In solid organ transplantation the HLA-A, -B, -DR, -DQ donor-recipient matching results are insufficient for highly sensitized patient. In fact, solid phase single antigen assays, used to define HLA antibodies in transplant candidates, show the presence of antibodies specific for all HLA molecules. Thus, an extended HLA typing of deceased donor is necessary to improve selection of the most suitable transplant candidate. Until July 2016, in our laboratory all donors were typed for HLA-A,-B,-C,-DR,-DQ loci by PCR-SSP technique; when a sensitized patient was selected, the donor typing was prospectively enlarged to pertinent HLA molecules. To simplify this procedure and improves organ allocation we introduced the new RT PCR-SSP technique, based on an innovative chemistry (Linkage Bioscience Inc.), it enables us to provide intermediate resolution typing of 11 HLA loci, in less than 90 minutes. Allele-specific amplification combined with SYBR Green and real-time PCR instruments are used to detect amplification products and to collect dissociation data for automatic interpretation by SureTyper software.Since August 2016, 76 potential deceased donors were typed by this technique. No allelic ambiguities were evidenced but rather high resolution typing were obtained in several cases: 11 HLA-A alleles, 55 HLA-B alleles, 48 HLA-C alleles, 41 HLA-DRB1 alleles, 37 HLA-DRB345 alleles, 20 HLA-DQA1 alleles, 30 HLA-DQB1 alleles, one HLA-DPA1 allele, and 50 HLA-DPB1 alleles. Moreover, the extended HLA typing obtained by RT PCR-SSP avoided additional HLA-C,-DRB1, -DQA1 and-DPB1 typing in 12 cases (15,8%) and allowed to define donor molecules against which 10 patients (13,2%) showed preformed high fluorescence intensity antibodies (MFI >5000).In conclusion, RT PCR-SSP is less hands-on and, considering the number of typed HLA loci, cheaper than traditional PCR-SSP techniques. The extended donor HLA typing gives useful information for a more precise pre-transplant virtual crossmatch and for a better donor-recipient selection to improve clinical transplant outcome.

FEASIBLE EXTENDED HLA TYPING OF DECEASED DONORS IN SOLID ORGAN TRANSPLANTATION

Ozzella Giuseppina
Primo
;
Poggi Elvira;Piazza Antonina
2017

Abstract

In solid organ transplantation the HLA-A, -B, -DR, -DQ donor-recipient matching results are insufficient for highly sensitized patient. In fact, solid phase single antigen assays, used to define HLA antibodies in transplant candidates, show the presence of antibodies specific for all HLA molecules. Thus, an extended HLA typing of deceased donor is necessary to improve selection of the most suitable transplant candidate. Until July 2016, in our laboratory all donors were typed for HLA-A,-B,-C,-DR,-DQ loci by PCR-SSP technique; when a sensitized patient was selected, the donor typing was prospectively enlarged to pertinent HLA molecules. To simplify this procedure and improves organ allocation we introduced the new RT PCR-SSP technique, based on an innovative chemistry (Linkage Bioscience Inc.), it enables us to provide intermediate resolution typing of 11 HLA loci, in less than 90 minutes. Allele-specific amplification combined with SYBR Green and real-time PCR instruments are used to detect amplification products and to collect dissociation data for automatic interpretation by SureTyper software.Since August 2016, 76 potential deceased donors were typed by this technique. No allelic ambiguities were evidenced but rather high resolution typing were obtained in several cases: 11 HLA-A alleles, 55 HLA-B alleles, 48 HLA-C alleles, 41 HLA-DRB1 alleles, 37 HLA-DRB345 alleles, 20 HLA-DQA1 alleles, 30 HLA-DQB1 alleles, one HLA-DPA1 allele, and 50 HLA-DPB1 alleles. Moreover, the extended HLA typing obtained by RT PCR-SSP avoided additional HLA-C,-DRB1, -DQA1 and-DPB1 typing in 12 cases (15,8%) and allowed to define donor molecules against which 10 patients (13,2%) showed preformed high fluorescence intensity antibodies (MFI >5000).In conclusion, RT PCR-SSP is less hands-on and, considering the number of typed HLA loci, cheaper than traditional PCR-SSP techniques. The extended donor HLA typing gives useful information for a more precise pre-transplant virtual crossmatch and for a better donor-recipient selection to improve clinical transplant outcome.
2017
FARMACOLOGIA TRASLAZIONALE - IFT
Inglese
Giuseppina Ozzella, Elvira Poggi, Silvia Sinopoli, Damiano Colasante, Maria Rosaria Fazio, Annarita Manfreda, Lucia Spano, Antonio Giuseppe Bianculli, Antonina Piazza.
Editor-in-Chief: Steven GE Marsh, Anthony Nolan Research Institute, Royal Free Hospital London NW3 2QG United Kingdom E: [email protected] Section Editors: Katharina Fleischhauer, Germany - HLA function, John Hammond, UK - Non-human MHC, Sebastiaan Heidt, The Netherlands - HLA in solid organ transplantation, Jill Hollenbach, USA - HLA and Disease, Neema Mayor, UK - HLA and diagnostic technology, Alicia Sanchez-Mazas,, Switzerland - HLA polymorphism in populations, James Robinson, UK - Bioinformatics, Luca Vago, Italy - HLA in hematopoietic stem cell transplantation, Carlos Vilches, Spain - KIR polymorphism, structure and function
HLA Volume 89, Issue 6 _ Special Issue: Abstracts for the 31st European Immunogenetics and Histocompatibility Conference (EFI) 25th Annual Meeting of the German Society for Immunogenetics (DGI)
HLA
Contributo
31st European Immunogenetics and Histocompatibility Conference (EFI) 25th Annual Meeting of the German Society for Immunogenetics (DGI)
89
Issue 6
409
409
1
https://onlinelibrary.wiley.com/toc/20592310/2017/89/6
John Wiley & Sons, Ltd.
Hoboken
STATI UNITI D'AMERICA
Comitato scientifico
30/05/2017-2/06/2017
Mannheim/Heidelberg, Germany
Internazionale
Organ Transplantation
HLA typing
HLA matching
RT PCR SSP.
Ruolo svolto: autore principale, primo autore, corresponding author
9
info:eu-repo/semantics/conferenceObject
open
274
04 Contributo in convegno::04.02 Abstract in Atti di convegno
Ozzella, Giuseppina; Poggi, Elvira; Sinopoli, Silvia; Colasante, Damiano; Fazio Maria, Rosaria; Manfreda, Annarita; Spano, Lucia; Bianculli Antonio, G...espandi
   Prestazioni diagnostiche nei confronti dell’Ospedale Pediatrico Bambino Gesù (OPBG)
   Ospedale Pediatrico Bambino Gesù - IRCCS
   Prot. 460/2014 del 30/09/2014, n. protocollo: 0002974
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/407541
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