Polysaccharides L900/2 and L900/3 isolated from Lactobacillus rhamnosus LOCK 0900 modulate allergic sensitization to ovalbumin in a mouse model
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
28165193
PubMed Central
PMC5404188
DOI
10.1111/1751-7915.12606
Knihovny.cz E-resources
- MeSH
- Allergens immunology MeSH
- Polysaccharides, Bacterial administration & dosage isolation & purification MeSH
- Basophils immunology MeSH
- Cytokines biosynthesis MeSH
- Cell Degranulation MeSH
- Immunization * MeSH
- Immunoglobulin E blood MeSH
- Immunoglobulin G blood MeSH
- Immunologic Factors administration & dosage isolation & purification MeSH
- Lacticaseibacillus rhamnosus chemistry MeSH
- Mice MeSH
- Serpins immunology MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Allergens MeSH
- Polysaccharides, Bacterial MeSH
- Cytokines MeSH
- Immunoglobulin E MeSH
- Immunoglobulin G MeSH
- Immunologic Factors MeSH
- SERPIN-B5 MeSH Browser
- Serpins MeSH
Here, we compared the abilities of polysaccharides L900/2 and L900/3, which were previously isolated from Lactobacillus rhamnosus LOCK 0900, to modulate the immune response to bystander antigens in a mouse model of ovalbumin (OVA) sensitization. In vivo, both polysaccharides reduced the levels of OVA-specific IgE, IgE-dependent basophil degranulation and IgG2a antibodies, but had no effect on the levels of OVA-specific IgA or IgG1. Interestingly, both polysaccharides triggered recall cellular responses with distinct properties. L900/3 significantly suppressed the OVA-induced upregulations of IL-4, IL-5, IL-10 and IL-13 in re-stimulated spleen cells and mesenteric lymph nodes. Our findings support and expand on our previous in vitro studies by demonstrating that polymer L900/3 might modulate the Th1/Th2 balance and could be a promising candidate molecule for preventing allergic sensitization.
See more in PubMed
Blumer, N. , Sel, S. , Virna, S. , Patrascan, C.C. , Zimmermann, S. , Herz, U. , et al (2007) Perinatal maternal application of Lactobacillus rhamnosus GG suppresses allergic airway inflammation in mouse offspring. Clin Exp Allergy 37: 348–357. PubMed
Christensen, H.R. , Frokiaer, H. , and Pestka, J.J. (2002) Lactobacilli differentially modulate expression of cytokines and maturation surface markers in murine dendritic cells. J Immunol 168: 171–178. PubMed
Ciszek‐Lenda, M. , Strus, M. , Górska‐Fraczek, S. , Targosz‐Korecka, M. , Śróttek, M. , Heczko, P.B. , et al (2011) Strain specific immunostimulatory potential of lactobacilli‐derived exopolysaccharides. Cent Eur J Immunol 36: 121–129.
Fanning, S. , Hall, L.J. , and van Sinderen, D. (2012) Bifidobacterium breve UCC2003 surface exopolysaccharide production is a beneficial trait mediating commensal‐host interaction through immune modulation and pathogen protection. Gut Microbes 3: 420–425. PubMed
Golias, J. , Schwarzer, M. , Wallner, M. , Kverka, M. , Kozakova, H. , Srutkova, D. , et al (2012) Heat‐induced structural changes affect OVA‐antigen processing and reduce allergic response in mouse model of food allergy. PLoS ONE 7: e37156. PubMed PMC
Górska, S. , Schwarzer, M. , Jachymek, W. , Srutkova, D. , Brzozowska, E. , Kozakova, H. , and Gamian, A. (2014) Distinct immunomodulation of bone marrow‐derived dendritic cell responses to Lactobacillus plantarum WCFS1 by two different polysaccharides isolated from Lactobacillus rhamnosus LOCK 0900. Appl Environ Microbiol 80: 6506–6516. PubMed PMC
Górska, S. , Hermanova, P. , Ciekot, J. , Schwarzer, M. , Srutkova, D. , Brzozowska, E. , et al (2016) Chemical characterization and immunomodulatory properties of polysaccharides isolated from probiotic Lactobacillus casei LOCK 0919. Glycobiology 26: 1014–1024. PubMed PMC
Ishida, Y. , Bandou, I. , Kanzato, H. , and Yamamoto, N. (2003) Decrease in ovalbumin specific IgE of mice serum after oral uptake of lactic acid bacteria. Biosci Biotechnol Biochem 67: 951–957. PubMed
Israel, E.J. , Wilsker, D.F. , Hayes, K.C. , Schoenfeld, D. , and Simiste, N.E. (1996) Increased clearance of IgG in mice that lack b2‐microglobulin: possible protective role of FcRn. Immunology 89: 573–578. PubMed PMC
Kim, J.Y. , Choi, Y.O. , and Ji, G.E. (2008) Effect of oral probiotics (Bifidobacterium lactis AD011 and Lactobacillus acidophilus AD031) administration on ovalbumin‐induced food allergy mouse model. J Microbiol Biotechnol 18: 1393–1400. PubMed
Liong, M. (2008) Safety of probiotics: translocation and infection. Nutr Rev 66: 192–202. PubMed
Maassen, C.B. , van Holten‐Neelen, C. , Balk, F. , den Bak‐Glashouwer, M.J. , Leer, R.J. , Laman, J.D. , et al (2000) Strain‐dependent induction of cytokine profiles in the gut by orally administered Lactobacillus strains. Vaccine 18: 2613–2623. PubMed
Ohno, H. , Tsunemine, S. , Isa, Y. , Shimakawa, M. , and Yamamura, H. (2005) Oral administration of Bifidobacterium bifidum G9‐1 suppresses total and antigen specific immunoglobulin E production in mice. Biol Pharm Bull 28: 1462–1466. PubMed
Rupa, P. , Schmied, J. , and Wilkie, B.N. (2011) Prophylaxis of experimentally induced ovomucoid allergy in neonatal pigs using Lactococcus lactis . Vet Immunol Immunopathol 140: 23–29. PubMed
Schabussova, I. , and Wiedermann, U. (2008) Lactic acid bacteria as novel adjuvant systems for prevention and treatment of atopic diseases. Curr Opin Allergy Clin Immunol 8: 557–564. PubMed
Schabussova, I. , Hufnagl, K. , Wild, C. , Nutten, S. , Zuercher, A.W. , Mercenier, A. , and Wiedermann, U. (2011) Distinctive anti‐allergy properties of two probiotic bacterial strains in a mouse model of allergic poly‐sensitization. Vaccine 29: 1981–1990. PubMed
Schabussova, I. , Hufnagl, K. , Tang, M.L.K. , Hoflehner, E. , Wagner, A. , Loupal, G. , et al (2012) Perinatal maternal administration of Lactobacillus paracasei NCC 2461 prevents allergic inflammation in a mouse model of birch pollen allergy. PLoS ONE 7: e40271. PubMed PMC
Schwarzer, M. , Srutkova, D. , Schabussova, I. , Hudcovic, T. , Akgün, J. , Wiedermann, U. , and Kozakova, H. (2013) Neonatal colonization of germ‐free mice with Bifidobacterium longum prevents allergic sensitization to major birch pollen allergen Bet v 1. Vaccine 31: 5405–5412. PubMed
Takahashi, N. , Kitazawa, H. , Iwabuchi, N. , Xiao, J.Z. , Miyaji, K. , Iwatsuki, K. , and Saito, T. (2006) Immunostimulatory oligodeoxynucleotide from Bifidobacterium longum suppresses Th2 immune responses in a murine model. Clin Exp Immunol 145: 130–138. PubMed PMC
Toh, Z.Q. , Anzela, A. , Tang, M.L.K. , and Licciardi, P.V. (2012) Probiotic therapy as a novel approach for allergic disease. Front Pharmacol 3: 171. PubMed PMC
Vighi, G. , Marcucci, F. , Sensi, L. , Di Cara, G. , and Fratis, F. (2008) Allergy and the gastrointestinal system. Clin Exp Immunol 153: 3–6. PubMed PMC
Whelan, K. , and Myers, C.E. (2010) Safety of probiotics in patients receiving nutritional support: a systematic review of case reports, randomized controlled trials, and nonrandomized trials. Am J Clin Nutr 91: 687–703. PubMed
Wiedermann, U. , Herz, U. , Baier, K. , Vrtala, S. , Neuhaus‐Steinmetz, U. , Bohle, B. , et al (2001) Intranasal treatment with a recombinant hypoallergenic derivative of the major birch pollen allergen Bet v 1 prevents allergic sensitization and airway inflammation in mice. Int Arch Allergy Immunol 126: 68–77. PubMed
Zuercher, A.W. , Weiss, M. , Holvoet, S. , Moser, M. , Moussu, H. , van Overtvelt, L. , et al (2012) Lactococcus lactis NCC 2287 alleviates food allergic manifestations in sensitized mice by reducing IL‐13 expression specifically in the ileum. Clin Dev Immunol. doi:10.1155/2012/485750 PubMed DOI PMC