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healthcare workers: a randomized, placebo-controlled trial. Nutrients. 2019;12(1):E4. https://pubmed.ncbi.nlm.nih.gov/31861349/

4606

Song JM, Lee KH, Seong BL. Antiviral effect of catechins in green tea on influenza virus. Antiviral Res. 2005;68:66–74. https://pubmed.ncbi.nlm.nih.gov/16137775/

4607

Furushima D, Otake Y, Koike N, et al. Investigation of the oral retention of tea catechins in humans: an exploratory interventional study. Nutrients. 2021;13(9):3024. https://pubmed.ncbi.nlm.nih.gov/34578903/

4608

Satomura K, Kitamura T, Kawamura T, et al. Prevention of upper respiratory tract infections by gargling: a randomized trial. Am J Prev Med. 2005;29(4):302–7. https://pubmed.ncbi.nlm.nih.gov/16242593/

4609

Rawangkan A, Kengkla K, Kanchanasurakit S, Duangjai A, Saokaew S. Anti-influenza with green tea catechins: a systematic review and meta-analysis. Molecules. 2021;26(13):4014. https://pubmed.ncbi.nlm.nih.gov/34209247/

4610

Ide K, Yamada H, Kawasaki Y. Effect of gargling with tea and ingredients of tea on the prevention of influenza infection: a meta-analysis. BMC Public Health. 2016;16:396. https://pubmed.ncbi.nlm.nih.gov/27175786/

4611

Goodall EC, Granados AC, Luinstra K, et al. Vitamin D3 and gargling for the prevention of upper respiratory tract infections: a randomized controlled trial. BMC Infect Dis. 2014;14:273. https://pubmed.ncbi.nlm.nih.gov/24885201/

4612

Chow EP, Howden BP, Walker S, et al. Antiseptic mouthwash against pharyngeal Neisseria gonorrhoeae: a randomised controlled trial and an in vitro study. Sex Transm Infect. 2017;93(2):88–93. https://pubmed.ncbi.nlm.nih.gov/27998950/

4613

Maddaford K, Fairley CK, Trumpour S, Chung M, Chow EPF. Sites in the oropharynx reached by different methods of using mouthwash: clinical implication for oropharyngeal gonorrhoea prevention. Sex Transm Infect. 2020;96(5):358–60. https://pubmed.ncbi.nlm.nih.gov/31628249/

4614

Phillips TR, Fairley C, Maddaford K, et al. Duration of gargling and rinsing among frequent mouthwash users: a cross-sectional study. BMJ Open. 2020;10(9):e040754. https://pubmed.ncbi.nlm.nih.gov/32994261/

4615

Kumari M, Kozyrskyj AL. Gut microbial metabolism defines host metabolism: an emerging perspective in obesity and allergic inflammation. Obes Rev. 2017;18(1):18–31. https://pubmed.ncbi.nlm.nih.gov/27862824/

4616

Brown AJ, Goldsworthy SM, Barnes AA, et al. The orphan G protein – coupled receptors GPR41 and GPR43 are activated by propionate and other short chain carboxylic acids. J Biol Chem. 2003;278(13):11312–9. https://pubmed.ncbi.nlm.nih.gov/12496283/

4617

Ang Z, Ding JL. GPR41 and GPR43 in obesity and inflammation – protective or causative? Front Immunol. 2016;7:28. https://pubmed.ncbi.nlm.nih.gov/26870043/

4618

Jiao J, Xu JY, Zhang W, Han S, Qin LQ. Effect of dietary fiber on circulating C-reactive protein in overweight and obese adults: a meta-analysis of randomized controlled trials. Int J Food Sci Nutr. 2015;66(1):114–9. https://pubmed.ncbi.nlm.nih.gov/25578759/

4619

Halnes I, Baines KJ, Berthon BS, MacDonald-Wicks LK, Gibson PG, Wood LG. Soluble fibre meal challenge reduces airway inflammation and expression of GPR43 and GPR41 in asthma. Nutrients. 2017;9(1):57. https://pubmed.ncbi.nlm.nih.gov/28075383/

4620

Van Landingham CB, Keast DR, Longnecker MP. Serum concentration of antibodies to mumps, but not measles, rubella, or varicella, is associated with intake of dietary fiber in the NHANES, 1999–2004. Nutrients. 2021;13(3):813. https://pubmed.ncbi.nlm.nih.gov/33801237/

4621

Hagan T, Cortese M, Rouphael N, et al. Antibiotics-driven gut microbiome perturbation alters immunity to vaccines in humans. Cell. 2019;178(6):1313–28.e13. https://pubmed.ncbi.nlm.nih.gov/31491384/

4622

Yeh TL, Shih PC, Liu SJ, et al. The influence of prebiotic or probiotic supplementation on antibody titers after influenza vaccination: a systematic review and meta-analysis of randomized controlled trials. Drug Des Devel Ther. 2018;12:217–30. https://pubmed.ncbi.nlm.nih.gov/29416317/

4623

Haak BW, Littmann ER, Chaubard JL, et al. Impact of gut colonization with butyrate-producing microbiota on respiratory viral infection following allo-HCT. Blood. 2018;131(26):2978–86. https://pubmed.ncbi.nlm.nih.gov/29674425/

4624

Williams LM, Stoodley IL, Berthon BS, Wood LG. The effects of prebiotics, synbiotics, and short-chain fatty acids on respiratory tract infections and immune function: a systematic review and meta-analysis. Adv Nutr. 2022;13(1):167–92. https://pubmed.ncbi.nlm.nih.gov/34543378/

4625

Hao Q, Dong BR, Wu T. Probiotics for preventing acute upper respiratory tract infections. Cochrane Database Syst Rev. 2015;(2):CD006895. https://pubmed.ncbi.nlm.nih.gov/25927096/

4626

Guillemard E, Tondu F, Lacoin F, Schrezenmeir J. Consumption of a fermented dairy product containing the probiotic Lactobacillus casei DN-114001 reduces the duration of respiratory infections in the elderly in a randomised controlled trial. Br J Nutr. 2010;103(1):58–68. https://pubmed.ncbi.nlm.nih.gov/19747410/

4627

Fujita R, Iimuro S, Shinozaki T, et al. Decreased duration of acute upper respiratory tract infections with daily intake of fermented milk: a multicenter, double-blinded, randomized comparative study in users of day care facilities for the elderly population. Am J Infect Control. 2013;41(12):1231–5. https://pubmed.ncbi.nlm.nih.gov/23890374/

4628

Turchet P, Laurenzano M, Auboiron S, Antoine JM. Effect of fermented milk containing the probiotic Lactobacillus casei DN-114001 on winter infections in free-living elderly subjects: a randomised, controlled pilot study. J Nutr Health Aging. 2003;7(2):75–7. https://pubmed.ncbi.nlm.nih.gov/12679825/

4629

Xu W, Wong G, Hwang YY, Larbi A. The untwining of immunosenescence and aging. Semin Immunopathol. 2020;42(5):559–72. https://pubmed.ncbi.nlm.nih.gov/33165716/

4630

Malter M, Schriever G, Eilber U. Natural killer cells, vitamins, and other blood components of vegetarian and omnivorous men. Nutr Cancer. 1989;12(3):271–8. https://pubmed.ncbi.nlm.nih.gov/2771803/

4631

Franco EL. The sexually transmitted disease model for cervical cancer: incoherent epidemiologic findings and the role of misclassification of human papillomavirus infection. Epidemiology. 1991;2(2):98–106. https://pubmed.ncbi.nlm.nih.gov/1657209/

4632

Skrabanek P. Cervical cancer in nuns and prostitutes: a plea for scientific continence. J Clin Epidemiol. 1988;41(6):577–82. https://pubmed.ncbi.nlm.nih.gov/3290397/

4633

Snijders PJF, Steenbergen RDM, Heideman DAM, Meijer CJLM. HPV-mediated cervical carcinogenesis: concepts and clinical implications. J Pathol. 2006;208(2):152–64. https://pubmed.ncbi.nlm.nih.gov/16362994/

4634

Goldstein MA, Goodman A, del Carmen MG, Wilbur DC. Case 10–2009: a 23-year-old woman with an abnormal Papanicolaou smear. Cabot RC, Harris NL, Shepard JAO, et al., eds. N Engl J Med. 2009;360(13):1337–44. https://pubmed.ncbi.nlm.nih.gov/19321871/