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  • Articles: DFG German National Licenses  (2)
  • Cyclosporine  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Research in experimental medicine 188 (1988), S. 305-317 
    ISSN: 1433-8580
    Keywords: Immune tolerance ; Thymocyte subpopulations ; Monoclonal antibodies ; Differentiation ratio ; Cyclosporine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary LEW with BDE-heart graft received 0 (control), 15, or 40 mg cyclosporine (CsA)/kg b. wt. per day. On postoperative days 3, 5, 7, 10, and 14 in four animals each weight and cell count of thymus and spleen were determined, and thymus and spleen cell subpopulations were examined with monoclonal antibodies. The same tests were performed in FiS heart graft recipients without immunosuppression and ungrafted LEW which received 15 or 40 mg CsA. We expressed alterations in thymocyte subpopulations by using the differentiation ratio (DR), i.e., differentiated in % of all T-cells and by the ratio of helper to suppressor/cytotoxic T-cells (Th-Ts/c). In graft rejection the thymus showed no significant change in DR or Th-Ts/c. However, in the CsA-induced graft tolerance DR was elevated and at the same time Th-Ts/c declined, both showing maximum values on days 5 and 7 and a return to normal thereafter. FiS graft recipients exhibited similar thymus alterations as tolerant recipients, but less marked. In CsA-treated ungrafted LEW, elevation of DR was slight after 15 mg but very strong after 40 mg CsA (93% on day 7), and it did not return to normal in the latter group. Th-Ts/c was decreased in these ungrafted animals, but not as strongly as in tolerant graft recipients. Such thymus alterations were not observed in graft rejection. Spleen weights were strongly increased in graft rejection and unchanged in graft tolerance. Splenic Ts/c and Th-Ts/s were increased in CsA-treated tolerant recipients but not in graft rejection. We conclude that elevation of DR and decline of thymic Th-Ts/c in the initial postoperative phase are indicators of graft tolerance in organ recipients.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Research in experimental medicine 185 (1985), S. 245-252 
    ISSN: 1433-8580
    Keywords: Liver ; Thymus ; Immune regulatory factor ; Cyclosporine ; Prednisolone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary This study was carried out to clarify the mechanism of the immune regulatory effect of factors which were liberated from the ischemic damaged liver. By occlusion of the hepatic vessels (hepatic artery and portal vein) for 40min daily during 5 days to induce the ischemic damage of the liver, reduced thymus weight (50 ± 5 mg; control, 274 ± 23 mg) and cell count (0.7 ± 0.3 × 107; control, 3.5 ± 0.3 × 108) and complete differentiation of thymocytes were observed, i.e., helper cells reacting to monoclonal antibody W3/25 were 34 ± 8% and suppressor/cytotoxic cells to OX-8, 49 ± 5% (in control W3/25:89 ± 1%, OX-8:89 ± 1%). These quantitative and qualitative changes of thymocytes were correspondent to those of animals treated with 40mg CsA/kg per day for 5 days; however, medication with 10mg prednisolone/day 5 times could not induce any alteration of thymocyte subpopulation (W3/25:89 ± 1%, OX-8:87 ± 1%) although the weight and cell count decreased to 92 ± 8mg and 4.1 ± 0.6 × 107, respectively. Furthermore, 5 days after liver allotransplantation (BDE to LEW), the weight and cell count of the thymus were extremely reduced (58 ± 6 mg, 2.7 ± 0.2 × 107), and thymocyte differentiation was observed (W3/25:56.6%, OX-8:61 ± 11%). On the other hand, in heart transplantation the atrophy of the thymus was not so strong (105 ± 28mg, 1.3 ± 0.6 × 108), and there was no change in the subpopulation (W3/25:89 ± 2%, OX-8:88 ± 1%). We conclude from these results that the liver should have an immune regulatory factor similar to CsA, which could stimulate formation of suppressor cells in the thymus, but different from prednisolone. This factor might be liberated from the damaged liver and responsible for immunologic benefit of hepatic grafts.
    Type of Medium: Electronic Resource
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