dc.contributor.author
Ekmekciu, Ira
dc.contributor.author
von Klitzing, Eliane
dc.contributor.author
Fiebiger, Ulrike
dc.contributor.author
Neumann, Christian
dc.contributor.author
Bacher, Petra
dc.contributor.author
Scheffold, Alexander
dc.contributor.author
Bereswill, Stefan
dc.contributor.author
Heimesaat, Markus M.
dc.date.accessioned
2018-06-08T10:31:05Z
dc.date.available
2017-05-29T11:24:13.681Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/20578
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-23879
dc.description.abstract
There is compelling evidence linking the commensal intestinal microbiota with
host health and, in turn, antibiotic induced perturbations of microbiota
composition with distinct pathologies. Despite the attractiveness of probiotic
therapy as a tool to beneficially alter the intestinal microbiota, its
immunological effects are still incompletely understood. The aim of the
present study was to assess the efficacy of the probiotic formulation VSL#3
consisting of eight distinct bacterial species (including Streptococcus
thermophilus, Bifidobacterium breve, B. longum, B. infantis, Lactobacillus
acidophilus, L. plantarum, L. paracasei, and L. delbrueckii subsp. Bulgaricus)
in reversing immunological effects of microbiota depletion as compared to
reassociation with a complex murine microbiota. To address this, conventional
mice were subjected to broad-spectrum antibiotic therapy for 8 weeks and
perorally reassociated with either VSL#3 bacteria or a complex murine
microbiota. VSL#3 recolonization resulted in restored CD4+ and CD8+ cell
numbers in the small and large intestinal lamina propria as well as in B220+
cell numbers in the former, whereas probiotic intervention was not sufficient
to reverse the antibiotic induced changes of respective cell populations in
the spleen. However, VSL#3 application was as efficient as complex microbiota
reassociation to attenuate the frequencies of regulatory T cells, activated
dendritic cells and memory/effector T cells in the small intestine, colon,
mesenteric lymph nodes, and spleen. Whereas broad-spectrum antibiotic
treatment resulted in decreased production of cytokines such as IFN-γ, IL-17,
IL-22, and IL-10 by CD4+ cells in respective immunological compartments, VSL#3
recolonization was sufficient to completely recover the expression of the
anti-inflammatory cytokine IL-10 without affecting pro-inflammatory mediators.
In summary, the probiotic compound VSL#3 has an extensive impact on mucosal,
peripheral, and systemic innate as well as adaptive immunity, exerting
beneficial anti-inflammatory effects in intestinal as well as systemic
compartments. Hence, VSL#3 might be considered a therapeutic immunomodulatory
tool following antibiotic therapy.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
innate and adaptive immunity
dc.subject
fecal microbiota transplantation
dc.subject
secondary abiotic (gnotobiotic) mice
dc.subject
mucosal and peripheral and central immunity
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
The Probiotic Compound VSL#3 Modulates Mucosal, Peripheral, and Systemic
Immunity Following Murine Broad-Spectrum Antibiotic Treatment
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Front. Cell. Infect. Microbiol. - 7 (2017), Artikel Nr. 167
dcterms.bibliographicCitation.doi
10.3389/fcimb.2017.00167
dcterms.bibliographicCitation.url
http://doi.org/10.3389/fcimb.2017.00167
refubium.affiliation
Charité - Universitätsmedizin Berlin
de
refubium.mycore.fudocsId
FUDOCS_document_000000027075
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000008244
dcterms.accessRights.openaire
open access