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Implementation of a Protocol for ABO-incompatible kidney transplantation--a three-center experience with 60 consecutive transplantations

Tydén, Gunnar (författare)
Karolinska Institutet
Donauer, Johannes (författare)
Wadström, Jonas (författare)
Uppsala universitet,Transplantationskirurgi
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Kumlien, Gunilla (författare)
Karolinska Institutet
Wilpert, Jochen (författare)
Nilsson, Thomas (författare)
Uppsala universitet,Transplantationskirurgi
Genberg, Helena (författare)
Karolinska Institutet
Pisarski, Przemislaw (författare)
Tufveson, Gunnar (författare)
Uppsala universitet,Transplantationskirurgi
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 (creator_code:org_t)
Ovid Technologies (Wolters Kluwer Health), 2007
2007
Engelska.
Ingår i: Transplantation. - : Ovid Technologies (Wolters Kluwer Health). - 0041-1337 .- 1534-6080. ; 7, s. 157-158
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background. A new protocol for ABO-incompatible kidney transplantation has recently been introduced. We report here on the joint experience of the implementation in Stockholm and Uppsala, Sweden and Freiburg, Germany. Methods. The new protocol utilizes antigen-specific immunoadsorption to remove existing ABO-antibodies, rituximab, and intravenous immunoglobulin to prevent the rebound of antibodies, and conventional tacrolimus, mycophenolate-mofetil, and prednisolone immunosuppression. Sixty consecutive ABO-incompatible kidney transplantations were included in the study. The outcome is compared with the results of 274 ABO-compatible live donor transplantations performed during the same period. Results. Two of the ABO-incompatible grafts have been lost (non-compliance and death with functioning graft). All the remaining 58 grafts had good renal function at a follow-up of up to 61 months. We did not observe any late rebound of antibodies and there were no humoral rejections. Graft survival was 97% for the ABO-incompatible compared with 95% for the ABO-compatible. Patient survival was 98% in both groups. There was a significant variation in preoperative A/B-antibody titer between the centers, with a median 1:8 in Uppsala, median 1:32 in Stockholm and median 1:128 in Freiburg. More preoperative antibody adsorptions were therefore needed in Freiburg than in Stockholm and Uppsala. Conclusions. The new protocol was easily implemented and there were no graft losses that could be related to ABO-incompatibility. A significant inter-institutional variation in the measurement of anti-AB-antibodies was found, having a substantial impact on the number of immunoadsorptions and consequently on the total cost for the procedure. A standardized fluorescence-activated cell sorting technique for antibody quantification is much needed.

Nyckelord

ABO-incompatible
Antigen-specific
Immunoadsorption
Rituximab
MEDICINE
MEDICIN

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