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MHC expression and chemokine production in the murine vagina following intra-vaginal administration of ligands to toll-like receptors 3, 7 and 9

Nurkkala, Merja, 1966 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning,Institute of Medicine, Department of Rheumatology and Inflammation Research
Nordström, Inger, 1958 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning,Institute of Medicine, Department of Rheumatology and Inflammation Research
Telemo, Esbjörn, 1953 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning,Institute of Medicine, Department of Rheumatology and Inflammation Research
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Eriksson, Kristina, 1962 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning,Institute of Medicine, Department of Rheumatology and Inflammation Research
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 (creator_code:org_t)
Elsevier BV, 2007
2007
Engelska.
Ingår i: J Reprod Immunol. - : Elsevier BV. - 0165-0378. ; 73:2, s. 148-57
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The expression of MHC class I, MHC class II and the chemokines IP-10, MIP-1alpha, RANTES, fractalkine and I-TAC has been analyzed after intra-vaginal treatment with three synthetic toll-like receptors (TLR) agonists-double-stranded RNA (poly I:C), imiquimod and CpG-rich oligonucleotides (CpG-ODN). These compounds act mainly through TLR3, TLR7 and TLR9, respectively. CpG-ODN induced an accumulation of leucocytes in the vagina, and a strong up-regulation of MHC class I expression on both leucocytes and epithelial cells. Imiquimod and poly I:C induced a weak MHC class I up-regulation in the epithelium but not in the lamina propria. Neither treatment had any profound effect on expression of MHC class II on epithelial cells but poly I:C and to a lesser extent CpG-ODN, up-regulated MHC class II staining intensity which, in the case of CpG-ODN, treatment, was associated with a strong accumulation of CD11c-positive dendritic cells. All three treatments induced an early (8h) but transient IP-10 response. Imiquimod and CpG-ODN, but not poly I:C induced an early MIP-1alpha response which remained for at least 7 days in CpG-ODN-treated animals but not in imiquimod-treated mice. Poly I:C and CpG-ODN, but not imiquimod, induced significant levels of RANTES at different time-points post-treatment. None of the treatments induced any significant changes in the levels of fractalkine, I-TAC or IFN-alpha. These studies have implications for the manipulation of the genital immune response and also improving the outcome of vaginal immunotherapy.

Nyckelord

Adjuvants
Immunologic/*pharmacology
Aminoquinolines/pharmacology
Animals
Antigens
CD11c/immunology/metabolism
Chemokines/*biosynthesis/immunology
Dendritic Cells/cytology/immunology/metabolism
Female
Histocompatibility Antigens/*biosynthesis/immunology
Interferon Inducers/*pharmacology
Leukocytes/cytology/immunology/metabolism
Ligands
Mice
Oligodeoxyribonucleotides/*pharmacology
Poly I-C/*pharmacology
Time Factors
Toll-Like Receptors/*agonists/immunology/metabolism
Up-Regulation/drug effects/immunology
Vagina/cytology/immunology/*metabolism

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