Similar Microvascular Inflammation and Tubulointerstitial Injury in ABO-Incompatible and Matched ABO-Compatible Kidney Allografts
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu srovnávací studie, časopisecké články
PubMed
29880350
DOI
10.1016/j.transproceed.2018.02.063
PII: S0041-1345(18)30214-8
Knihovny.cz E-zdroje
- MeSH
- ABO systém krevních skupin imunologie MeSH
- alografty imunologie zásobování a distribuce MeSH
- biopsie MeSH
- desenzibilizace imunologická MeSH
- dospělí MeSH
- histokompatibilita imunologie MeSH
- hodnoty glomerulární filtrace MeSH
- ledviny krevní zásobení imunologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mikrocévy MeSH
- nekompatibilita krevních skupin komplikace imunologie MeSH
- rejekce štěpu imunologie MeSH
- transplantace ledvin metody MeSH
- vaskulitida imunologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- srovnávací studie MeSH
- Názvy látek
- ABO systém krevních skupin MeSH
ABO-incompatible (ABOi) kidney transplantation represents a viable tool to increase the donor pool for kidney transplantation, however, increased alloimmune response has been debated. The early outcomes of 25 low-risk ABOi kidney transplant recipients were compared with thoroughly matched 50 ABO-compatible (ABOc) ones. The matching process was based on gender and age of recipients and immunologic parameters, such as panel reactive antibodies, number of human leukocyte antigen mismatches, and transplantation era. Three-month protocol kidney graft biopsy Banff scores and 1-year clinical outcomes were compared. Apart from C4d positivity, no statistically significant differences were found regarding the Banff scores between the two groups. Similarly, microvascular inflammation and tubulointerstitial injury revealed no differences either. The eGFR at 3 months and 1 year was similar in both groups. In conclusion, blood group incompatibility yields no additional microvascular and tubulointerstitial graft injury if desensitization protocol was applied to low-risk kidney transplant recipients.
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