Lactobacillus rhamnosus GG: современные возможности применения в пульмонологии, нефрологии, аллергологии, детской гастроэнтерологической практике
Lactobacillus rhamnosus GG: современные возможности применения в пульмонологии, нефрологии, аллергологии, детской гастроэнтерологической практике
Захарова И.Н., Борзова Е.Ю., Симакова М.А. Lactobacillus rhamnosus GG: современные возможности применения в пульмонологии, нефрологии, аллергологии, детской гастроэнтерологической практике. Педиатрия. Consilium Medicum. 2019; 3: 52–60.
DOI: 10.26442/26586630.2019.3.190601
________________________________________________
Zakharova I.N., Borzova E.Iu., Simakova M.A. Lactobacillus rhamnosus GG: current opportunities of their use in pulmonology, nephrology, allergology and pediatric gastroenterological practice. Pediatrics. Consilium Medicum. 2019; 3: 52–60.
DOI: 10.26442/26586630.2019.3.190601
Lactobacillus rhamnosus GG: современные возможности применения в пульмонологии, нефрологии, аллергологии, детской гастроэнтерологической практике
Захарова И.Н., Борзова Е.Ю., Симакова М.А. Lactobacillus rhamnosus GG: современные возможности применения в пульмонологии, нефрологии, аллергологии, детской гастроэнтерологической практике. Педиатрия. Consilium Medicum. 2019; 3: 52–60.
DOI: 10.26442/26586630.2019.3.190601
________________________________________________
Zakharova I.N., Borzova E.Iu., Simakova M.A. Lactobacillus rhamnosus GG: current opportunities of their use in pulmonology, nephrology, allergology and pediatric gastroenterological practice. Pediatrics. Consilium Medicum. 2019; 3: 52–60.
DOI: 10.26442/26586630.2019.3.190601
Пробиотики исторически рассматривались как лекарственные препараты или пищевые добавки, способные предупреждать либо помогать лечить некоторые заболевания желудочно-кишечного тракта. Однако в исследованиях на моделях животных, дальнейших исследованиях, проведенных у взрослых и детей, установлено положительное иммунологическое, метаболическое влияние определенных штаммов не только при гастроэнтерологической патологии, но и при заболеваниях других органов и систем. В настоящее время проводится большое количество исследований, показывающих негативное влияние нарушений состава микробиома определенных участков нашего организма на риск формирования и течение различных заболеваний. Нормальный микробиом кишечника влияет практически на все аспекты здоровья человека, но степень доказательности научных данных, используемых технологий, а также понимание механизмов действия значительно варьируют в различных исследованиях. Лактобациллы являются представителями здоровой микробиоты человека. Было показано положительное влияние штамма Lactobacillus rhamnosus GG (LGG) на иммунный ответ организма. Наибольший интерес исследователей в последние 40 лет отмечается к изучению этого пробиотического штамма в отношении профилактики и лечения многих заболеваний. В статье собраны данные о применении LGG с целью профилактики респираторных инфекций, инфекций мочевых путей, кариеса, лечения инфекционных и антибиотикоассоциированных диарей, неалкогольной жировой болезни печени, а также предварительные данные исследования LGG в комбинации с Bifidobacterium lactis Bb-12 у детей с впервые выявленным сахарным диабетом 1-го типа.
Ключевые слова: Lactobacillus rhamnosus GG, пробиотики, кишечная микробиота, дети, профилактика, терапия.
________________________________________________
Probiotics was historically considered to be drugs or dietary supplements that can prevent or treat certain gastrointestinal diseases. However, in studies on animal models and subsequent studies in adults and children, the positive immunological and metabolic effects of certain strains were established not only for gastroenterological pathology but also for diseases of other organs and systems. Currently, a large number of studies are being conducted which show a negative effect of alterations in the microbiome composition in certain areas of our body on the risk of occurrence and course of various diseases. Normal intestinal microbiota affects almost all aspects of human health, but the levels of evidence of scientific data, the technologies used, as well as an understanding of mechanisms of action vary significantly in different studies. Lactobacilli are members of a healthy human microbiota. It was shown that Lactobacillus rhamnosus GG (LGG) strain has a positive effect on the body's immune response. To study this probiotic strain for the prevention and treatment of many diseases has been of the greatest interest to researchers in the last 40 years. The article provides data on the use of LGG for the prevention of respiratory infections, urinary tract infections, caries and for the treatment of infectious and antibiotic-associated diarrhea, non-alcoholic fatty liver disease, as well as preliminary data from the study on LGG in combination with Bifidobacterium lactis Bb-12 in children with new-onset type1 diabetes mellitus. Key words: Lactobacillus rhamnosus GG, probiotics, intestinal microbiota, children, prevention, therapy.
Список литературы
1. Capurso L. Thirty Years of Lactobacillus rhamnosus GG: A Review. J Clin Gastroenterol 2019; 53: 1–41. DOI: 10.1097/mcg.0000000000001170
2. Segers ME, Lebeer S. Towards a better understanding of Lactobacillus rhamnosus GG – host interactions. Microbial Cell Factories 2014; 13 (Suppl. 1): 7. DOI: 10.1186/1475-2859-13-s1-s7
3. Lu R, Fasano S, Madayiputhiya N et al. Isolation, Identification, and Characterization of Small Bioactive Peptides From Lactobacillus GG Conditional Media That Exert Both Anti-Gram-negative and Gram-positive Bactericidal Activity. J Pediatr Gastroenterol Nutr 2009; 49 (1): 23–30. DOI: 10.1097/mpg.0b013e3181924d1e
4. Vélez MP, Petrova MI, Lebeer S et al. Characterization of MabA, a modulator of Lactobacillus rhamnosus GG adhesion and biofilm formation. FEMS Immunol Med Microbiol 2010; 59 (3): 386–98. DOI: 10.1111/j.1574-695x.2010.00680.x
5. Landersjo C, Yang Z, Huttunen E, Widmalm G. Structural studies of the exopolysaccharide produced by Lactobacillus rhamnosus strain GG (ATCC 53103). Biomacromolecules 2002; 3: 880–4.
6. Wang Y, Liu L, Moore DJ et al. An LGG-derived protein promotes IgA production through upregulation of APRIL expression in intestinal epithelial cells. Mucosal Immunol 2016; 10 (2): 373–84. DOI: 10.1038/mi.2016.57
7. Claes IJ, Segers ME, Verhoeven TL et al. Lipoteichoic acid is an important microbe-associated molecular pattern of Lactobacillus rhamnosus GG. Microb Cell Fact 2012; 11: 161. DOI: 10.1186/1475-2859-11-161
8. Van Baarlen P, Troost FJ, Van der Meer C et al. Human mucosal in vivo transcriptome responses to three lactobacilli indicate how probiotics may modulate human cellular pathways. PNAS 2011; 108: 4562–9. DOI: 10.1073/pnas.1000079107
9. Bron PA, van Baarlen P, Kleerebezem M. Emerging molecular insights into the interaction between probiotics and the host intestinal mucosa. Nature Rev Microbiol 2011; 10 (1): 66–78. DOI: 10.1038/nrmicro2690
10. Korterink J, Devanarayana NM, Rajindrajith S et al. Childhood functional abdominal pain: mechanisms and management. Nat Rev Gastroenterol Hepatol 2015; 12 (3): 159–71. https: //doi.org/10.1038/nrgastro.2015.21
11. GBD Diarrhoeal Diseases Collaborators. Estimates of global, regional, and national morbidity, mortality, and aetiologies of diarrhoeal diseases: a systematic analysis for the Global Burden of Disease Study. Lancet Infect Dis 2017; 17: 909–48. Erratum in: Lancet Infect Dis 2017; 17: 897.
12. Huang J, Bousvaros A, Lee J et al. Efficacy of probiotic use in acute diarrhea in children, a meta-analysis. Dig Dis Sci 2002; 47 (11): 2625–34.
13. Guarino A, Ashkenazi S, Gendrel D et al. European Society for Pediatric Gastroenterology, Hepatology, and Nutrition/European Society for Pediatric Infectious Diseases evidence-based guidelines for the management of acute gastroenteritis in children in Europe: update 2014. J Pediatr Gastroenterol Nutr 2014; 59: 132–52.
14. Allen SJ, Martinez EG, Gregorio GV, Dans LF. Probiotics for treating acute infectious diarrhoea. Cochrane Database System Rev 2010. Issue 11. Art. No.: CD003048. DOI: 10.1002/14651858.CD003048.pub3
15. Szajewska H, Kołodziej M, Gieruszczak‐Białek D et al. Systematic review with meta‐analysis: Lactobacillus rhamnosus GG for treating acute gastroenteritis in children – a 2019 update. Aliment Pharmacol Ther 2019; 49: 1376–84.
16. Arvola T, Laiho K, Torkkeli S et al. Prophylactic Lactobacillus GG reduces antibiotic-associated diarrhea in children with respiratory infections: a randomized study. Pediatrics 1999; 104: 64.
17. Johnston BC, Supina AL, Vohra S. Probiotics for pediatric antibiotic-associated diarrhea: a meta-analysis of randomized placebo-controlled trials. CMAJ 2006; 175 (4): 377–83.
18. McFarland LV. Meta-analysis of probiotics for the prevention of antibiotic associated diarrhea and the treatment of Clostridium difficile disease. Am J Gastroenterol 2006; 101: 812–22.
19. Johnston BC, Goldenberg JZ, Vandvik PO et al. Probiotics for the prevention of pediatric antibiotic-associated diarrhea. Cochrane Database Syst Rev 2011; 11: CD004827. DOI: 10.1002/14651858.CD004827.pub3
20. Goldenberg JZ, Lytvyn L, Steurich J et al. Probiotics for the prevention of pediatric antibiotic-associated diarrhea. Cochrane Database Syst Rev 2015; 12: CD004827.
21. Szajewska H, Canani RB, Guarino A et al. ESPGHAN Working Group for Probiotics Prebiotics. Probiotics for the Prevention of Antibiotic-Associated Diarrhea in Children. J Pediatr Gastroenterol Nutr 2016; 62 (3): 495–506. DOI: 10.1097/MPG.0000000000001081
22. Guo Q, Goldenberg JZ, Humphrey C et al. Probiotics for the prevention of pediatric antibiotic-associated diarrhea. Cochrane Database Syst Rev 2019; 4: CD004827. DOI: 10.1002/14651858.CD004827.pub5
23. Abarca-Gómez L, Abdeen ZA, Hamid ZA et al. NCD Risk Factor Collaboration (NCD-RisC). Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults. Lancet 2017; 390 (10113): 2627–42. DOI: 10.1016/S0140-6736 (17)32129-3
24. Kumar S, Kelly AS. Review of Childhood Obesity. Mayo Clinic Proceedings 2017; 92 (2): 251–65. DOI: 10.1016/j.mayocp.2016.09.017
25. Machado MV, Cortez-Pinto H. Gut microbiota and nonalcoholic fatty liver disease. Ann Hepatol 2012; 11: 440–9.
26. Frost G, Sleeth ML, Sahuri-Arisoylu M et al. The short-chain fatty acid acetate reduces appetite via a central homeostatic mechanism. Nat Commun 2014; 5: 3611.
27. Zhu L, Baker SS, Gill C et al. Characterization of gut microbiomes in nonalcoholic steatohepatitis (NASH) patients: a connection between endogenous alcohol and NASH. Hepatology 2013; 57: 601–9.
28. Zhang H, DiBaise JK, Zuccolo A et al. Human gut microbiota in obesity and after gastric bypass. P Natl Acad Sci USA 2009; 106: 2365–70.
29. Michail S, Lin M, Frey MR et al. Altered gut microbial energy and metabolism in children with non-alcoholic fatty liver disease. FEMS Microbiol Ecol 2014; 91 (2): 1–9. DOI: 10.1093/femsec/fiu002
30. Vajro P, Mandato C, Licenziati MR et al. Effects of Lactobacillus rhamnosus Strain GG in Pediatric Obesity-related Liver Disease. J Pediatr Gastroenterol Nutr 2011; 52 (6): 740–3. DOI: 10.1097/mpg.0b013e31821f9b85
31. Sharpton SR, Maraj B, Harding-Theobald E et al. Gut microbiome – targeted therapies in nonalcoholic fatty liver disease: a systematic review, meta-analysis, and meta-regression. Am J Clin Nutr 2019; 110 (1): 139–49. DOI: 10.1093/ajcn/nqz042
32. Lloyd-Price J, Abu-Ali G, Huttenhower C. The healthy human microbiome. Genome Med 2016; 8: 51.
33. Man WH, de Steenhuijsen Piters WAA, Bogaert D. The microbiota of the respiratory tract: gatekeeper to respiratory health. Nature Rev Microbiol 2017; 15 (5): 259–70. DOI: 10.1038/nrmicro.2017.14
34. Esposito S, Principi N. Impact of nasopharyngeal microbiota on the development of respiratory tract diseases. Eur J Clin Microbiol Infect Dis 2017; 37 (1): 1–7. DOI: 10.1007/s10096-017-3076-7
35. Hatakka K, Savilahti E, Ponka A et al. Effect of long-term consumption of probiotic milk on infections in children attending day care centres: double blind, randomised trial. BMJ 2001; 322 (7298): 1327.
36. Hojsak I, Snovak N, Abdovic S et al. Lactobacillus GG in the prevention of gastrointestinal and respiratory tract infections in children who attend day care centers: a randomized, double-blind, placebo-controlled trial. Clin Nutr 2010; 29 (3): 312–6.
37. Rautava S, Salminen S, Isolauri E. Specific probiotics in reducing the risk of acute infections in infancy – a randomised, double-blind, placebo-controlled study. Br J Nutr 2009; 101 (11): 1722–6.
38. Liu S, Hu P, Du X et al. Lactobacillus rhamnosus GG supplementation for preventing respiratory infections in children: a meta-analysis of randomized, placebo-controlled trials. Indian Pediatr 2013; 50: 377–81.
39. Hao Q, Dong BR, Wu T. Probiotics for preventing acute upper respiratory tract infections. Cochrane Database Syst Rev 2015; 2: CD006895.
40. Laursen RP, Hojsak I. Probiotics for respiratory tract infections in children attending day care centers – a systematic review. Eur J Pediatr 2018; 177 (7): 979–94. DOI: 10.1007/s00431-018-3167-1
41. Kumpu M, Kekkonen RA, Kautiainen H et al. Milk containing probiotic Lactobacillus rhamnosus GG and respiratory illness in children: a randomized, double-blind, placebo-controlled trial. Eur J Clin Nutr 2012; 66: 1020–3. DOI: doi.org/10.1038/ejcn. 2012.62
42. Scott AM, Clark J, Julien B et al. Probiotics for preventing acute otitis media in children. Cochrane Database Syst Rev 2019; Issue 6. Art. No.: CD012941. DOI: 10.1002/14651858.CD012941.pub2
43. Van den Broek MFL, De Boeck I, Claes IJJ et al. Multifactorial inhibition of lactobacilli against the respiratory tract pathogen Moraxella catarrhalis. Benef Microb 2018; 9 (3): 429–39. DOI: 10.3920/bm2017.0101
44. Schwenger EM, Tejani AM, Loewen PS. Probiotics for preventing urinary tract infections in adults and children. Cochrane Database System Rev 2015; Issue 12. Art. No.: CD008772. DOI: 10.1002/14651858.cd008772.pub2
45. Kara SS, Volkan B, Erten I. Lactobacillus rhamnosus GG can protect malnourished children. Benef Microb 2019; 10 (3): 237–44. DOI: 10.3920/BM2018.0071
46. http: //raaci.ru/education/clinic_recomendations/97.html
47. Williams HC. Clinical practice. Atopic dermatitis. N Engl J Med 2005; 352: 2314–24.
48. Mastrorilli C, Caffarelli C, Hoffmann-Sommergruber K. Food allergy and atopic dermatitis: Prediction, progression, and prevention. Pediatr Allergy Immunol 2017; 28 (8): 831–40. DOI: 10.1111/pai.12831
49. Zhao W, Ho H, Bunyavanich S. The Gut Microbiome in Food Allergy. Ann Allergy, Asthma Immunol 2018; 122 (3): 276–82. DOI: 10.1016/j.anai.2018.12.012
50. Pascal M, Perez-Gordo M, Caballero T et al. Microb Allergic Dis Front Immunol 2018; 9: 1584. DOI: 10.3389/fimmu.2018.01584
51. Cosenza L, Nocerino R, Di Scala C et al. Bugs for atopy: the Lactobacillus rhamnosus GG strategy for food allergy prevention and treatment in children. Benef Microb 2015; 6 (2): 225–32. DOI: 10.3920/bm2014.0158
52. Isolauri E. Studies on Lactobacillus GG in food hypersensitivity disorders. Nutr Today (Suppl.) 1996; 31: 285–315.
53. Kalliomaki M, Salminen S, Arvilommi H et al. Probiotics in primary prevention of atopic disease: a randomised placebo-controlled trial. Lancet 2001; 357: 1076–9. DOI: 10.1016/S0140-6736 (00)04259-8
54. Kalliomaki M, Salminen S, Poussa T et al. Probiotics and prevention of atopic disease: 4-year follow-up of a randomised placebo-controlled trial. Lancet 2003; 361: 1869–71. DOI: 10.1016/S0140-6736 (03)13490-3
55. Kalliomaki M, Salminen S, Poussa T, Isolauri E. Probiotics during the first 7 years of life: a cumulative risk reduction of eczema in a randomized, placebo- controlled trial. J Allergy Clin Immunol 2007; 119: 1019–21. DOI: 10.1016/j. jaci.2006.12.608
56. Rautava S, Kalliomaki M, Isolauri E. Probiotics during pregnancy and breast-feeding might confer immnomodulatory protection against atopic disease in the infant. J Allergy Clin Immunol 2002; 109 (1): 119–21.
57. Kalliomäki M, Antoine JM, Herz U et al. Guidance for Substantiating the Evidence for Beneficial Effects of Probiotics: Prevention and Management of Allergic Diseases by Probiotics. J Nutr 2010; 140 (3): 713S–721S. DOI: 10.3945/jn.109.113761
58. Fiocchi A, Pawankar R, Cuello-Garcia C et al. World allergy organization-McMaster university guidelines for allergic disease prevention (GLAD-P): Probiotics. World Allergy Organ J 2015; 8 (1): 4.
59. Szajewska H, Horvath A. Lactobacillus rhamnosus GG in the Primary Prevention of Eczema in Children: A Systematic Review and Meta-Analysis. Nutrients 2018; 10 (9): 1319. DOI: 10.3390/nu10091319
60. Berni Canani R, Di Costanzo M, Pezzella V et al. The potential therapeutic efficacy of Lactobacillus GG in children with food allergies. Pharmaceuticals 2012; 5: 655–64.
61. Murch SH. Toll of allergy reduced by probiotics. Lancet 2001; 357: 1057–9.
62. Majamaa H, Isolauri E. Probiotics: a novel approach in the management of food allergy. J Allergy Clin Immunol 1997; 99 (2): 179–85.
63. Isolauri E, Arvola T, Sutas Y et al. Probiotics in the management of atopic eczema. Clin Exp Allergy 2000; 30 (11): 1604–10.
64. Rosenfeldt V, Benfeldt E, Nielsen SD et al. Effect of probiotic Lactobacillus strains in children with atopic dermatitis. J Allergy Clin Immunol 2003; 111 (2): 389–95. DOI: 10.1067/mai.2003.389
65. Kirjavainen PV, Salminen SJ, Isolauri E. Probiotic Bacteria in the Management of Atopic Disease: Underscoring the Importance of Viability. J Pediatr Gastroenterol Nutr 2003; 36 (2): 223–7. DOI: 10.1097/00005176-200302000-00012
66. Viljanen M, Savilahti E, Haahtela T et al. Probiotics in the treatment of atopic eczema/ dermatitis syndrome in infants: a double-blind placebo-controlled trial. Allergy 2005; 60: 494–500. DOI: 10.1111/j.1398-9995.2004.00514.x
67. Brouwer ML, Wolt-Plompen SAA, Dubois AEJ et al. No effects of probiotics on atopic dermatitis in infancy: a randomized placebo-controlled trial. Clin Exper Allergy 2006; 36 (7): 899–906. DOI: 10.1111/j.1365-2222.2006.02513.x
68. Fölster-Holst R, Müller F, Schnopp N et al. Prospective, randomized controlled trial on Lactobacillus rhamnosus in infants with moderate to severe atopic dermatitis. Br J Dermatol 2006; 155 (6): 1256–61. DOI: 10.1111/j.1365-2133.2006.07558.x
69. Grüber C, Wendt M, Sulser C et al. Randomized, placebo-controlled trial of Lactobacillus rhamnosus GG as treatment of atopic dermatitis in infancy. Allergy 2007; 62 (11): 1270–6. DOI: 10.1111/j.1398-9995.2007.01543.x
70. Baldassarre ME, Laforgia N, Fanelli M et al. Lactobacillus GG improve recovery in infants with blood in the stools and presumptive allergic colitis compared with extensively hydrolyzed formula alone. J Pediatr 2010; 156: 397–401.
71. Berni Canani R, Di Costanzo M, Bedogni G et al. Extensively hydrolyzed casein formula containing Lactobacillus rhamnosus GG reduces the occurrence of other allergic manifestations in children with cow’s milk allergy: 3-year randomized controlled trial. J Allergy Clin Immunol 2017; 139 (6): 1906–13. DOI: 10.1016/j.jaci.2016.10.050
72. Qamer S, Deshmukh M, Patole S. Probiotics for cow’s milk protein allergy: a systematic review of randomized controlled trials. Eur J Pediatr 2019; 178 (8): 1139–49. DOI: 10.1007/s00431-019-03397-6
73. Nase L, Hatakka K, Savilahti E et al. Effect of long-term consumption of a probiotic bacterium, Lactobacillus rhamnosus GG, in milk on dental caries and caries risk in children. Caries Res 2001; 35 (6): 412–20.
74. Schwendicke F, Dörfer C, Kneist S et al. Cariogenic Effects of Probiotic Lactobacillus rhamnosus GG in a Dental Biofilm Model. Caries Res 2014; 48 (3): 186–92. DOI: 10.1159/000355907
75. Gungor OE, Kirzioglu Z, Kivanc M. Probiotics: can they be used to improve oral health? Benef Microb 2015; 6 (5): 647–56. DOI: 10.3920/bm2014.0167
76. Knip M, Siljander H. The role of the intestinal microbiota in type 1 diabetes mellitus. Nat Rev Endocrinol 2016; 12: 154–67. DOI: 10.1038/nrendo.2015.218
77. Vatanen T, Franzosa EA, Schwager R et al. The human gut microbiome in early-onset type 1 diabetes from the TEDDY study. Nature 2018; 562 (7728): 589–94. DOI: 10.1038/s41586-018-0620-2
78. Groele L, Szajewska H, Szypowska A. Effects of Lactobacillus rhamnosus GG and Bifidobacterium lactis Bb12 on beta-cell function in children with newly diagnosed type 1 diabetes: protocol of a randomised controlled trial. BMJ Open 2017; 7 (10): e017178. DOI: 10.1136/bmjopen-2017-017178
79. Abstracts for the 44th Annual Meeting of the International Society for Pediatric and Adolescent Diabetes (ISPAD), 11–14 October 2018, Hyderabad, India, Vol. 19, Issue S26: 33. doi.org/10.1111/pedi.12745
________________________________________________
1. Capurso L. Thirty Years of Lactobacillus rhamnosus GG: A Review. J Clin Gastroenterol 2019; 53: 1–41. DOI: 10.1097/mcg.0000000000001170
2. Segers ME, Lebeer S. Towards a better understanding of Lactobacillus rhamnosus GG – host interactions. Microbial Cell Factories 2014; 13 (Suppl. 1): 7. DOI: 10.1186/1475-2859-13-s1-s7
3. Lu R, Fasano S, Madayiputhiya N et al. Isolation, Identification, and Characterization of Small Bioactive Peptides From Lactobacillus GG Conditional Media That Exert Both Anti-Gram-negative and Gram-positive Bactericidal Activity. J Pediatr Gastroenterol Nutr 2009; 49 (1): 23–30. DOI: 10.1097/mpg.0b013e3181924d1e
4. Vélez MP, Petrova MI, Lebeer S et al. Characterization of MabA, a modulator of Lactobacillus rhamnosus GG adhesion and biofilm formation. FEMS Immunol Med Microbiol 2010; 59 (3): 386–98. DOI: 10.1111/j.1574-695x.2010.00680.x
5. Landersjo C, Yang Z, Huttunen E, Widmalm G. Structural studies of the exopolysaccharide produced by Lactobacillus rhamnosus strain GG (ATCC 53103). Biomacromolecules 2002; 3: 880–4.
6. Wang Y, Liu L, Moore DJ et al. An LGG-derived protein promotes IgA production through upregulation of APRIL expression in intestinal epithelial cells. Mucosal Immunol 2016; 10 (2): 373–84. DOI: 10.1038/mi.2016.57
7. Claes IJ, Segers ME, Verhoeven TL et al. Lipoteichoic acid is an important microbe-associated molecular pattern of Lactobacillus rhamnosus GG. Microb Cell Fact 2012; 11: 161. DOI: 10.1186/1475-2859-11-161
8. Van Baarlen P, Troost FJ, Van der Meer C et al. Human mucosal in vivo transcriptome responses to three lactobacilli indicate how probiotics may modulate human cellular pathways. PNAS 2011; 108: 4562–9. DOI: 10.1073/pnas.1000079107
9. Bron PA, van Baarlen P, Kleerebezem M. Emerging molecular insights into the interaction between probiotics and the host intestinal mucosa. Nature Rev Microbiol 2011; 10 (1): 66–78. DOI: 10.1038/nrmicro2690
10. Korterink J, Devanarayana NM, Rajindrajith S et al. Childhood functional abdominal pain: mechanisms and management. Nat Rev Gastroenterol Hepatol 2015; 12 (3): 159–71. https: //doi.org/10.1038/nrgastro.2015.21
11. GBD Diarrhoeal Diseases Collaborators. Estimates of global, regional, and national morbidity, mortality, and aetiologies of diarrhoeal diseases: a systematic analysis for the Global Burden of Disease Study. Lancet Infect Dis 2017; 17: 909–48. Erratum in: Lancet Infect Dis 2017; 17: 897.
12. Huang J, Bousvaros A, Lee J et al. Efficacy of probiotic use in acute diarrhea in children, a meta-analysis. Dig Dis Sci 2002; 47 (11): 2625–34.
13. Guarino A, Ashkenazi S, Gendrel D et al. European Society for Pediatric Gastroenterology, Hepatology, and Nutrition/European Society for Pediatric Infectious Diseases evidence-based guidelines for the management of acute gastroenteritis in children in Europe: update 2014. J Pediatr Gastroenterol Nutr 2014; 59: 132–52.
14. Allen SJ, Martinez EG, Gregorio GV, Dans LF. Probiotics for treating acute infectious diarrhoea. Cochrane Database System Rev 2010. Issue 11. Art. No.: CD003048. DOI: 10.1002/14651858.CD003048.pub3
15. Szajewska H, Kołodziej M, Gieruszczak‐Białek D et al. Systematic review with meta‐analysis: Lactobacillus rhamnosus GG for treating acute gastroenteritis in children – a 2019 update. Aliment Pharmacol Ther 2019; 49: 1376–84.
16. Arvola T, Laiho K, Torkkeli S et al. Prophylactic Lactobacillus GG reduces antibiotic-associated diarrhea in children with respiratory infections: a randomized study. Pediatrics 1999; 104: 64.
17. Johnston BC, Supina AL, Vohra S. Probiotics for pediatric antibiotic-associated diarrhea: a meta-analysis of randomized placebo-controlled trials. CMAJ 2006; 175 (4): 377–83.
18. McFarland LV. Meta-analysis of probiotics for the prevention of antibiotic associated diarrhea and the treatment of Clostridium difficile disease. Am J Gastroenterol 2006; 101: 812–22.
19. Johnston BC, Goldenberg JZ, Vandvik PO et al. Probiotics for the prevention of pediatric antibiotic-associated diarrhea. Cochrane Database Syst Rev 2011; 11: CD004827. DOI: 10.1002/14651858.CD004827.pub3
20. Goldenberg JZ, Lytvyn L, Steurich J et al. Probiotics for the prevention of pediatric antibiotic-associated diarrhea. Cochrane Database Syst Rev 2015; 12: CD004827.
21. Szajewska H, Canani RB, Guarino A et al. ESPGHAN Working Group for Probiotics Prebiotics. Probiotics for the Prevention of Antibiotic-Associated Diarrhea in Children. J Pediatr Gastroenterol Nutr 2016; 62 (3): 495–506. DOI: 10.1097/MPG.0000000000001081
22. Guo Q, Goldenberg JZ, Humphrey C et al. Probiotics for the prevention of pediatric antibiotic-associated diarrhea. Cochrane Database Syst Rev 2019; 4: CD004827. DOI: 10.1002/14651858.CD004827.pub5
23. Abarca-Gómez L, Abdeen ZA, Hamid ZA et al. NCD Risk Factor Collaboration (NCD-RisC). Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults. Lancet 2017; 390 (10113): 2627–42. DOI: 10.1016/S0140-6736 (17)32129-3
24. Kumar S, Kelly AS. Review of Childhood Obesity. Mayo Clinic Proceedings 2017; 92 (2): 251–65. DOI: 10.1016/j.mayocp.2016.09.017
25. Machado MV, Cortez-Pinto H. Gut microbiota and nonalcoholic fatty liver disease. Ann Hepatol 2012; 11: 440–9.
26. Frost G, Sleeth ML, Sahuri-Arisoylu M et al. The short-chain fatty acid acetate reduces appetite via a central homeostatic mechanism. Nat Commun 2014; 5: 3611.
27. Zhu L, Baker SS, Gill C et al. Characterization of gut microbiomes in nonalcoholic steatohepatitis (NASH) patients: a connection between endogenous alcohol and NASH. Hepatology 2013; 57: 601–9.
28. Zhang H, DiBaise JK, Zuccolo A et al. Human gut microbiota in obesity and after gastric bypass. P Natl Acad Sci USA 2009; 106: 2365–70.
29. Michail S, Lin M, Frey MR et al. Altered gut microbial energy and metabolism in children with non-alcoholic fatty liver disease. FEMS Microbiol Ecol 2014; 91 (2): 1–9. DOI: 10.1093/femsec/fiu002
30. Vajro P, Mandato C, Licenziati MR et al. Effects of Lactobacillus rhamnosus Strain GG in Pediatric Obesity-related Liver Disease. J Pediatr Gastroenterol Nutr 2011; 52 (6): 740–3. DOI: 10.1097/mpg.0b013e31821f9b85
31. Sharpton SR, Maraj B, Harding-Theobald E et al. Gut microbiome – targeted therapies in nonalcoholic fatty liver disease: a systematic review, meta-analysis, and meta-regression. Am J Clin Nutr 2019; 110 (1): 139–49. DOI: 10.1093/ajcn/nqz042
32. Lloyd-Price J, Abu-Ali G, Huttenhower C. The healthy human microbiome. Genome Med 2016; 8: 51.
33. Man WH, de Steenhuijsen Piters WAA, Bogaert D. The microbiota of the respiratory tract: gatekeeper to respiratory health. Nature Rev Microbiol 2017; 15 (5): 259–70. DOI: 10.1038/nrmicro.2017.14
34. Esposito S, Principi N. Impact of nasopharyngeal microbiota on the development of respiratory tract diseases. Eur J Clin Microbiol Infect Dis 2017; 37 (1): 1–7. DOI: 10.1007/s10096-017-3076-7
35. Hatakka K, Savilahti E, Ponka A et al. Effect of long-term consumption of probiotic milk on infections in children attending day care centres: double blind, randomised trial. BMJ 2001; 322 (7298): 1327.
36. Hojsak I, Snovak N, Abdovic S et al. Lactobacillus GG in the prevention of gastrointestinal and respiratory tract infections in children who attend day care centers: a randomized, double-blind, placebo-controlled trial. Clin Nutr 2010; 29 (3): 312–6.
37. Rautava S, Salminen S, Isolauri E. Specific probiotics in reducing the risk of acute infections in infancy – a randomised, double-blind, placebo-controlled study. Br J Nutr 2009; 101 (11): 1722–6.
38. Liu S, Hu P, Du X et al. Lactobacillus rhamnosus GG supplementation for preventing respiratory infections in children: a meta-analysis of randomized, placebo-controlled trials. Indian Pediatr 2013; 50: 377–81.
39. Hao Q, Dong BR, Wu T. Probiotics for preventing acute upper respiratory tract infections. Cochrane Database Syst Rev 2015; 2: CD006895.
40. Laursen RP, Hojsak I. Probiotics for respiratory tract infections in children attending day care centers – a systematic review. Eur J Pediatr 2018; 177 (7): 979–94. DOI: 10.1007/s00431-018-3167-1
41. Kumpu M, Kekkonen RA, Kautiainen H et al. Milk containing probiotic Lactobacillus rhamnosus GG and respiratory illness in children: a randomized, double-blind, placebo-controlled trial. Eur J Clin Nutr 2012; 66: 1020–3. DOI: doi.org/10.1038/ejcn. 2012.62
42. Scott AM, Clark J, Julien B et al. Probiotics for preventing acute otitis media in children. Cochrane Database Syst Rev 2019; Issue 6. Art. No.: CD012941. DOI: 10.1002/14651858.CD012941.pub2
43. Van den Broek MFL, De Boeck I, Claes IJJ et al. Multifactorial inhibition of lactobacilli against the respiratory tract pathogen Moraxella catarrhalis. Benef Microb 2018; 9 (3): 429–39. DOI: 10.3920/bm2017.0101
44. Schwenger EM, Tejani AM, Loewen PS. Probiotics for preventing urinary tract infections in adults and children. Cochrane Database System Rev 2015; Issue 12. Art. No.: CD008772. DOI: 10.1002/14651858.cd008772.pub2
45. Kara SS, Volkan B, Erten I. Lactobacillus rhamnosus GG can protect malnourished children. Benef Microb 2019; 10 (3): 237–44. DOI: 10.3920/BM2018.0071
46. http: //raaci.ru/education/clinic_recomendations/97.html
47. Williams HC. Clinical practice. Atopic dermatitis. N Engl J Med 2005; 352: 2314–24.
48. Mastrorilli C, Caffarelli C, Hoffmann-Sommergruber K. Food allergy and atopic dermatitis: Prediction, progression, and prevention. Pediatr Allergy Immunol 2017; 28 (8): 831–40. DOI: 10.1111/pai.12831
49. Zhao W, Ho H, Bunyavanich S. The Gut Microbiome in Food Allergy. Ann Allergy, Asthma Immunol 2018; 122 (3): 276–82. DOI: 10.1016/j.anai.2018.12.012
50. Pascal M, Perez-Gordo M, Caballero T et al. Microb Allergic Dis Front Immunol 2018; 9: 1584. DOI: 10.3389/fimmu.2018.01584
51. Cosenza L, Nocerino R, Di Scala C et al. Bugs for atopy: the Lactobacillus rhamnosus GG strategy for food allergy prevention and treatment in children. Benef Microb 2015; 6 (2): 225–32. DOI: 10.3920/bm2014.0158
52. Isolauri E. Studies on Lactobacillus GG in food hypersensitivity disorders. Nutr Today (Suppl.) 1996; 31: 285–315.
53. Kalliomaki M, Salminen S, Arvilommi H et al. Probiotics in primary prevention of atopic disease: a randomised placebo-controlled trial. Lancet 2001; 357: 1076–9. DOI: 10.1016/S0140-6736 (00)04259-8
54. Kalliomaki M, Salminen S, Poussa T et al. Probiotics and prevention of atopic disease: 4-year follow-up of a randomised placebo-controlled trial. Lancet 2003; 361: 1869–71. DOI: 10.1016/S0140-6736 (03)13490-3
55. Kalliomaki M, Salminen S, Poussa T, Isolauri E. Probiotics during the first 7 years of life: a cumulative risk reduction of eczema in a randomized, placebo- controlled trial. J Allergy Clin Immunol 2007; 119: 1019–21. DOI: 10.1016/j. jaci.2006.12.608
56. Rautava S, Kalliomaki M, Isolauri E. Probiotics during pregnancy and breast-feeding might confer immnomodulatory protection against atopic disease in the infant. J Allergy Clin Immunol 2002; 109 (1): 119–21.
57. Kalliomäki M, Antoine JM, Herz U et al. Guidance for Substantiating the Evidence for Beneficial Effects of Probiotics: Prevention and Management of Allergic Diseases by Probiotics. J Nutr 2010; 140 (3): 713S–721S. DOI: 10.3945/jn.109.113761
58. Fiocchi A, Pawankar R, Cuello-Garcia C et al. World allergy organization-McMaster university guidelines for allergic disease prevention (GLAD-P): Probiotics. World Allergy Organ J 2015; 8 (1): 4.
59. Szajewska H, Horvath A. Lactobacillus rhamnosus GG in the Primary Prevention of Eczema in Children: A Systematic Review and Meta-Analysis. Nutrients 2018; 10 (9): 1319. DOI: 10.3390/nu10091319
60. Berni Canani R, Di Costanzo M, Pezzella V et al. The potential therapeutic efficacy of Lactobacillus GG in children with food allergies. Pharmaceuticals 2012; 5: 655–64.
61. Murch SH. Toll of allergy reduced by probiotics. Lancet 2001; 357: 1057–9.
62. Majamaa H, Isolauri E. Probiotics: a novel approach in the management of food allergy. J Allergy Clin Immunol 1997; 99 (2): 179–85.
63. Isolauri E, Arvola T, Sutas Y et al. Probiotics in the management of atopic eczema. Clin Exp Allergy 2000; 30 (11): 1604–10.
64. Rosenfeldt V, Benfeldt E, Nielsen SD et al. Effect of probiotic Lactobacillus strains in children with atopic dermatitis. J Allergy Clin Immunol 2003; 111 (2): 389–95. DOI: 10.1067/mai.2003.389
65. Kirjavainen PV, Salminen SJ, Isolauri E. Probiotic Bacteria in the Management of Atopic Disease: Underscoring the Importance of Viability. J Pediatr Gastroenterol Nutr 2003; 36 (2): 223–7. DOI: 10.1097/00005176-200302000-00012
66. Viljanen M, Savilahti E, Haahtela T et al. Probiotics in the treatment of atopic eczema/ dermatitis syndrome in infants: a double-blind placebo-controlled trial. Allergy 2005; 60: 494–500. DOI: 10.1111/j.1398-9995.2004.00514.x
67. Brouwer ML, Wolt-Plompen SAA, Dubois AEJ et al. No effects of probiotics on atopic dermatitis in infancy: a randomized placebo-controlled trial. Clin Exper Allergy 2006; 36 (7): 899–906. DOI: 10.1111/j.1365-2222.2006.02513.x
68. Fölster-Holst R, Müller F, Schnopp N et al. Prospective, randomized controlled trial on Lactobacillus rhamnosus in infants with moderate to severe atopic dermatitis. Br J Dermatol 2006; 155 (6): 1256–61. DOI: 10.1111/j.1365-2133.2006.07558.x
69. Grüber C, Wendt M, Sulser C et al. Randomized, placebo-controlled trial of Lactobacillus rhamnosus GG as treatment of atopic dermatitis in infancy. Allergy 2007; 62 (11): 1270–6. DOI: 10.1111/j.1398-9995.2007.01543.x
70. Baldassarre ME, Laforgia N, Fanelli M et al. Lactobacillus GG improve recovery in infants with blood in the stools and presumptive allergic colitis compared with extensively hydrolyzed formula alone. J Pediatr 2010; 156: 397–401.
71. Berni Canani R, Di Costanzo M, Bedogni G et al. Extensively hydrolyzed casein formula containing Lactobacillus rhamnosus GG reduces the occurrence of other allergic manifestations in children with cow’s milk allergy: 3-year randomized controlled trial. J Allergy Clin Immunol 2017; 139 (6): 1906–13. DOI: 10.1016/j.jaci.2016.10.050
72. Qamer S, Deshmukh M, Patole S. Probiotics for cow’s milk protein allergy: a systematic review of randomized controlled trials. Eur J Pediatr 2019; 178 (8): 1139–49. DOI: 10.1007/s00431-019-03397-6
73. Nase L, Hatakka K, Savilahti E et al. Effect of long-term consumption of a probiotic bacterium, Lactobacillus rhamnosus GG, in milk on dental caries and caries risk in children. Caries Res 2001; 35 (6): 412–20.
74. Schwendicke F, Dörfer C, Kneist S et al. Cariogenic Effects of Probiotic Lactobacillus rhamnosus GG in a Dental Biofilm Model. Caries Res 2014; 48 (3): 186–92. DOI: 10.1159/000355907
75. Gungor OE, Kirzioglu Z, Kivanc M. Probiotics: can they be used to improve oral health? Benef Microb 2015; 6 (5): 647–56. DOI: 10.3920/bm2014.0167
76. Knip M, Siljander H. The role of the intestinal microbiota in type 1 diabetes mellitus. Nat Rev Endocrinol 2016; 12: 154–67. DOI: 10.1038/nrendo.2015.218
77. Vatanen T, Franzosa EA, Schwager R et al. The human gut microbiome in early-onset type 1 diabetes from the TEDDY study. Nature 2018; 562 (7728): 589–94. DOI: 10.1038/s41586-018-0620-2
78. Groele L, Szajewska H, Szypowska A. Effects of Lactobacillus rhamnosus GG and Bifidobacterium lactis Bb12 on beta-cell function in children with newly diagnosed type 1 diabetes: protocol of a randomised controlled trial. BMJ Open 2017; 7 (10): e017178. DOI: 10.1136/bmjopen-2017-017178
79. Abstracts for the 44th Annual Meeting of the International Society for Pediatric and Adolescent Diabetes (ISPAD), 11–14 October 2018, Hyderabad, India, Vol. 19, Issue S26: 33. doi.org/10.1111/pedi.12745
Авторы
И.Н. Захарова*, Е.Ю. Борзова, М.А. Симакова
ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России, Москва, Россия
*zakharova-rmapo@yandex.ru
________________________________________________
Irina N. Zakharova*, Elena Iu. Borzova, Mariia A. Simakova
Russian Medical Academy of Continuous Professional Education, Moscow, Russia
*zakharova-rmapo@yandex.ru