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  • 1
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Gene Structure and Expression 1130 (1992), S. 333-335 
    ISSN: 0167-4781
    Schlagwort(e): (B. subtilis) ; 1-Methyladenosine ; 5-Methoxyuridine ; Modified nucleoside ; Serine tRNA
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Biologie , Chemie und Pharmazie , Medizin , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1434-0879
    Schlagwort(e): Key words Kidney transplantation ; Dendritic cell ; Antigen presentation ; CTLA4Ig ; Donor-specific tolerance
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Donor dendritic cells (DCs) within allografts initiate the induction of an allospecific T cell response, while an abortive alloantigen presentation by DCs may induce allospecific unresponsiveness. We thus investigated the tolerogenic effect of donor DCs that were made incompetent in alloantigen presentation by treatment of CTLA4Ig. When we treated rats with donor DCs (2 × 106/rat i.v.) on the preoperative day, nine rejected allografts in an accelerated manner (5.0 ± 2.2 vs. 8.2 ± 1.6 days in the control group). Preoperative inoculation of DCs pulsed with CTLA4Ig, a procedure which suppresses an allogeneic mixed lymphocyte reaction (MLR), also provoked an accelerated rejection (5.6 ± 1.7 days). When DCs and CTLA4Ig (500 μg/rat i.p. on days −9, −7 and −5) were concomitantly inoculated, allograft survival was significantly prolonged (〉38.7 ± 40.0 days); a preoperative CTLA4Ig inoculation alone failed to do so (7.5 ± 1.2 days). Long-term graft survivors tolerated skin grafts from the donor but not from those from a third party. These results indicate that abortive alloantigen presentation by donor DCs, upon which an accessory signal pathway is suppressed by CTLA4Ig, leads to prolonged graft survival and donor-specific tolerance.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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