Probiotics and Lung Diseases

Ido expression by dendritic cells: tolerance and tryptophan catabolism

Mellor, A. L., & Munn, D. H. (2004) · Nature Reviews Immunology · doi:10.1038/nri1457 · Cited by 2,341 · see citing works

A microbial symbiosis factor prevents intestinal inflammatory disease

Mazmanian, S. K., Round, J. L., & Kasper, D. L. (2008) · Nature · doi:10.1038/nature07008 · Cited by 2,340 · see citing works

Probiotics and prevention of atopic disease: 4-year follow-up of a randomised placebo-controlled trial

Kalliomäki, M. A., Salminen, S., Poussa, T. A., Arvilommi, H. S., & Isolauri, E. (2003) · The Lancet · doi:10.1016/s0140-6736(03)13490-3 · Cited by 1,340 · see citing works

Distinct patterns of neonatal gut microflora in infants in whom atopy was and was not developing

Kalliomäki, M., Kirjavainen, P., Eerola, E., Kero, P., Salminen, S., & Isolauri, E. (2001) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2001.111237 · Cited by 1,255 · see citing works

The Foxp3+ regulatory T cell: a jack of all trades, master of regulation

Tang, Q., & Bluestone, J. A. (2008) · Nature Immunology · doi:10.1038/ni1572 · Cited by 1,026 · see citing works

Lactobacilli Differentially Modulate Expression of Cytokines and Maturation Surface Markers in Murine Dendritic Cells

Christensen, H. R., Frøkiær, H., & Pestka, J. J. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.1.171 · Cited by 905 · see citing works

Effect of long term consumption of probiotic milk on infections in children attending day care centres: double blind, randomised trial

Hatakka, K., Savilahti, E., Pönkä, A., Meurman, J. H., Poussa, T., Näse, L., Saxelin, M., & Korpela, R. (2001) · BMJ · doi:10.1136/bmj.322.7298.1327 · Cited by 645 · see citing works

Generation of regulatory dendritic cells and CD4 + Foxp3 + T cells by probiotics administration suppresses immune disorders

Kwon, H., Lee, C., So, J., Chae, C.-S., Hwang, J.-S., Sahoo, A., Nam, J. H., Rhee, J. H., Hwang, K.-C., & Im, S. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904055107 · Cited by 627 · see citing works

Suppression of allergic airway inflammation by helminth-induced regulatory T cells

Wilson, M. S., Taylor, M. D., Balic, A., Finney, C. A. M., Lamb, J. R., & Maizels, R. M. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20042572 · Cited by 611 · see citing works

Enhanced antiinflammatory capacity of a Lactobacillus plantarum mutant synthesizing modified teichoic acids

Grangette, C., Nutten, S., Palumbo, E., Morath, S., Hermann, C., Dewulf, J., Pot, B., Härtung, T., Pascal Hols, A., & Mercenier, A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504084102 · Cited by 443 · see citing works

Probiotics prevent IgE-associated allergy until age 5 years in cesarean-delivered children but not in the total cohort

Kuitunen, M., Kukkonen, A. K., Juntunen‐Backman, K., Korpela, R., Poussa, T. A., Tuure, T., Haahtela, T., & Savilahti, E. (2009) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2008.11.019 · Cited by 408 · see citing works

Effects of probiotics on atopic dermatitis: a randomised controlled trial

Weston, S. (2005) · Archives of Disease in Childhood · doi:10.1136/adc.2004.060673 · Cited by 408 · see citing works

The ‘microflora hypothesis’ of allergic diseases

Noverr, M. C., & Huffnagle, G. B. (2005) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2005.02379.x · Cited by 394 · see citing works

Commensal-Induced Regulatory T Cells Mediate Protection against Pathogen-Stimulated NF-κB Activation

O’Mahony, C., Scully, P., O'Mahony, D., Murphy, S., O'Brien, F., Lyons, A., Sherlock, G., MacSharry, J. A., Kiely, B., Shanahan, F., et al. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.1000112 · Cited by 365 · see citing works

Lactobacillus reuteri –induced Regulatory T cells Protect against an Allergic Airway Response in Mice

Karimi, K., Inman, M. D., Bienenstock, J., & Forsythe, P. (2008) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200806-951oc · Cited by 361 · see citing works

Probiotic Prophylaxis of Ventilator-associated Pneumonia: A Blinded, Randomized, Controlled Trial

Morrow, L. E., Kollef, M. H., & Casale, T. B. (2010) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200912-1853oc · Cited by 347 · see citing works

Inhibition of experimental asthma by indoleamine 2,3-dioxygenase

Hayashi, T., Beck, L., Rossetto, C. C., Gong, X., Takikawa, O., Takabayashi, K., Broide, D. H., Carson, D. A., & Raz, E. (2004) · Journal of Clinical Investigation · doi:10.1172/jci21275 · Cited by 344 · see citing works

Probiotic‐induced suppression of allergic sensitization and airway inflammation is associated with an increase of T regulatory‐dependent mechanisms in a murine model of asthma

Feleszko, W., Jaworska, J., Rha, R.-D., Steinhausen, S., Avagyan, A., Jaudszus, A., Ahrens, B., Groneberg, D. A., Wahn, U., & Hamelmann, E. H. (2006) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2006.02629.x · Cited by 339 · see citing works

Oral Treatment with Live Lactobacillus reuteri Inhibits the Allergic Airway Response in Mice

Forsythe, P., Inman, M. D., & Bienenstock, J. (2007) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200606-821oc · Cited by 306 · see citing works

Interference of Lactobacillus plantarum with Pseudomonas aeruginosa in vitro and in infected burns: the potential use of probiotics in wound treatment

Valdéz, J. C., Peral, M. C., Rachid, M., Santana, M., & Perdigón, G. (2005) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2005.01142.x · Cited by 301 · see citing works

A Key Role of Dendritic Cells in Probiotic Functionality

Foligné, B., Ζουμποπούλου, Γ., Dewulf, J., Younes‐Chennoufi, A. B., Chareyre, F., Sirard, J., Pot, B., & Grangette, C. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000313 · Cited by 278 · see citing works

Bacterial strain‐specific induction of Foxp3+ T regulatory cells is protective in murine allergy models

Lyons, A., O'Mahony, D., O'Brien, F., MacSharry, J. A., Sheil, B., Ceddia, M. A., Russell, W. M., Forsythe, P., Bienenstock, J., Kiely, B., et al. (2010) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2009.03437.x · Cited by 233 · see citing works

Clinical Indications for Probiotics: An Overview

Goldin, B., & Gorbach, S. L. (2008) · Clinical Infectious Diseases · doi:10.1086/523333 · Cited by 231 · see citing works

Lactobacillus GG in the Prevention of Nosocomial Gastrointestinal and Respiratory Tract Infections

Hojsak, I., Abdović, S., Szajewska, H., Milošević, M., Krznarić, Ž., & Kolaček, S. (2010) · PEDIATRICS · doi:10.1542/peds.2009-2568 · Cited by 214 · see citing works

Probiotic bacteria reduced duration and severity but not the incidence of common cold episodes in a double blind, randomized, controlled trial

de Vrese, M., Winkler, P., Rautenberg, P., Harder, T., Noah, C., Laue, C., Ott, S., Hampe, J., Schreiber, S., Heller, K., et al. (2006) · Vaccine · doi:10.1016/j.vaccine.2006.05.048 · Cited by 201 · see citing works

Effects of intestinal microflora and the environment on the development of asthma and allergy

n, B. B. R. (2004) · Springer Seminars in Immunopathology · doi:10.1007/s00281-003-0142-2 · Cited by 187 · see citing works

Intranasal administration of Lactobacillus rhamnosus GG protects mice from H1N1 influenza virus infection by regulating respiratory immune responses

Harata, G., He, F., Hiruta, N., Kawase, M., Kubota, A., Hiramatsu, M., & Yausi, H. (2010) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.2010.02844.x · Cited by 186 · see citing works

Antibiotic use during infancy promotes a shift in the TH1/TH2 balance toward TH2-dominant immunity in mice

Oyama, N., Sudo, N., Sogawa, H., & Kubo, C. (2001) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2001.111142 · Cited by 179 · see citing works

Bifidobacterium longum lysate, a new ingredient for reactive skin

Guéniche, A., Bastien, P., Ovigne, J.-M., Kermici, M., Courchay, G., Chevalier, V., Breton, L., & Castiel‐Higounenc, I. (2009) · Experimental Dermatology · doi:10.1111/j.1600-0625.2009.00932.x · Cited by 169 · see citing works

Perinatal maternal application of Lactobacillus rhamnosus GG suppresses allergic airway inflammation in mouse offspring

Blümer, N., Sel, S., Virna, S., Patrascan, C. C., Zimmermann, S., Herz, U., Renz, H. E., & Garn, H. (2007) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2007.02671.x · Cited by 168 · see citing works

Oral Treatment with Probiotics Reduces Allergic Symptoms in Ovalbumin-Sensitized Mice: A Bacterial Strain Comparative Study

Hougee, S., Vriesema, A. J. M., Wijering, S. C., Knippels, L. M. J., Folkerts, G., Nijkamp, F. P., Knol, J., & Garssen, J. (2009) · International Archives of Allergy and Immunology · doi:10.1159/000236000 · Cited by 162 · see citing works

In vitro immunomodulatory activity of Lactobacillus fermentum CECT5716 and Lactobacillus salivarius CECT5713: two probiotic strains isolated from human breast milk

Pérez-Cano, F. J., Dong, H., & Yaqoob, P. (2010) · Immunobiology · doi:10.1016/j.imbio.2010.01.004 · Cited by 156 · see citing works

Probiotics for the treatment of allergic rhinitis and asthma: systematic review of randomized controlled trials

Vliagoftis, H., Kouranos, V., Betsi, G. I., & Falagas, M. E. (2008) · Annals of Allergy Asthma & Immunology · doi:10.1016/s1081-1206(10)60219-0 · Cited by 146 · see citing works

Effect of intranasal administration of Lactobacillus pentosus S-PT84 on influenza virus infection in mice

Izumo, T., Maekawa, T., Ida, M., Noguchi, A., Kitagawa, Y., Shibata, H., Yasui, H., & Kiso, Y. (2010) · International Immunopharmacology · doi:10.1016/j.intimp.2010.06.012 · Cited by 134 · see citing works

An oral introduction of intestinal bacteria prevents the development of a long‐term Th2‐skewed immunological memory induced by neonatal antibiotic treatment in mice

Sudo, N., Yu, X.-N., Aiba, Y., Oyama, N., Sonoda, J., Koga, Y., & Kubo, C. (2002) · Clinical & Experimental Allergy · doi:10.1046/j.1365-2222.2002.01430.x · Cited by 130 · see citing works

Immunomodulatory function of lactic acid bacteria

Yasui, H., Shida, K., Matsuzaki, T., & Yokokura, T. (1999) · Springer eBooks · doi:10.1007/978-94-017-2027-4_24 · Cited by 126 · see citing works

Distinct gut-derived lactic acid bacteria elicit divergent dendritic cell-mediated NK cell responses

Fink, L. N., Zeuthen, L., Christensen, H. R., Morandi, B., Frøkiær, H., & Ferlazzo, G. (2007) · International Immunology · doi:10.1093/intimm/dxm103 · Cited by 115 · see citing works

Lactic acid bacteria enhance autophagic ability of mononuclear phagocytes by increasing Th1 autophagy-promoting cytokine (IFN-γ) and nitric oxide (NO) levels and reducing Th2 autophagy-restraining cytokines (IL-4 and IL-13) in response to Mycobacterium tuberculosis antigen

Ghadimi, D., de Vrese, M., Heller, K. J., & Schrezenmeir, J. (2010) · International Immunopharmacology · doi:10.1016/j.intimp.2010.03.014 · Cited by 110 · see citing works

Immunomodulatory function of lactic acid bacteria

Yasui, H., Shida, K., Matsuzaki, T., & Yokokura, T. (1999) · Antonie van Leeuwenhoek · doi:10.1023/a:1002041616085 · Cited by 106 · see citing works

Effect of Lactobacillus casei and Yogurt Administration on Prevention of Pseudomonas aeruginosa Infection in Young Mice

Alvarez, S., Herrero, C., Bru, E., & Perdigón, G. (2001) · Journal of Food Protection · doi:10.4315/0362-028x-64.11.1768 · Cited by 104 · see citing works

Lactobacillus casei Improves Resistance to Pneumococcal Respiratory Infection in Malnourished Mice

Villena, J., Racedo, S., Agüero, G., Bru, E., Medina, M., & Alvarez, S. (2005) · Journal of Nutrition · doi:10.1093/jn/135.6.1462 · Cited by 102 · see citing works

Effect of long-term continuous consumption of fermented milk containing probiotic bacteria on mucosal immunity and the activity of peritoneal macrophages

de LeBlanc, A. D. M., Chaves, S., Carmuega, E., Weill, R., Antoine, J. M., & Perdigón, G. (2007) · Immunobiology · doi:10.1016/j.imbio.2007.07.002 · Cited by 98 · see citing works

Resolution of Der p1-Induced Allergic Airway Inflammation Is Dependent on CD4+CD25+Foxp3+ Regulatory Cells

Leech, M. D., Benson, R. A., deVries, A., Fitch, P. M., & Howie, S. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.10.7050 · Cited by 97 · see citing works

Probiotics as Drugs Against Human Gastrointestinal Infections

Sanz, Y., Nadal, I., & Sánchez, E. (2007) · Recent Patents on Anti-Infective Drug Discovery · doi:10.2174/157489107780832596 · Cited by 96 · see citing works

Growth phase of orally administered Lactobacillus strains differentially affects IgG1/IgG2a ratio for soluble antigens: implications for vaccine development

Maassen, C. B. M., Boersma, W. J. A., van Holten-Neelen, C., Claassen, E., & Laman, J. D. (2003) · Vaccine · doi:10.1016/s0264-410x(03)00220-2 · Cited by 96 · see citing works

Asymptomatic atopy is associated with increased indoleamine 2,3‐dioxygenase activity and interleukin‐10 production during seasonal allergen exposure

von Bubnoff, D., Fimmers, R., Bogdanow, M., Matz, H., Koch, S., & Bieber, T. R. M. (2004) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2004.01984.x · Cited by 80 · see citing works

Essential role of Toll-like receptors for dendritic cell and NK1.1+ cell-dependent activation of type 1 immunity by Lactobacillus pentosus strain S-PT84

Koizumi, S.-I., Wakita, D., Sato, T., Mitamura, R., Izumo, T., Shibata, H., Kiso, Y., Chamoto, K., Togashi, Y., Kitamura, H., et al. (2008) · Immunology Letters · doi:10.1016/j.imlet.2008.06.003 · Cited by 76 · see citing works

Lactobacillus caseiShirota administered during lactation increases the duration of autoimmunity in rats and enhances lung inflammation in mice

Ezendam, J., & Loveren, H. V. (2007) · British Journal Of Nutrition · doi:10.1017/s0007114507803412 · Cited by 61 · see citing works

Enhanced immune response to pneumococcal infection in malnourished mice nasally treated with heat‐killed Lactobacillus casei

Villena, J., Barbieri, N., Salva, S., Herrera, M., & Alvarez, S. (2009) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2009.00171.x · Cited by 56 · see citing works

Microbial Manipulation of Immune Function for Asthma Prevention: Inferences from Clinical Trials

Yoo, J., Tcheurekdjian, H., Lynch, S. V., Cabana, M. D., & Boushey, H. A. (2007) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200702-033aw · Cited by 55 · see citing works

Chapter 5 Immune Pathways for Translating Viral Infection into Chronic Airway Disease

Holtzman, M. J., Byers, D. E., Benoît, L. A., Battaile, J. T., You, Y., Agapov, E. V., Park, C., Grayson, M. H., Kim, E. Y., & Patel, A. C. (2009) · Advances in immunology · doi:10.1016/s0065-2776(09)01205-x · Cited by 46 · see citing works

Differentiated implication of Lactobacillus GG and L. gasseri TMC0356 to immune responses of murine Peyer's patch

Harata, G., He, F., Kawase, M., Hosono, A., Takahashi, K., & Kaminogawa, S. (2009) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2009.00146.x · Cited by 41 · see citing works

Administration of polysaccharides from Antrodia camphorata modulates dendritic cell function and alleviates allergen‐induced T helper type 2 responses in a mouse model of asthma

Liu, K., Leu, S., Su, C., Chiang, B., Chen, Y., & Lee, Y. (2009) · Immunology · doi:10.1111/j.1365-2567.2009.03175.x · Cited by 28 · see citing works

Dyella jejuensis sp. nov., isolated from soil of Hallasan Mountain in Jeju Island

Kim, M., Hyun, D., Kim, J. Y., Kim, S., Bae, J., & Park, E. J. (2014) · The Journal of Microbiology · doi:10.1007/s12275-014-3670-7 · Cited by 22 · see citing works

Induction of cytokines and nitric oxide in murine macrophages stimulated with enzymatically digested lactobacillus strains.

Kim, D. W., Cho, S. B., Yun, C., Jeong, H. Y., Chung, W. T., Choi, C. W., Lee, H. J., Nam, I. S., Suh, G. H., Lee, S., et al. (2007) · PubMed · Cited by 18 · see citing works

Early life antibiotic‐driven changes in microbiota enhance susceptibility to allergic asthma

Russell, S. L., Gold, M. J., Hartmann, M., Willing, B. P., Thorson, L., Wlodarska, M., Gill, N., Blanchet, M., Mohn, W. W., McNagny, K. M., et al. (2012) · The EMBO Reports · doi:10.1038/embor.2012.32 · Cited by 883 · see citing works

Intestinal microbiota in health and disease: Role of bifidobacteria in gut homeostasis

Tojo, R. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i41.15163 · Cited by 533 · see citing works

Regulation of lung immunity and host defense by the intestinal microbiota

Samuelson, D. R., Welsh, D. A., & Shellito, J. E. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01085 · Cited by 434 · see citing works

The role of the bacterial microbiome in lung disease

Dickson, R. P., Erb‐Downward, J. R., & Huffnagle, G. B. (2013) · Expert Review of Respiratory Medicine · doi:10.1586/ers.13.24 · Cited by 412 · see citing works

Pediococcus spp.: An important genus of lactic acid bacteria and pediocin producers

Porto, M. C. W., Kuniyoshi, T. M., Azevedo, P. O. S., Vitolo, M., & Oliveira, R. P. S. (2017) · Biotechnology Advances · doi:10.1016/j.biotechadv.2017.03.004 · Cited by 262 · see citing works

A Clinician's Primer on the Role of the Microbiome in Human Health and Disease

Khanna, S., & Tosh, P. K. (2014) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2013.10.011 · Cited by 231 · see citing works

The Innate Immune Protein Nod2 Binds Directly to MDP, a Bacterial Cell Wall Fragment

Grimes, C. L., Ariyananda, L. D. Z., Melnyk, J. E., & O’Shea, E. K. (2012) · Journal of the American Chemical Society · doi:10.1021/ja303883c · Cited by 194 · see citing works

Assembly of a Three-Dimensional Multitype Bronchiole Coculture Model Using Magnetic Levitation

Tseng, H., Gage, J. A., Raphael, R. M., Moore, R. H., Killian, T. C., Grande-Allen, K. J., & Souza, G. R. (2013) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2012.0157 · Cited by 138 · see citing works

Gut microbiota in various childhood disorders: Implication and indications

Saeed, N. K., Al‐Beltagi, M., Bediwy, A. S., El-Sawaf, Y., & Toema, O. (2022) · World Journal of Gastroenterology · doi:10.3748/wjg.v28.i18.1875 · Cited by 147 · see citing works

Limosilactobacillus reuteri in Health and Disease

Abuqwider, J., Altamimi, M., & Mauriello, G. (2022) · Microorganisms · doi:10.3390/microorganisms10030522 · Cited by 124 · see citing works

SARS-CoV-2 microbiome dysbiosis linked disorders and possible probiotics role

Din, A. U., Mazhar, M., Waseem, M., Ahmad, W., Bibi, A., Hassan, A., Ali, N., Wang, G., Gao, Q., Ullah, R., et al. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110947 · Cited by 119 · see citing works

Non dairy probiotic beverages.

Vasudha, S., & Mishra, H. (2013) · International Food Research Journal · Cited by 116 · see citing works

Perinatal Programming of Asthma: The Role of Gut Microbiota

Azad, M. B., & Kozyrskyj, A. L. (2011) · Clinical and Developmental Immunology · doi:10.1155/2012/932072 · Cited by 102 · see citing works

Human Pharyngeal Microbiome May Play A Protective Role in Respiratory Tract Infections

Gao, Z., Kang, Y., Yu, J. M., & Ren, L. (2014) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2014.06.001 · Cited by 95 · see citing works

Oral administration of Lactobacillus paracasei L9 attenuates PM2.5-induced enhancement of airway hyperresponsiveness and allergic airway response in murine model of asthma

Wang, X., Yan, H., Zhao, L., Hao, Y., Guo, H., & Ren, F. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171721 · Cited by 85 · see citing works

Effect of 3 lactobacilli on immunoregulation and intestinal microbiota in a β-lactoglobulin–induced allergic mouse model

Fu, G., Zhao, K., Chen, H., Wang, Y., Nie, L., Wei, H., & Wan, C. (2019) · Journal of Dairy Science · doi:10.3168/jds.2018-15683 · Cited by 86 · see citing works

Augmented IFN-γ and TNF-α Induced by Probiotic Bacteria in NK Cells Mediate Differentiation of Stem-Like Tumors Leading to Inhibition of Tumor Growth and Reduction in Inflammatory Cytokine Release; Regulation by IL-10

Bui, V. T., Tseng, H.-C., Kozłowska, A. K., Maung, P. O., Kaur, K., Topchyan, P., & Jewett, A. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00576 · Cited by 83 · see citing works

Gut Microbiota: the Emerging Link to Lung Homeostasis and Disease

Zhou, A., Lei, Y., Tang, L., Hu, S., Yang, M., Wu, L., Yang, S., & Tang, B. (2020) · Journal of Bacteriology · doi:10.1128/jb.00454-20 · Cited by 78 · see citing works

The impact of gut microbes in allergic diseases

Russell, S., & Finlay, B. B. (2012) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e3283573017 · Cited by 74 · see citing works

Oral feeding with probiotic Lactobacillus rhamnosus attenuates cigarette smoke-induced COPD in C57Bl/6 mice: Relevance to inflammatory markers in human bronchial epithelial cells

Carvalho, J. L., Miranda, M., FIALHO, A. K. C. D. S., Castro-Faria-Neto, H., Anatriello, E., Keller, A. C., & Aimbire, F. (2020) · PLoS ONE · doi:10.1371/journal.pone.0225560 · Cited by 73 · see citing works

Probiotics' effects on the incidence of nosocomial pneumonia in critically ill patients: a systematic review and meta-analysis

Liu, K., Zhu, Y., Zhang, J., Tao, L., Lee, J. W., Wang, X., & Qu, J. (2012) · Critical Care · doi:10.1186/cc11398 · Cited by 72 · see citing works

Lactobacillus reuteri ATCC55730 in Cystic Fibrosis

Nardo, G. D., Oliva, S., Menichella, A., Pistelli, R., Biase, R. V. D., Patriarchi, F., Cucchiara, S., & Stronati, L. (2013) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000000187 · Cited by 71 · see citing works

The Airway Microbiome and Disease

Marsland, B. J., Yadava, K., & Nicod, L. P. (2013) · CHEST Journal · doi:10.1378/chest.12-2854 · Cited by 69 · see citing works

Exposure to diesel exhaust particles results in altered lung microbial profiles, associated with increased reactive oxygen species/reactive nitrogen species and inflammation, in C57Bl/6 wildtype mice on a high-fat diet

Daniel, S., Phillippi, D., Schneider, L. J., Nguyen, K. N., Mirpuri, J., & Lund, A. K. (2021) · Particle and Fibre Toxicology · doi:10.1186/s12989-020-00393-9 · Cited by 67 · see citing works

The Murine Lung Microbiome Changes During Lung Inflammation and Intranasal Vancomycin Treatment

Barfod, K. K., Vrankx, K., Mirsepasi‐Lauridsen, H. C., Hansen, J. S., ­Hougaard, K. S., Larsen, S. T., Ouwenhand, A. C., & Krogfelt, K. A. (2015) · The Open Microbiology Journal · doi:10.2174/1874285801509010167 · Cited by 64 · see citing works

Probiotics: A new way to fight bacterial pulmonary infections?

Alexandre, Y., Blay, G. L., Boisramé, S., Gall, F. L., Héry-Arnaud, G., Gouriou, S., Vallet, S., & Berre, R. L. (2013) · Médecine et Maladies Infectieuses · doi:10.1016/j.medmal.2013.05.001 · Cited by 64 · see citing works

Respiratory Microbiome of New-Born Infants

Gallacher, D. J., & Kotecha, S. (2016) · Frontiers in Pediatrics · doi:10.3389/fped.2016.00010 · Cited by 64 · see citing works

Oral administration of Enterococcus faecalis FK-23 suppresses Th17 cell development and attenuates allergic airway responses in mice

Zhang, B., An, J., Shimada, T., Liu, S., & Maeyama, K. (2012) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2012.1010 · Cited by 61 · see citing works

The combination of Bifidobacterium breve with non-digestible oligosaccharides suppresses airway inflammation in a murine model for chronic asthma

Sagar, S., Vos, A. P., Morgan, M. E., Garssen, J., Georgiou, N., Boon, L., Kraneveld, A. D., & Folkerts, G. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.01.005 · Cited by 60 · see citing works

Respiratory viral infections in children with asthma: do they matter and can we prevent them?

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Emerging importance of holobionts in evolution and in probiotics

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