food components and dietary habits: keys for a healthy gut microbiota composition Nutrients 11 2019 2393 10.3390/nu11102393 31591348 PMC6835969 · DOI
  23. [27]Dimidi E. Cox S.R. Rossi M. Whelan K. Fermented foods: definitions and characteristics, impact on the gut microbiota and effects on gastrointestinal health and disease Nutrients 11 2019 1806 10.3390/nu11081806 31387262 PMC6723656 · DOI · Paper page
  24. [28]Klingbeil E.A. Serre C.B.D.L. Microbiota modulation by eating patterns, dietary and macronutrient composition; impact on food intake Am. J. Phys. Regul. Integr. Comp. Phys. 315 2018 R1254 R1260 10.1152/ajpregu.00037.2018 30230934 · DOI
  25. [29]Pereira J.D.C. Rea K. Nolan Y.M. O'Leary O.F. Dinan T.G. Cryan J.F. Depression's unholy trinity: dysregulated stress, immunity, and the microbiome Annu. Rev. Psychol. 71 2020 49 78 10.1146/annurev-psych-122216-011613 31567042 · DOI · Paper page
  26. [30]Rea K. Dinan T.G. Cryan John F. The microbiome: a key regulator of stress and neuroinflammation Neurobiol. Stress 2016 1 11 10.1016/j.ynstr.2016.03.001 PMC5146205 27981187 · DOI · Paper page
  27. [31]Mailing L.J. Allen J.M. Buford T.W. Fields C.J. Woods J.A. Exercise and the gut microbiome: a review of the evidence, potential mechanisms, and implications for human health Exerc. Sport Sci. Rev. 47 2019 75 85 10.1249/jes.0000000000000183 30883471 · DOI · Paper page
  28. [32]Perdijk O. Marsland B.J. The microbiome: toward preventing allergies and asthma by nutritional intervention Curr. Opin. Immunol. 60 2019 10 18 10.1016/j.coi.2019.04.001 31078013 · DOI
  29. [33]McCall L.-I. Callewaert C. Zhu Q. Song S.J. Bouslimani A. Minich J.J. Ernst M. Ruiz-Calderon J.F. Cavallin H. Pereira H.S. Novoselac A. Hernandez J. Rios R. Branch O.H. Blaser M.J. Paulino L.C. Dorrestein P.C. Knight R. Dominguez-Bello M.G. Home chemical and microbial transitions across urbanization Nat. Microbiol. 5 2020 108 115 10.1038/s41564-019-0593-4 31686026 PMC7895447 · DOI
  30. [34]Zmora N. Suez J. Elinav E. You are what you eat: diet, health and the gut microbiota Nat. Rev. Gastroenterol. Hepatol. 16 2019 35 56 10.1038/s41575-018-0061-2 30262901 · DOI · Paper page
  31. [35]Buchta V. Vaginal microbiome Ceska Gynekol. 83 2018 371 379 30848142
  32. [36]Lyon J. Even the eye has a microbiome JAMA 318 2017 689 10.1001/jama.2017.10599 28829856 · DOI
  33. [38]Belkaid Y. Timothy W. Hand, role of the microbiota in immunity and inflammation Cell 157 2014 121 141 10.1016/j.cell.2014.03.011 24679531 PMC4056765 · DOI · Paper page
  34. [39]Herwald H. Egesten A. On PAMPs and DAMPs J. Innate Immun. 8 2016 427 428 10.1159/000448437 27522675 PMC6738819 · DOI
  35. [40]Thursby E. Juge N. Introduction to the human gut microbiota Biochem. J. 474 2017 1823 1836 10.1042/BCJ20160510 28512250 PMC5433529 · DOI · Paper page
  36. [42]Kałużna-Czaplińska J. Gątarek P. Chartrand M.S. Dadar M. Bjørklund G. Is there a relationship between intestinal microbiota, dietary compounds, and obesity? Trends Food Sci. Technol. 70 2017 105 113 10.1016/j.tifs.2017.10.010 · DOI
  37. [44]Venegas D.P. Marjorie K. Landskron G. González M.J. Quera R. Dijkstra G. Harmsen H.J. Faber K.N. Hermoso M.A. Short chain fatty acids (SCFAs)-mediated gut epithelial and immune regulation and its relevance for inflammatory bowel diseases Front. Immunol. 10 2019 10.3389/fimmu.2019.00277 PMC6421268 30915065 · DOI · Paper page
  38. [45]Morrison D.J. Preston T. Formation of short chain fatty acids by the gut microbiota and their impact on human metabolism Gut Microbes 7 2016 189 200 10.1080/19490976.2015.1134082 26963409 PMC4939913 · DOI · Paper page
  39. [46]Sencio V. Barthelemy A. Tavares L.P. Machado M.G. Soulard D. Cuinat C. Queiroz-Junior C.M. Noordine M.-L. Salomé-Desnoulez S. Deryuter L. Gut Dysbiosis during influenza contributes to pulmonary pneumococcal superinfection through altered short-chain fatty acid production Cell Rep. 30 2020 2934 2947 e2936 10.1016/j.celrep.2020.02.013 32130898 · DOI
  40. [47]Dickson R.P. Erb-Downward J.R. Martinez F.J. Huffnagle G.B. The microbiome and the respiratory tract Annu. Rev. Physiol. 78 2016 481 504 10.1146/annurev-physiol-021115-105238 26527186 PMC4751994 · DOI · Paper page
  41. [48]Lynch S.V. The lung microbiome and airway disease Ann. Am. Thorac. Soc. 13 2016 S462 S465 10.1513/AnnalsATS.201605-356AW 28005424 PMC5291470 · DOI
  42. [50]Li K.-j. Chen Z.-l. Huang Y. Zhang R. Luan X.-q. Lei T.-t. Chen L. Dysbiosis of lower respiratory tract microbiome are associated with inflammation and microbial function variety Respir. Res. 20 2019 1 16 10.1186/s12931-019-1246-0 31796027 PMC6892239 · DOI
  43. [51]Vardavas C.I. Nikitara K. COVID-19 and smoking: a systematic review of the evidence Tob. Induc. Dis. 18 20 2020 1 4 10.18332/tid/119324 PMC7083240 32206052 · DOI
  44. [53]Marsland B.J. Trompette A. Gollwitzer E.S. The gut-lung Axis in respiratory disease Ann. Am. Thorac. Soc. 12 2015 S150 S156 10.1513/AnnalsATS.201503-133AW 26595731 · DOI
  45. [54]Budden K.F. Gellatly S.L. Wood D.L. Cooper M.A. Morrison M. Hugenholtz P. Hansbro P.M. Emerging pathogenic links between microbiota and the gut-lung axis Nat. Rev. Microbiol. 15 2017 55 63 10.1038/nrmicro.2016.142 27694885 · DOI · Paper page
  46. [55]Ichinohe T. Pang I.K. Kumamoto Y. Peaper D.R. Ho J.H. Murray T.S. Iwasaki A. Microbiota regulates immune defense against respiratory tract influenza A virus infection Proc. Natl. Acad. Sci. U. S. A. 108 2011 5354 5359 10.1073/pnas.1019378108 21402903 PMC3069176 · DOI · Paper page
  47. [57]Gollwitzer E.S. Saglani S. Trompette A. Yadava K. Sherburn R. McCoy K.D. Nicod L.P. Lloyd C.M. Marsland B.J. Lung microbiota promotes tolerance to allergens in neonates via PD-L1 Nat. Med. 20 2014 642 10.1038/nm.3568 24813249 · DOI · Paper page
  48. [58]Zhang D. Li S. Wang N. Tan H.-Y. Zhang Z. Feng Y. The cross-talk between gut microbiota and lungs in common lung diseases Front. Microbiol. 11 2020 301 10.3389/fmicb.2020.00301 32158441 PMC7052046 · DOI
  49. [59]Wilks J. Golovkina T. Influence of microbiota on viral infections PLoS Pathog. 8 2012 10.1371/journal.ppat.1002681 PMC3355081 22615558 · DOI
  50. [60]Monedero V. Collado M.C. Rodríguez-Díaz J. Therapeutic opportunities in intestinal microbiota–virus interactions Trends Biotechnol. 36 2018 645 648 10.1016/j.tibtech.2017.12.009 29395344 · DOI
  51. [61]Garg R.R. Karst S.M. Chapter 5.2 - interactions between enteric viruses and the gut microbiota Svensson L. Desselberger U. Greenberg H.B. Estes M.K. Viral Gastroenteritis 2016 Academic Press Boston 535 544
  52. [62]Vignesh R. Swathirajan C.R. Tun Z.H. Rameshkumar M.R. Solomon S.S. Balakrishnan P. Could perturbation of gut microbiota possibly exacerbate the severity of COVID-19 via cytokine storm? Front. Immunol. 11 2020 607734 10.3389/fimmu.2020.607734 33569053 PMC7868418 · DOI
  53. [63]Venema K. Foreword - the importance of a healthy microbiota in the era of COVID-19 Benefic. Microbes 12 2021 1 3 10.3920/BM2021.x001 33627060 · DOI
  54. [64]Luo J. Liang S. Jin F. Gut microbiota in antiviral strategy from bats to humans: a missing link in COVID-19 Sci. China Life Sci. 2021 10.1007/s11427-020-1847-7 PMC7847806 33521857 · DOI
  55. [65]Littlejohn P. Finlay B.B. When a pandemic and an epidemic collide: COVID-19, gut microbiota, and the double burden of malnutrition BMC Med. 19 2021 31 10.1186/s12916-021-01910-z 33504332 PMC7840385 · DOI
  56. [66]Kim H.S. Do an altered gut microbiota and an associated leaky gut affect COVID-19 severity? mBio 12 2021 10.1128/mBio.03022-20 e03022–03020 PMC7845625 33436436 · DOI
  57. [67]Bradley K.C. Finsterbusch K. Schnepf D. Crotta S. Llorian M. Davidson S. Fuchs S.Y. Staeheli P. Wack A. Microbiota-driven tonic interferon signals in lung stromal cells protect from influenza virus infection Cell Rep. 28 2019 245 256 e244 10.1016/j.celrep.2019.05.105 31269444 · DOI · Paper page
  58. [70]Wu S. Jiang Z.-Y. Sun Y.-F. Yu B. Chen J. Dai C.-Q. Wu X.-L. Tang X.-L. Chen X.-Y. Microbiota regulates the TLR7 signaling pathway against respiratory tract influenza A virus infection Curr. Microbiol. 67 2013 414 422 10.1007/s00284-013-0380-z 23677145 · DOI · Paper page
  59. [71]Trompette A. Gollwitzer E.S. Pattaroni C. Lopez-Mejia I.C. Riva E. Pernot J. Ubags N. Fajas L. Nicod L.P. Marsland B.J. Dietary fiber confers protection against flu by shaping Ly6c− patrolling monocyte hematopoiesis and CD8+ T cell metabolism Immunity 48 2018 992 1005 e1008 10.1016/j.immuni.2018.04.022 29768180 · DOI · Paper page
  60. [72]Moriyama M. Ichinohe T. High ambient temperature dampens adaptive immune responses to influenza A virus infection Proc. Natl. Acad. Sci. U. S. A. 116 2019 3118 3125 10.1073/pnas.1815029116 30718396 PMC6386664 · DOI
  61. [73]Vieira R.D.S. Castoldi A. Basso P.J. Hiyane M.I. Câmara N.O.S. Almeida R.R. Butyrate attenuates lung inflammation by negatively modulating Th9 cells Front. Immunol. 10 2019 67 10.3389/fimmu.2019.00067 30761137 PMC6361737 · DOI
  62. [74]Haak B.W. Littmann E.R. Chaubard J.-L. Pickard A.J. Fontana E. Adhi F. Gyaltshen Y. Ling L. Morjaria S.M. Peled J.U. Impact of gut colonization with butyrate-producing microbiota on respiratory viral infection following allo-HCT Blood 131 2018 2978 2986 10.1182/blood-2018-01-828996 29674425 PMC6024637 · DOI · Paper page
  63. [75]Kim H. Jang M. Kim Y. Choi J. Jeon J. Kim J. Hwang Y.I. Kang J.S. Lee W.J. Red ginseng and vitamin C increase immune cell activity and decrease lung inflammation induced by influenza A virus/H1N1 infection J. Pharm. Pharmacol. 68 2016 406 420 10.1111/jphp.12529 26898166 · DOI
  64. [76]Hemilä H. Vitamin C and SARS coronavirus J. Antimicrob. Chemother. 52 2003 1049 1050 10.1093/jac/dkh002 14613951 PMC7110025 · DOI
  65. [77]Hansdottir S. Monick M.M. Lovan N. Powers L. Gerke A. Hunninghake G.W. Vitamin D decreases respiratory syncytial virus induction of NF-κB–linked chemokines and cytokines in airway epithelium while maintaining the antiviral state J. Immunol. 184 2010 965 974 10.4049/jimmunol.0902840 20008294 PMC3035054 · DOI
  66. [78]Hughes D. Norton R. Vitamin D and respiratory health Clin. Exp. Immunol. 158 2009 20 25 10.1111/j.1365-2249.2009.04001.x 19737226 PMC2759054 · DOI
  67. [80]Read S.A. Obeid S. Ahlenstiel C. Ahlenstiel G. The role of zinc in antiviral immunity Adv. Nutr. 10 2019 696 710 10.1093/advances/nmz013 31305906 PMC6628855 · DOI
  68. [81]Li Y. Lin Z. Guo M. Xia Y. Zhao M. Wang C. Xu T. Chen T. Zhu B. Inhibitory activity of selenium nanoparticles functionalized with oseltamivir on H1N1 influenza virus Int. J. Nanomedicine 12 2017 5733 10.2147/IJN.S140939 28848350 PMC5557909 · DOI
  69. [82]Gasmi A. Tippairote T. Mujawdiya P.K. Peana M. Menzel A. Dadar M. Gasmi Benahmed A. Bjorklund G. Micronutrients as immunomodulatory tools for COVID-19 management Clin. Immunol. 220 2020 108545 10.1016/j.clim.2020.108545 32710937 PMC7833875 · DOI
  70. [83]Cory H. Passarelli S. Szeto J. Tamez M. Mattei J. The role of polyphenols in human health and food systems: a mini-review Front. Nutr. 5 2018 87 10.3389/fnut.2018.00087 30298133 PMC6160559 · DOI · Paper page
  71. [84]Lin S.-C. Ho C.-T. Chuo W.-H. Li S. Wang T.T. Lin C.-C. Effective inhibition of MERS-CoV infection by resveratrol BMC Infect. Dis. 17 2017 144 10.1186/s12879-017-2253-8 28193191 PMC5307780 · DOI
  72. [85]Davani-Davari D. Negahdaripour M. Karimzadeh I. Seifan M. Mohkam M. Masoumi S.J. Berenjian A. Ghasemi Y. Prebiotics: definition, types, sources, mechanisms, and clinical applications Foods 8 2019 92 10.3390/foods8030092 30857316 PMC6463098 · DOI
  73. [86]Visan I. Fiber against flu Nat. Immunol. 19 2018 647 10.1038/s41590-018-0147-6 29925990 · DOI
  74. [87]Luoto R. Ruuskanen O. Waris M. Kalliomäki M. Salminen S. Isolauri E. Prebiotic and probiotic supplementation prevents rhinovirus infections in preterm infants: a randomized, placebo-controlled trial J. Allergy Clin. Immunol. 133 2014 405 413 10.1016/j.jaci.2013.08.020 24131826 PMC7112326 · DOI
  75. [88]Langkamp-Henken B. Bender B.S. Gardner E.M. Herrlinger-garcia K.A. Kelley M.J. Murasko D.M. Schaller J.P. Stechmiller J.K. Thomas D.J. Wood S.M. Nutritional formula enhanced immune function and reduced days of symptoms of upper respiratory tract infection in seniors J. Am. Geriatr. Soc. 52 2004 3 12 10.1093/jac/dkh002 14687308 · DOI
  76. [89]Olaimat A.N. Aolymat I. Al-Holy M. Ayyash M. Abu Ghoush M. Al-Nabulsi A.A. Osaili T. Apostolopoulos V. Liu S.Q. Shah N.P. The potential application of probiotics and prebiotics for the prevention and treatment of COVID-19 NPJ Sci. Food 4 2020 17 10.1038/s41538-020-00078-9 33083549 PMC7536434 · DOI
  77. [90]Zhang H. Yeh C. Jin Z. Ding L. Liu B.Y. Zhang L. Dannelly H.K. Prospective study of probiotic supplementation results in immune stimulation and improvement of upper respiratory infection rate Synth. Syst. Biotechnol. 3 2018 113 120 10.1016/j.synbio.2018.03.001 29900424 PMC5995450 · DOI
  78. [92]Park M.-K. Vu N. Kwon Y.-M. Lee Y.-T. Yoo S. Cho Y.-H. Hong S.-M. Hwang H.S. Ko E.-J. Jung Y.-J. Lactobacillus plantarum DK119 as a probiotic confers protection against influenza virus by modulating innate immunity PLoS One 8 2013 10.1371/journal.pone.0075368 PMC3790790 24124485 · DOI
  79. [93]Rocha-Ramírez L.M. Hernández-Ochoa B. Gómez-Manzo S. Marcial-Quino J. Cárdenas-Rodríguez N. Centeno-Leija S. García-Garibay M. Evaluation of immunomodulatory activities of the heat-killed probiotic strain lactobacillus casei IMAU60214 on macrophages in vitro Microorganisms 8 2020 79 10.3390/microorganisms8010079 31936101 PMC7022880 · DOI
  80. [94]Guillemard E. Tondu F. Lacoin F. Schrezenmeir J. Consumption of a fermented dairy product containing the probiotic lactobacillus casei DN-114 001 reduces the duration of respiratory infections in the elderly in a randomised controlled trial Br. J. Nutr. 103 2010 58 68 10.1017/S0007114509991395 19747410 · DOI
  81. [95]Hu J. Zhang L. Lin W. Tang W. Chan F.K.L. Ng S.C. Review article: probiotics, prebiotics and dietary approaches during COVID-19 pandemic Trends Food Sci. Technol. 108 2021 187 196 10.1016/j.tifs.2020.12.009 33519087 PMC7833886 · DOI
  82. [96]Antunes A.E.C. Vinderola G. Xavier-Santos D. Sivieri K. Potential contribution of beneficial microbes to face the COVID-19 pandemic Food Res. Int. 136 2020 109577 10.1016/j.foodres.2020.109577 32846611 PMC7378002 · DOI
  83. [98]Chan M. Baxter H. Larsen N. Jespersen L. Ekinci E.I. Howell K. Impact of botanical fermented foods on metabolic biomarkers and gut microbiota in adults with metabolic syndrome and type 2 diabetes: a systematic review protocol BMJ Open 9 2019 e029242 10.1136/bmjopen-2019-029242 PMC6678017 31366656 · DOI
  84. [99]Bell V. Ferrão J. Pimentel L. Pintado M. Fernandes T. One health, fermented foods, and gut microbiota Foods (Basel, Switzerland) 7 2018 195 10.3390/foods7120195 30513869 PMC6306734 · DOI · Paper page
  85. [100]Bourrie B.C. Willing B.P. Cotter P.D. The microbiota and health promoting characteristics of the fermented beverage kefir Front. Microbiol. 7 2016 647 10.3389/fmicb.2016.00647 27199969 PMC4854945 · DOI
  86. [101]Walsh A.M. Crispie F. Kilcawley K. O’Sullivan O. O’Sullivan M.G. Claesson M.J. Cotter P.D. Microbial succession and flavor production in the fermented dairy beverage kefir mSystems 1 2016 10.1128/mSystems.00052-16 e00052–00016 PMC5080400 27822552 · DOI
  87. [103]de Andrade G.R. Neves I.V. Marques V.D. Borges M.M. Broring T.A.M. dos Anjos M.T. Astray R.M. de Oliveira M. Influence of a Kefir-derived antimicrobial fraction on Zika virus cytopathic effects and lymphocyte proliferation J. Virol. Curr. Res. 2 2017 555584 10.19080/004JOJIV.2017.02.555584 · DOI
  88. [104]Ghoneum M. Felo N. Agrawal S. Agrawal A. A novel kefir product (PFT) activates dendritic cells to induce CD4+ T and CD8+ T cell responses in vitro Int. J. Immunopathol. Pharmacol. 28 2015 488 496 10.1177/0394632015599447 26384392 · DOI
  89. [105]Caminero A. Meisel M. Jabri B. Verdu E.F. Mechanisms by which gut microorganisms influence food sensitivities Nat. Rev. Gastroenterol. Hepatol. 16 2019 7 18 10.1038/s41575-018-0064-z 30214038 PMC6767923 · DOI
  90. [106]Bouziat R. Hinterleitner R. Brown J.J. Stencel-Baerenwald J.E. Ikizler M. Mayassi T. Meisel M. Kim S.M. Discepolo V. Pruijssers A.J. Ernest J.D. Iskarpatyoti J.A. Costes L.M. Lawrence I. Palanski B.A. Varma M. Zurenski M.A. Khomandiak S. McAllister N. Aravamudhan P. Boehme K.W. Hu F. Samsom J.N. Reinecker H.C. Kupfer S.S. Guandalini S. Semrad C.E. Abadie V. Khosla C. Barreiro L.B. Xavier R.J. Ng A. Dermody T.S. Jabri B. Reovirus infection triggers inflammatory responses to dietary antigens and development of celiac disease Science 356 2017 44 50 10.1126/science.aah5298 28386004 PMC5506690 · DOI
  91. [107]Tye-Din J.A. Galipeau H.J. Agardh D. Celiac disease: a review of current concepts in pathogenesis, prevention, and novel therapies Front. Pediatr. 6 2018 350 10.3389/fped.2018.00350 30519552 PMC6258800 · DOI
  92. [108]Brown J.J. Jabri B. Dermody T.S. A viral trigger for celiac disease PLoS Pathog. 14 2018 e1007181 10.1371/journal.ppat.1007181 PMC6147651 30235320 · DOI
  93. [109]Plot L. Amital H. Infectious associations of celiac disease Autoimmun. Rev. 8 2009 316 319 10.1016/j.autrev.2008.10.001 18973831 · DOI
  94. [110]Stene L.C. Honeyman M.C. Hoffenberg E.J. Haas J.E. Sokol R.J. Emery L. Taki I. Norris J.M. Erlich H.A. Eisenbarth G.S. Rotavirus infection frequency and risk of celiac disease autoimmunity in early childhood: a longitudinal study Am. J. Gastroenterol. 101 2006 2333 2340 10.1111/j.1572-0241.2006.00741.x 17032199 · DOI
  95. [111]Beck M.A. Selenium as an antiviral agent Hatfield D.L. Selenium: Its Molecular Biology and Role in Human Health 2001 Springer US Boston, MA 235 245

Authors
Gasmi, A., Tippairote, T., Mujawdiya, P. K., Peana, M., Menzel, A., Dadar, M., Gasmi Benahmed, A., & Bjørklund, G.
Affiliations
  • Société Francophone de Nutrithérapie et de Nutrigénétique Appliquée (FR)
  • Mahidol University (TH)
  • Birla Institute of Technology and Science, Pilani (IN)
  • University of Sassari (IT)
  • Razi Vaccine and Serum Research Institute (IR)
  • Council for Nutritional and Environmental Medicine (NO)
Corresponding author
Bjørklund, Geir
Venue
Clinical Immunology
Publisher
Elsevier BV
Published
2021-05
Volume
226
Pages
108725
ISSN
1521-6616 (ISSN-L)
OpenAlex
W3155330492
Cited by
42
References
123
Citations by year
2025: 5 · 2024: 5 · 2023: 11 · 2022: 14 · 2021: 7
FWCI
0.97
Type
journal article
Language
en
Open access
Locations
  • Clinical Immunology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • UnissResearch (Università degli Studi di Sassari) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Nutritional Studies and Diet
Keywords
COVID-19 pandemic, SARS-CoV-2, gut microbiota, airway microbiome, dietary intervention, lifestyle intervention, immunomodulation, cigarette smoking, prebiotics, fermented foods, phytochemicals, innate and adaptive immunity, severe COVID-19 prevention
MeSH terms
Gastrointestinal Microbiome, Host Microbial Interactions, COVID-19, SARS-CoV-2, Anti-Inflammatory Agents, Antioxidants, Humans, Immunity, Innate, Life Style, Lung, Probiotics, Prebiotics, Adaptive Immunity

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