Probiotic Lactobacilli Modulate Staphylococcus aureus-Induced Activation of Conventional and Unconventional T cells and NK Cells
Lactobacilli are probiotic commensal bacteria and potent modulators of immunity. When present in the gut or supplemented as probiotics, they beneficially modulate ex vivo immune responsiveness. Further, factors derived from several lactobacilli strains act immune regulatory in vitro. In contrast, St...
Saved in:
Published in | Frontiers in immunology Vol. 7; p. 273 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
11.07.2016
|
Subjects | |
Online Access | Get full text |
ISSN | 1664-3224 1664-3224 |
DOI | 10.3389/fimmu.2016.00273 |
Cover
Abstract | Lactobacilli are probiotic commensal bacteria and potent modulators of immunity. When present in the gut or supplemented as probiotics, they beneficially modulate ex vivo immune responsiveness. Further, factors derived from several lactobacilli strains act immune regulatory in vitro. In contrast, Staphylococcus aureus (S. aureus) is known to induce excessive T cell activation. In this study, we aimed to investigate S. aureus-induced activation of human mucosal-associated invariant T cells (MAIT cells), γδ T cells, NK cells, as well as of conventional CD4(+) and CD8(+) T cells in vitro. Further, we investigated if lactobacilli-derived factors could modulate their activation. PBMC were cultured with S. aureus 161:2 cell-free supernatants (CFS), staphylococcal enterotoxin A or CD3/CD28-beads alone, or in combination with Lactobacillus rhamnosus GG-CFS or Lactobacillus reuteri DSM 17938-CFS and activation of T and NK cells was evaluated. S. aureus-CFS induced IFN-γ and CD107a expression as well as proliferation. Costimulation with lactobacilli-CFS dampened lymphocyte-activation in all cell types analyzed. Preincubation with lactobacilli-CFS was enough to reduce subsequent activation, and the absence of APC or APC-derived IL-10 did not prevent lactobacilli-mediated dampening. Finally, lactate selectively dampened activation of unconventional T cells and NK cells. In summary, we show that molecules present in the lactobacilli-CFS are able to directly dampen in vitro activation of conventional and unconventional T cells and of NK cells. This study provides novel insights on the immune-modulatory nature of probiotic lactobacilli and suggests a role for lactobacilli in the modulation of induced T and NK cell activation. |
---|---|
AbstractList | Lactobacilli are probiotic commensal bacteria and potent modulators of immunity. When present in the gut or supplemented as probiotics, they beneficially modulate ex vivo immune responsiveness. Further, factors derived from several lactobacilli strains act immune regulato-ry in vitro. In contrast, Staphylococcus aureus (S. aureus) is known to induce excessive T cell activation. In this study we aimed to investigate S. aureus-induced activation of human muco-sal associated invariant T cells (MAIT cells), γδ T cells, NK cells, as well as of conventional CD4+ and CD8+ T cells in vitro. Further, we investigated if lactobacilli-derived factors could modulate their activation.PBMC were cultured with S. aureus 161:2 cell free supernatant (CFS), staphylococcal en-terotoxin A or CD3/CD28-beads alone or in combination with Lactobacillus rhamnosus (L. rhamnosus) GG-CFS or Lactobacillus reuteri (L. reuteri) DSM 17938-CFS, and activation of T and NK cells was evaluated. S. aureus-CFS induced IFN-γ and CD107a expression as well as proliferation. Co-stimulation with lactobacilli-CFS dampened lymphocyte activation in all cell types analysed. Pre-incubation with lactobacilli-CFS was enough to reduce subsequent activation and the ab-sence of APC or APC-derived IL-10 did not prevent lactobacilli-mediated dampening. Final-ly, lactate selectively dampened activation of unconventional T cells and NK cells. In summary, we show that molecules present in the lactobacilli-CFS are able to directly dampen in vitro activation of conventional and unconventional T cells and of NK cells. This study provides novel insights on the immune modulatory nature of probiotic lactobacilli and suggests a role for lactobacilli in modulation of induced T and NK cell activation. Lactobacilli are probiotic commensal bacteria and potent modulators of immunity. When present in the gut or supplemented as probiotics, they beneficially modulate ex vivo immune responsiveness. Further, factors derived from several lactobacilli strains act immune regulatory in vitro. In contrast, Staphylococcus aureus (S. aureus) is known to induce excessive T cell activation. In this study, we aimed to investigate S. aureus-induced activation of human mucosal-associated invariant T cells (MAIT cells), γδ T cells, NK cells, as well as of conventional CD4(+) and CD8(+) T cells in vitro. Further, we investigated if lactobacilli-derived factors could modulate their activation. PBMC were cultured with S. aureus 161:2 cell-free supernatants (CFS), staphylococcal enterotoxin A or CD3/CD28-beads alone, or in combination with Lactobacillus rhamnosus GG-CFS or Lactobacillus reuteri DSM 17938-CFS and activation of T and NK cells was evaluated. S. aureus-CFS induced IFN-γ and CD107a expression as well as proliferation. Costimulation with lactobacilli-CFS dampened lymphocyte-activation in all cell types analyzed. Preincubation with lactobacilli-CFS was enough to reduce subsequent activation, and the absence of APC or APC-derived IL-10 did not prevent lactobacilli-mediated dampening. Finally, lactate selectively dampened activation of unconventional T cells and NK cells. In summary, we show that molecules present in the lactobacilli-CFS are able to directly dampen in vitro activation of conventional and unconventional T cells and of NK cells. This study provides novel insights on the immune-modulatory nature of probiotic lactobacilli and suggests a role for lactobacilli in the modulation of induced T and NK cell activation.Lactobacilli are probiotic commensal bacteria and potent modulators of immunity. When present in the gut or supplemented as probiotics, they beneficially modulate ex vivo immune responsiveness. Further, factors derived from several lactobacilli strains act immune regulatory in vitro. In contrast, Staphylococcus aureus (S. aureus) is known to induce excessive T cell activation. In this study, we aimed to investigate S. aureus-induced activation of human mucosal-associated invariant T cells (MAIT cells), γδ T cells, NK cells, as well as of conventional CD4(+) and CD8(+) T cells in vitro. Further, we investigated if lactobacilli-derived factors could modulate their activation. PBMC were cultured with S. aureus 161:2 cell-free supernatants (CFS), staphylococcal enterotoxin A or CD3/CD28-beads alone, or in combination with Lactobacillus rhamnosus GG-CFS or Lactobacillus reuteri DSM 17938-CFS and activation of T and NK cells was evaluated. S. aureus-CFS induced IFN-γ and CD107a expression as well as proliferation. Costimulation with lactobacilli-CFS dampened lymphocyte-activation in all cell types analyzed. Preincubation with lactobacilli-CFS was enough to reduce subsequent activation, and the absence of APC or APC-derived IL-10 did not prevent lactobacilli-mediated dampening. Finally, lactate selectively dampened activation of unconventional T cells and NK cells. In summary, we show that molecules present in the lactobacilli-CFS are able to directly dampen in vitro activation of conventional and unconventional T cells and of NK cells. This study provides novel insights on the immune-modulatory nature of probiotic lactobacilli and suggests a role for lactobacilli in the modulation of induced T and NK cell activation. Lactobacilli are probiotic commensal bacteria and potent modulators of immunity. When present in the gut or supplemented as probiotics, they beneficially modulate ex vivo immune responsiveness. Further, factors derived from several lactobacilli strains act immune regulatory in vitro. In contrast, Staphylococcus aureus (S. aureus) is known to induce excessive T cell activation. In this study, we aimed to investigate S. aureus-induced activation of human mucosal-associated invariant T cells (MAIT cells), gamma delta T cells, NK cells, as well as of conventional CD4(+) and CD8(+) T cells in vitro. Further, we investigated if lactobacilli-derived factors could modulate their activation. PBMC were cultured with S. aureus 161: 2 cell-free supernatants (CFS), staphylococcal enterotoxin A or CD3/CD28-beads alone, or in combination with Lactobacillus rhamnosus GG-CFS or Lactobacillus reuteri DSM 17938-CFS and activation of T and NK cells was evaluated. S. aureus-CFS induced IFN-gamma and CD107a expression as well as proliferation. Costimulation with lactobacilli-CFS dampened lymphocyte-activation in all cell types analyzed. Preincubation with lactobacilli-CFS was enough to reduce subsequent activation, and the absence of APC or APC-derived IL-10 did not prevent lactobacilli-mediated dampening. Finally, lactate selectively dampened activation of unconventional T cells and NK cells. In summary, we show that molecules present in the lactobacilli-CFS are able to directly dampen in vitro activation of conventional and unconventional T cells and of NK cells. This study provides novel insights on the immune-modulatory nature of probiotic lactobacilli and suggests a role for lactobacilli in the modulation of induced T and NK cell activation. Lactobacilli are probiotic commensal bacteria and potent modulators of immunity. When present in the gut or supplemented as probiotics, they beneficially modulate ex vivo immune responsiveness. Further, factors derived from several lactobacilli strains act immune regulatory in vitro . In contrast, Staphylococcus aureus ( S. aureus ) is known to induce excessive T cell activation. In this study, we aimed to investigate S. aureus -induced activation of human mucosal-associated invariant T cells (MAIT cells), γδ T cells, NK cells, as well as of conventional CD4 + and CD8 + T cells in vitro . Further, we investigated if lactobacilli-derived factors could modulate their activation. PBMC were cultured with S. aureus 161:2 cell-free supernatants (CFS), staphylococcal enterotoxin A or CD3/CD28-beads alone, or in combination with Lactobacillus rhamnosus GG-CFS or Lactobacillus reuteri DSM 17938-CFS and activation of T and NK cells was evaluated. S. aureus -CFS induced IFN-γ and CD107a expression as well as proliferation. Costimulation with lactobacilli-CFS dampened lymphocyte-activation in all cell types analyzed. Preincubation with lactobacilli-CFS was enough to reduce subsequent activation, and the absence of APC or APC-derived IL-10 did not prevent lactobacilli-mediated dampening. Finally, lactate selectively dampened activation of unconventional T cells and NK cells. In summary, we show that molecules present in the lactobacilli-CFS are able to directly dampen in vitro activation of conventional and unconventional T cells and of NK cells. This study provides novel insights on the immune-modulatory nature of probiotic lactobacilli and suggests a role for lactobacilli in the modulation of induced T and NK cell activation. Lactobacilli are probiotic commensal bacteria and potent modulators of immunity. When present in the gut or supplemented as probiotics, they beneficially modulate ex vivo immune responsiveness. Further, factors derived from several lactobacilli strains act immune regulatory in vitro. In contrast, Staphylococcus aureus (S. aureus) is known to induce excessive T cell activation. In this study, we aimed to investigate S. aureus-induced activation of human mucosal-associated invariant T cells (MAIT cells), γδ T cells, NK cells, as well as of conventional CD4(+) and CD8(+) T cells in vitro. Further, we investigated if lactobacilli-derived factors could modulate their activation. PBMC were cultured with S. aureus 161:2 cell-free supernatants (CFS), staphylococcal enterotoxin A or CD3/CD28-beads alone, or in combination with Lactobacillus rhamnosus GG-CFS or Lactobacillus reuteri DSM 17938-CFS and activation of T and NK cells was evaluated. S. aureus-CFS induced IFN-γ and CD107a expression as well as proliferation. Costimulation with lactobacilli-CFS dampened lymphocyte-activation in all cell types analyzed. Preincubation with lactobacilli-CFS was enough to reduce subsequent activation, and the absence of APC or APC-derived IL-10 did not prevent lactobacilli-mediated dampening. Finally, lactate selectively dampened activation of unconventional T cells and NK cells. In summary, we show that molecules present in the lactobacilli-CFS are able to directly dampen in vitro activation of conventional and unconventional T cells and of NK cells. This study provides novel insights on the immune-modulatory nature of probiotic lactobacilli and suggests a role for lactobacilli in the modulation of induced T and NK cell activation. |
Author | Johansson, Maria A. Bittmann, Julia Eberl, Matthias Qazi, Khaleda Rahman Mata Forsberg, Manuel Sverremark-Ekström, Eva Björkander, Sophia Salvany Celades, Maria |
AuthorAffiliation | 3 Systems Immunity Research Institute, Cardiff University , Cardiff , UK 1 Arrhenius Laboratories for Natural Sciences, Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University , Stockholm , Sweden 2 Division of Infection and Immunity, School of Medicine, Cardiff University , Cardiff , UK |
AuthorAffiliation_xml | – name: 1 Arrhenius Laboratories for Natural Sciences, Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University , Stockholm , Sweden – name: 2 Division of Infection and Immunity, School of Medicine, Cardiff University , Cardiff , UK – name: 3 Systems Immunity Research Institute, Cardiff University , Cardiff , UK |
Author_xml | – sequence: 1 givenname: Maria A. surname: Johansson fullname: Johansson, Maria A. – sequence: 2 givenname: Sophia surname: Björkander fullname: Björkander, Sophia – sequence: 3 givenname: Manuel surname: Mata Forsberg fullname: Mata Forsberg, Manuel – sequence: 4 givenname: Khaleda Rahman surname: Qazi fullname: Qazi, Khaleda Rahman – sequence: 5 givenname: Maria surname: Salvany Celades fullname: Salvany Celades, Maria – sequence: 6 givenname: Julia surname: Bittmann fullname: Bittmann, Julia – sequence: 7 givenname: Matthias surname: Eberl fullname: Eberl, Matthias – sequence: 8 givenname: Eva surname: Sverremark-Ekström fullname: Sverremark-Ekström, Eva |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27462316$$D View this record in MEDLINE/PubMed https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-132953$$DView record from Swedish Publication Index |
BookMark | eNp1Uktv1DAQjlARLaV3TshHDmTxK45zQVotrxXLQ6Llak1sp3XlxEucLOqNn46TbdEuEr7YM_4e0sz3NDvpQmez7DnBC8Zk9bpxbTsuKCZigTEt2aPsjAjBc0YpPzl4n2YXMd7idHjFGCueZKe05IIyIs6y39_6ULswOI02oIdQg3beO_Q5mNHDYNH3AbY3dz7ooPUYEYy9HWO-7syorUFLPbgdDC50KDRoFbqd7aYKPILOoKtOH7Yukbbex_nryye0mopn2eMGfLQX9_d5dvX-3eXqY775-mG9Wm5yzatqyLmVxFBJipJTbBoJlWlAF4I3NVgiaio1ptBwkiCMskKbRmgqgGFZNZLW7Dxb73VNgFu17V0L_Z0K4NTcCP21gj6NwVslC4IZqyVhXHJKdGUw6EpIIwqNGSdJ69VeK_6y27E-UnvrfixntTgqwmhVsAR_s4cnbGuNTvPowR-xjn86d6Ouw06lfVWcTH4v7wX68HO0cVCti9MoobNhjIpIXBaMl7hM0BeHXn9NHjaeAGIP0H2IsbeN0m6YN5isnVcEqyldak6XmtKl5nQlIv6H-KD9X8ofoEbUvQ |
CitedBy_id | crossref_primary_10_1515_jbcpp_2021_0320 crossref_primary_10_3390_ijms25063340 crossref_primary_10_3390_ijms22052453 crossref_primary_10_4049_jimmunol_1900941 crossref_primary_10_3390_ijms21093303 crossref_primary_10_3390_biom14020225 crossref_primary_10_1016_j_micres_2024_127913 crossref_primary_10_3389_fnut_2022_1000517 crossref_primary_10_3390_microbiolres14030082 crossref_primary_10_1016_j_jbc_2024_107748 crossref_primary_10_1016_j_aqrep_2024_102384 crossref_primary_10_3389_fmicb_2020_607735 crossref_primary_10_1007_s00005_017_0500_8 crossref_primary_10_1093_postmj_qgae030 crossref_primary_10_1093_femsre_fuab041 crossref_primary_10_1038_s41598_019_53576_6 crossref_primary_10_3389_fimmu_2024_1298971 crossref_primary_10_1017_S0029665121003207 crossref_primary_10_3389_fmicb_2019_00977 crossref_primary_10_1016_j_nutres_2024_09_018 crossref_primary_10_1016_j_aquatox_2023_106671 crossref_primary_10_4049_jimmunol_2000143 crossref_primary_10_3389_fimmu_2021_578386 crossref_primary_10_1016_j_intimp_2024_111937 crossref_primary_10_3389_fmicb_2018_02532 crossref_primary_10_3389_fmicb_2017_02705 crossref_primary_10_1002_JLB_3A1020_630RR crossref_primary_10_3389_fmicb_2022_886206 crossref_primary_10_3389_fimmu_2017_01837 crossref_primary_10_1080_1547691X_2019_1706672 crossref_primary_10_3389_fimmu_2023_1073788 crossref_primary_10_1111_imcb_70012 crossref_primary_10_4049_jimmunol_1900681 crossref_primary_10_3389_fimmu_2018_01602 crossref_primary_10_2147_JAA_S382978 crossref_primary_10_1007_s12602_024_10247_x crossref_primary_10_1016_j_archoralbio_2017_04_026 crossref_primary_10_3390_microorganisms8010019 crossref_primary_10_3390_microorganisms10010148 crossref_primary_10_1016_j_schres_2019_08_013 crossref_primary_10_1155_2019_1603758 crossref_primary_10_3389_fimmu_2020_584521 crossref_primary_10_1007_s00284_021_02442_8 crossref_primary_10_3920_BM2021_0151 crossref_primary_10_3390_metabo13030415 crossref_primary_10_3389_fimmu_2021_639291 crossref_primary_10_3892_mmr_2017_7492 crossref_primary_10_1159_000499184 crossref_primary_10_3390_pathophysiology31010002 crossref_primary_10_3390_ijms242115584 crossref_primary_10_3390_nu16223830 crossref_primary_10_1080_19490976_2022_2045046 crossref_primary_10_3389_fmicb_2019_01972 crossref_primary_10_1021_acsami_1c23713 crossref_primary_10_3390_vaccines9070775 |
Cites_doi | 10.1136/gut.2003.026252 10.3389/fimmu.2016.00096 10.1038/nri1001 10.1111/j.1462-5822.2006.00763.x 10.4049/jimmunol.172.8.4661 10.1126/science.2185544 10.1038/nature11605 10.1099/mic.0.042069-0 10.4049/jimmunol.174.6.3237 10.4049/jimmunol.1202702 10.1007/s40272-015-0124-6 10.1371/journal.pone.0077893 10.1046/j.1365-2249.2002.01854.x 10.1016/j.jaci.2015.08.033 10.1038/srep22845 10.1038/mi.2012.138 10.1371/journal.pone.0000313 10.4049/jimmunol.1401018 10.1038/nchembio744 10.1371/journal.pone.0023031 10.1111/j.1440-1746.2010.06498.x 10.1111/j.1365-2222.2005.02375.x 10.1371/journal.pone.0049315 10.1111/cea.12047 10.1111/j.1365-2222.2008.03025.x 10.1371/journal.pbio.1001149 10.1128/IAI.01172-06 10.1371/journal.pone.0031951 10.1177/0148607115588113 10.1038/mi.2016.43 10.1067/mai.2001.118130 10.1186/2045-7022-4-21 10.1111/j.1365-2249.2011.04408.x 10.3389/fcimb.2012.00052 10.1097/00054725-200203000-00001 10.1371/journal.pbio.1000407 10.1016/j.jaci.2013.08.020 10.3389/fimmu.2013.00507 10.1084/jem.20151159 10.3748/wjg.v17.i5.557 10.1371/journal.pone.0056547 10.1128/CVI.05642-11 10.1038/nature12726 10.1016/0008-8749(85)90355-7 10.1067/mai.2002.128528 10.1038/srep22083 10.1038/ni.1890 10.1111/cea.12253 10.1371/journal.pone.0047244 10.1016/j.jff.2013.11.006 10.1002/ibd.20448 10.1093/intimm/dxm103 10.1186/1475-2859-13-S1-S7 10.3168/jds.2013-7459 10.1111/j.1365-2222.2009.03344.x 10.1111/j.1365-2567.2011.03455.x 10.1371/journal.pone.0108360 10.1203/01.pdr.0000191137.12774.b2 10.4161/gmic.19245 10.1093/ajcn/80.6.1618 10.1128/CDLI.9.3.649-647.2002 10.1111/j.1365-2222.2008.03156.x 10.5402/2011/892971 10.1371/journal.pone.0130155 10.1016/S0165-2478(01)00182-1 10.1182/blood-2006-07-035972 10.1016/j.jff.2013.01.028 10.1016/j.imbio.2008.02.001 |
ContentType | Journal Article |
Copyright | Copyright © 2016 Johansson, Björkander, Mata Forsberg, Qazi, Salvany Celades, Bittmann, Eberl and Sverremark-Ekström. 2016 Johansson, Björkander, Mata Forsberg, Qazi, Salvany Celades, Bittmann, Eberl and Sverremark-Ekström |
Copyright_xml | – notice: Copyright © 2016 Johansson, Björkander, Mata Forsberg, Qazi, Salvany Celades, Bittmann, Eberl and Sverremark-Ekström. 2016 Johansson, Björkander, Mata Forsberg, Qazi, Salvany Celades, Bittmann, Eberl and Sverremark-Ekström |
DBID | AAYXX CITATION NPM 7X8 5PM ABAVF ADTPV AOWAS D8T DG7 ZZAVC DOA |
DOI | 10.3389/fimmu.2016.00273 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) SWEPUB Stockholms universitet full text SwePub SwePub Articles SWEPUB Freely available online SWEPUB Stockholms universitet SwePub Articles full text Directory of Open Access Journals (DOAJ) (Open Access) |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
EISSN | 1664-3224 |
ExternalDocumentID | oai_doaj_org_article_851033b81348421c9d0ac968d65c0341 oai_DiVA_org_su_132953 PMC4939411 27462316 10_3389_fimmu_2016_00273 |
Genre | Journal Article |
GrantInformation_xml | – fundername: Medical Research Council grantid: MR/N023145/1 – fundername: Vetenskapsrådet grantid: 57X-15160-10-4 – fundername: Hjärt-Lungfonden – fundername: Carl Tryggers Stiftelse för Vetenskaplig Forskning – fundername: Torsten Söderbergs Stiftelse |
GroupedDBID | 53G 5VS 9T4 AAFWJ AAKDD AAYXX ACGFO ACGFS ACXDI ADBBV ADRAZ AENEX AFPKN ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BCNDV CITATION DIK EBS EMOBN GROUPED_DOAJ GX1 HYE IPNFZ KQ8 M48 M~E OK1 PGMZT RIG RNS RPM NPM 7X8 5PM ABAVF ADTPV AOWAS D8T DG7 ZZAVC |
ID | FETCH-LOGICAL-c499t-4e81d28157420df8a9dfac564fbae16b28c02af418153235cdf6c26a3089f82b3 |
IEDL.DBID | M48 |
ISSN | 1664-3224 |
IngestDate | Wed Aug 27 01:30:18 EDT 2025 Thu Aug 21 06:23:29 EDT 2025 Thu Aug 21 18:43:16 EDT 2025 Thu Sep 04 19:38:47 EDT 2025 Sat May 31 02:09:31 EDT 2025 Tue Jul 01 01:57:32 EDT 2025 Thu Apr 24 23:05:00 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | NK cells probiotic superantigens cell-free supernatant lactobacilli immune modulation T cells Staphylococcus aureus |
Language | English |
License | This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c499t-4e81d28157420df8a9dfac564fbae16b28c02af418153235cdf6c26a3089f82b3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Diego A. Vargas-Inchaustegui, National Institute of Allergy and Infectious Diseases, USA; Geoffrey A. Preidis, Baylor College of Medicine, USA; Texas Children’s Hospital, USA Edited by: Michael Harrison Hsieh, Children’s National Medical Center, USA Maria A. Johansson and Sophia Björkander contributed equally to this work. Specialty section: This article was submitted to Microbial Immunology, a section of the journal Frontiers in Immunology |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.3389/fimmu.2016.00273 |
PMID | 27462316 |
PQID | 1807534707 |
PQPubID | 23479 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_851033b81348421c9d0ac968d65c0341 swepub_primary_oai_DiVA_org_su_132953 pubmedcentral_primary_oai_pubmedcentral_nih_gov_4939411 proquest_miscellaneous_1807534707 pubmed_primary_27462316 crossref_citationtrail_10_3389_fimmu_2016_00273 crossref_primary_10_3389_fimmu_2016_00273 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2016-07-11 |
PublicationDateYYYYMMDD | 2016-07-11 |
PublicationDate_xml | – month: 07 year: 2016 text: 2016-07-11 day: 11 |
PublicationDecade | 2010 |
PublicationPlace | Switzerland |
PublicationPlace_xml | – name: Switzerland |
PublicationTitle | Frontiers in immunology |
PublicationTitleAlternate | Front Immunol |
PublicationYear | 2016 |
Publisher | Frontiers Media S.A |
Publisher_xml | – name: Frontiers Media S.A |
References | Braat (B18) 2004; 80 Brown (B10) 2014; 4 Ivory (B5) 2008; 38 Yan (B21) 2016 Liu (B17) 2013; 8 Frauwirth (B63) 2004; 172 Ménard (B25) 2004; 53 Petersson (B8) 2003; 170 Peluso (B50) 2007; 75 Björkstén (B68) 2001; 108 Johansson (B1) 2011; 6 Foligne (B19) 2007; 2 Luoto (B65) 2014; 133 Johansson (B11) 2012; 7 Demont (B48) 2016; 137 Husain (B61) 2013; 191 Cruchet (B33) 2015; 17 Trinchieri (B30) 2003; 3 Haller (B39) 2002; 9 Pochard (B3) 2002; 110 Yan (B27) 2012; 3 Schultz (B57) 2002; 8 Kjer-Nielsen (B36) 2012; 491 Di Giacinto (B13) 2005; 174 Kim (B22) 2006; 8 Marrack (B7) 1990; 248 Ashraf (B24) 2014; 97 Gold (B37) 2010; 8 Athalye-Jape (B32) 2015 Sjögren (B69) 2009; 39 Le Bourhis (B35) 2010; 11 Thomas (B28) 2012; 7 Buck (B62) 2015; 212 Hsieh (B47) 2013; 36 Forsberg (B64) 2014; 4 Penders (B70) 2010; 156 Reinhardt (B40) 2015; 10 Xia (B58) 2011; 26 Yoshida (B52) 2011; 133 Björkander (B29) 2016; 6 Smelt (B16) 2012; 7 Segers (B31) 2014; 13 Chiu (B55) 2013; 5 Ghadimi (B4) 2008; 213 Fong (B49) 2016; 6 Latvala (B54) 2011; 165 de Roock (B15) 2010; 40 Ashraf (B45) 2014; 6 Mihm (B60) 1985; 96 Murray (B51) 2005; 1 Kumar (B42) 2013; 6 Haileselassie (B12) 2013; 8 Davey (B38) 2014; 193 Niers (B56) 2005; 35 de Moreno de Leblanc (B14) 2011; 2011 Hosoya (B53) 2014; 9 Fischer (B59) 2007; 109 Ami (B41) 2002; 128 Haileselassie (B20) 2016; 7 Fikri (B43) 2001; 77 Abrahamsson (B67) 2014; 44 Arad (B44) 2011; 9 Arpaia (B26) 2013; 504 Fink (B46) 2007; 19 Fava (B66) 2011; 17 Xu (B9) 2012; 2 Lin (B23) 2008; 14 Lawrence (B34) 2012; 19 Harb (B2) 2013; 43 Adlerberth (B6) 2006; 59 |
References_xml | – volume: 53 start-page: 821 year: 2004 ident: B25 article-title: Lactic acid bacteria secrete metabolites retaining anti-inflammatory properties after intestinal transport publication-title: Gut doi: 10.1136/gut.2003.026252 – volume: 7 start-page: 96 year: 2016 ident: B20 article-title: Postbiotic modulation of retinoic acid imprinted mucosal-like dendritic cells by probiotic Lactobacillus reuteri 17938 in vitro publication-title: Front Immunol doi: 10.3389/fimmu.2016.00096 – volume: 3 start-page: 133 year: 2003 ident: B30 article-title: Interleukin-12 and the regulation of innate resistance and adaptive immunity publication-title: Nat Rev Immunol doi: 10.1038/nri1001 – volume: 8 start-page: 1958 year: 2006 ident: B22 article-title: G-CSF-mediated inhibition of JNK is a key mechanism for Lactobacillus rhamnosus-induced suppression of TNF production in macrophages publication-title: Cell Microbiol doi: 10.1111/j.1462-5822.2006.00763.x – volume: 172 start-page: 4661 year: 2004 ident: B63 article-title: Regulation of T lymphocyte metabolism publication-title: J Immunol doi: 10.4049/jimmunol.172.8.4661 – volume: 170 start-page: 4148 year: 2003 ident: B8 article-title: Staphylococcal enterotoxin H induces V alpha-specific expansion of T cells publication-title: J Immunol doi: 10.1126/science.2185544 – volume: 491 start-page: 717 year: 2012 ident: B36 article-title: MR1 presents microbial vitamin B metabolites to MAIT cells publication-title: Nature doi: 10.1038/nature11605 – volume: 156 start-page: 3298 year: 2010 ident: B70 article-title: Intestinal lactobacilli and the DC-SIGN gene for their recognition by dendritic cells play a role in the aetiology of allergic manifestations publication-title: Microbiology doi: 10.1099/mic.0.042069-0 – volume: 36 start-page: 167 year: 2013 ident: B47 article-title: Potential of probiotic strains to modulate the inflammatory responses of epithelial and immune cells in vitro publication-title: New Microbiol – volume: 174 start-page: 3237 year: 2005 ident: B13 article-title: Probiotics ameliorate recurrent Th1-mediated murine colitis by inducing IL-10 and IL-10-dependent TGF-beta-bearing regulatory cells publication-title: J Immunol doi: 10.4049/jimmunol.174.6.3237 – volume: 191 start-page: 1486 year: 2013 ident: B61 article-title: Tumor-derived lactate modifies antitumor immune response: effect on myeloid-derived suppressor cells and NK cells publication-title: J Immunol doi: 10.4049/jimmunol.1202702 – volume: 17 start-page: 199 year: 2015 ident: B33 article-title: The use of probiotics in pediatric gastroenterology: a review of the literature and recommendations by Latin-American experts publication-title: Paediatr Drugs doi: 10.1007/s40272-015-0124-6 – volume: 8 start-page: e77893 year: 2013 ident: B12 article-title: Lactobacilli regulate Staphylococcus aureus 161:2-induced pro-inflammatory T-cell responses in vitro publication-title: PLoS One doi: 10.1371/journal.pone.0077893 – volume: 128 start-page: 453 year: 2002 ident: B41 article-title: Activation of human T cells with NK cell markers by staphylococcal enterotoxin A via IL-12 but not via IL-18 publication-title: Clin Exp Immunol doi: 10.1046/j.1365-2249.2002.01854.x – volume: 137 start-page: 1264.e year: 2016 ident: B48 article-title: Live and heat-treated probiotics differently modulate IL10 mRNA stabilization and microRNA expression publication-title: J Allergy Clin Immunol doi: 10.1016/j.jaci.2015.08.033 – volume: 6 start-page: 22845 year: 2016 ident: B49 article-title: Immunomodulation of Lactobacillus rhamnosus GG (LGG)-derived soluble factors on antigen-presenting cells of healthy blood donors publication-title: Sci Rep doi: 10.1038/srep22845 – volume: 6 start-page: 1006 year: 2013 ident: B42 article-title: Rapid αβ T-cell responses orchestrate innate immunity in response to Staphylococcal enterotoxin A publication-title: Mucosal Immunol doi: 10.1038/mi.2012.138 – volume: 2 start-page: e313 year: 2007 ident: B19 article-title: A key role of dendritic cells in probiotic functionality publication-title: PLoS One doi: 10.1371/journal.pone.0000313 – volume: 193 start-page: 3704 year: 2014 ident: B38 article-title: Microbe-specific unconventional T cells induce human neutrophil differentiation into antigen cross-presenting cells publication-title: J Immunol doi: 10.4049/jimmunol.1401018 – volume: 1 start-page: 371 year: 2005 ident: B51 article-title: Monocarboxylate transporter MCT1 is a target for immunosuppression publication-title: Nat Chem Biol doi: 10.1038/nchembio744 – volume: 6 start-page: e23031 year: 2011 ident: B1 article-title: Early colonization with a group of Lactobacilli decreases the risk for allergy at five years of age despite allergic heredity publication-title: PLoS One doi: 10.1371/journal.pone.0023031 – volume: 26 start-page: 405 year: 2011 ident: B58 article-title: Effect of Lactobacillus plantarum LP-Onlly on gut flora and colitis in interleukin-10 knockout mice publication-title: J Gastroenterol Hepatol doi: 10.1111/j.1440-1746.2010.06498.x – volume: 35 start-page: 1481 year: 2005 ident: B56 article-title: Identification of strong interleukin-10 inducing lactic acid bacteria which down-regulate T helper type 2 cytokines publication-title: Clin Exp Allergy doi: 10.1111/j.1365-2222.2005.02375.x – volume: 7 start-page: e49315 year: 2012 ident: B11 article-title: Early-life gut bacteria associate with IL-4-, IL-10- and IFN-γ production at two years of age publication-title: PLoS One doi: 10.1371/journal.pone.0049315 – volume: 43 start-page: 353 year: 2013 ident: B2 article-title: Neonatal supplementation of processed supernatant from Lactobacillus rhamnosus GG improves allergic airway inflammation in mice later in life publication-title: Clin Exp Allergy doi: 10.1111/cea.12047 – volume: 38 start-page: 1282 year: 2008 ident: B5 article-title: Oral delivery of Lactobacillus casei Shirota modifies allergen-induced immune responses in allergic rhinitis publication-title: Clin Exp Allergy doi: 10.1111/j.1365-2222.2008.03025.x – volume: 9 start-page: e1001149 year: 2011 ident: B44 article-title: Binding of superantigen toxins into the CD28 homodimer interface is essential for induction of cytokine genes that mediate lethal shock publication-title: PLoS Biol doi: 10.1371/journal.pbio.1001149 – volume: 75 start-page: 1730 year: 2007 ident: B50 article-title: Lactobacillus paracasei subsp. paracasei B21060 suppresses human T-cell proliferation publication-title: Infect Immun doi: 10.1128/IAI.01172-06 – volume: 7 start-page: e31951 year: 2012 ident: B28 article-title: Histamine derived from probiotic Lactobacillus reuteri suppresses TNF via modulation of PKA and ERK signaling publication-title: PLoS One doi: 10.1371/journal.pone.0031951 – year: 2015 ident: B32 article-title: Lactobacillus reuteri DSM 17938 as a probiotic for preterm neonates: a strain-specific systematic review publication-title: JPEN J Parenter Enteral Nutr doi: 10.1177/0148607115588113 – year: 2016 ident: B21 article-title: Neonatal colonization of mice with LGG promotes intestinal development and decreases susceptibility to colitis in adulthood publication-title: Mucosal Immunol doi: 10.1038/mi.2016.43 – volume: 108 start-page: 516 year: 2001 ident: B68 article-title: Allergy development and the intestinal microflora during the first year of life publication-title: J Allergy Clin Immunol doi: 10.1067/mai.2001.118130 – volume: 4 start-page: 21 year: 2014 ident: B64 article-title: Pre- and postnatal administration of Lactobacillus reuteri decreases TLR2 responses in infants publication-title: Clin Transl Allergy doi: 10.1186/2045-7022-4-21 – volume: 165 start-page: 94 year: 2011 ident: B54 article-title: Lactobacillus rhamnosus GG and Streptococcus thermophilus induce suppressor of cytokine signalling 3 (SOCS3) gene expression directly and indirectly via interleukin-10 in human primary macrophages publication-title: Clin Exp Immunol doi: 10.1111/j.1365-2249.2011.04408.x – volume: 248 start-page: 705 year: 1990 ident: B7 article-title: The staphylococcal enterotoxins and their relatives publication-title: Science doi: 10.1126/science.2185544 – volume: 2 start-page: 52 year: 2012 ident: B9 article-title: Staphylococcal superantigens in colonization and disease publication-title: Front Cell Infect Microbiol doi: 10.3389/fcimb.2012.00052 – volume: 8 start-page: 71 year: 2002 ident: B57 article-title: Lactobacillus plantarum 299V in the treatment and prevention of spontaneous colitis in interleukin-10-deficient mice publication-title: Inflamm Bowel Dis doi: 10.1097/00054725-200203000-00001 – volume: 8 start-page: e1000407 year: 2010 ident: B37 article-title: Human mucosal associated invariant T cells detect bacterially infected cells publication-title: PLoS Biol doi: 10.1371/journal.pbio.1000407 – volume: 133 start-page: 405 year: 2014 ident: B65 article-title: Prebiotic and probiotic supplementation prevents rhinovirus infections in preterm infants: a randomized, placebo-controlled trial publication-title: J Allergy Clin Immunol doi: 10.1016/j.jaci.2013.08.020 – volume: 4 start-page: 507 year: 2014 ident: B10 article-title: Staphylococcus aureus colonization: modulation of host immune response and impact on human vaccine design publication-title: Front Immunol doi: 10.3389/fimmu.2013.00507 – volume: 212 start-page: 1345 year: 2015 ident: B62 article-title: T cell metabolism drives immunity publication-title: J Exp Med doi: 10.1084/jem.20151159 – volume: 17 start-page: 557 year: 2011 ident: B66 article-title: Intestinal microbiota in inflammatory bowel disease: friend of foe? publication-title: World J Gastroenterol doi: 10.3748/wjg.v17.i5.557 – volume: 8 start-page: e56547 year: 2013 ident: B17 article-title: Lactobacillus reuteri DSM 17938 changes the frequency of Foxp3+ regulatory T cells in the intestine and mesenteric lymph node in experimental necrotizing enterocolitis publication-title: PLoS One doi: 10.1371/journal.pone.0056547 – volume: 19 start-page: 477 year: 2012 ident: B34 article-title: CD4 T cell antigens from Staphylococcus aureus Newman strain identified following immunization with heat-killed bacteria publication-title: Clin Vaccine Immunol doi: 10.1128/CVI.05642-11 – volume: 504 start-page: 451 year: 2013 ident: B26 article-title: Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation publication-title: Nature doi: 10.1038/nature12726 – volume: 96 start-page: 235 year: 1985 ident: B60 article-title: Regulation of cytotoxic T-lymphocyte activation by l-lactate and pyruvate publication-title: Cell Immunol doi: 10.1016/0008-8749(85)90355-7 – volume: 110 start-page: 617 year: 2002 ident: B3 article-title: Lactic acid bacteria inhibit TH2 cytokine production by mononuclear cells from allergic patients publication-title: J Allergy Clin Immunol doi: 10.1067/mai.2002.128528 – volume: 6 start-page: 22083 year: 2016 ident: B29 article-title: Staphylococcus aureus-derived factors induce IL-10, IFN-γ and IL-17A-expressing FOXP3+CD161+ T-helper cells in a partly monocyte-dependent manner publication-title: Sci Rep doi: 10.1038/srep22083 – volume: 11 start-page: 701 year: 2010 ident: B35 article-title: Antimicrobial activity of mucosal-associated invariant T cells publication-title: Nat Immunol doi: 10.1038/ni.1890 – volume: 44 start-page: 842 year: 2014 ident: B67 article-title: Low gut microbiota diversity in early infancy precedes asthma at school age publication-title: Clin Exp Allergy doi: 10.1111/cea.12253 – volume: 7 start-page: e47244 year: 2012 ident: B16 article-title: L. plantarum, L. salivarius, and L. lactis attenuate Th2 responses and increase Treg frequencies in healthy mice in a strain dependent manner publication-title: PLoS One doi: 10.1371/journal.pone.0047244 – volume: 6 start-page: 395 year: 2014 ident: B45 article-title: Lactic acid bacteria and probiotic organisms induce different cytokine profile and regulatory T cells mechanisms publication-title: J Funct Foods doi: 10.1016/j.jff.2013.11.006 – volume: 14 start-page: 1068 year: 2008 ident: B23 article-title: Probiotic Lactobacillus reuteri suppress proinflammatory cytokines via c-Jun publication-title: Inflamm Bowel Dis doi: 10.1002/ibd.20448 – volume: 19 start-page: 1319 year: 2007 ident: B46 article-title: Distinct gut-derived lactic acid bacteria elicit divergent dendritic cell-mediated NK cell responses publication-title: Int Immunol doi: 10.1093/intimm/dxm103 – volume: 13 start-page: S7 issue: Suppl 1 year: 2014 ident: B31 article-title: Towards a better understanding of Lactobacillus rhamnosus GG – host interactions publication-title: Microb Cell Fact doi: 10.1186/1475-2859-13-S1-S7 – volume: 97 start-page: 2542 year: 2014 ident: B24 article-title: Effect of cell-surface components and metabolites of lactic acid bacteria and probiotic organisms on cytokine production and induction of CD25 expression in human peripheral mononuclear cells publication-title: J Dairy Sci doi: 10.3168/jds.2013-7459 – volume: 40 start-page: 103 year: 2010 ident: B15 article-title: Lactic acid bacteria differ in their ability to induce functional regulatory T cells in humans publication-title: Clin Exp Allergy doi: 10.1111/j.1365-2222.2009.03344.x – volume: 133 start-page: 442 year: 2011 ident: B52 article-title: Lactobacillus gasseri OLL2809 and its RNA suppress proliferation of CD4(+) T cells through a MyD88-dependent signalling pathway publication-title: Immunology doi: 10.1111/j.1365-2567.2011.03455.x – volume: 9 start-page: e108360 year: 2014 ident: B53 article-title: Lactobacillus helveticus SBT2171 inhibits lymphocyte proliferation by regulation of the JNK signaling pathway publication-title: PLoS One doi: 10.1371/journal.pone.0108360 – volume: 59 start-page: 96 year: 2006 ident: B6 article-title: Reduced enterobacterial and increased staphylococcal colonization of the infantile bowel: an effect of hygienic lifestyle? publication-title: Pediatr Res doi: 10.1203/01.pdr.0000191137.12774.b2 – volume: 3 start-page: 25 year: 2012 ident: B27 article-title: Characterization of a probiotic-derived soluble protein which reveals a mechanism of preventive and treatment effects of probiotics on intestinal inflammatory diseases publication-title: Gut Microbes doi: 10.4161/gmic.19245 – volume: 80 start-page: 1618 year: 2004 ident: B18 article-title: Lactobacillus rhamnosus induces peripheral hyporesponsiveness in stimulated CD4+ T cells via modulation of dendritic cell function publication-title: Am J Clin Nutr doi: 10.1093/ajcn/80.6.1618 – volume: 9 start-page: 649 year: 2002 ident: B39 article-title: Activation of human NK cells by staphylococci and lactobacilli requires cell contact-dependent costimulation by autologous monocytes publication-title: Clin Diagn Lab Immunol doi: 10.1128/CDLI.9.3.649-647.2002 – volume: 39 start-page: 518 year: 2009 ident: B69 article-title: Altered early infant gut microbiota in children developing allergy up to 5 years of age publication-title: Clin Exp Allergy doi: 10.1111/j.1365-2222.2008.03156.x – volume: 2011 start-page: 892971 year: 2011 ident: B14 article-title: Importance of IL-10 modulation by probiotic microorganisms in gastrointestinal inflammatory diseases publication-title: ISRN Gastroenterol doi: 10.5402/2011/892971 – volume: 10 start-page: e0130155 year: 2015 ident: B40 article-title: Invasive surgery impairs the regulatory function of human CD56 bright natural killer cells in response to Staphylococcus aureus. Suppression of interferon-γ synthesis publication-title: PLoS One doi: 10.1371/journal.pone.0130155 – volume: 77 start-page: 87 year: 2001 ident: B43 article-title: Purified bovine WC1+ gamma delta T lymphocytes are activated by staphylococcal enterotoxins and toxic shock syndrome toxin-1 superantigens: proliferation response, TCR V gamma profile and cytokines expression publication-title: Immunol Lett doi: 10.1016/S0165-2478(01)00182-1 – volume: 109 start-page: 3812 year: 2007 ident: B59 article-title: Inhibitory effect of tumor cell-derived lactic acid on human T cells publication-title: Blood doi: 10.1182/blood-2006-07-035972 – volume: 5 start-page: 820 year: 2013 ident: B55 article-title: Anti-inflammatory effect of lactobacilli bacteria on HepG2 cells is through cross-regulation of TLR4 and NOD2 signalling publication-title: J Funct Foods doi: 10.1016/j.jff.2013.01.028 – volume: 213 start-page: 677 year: 2008 ident: B4 article-title: Effects of probiotic bacteria and their genomic DNA on TH1/TH2-cytokine production by peripheral blood mononuclear cells (PBMCs) of healthy and allergic subjects publication-title: Immunobiology doi: 10.1016/j.imbio.2008.02.001 |
SSID | ssj0000493335 |
Score | 2.3553061 |
Snippet | Lactobacilli are probiotic commensal bacteria and potent modulators of immunity. When present in the gut or supplemented as probiotics, they beneficially... |
SourceID | doaj swepub pubmedcentral proquest pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 273 |
SubjectTerms | cell-free supernatant Immune Modulation Immunology lactobacilli Molecular Bioscience molekylär biovetenskap NK cells probiotic Staphylococcus aureus Superantigens T cells |
SummonAdditionalLinks | – databaseName: Directory of Open Access Journals (DOAJ) (Open Access) dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELZQJSQuiPJcXjISHDhEG9uxYx-XQlUBrTh0UW-Wn2IrmqBmc-iNn87Y3l1tBIILpyixLTszY_kbe_wNQq9hxRXBx7ZynKqq8cpUNjpTsdpyJyQ8VLo7fHomTpbNxwt-sZfqK8WEFXrgIri5TJRvzErCGtlQ4pSvjVNCesFdzfKVdVqres-Zuiy4lzHGy7kkeGFqHldXV2MK5UqHD7Rlk3Uo0_X_CWP-Hio5IRTNi9DxPXR3gx7xooz6EN0K3X10u-STvHmAfn7JrEpQiD-nPDrWuLSdgk97n7J0BQzQEsQK61fv3DhgM16HcahS-g4XPF64ba4z3Ed8tBePjk3n8bLbD1HH5zht-g-56OxTeXmIlscfzo9Oqk2KhcqBq7OumgB4lUrCwUOufZRG-WgcF020JhBhqXQ1NbEBHMAZZdz5KBwVhtVSRUkte4QOur4LTxAGKOFpa5lJZ3XSBmkpa4ORUgFIaomZoflW4Npt-MdTGozvGvyQpCKdVaSTinRW0Qy93bX4Ubg3_lL3XdLhrl5izc4fwJb0xpb0v2xphl5tLUDDLEuCM13ox0GTxNnMmrZuZ-hxsYhdV-DXA4YkYobaia1MxjIt6VbfMpM3WKlqCPT7pljVpMn71ddFHv4wasKo4uzp__jJZ-hOElvanybkOTpYX4_hBQCrtX2Z59AvUqwhlQ priority: 102 providerName: Directory of Open Access Journals |
Title | Probiotic Lactobacilli Modulate Staphylococcus aureus-Induced Activation of Conventional and Unconventional T cells and NK Cells |
URI | https://www.ncbi.nlm.nih.gov/pubmed/27462316 https://www.proquest.com/docview/1807534707 https://pubmed.ncbi.nlm.nih.gov/PMC4939411 https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-132953 https://doaj.org/article/851033b81348421c9d0ac968d65c0341 |
Volume | 7 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELagCIkL4s3yqIwEBw6hsZ049gGhpVAqoBWHLtpb5FdgUZvAZiPRGz-dGSe7NGLFiUtWiWMlOzPWfOOZfEPIU_C4MviqSFzOdZJ5bRJbOZOI1OZOKvjR-O3w0bE8nGXv5_n8z-fRgwDbraEd9pOaLU9f_Pxx_goW_EuMOMHf7lWLs7MOq7QwrwDu-DK5ErNFWMg3gP1vPRYWQuR9rnLrxJFvihT-23Dn3-WTI5LR6JgObpDrA6Kk094EbpJLob5FrvY9Js9vk1-fItMSDNKP2FvHGodbLPSo8di5K1CAmyBq8GmNc11LTbcMXZtgSw8XPJ26df8z2lR0_0KNOjW1p7P6Ytk6PaGYCGjj0PGH_uQOmR28Pdk_TIa2C4mD8GeVZAEwLFcsh6g59ZUy2lfG5TKrrAlMWq5cyk2VATbIBRe585V0XBqRKl0pbsVdslM3dbhPKMALzwsrDObvlA3KclEEo5QG4FQwMyF7a4GXbuAkx9YYpyXEJqiiMqqoRBWVUUUT8nwz43vPx_GPe1-jDjf3IZN2vNAsv5TDwiwVUgoKq5jIVMaZ0z41TkvlZe5ScPET8mRtASWsPBScqUPTtSVDHmeRFWkxIfd6i9g8CmJ9wJVMTkgxspXRu4xH6sXXyO4NVqozBs991lvVaMqbxedpfP22K5ngOhcP_seffEiuodhwz5qxR2RntezCYwBbK7sbNyng-G7OduN6-g0cYiyM |
linkProvider | Scholars Portal |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Probiotic+Lactobacilli+Modulate+Staphylococcus+aureus-Induced+Activation+of+Conventional+and+Unconventional+T+cells+and+NK+cells&rft.jtitle=Frontiers+in+immunology&rft.au=Maria+A+Johansson&rft.au=Sophia+Bj%C3%B6rkander&rft.au=Manuel+Mata+Forsberg&rft.au=Khaleda+Rahman+Qazi&rft.date=2016-07-11&rft.pub=Frontiers+Media+S.A&rft.eissn=1664-3224&rft.volume=7&rft_id=info:doi/10.3389%2Ffimmu.2016.00273&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_851033b81348421c9d0ac968d65c0341 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-3224&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-3224&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-3224&client=summon |