Antibody-mediated rejection of arterialised venous allografts is inhibited by immunosuppression in rats
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24618652
PubMed Central
PMC3949981
DOI
10.1371/journal.pone.0091212
PII: PONE-D-13-40263
Knihovny.cz E-zdroje
- MeSH
- alografty imunologie MeSH
- arterie transplantace MeSH
- buněčná cytotoxicita závislá na protilátkách účinky léků imunologie MeSH
- časové faktory MeSH
- imunosupresivní léčba * MeSH
- isoprotilátky imunologie MeSH
- krysa rodu Rattus MeSH
- MHC antigeny I. třídy imunologie metabolismus MeSH
- MHC antigeny II. třídy imunologie metabolismus MeSH
- podskupiny lymfocytů imunologie metabolismus MeSH
- rejekce štěpu farmakoterapie imunologie MeSH
- slezina cytologie imunologie metabolismus MeSH
- transplantační imunologie MeSH
- vény imunologie transplantace MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- isoprotilátky MeSH
- MHC antigeny I. třídy MeSH
- MHC antigeny II. třídy MeSH
OBJECTIVES AND DESIGN: We determined in a rat model (1) the presence and dynamics of alloantibodies recognizing MHC complexes on quiescent Brown-Norway (BN) splenic cells in the sera of Lewis (LEW) recipients of Brown-Norway iliolumbar vein grafts under tacrolimus immunosuppression; and (2) the presence of immunoglobulins in the wall of acute rejected vein allografts. MATERIALS AND METHODS: Flow cytometry was used for the analysis of day 0, 14 and 30 sera obtained from Lewis recipients of isogeneic iliolumbar vein grafts (group A) or Brown-Norway grafts (group B, C) for the presence of donor specific anti-MHC class I and II antibodies. Tacrolimus 0.2 mg/kg daily was administered from day 1 to day 30 (group C). Histology was performed on day 30. RESULTS: Sera obtained preoperatively and on day 30 were compared in all groups. The statistically significant decrease of anti MHC class I and II antibody binding was observed only in allogenic non-immunosuppressed group B (splenocytes: MHC class I - day 0 (93% ± 7% ) vs day 30 (66% ± 7%), p = 0.02, MHC class II - day 0 (105% ± 3% ) vs day 30 (83% ± 5%), p = 0.003; B-cells: MHC class I - day 0 (83% ± 5%) vs day 30 (55% ± 6%), p = 0.003, MHC class II - day 0 (101% ± 1%) vs day 30 (79% ± 6%), p = 0.006; T-cells: MHC class I - day 0 (71% ± 7%) vs day 30 (49% ± 5%), p = 0.04). No free clusters of immunoglobulin G deposition were detected in any experimental group. CONCLUSION: Arterialized venous allografts induce strong donor-specific anti-MHC class I and anti-MHC class II antibody production with subsequent immune-mediated destruction of these allografts with no evidence of immunoglobulin G deposition. Low-dose tacrolimus suppress the donor-specific antibody production.
Translational Centre for Regenerative Medicine University of Leipzig Leipzig Germany
Transplant Surgery Department Institute for Clinical und Experimental Medicine Prague Czech Republic
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