Barcelona Consensus on Biomarker-Based Immunosuppressive Drugs Management in Solid Organ Transplantation

被引:74
|
作者
Brunet, Merce [1 ]
Shipkova, Maria [2 ]
van Gelder, Teun [3 ,4 ]
Wieland, Eberhard [2 ]
Sommerer, Claudia [5 ]
Budde, Klemens [6 ]
Haufroid, Vincent [7 ,8 ]
Christians, Uwe [9 ]
Lopez-Hoyos, Marcos [10 ]
Barten, Markus J. [11 ]
Bergan, Stein [12 ]
Picard, Nicolas [13 ]
Millan Lopez, Olga [1 ]
Marquet, Pierre [13 ]
Hesselink, Dennis A. [14 ]
Noceti, Ofelia [13 ,15 ]
Pawinski, Tomasz [16 ]
Wallemacq, Pierre [7 ,8 ]
Oellerich, Michael [17 ]
机构
[1] Univ Barcelona, Hosp Clin Barcelona, Biomed Diagnost Ctr CDB, Pharmacol & Toxicol Lab, Villarroel 170, E-08036 Barcelona, Spain
[2] Klinikum Stuttgart, Zent Inst Klin Chem & Lab Med, Stuttgart, Germany
[3] Univ Med Ctr Rotterdam, Erasmus MC, Dept Internal Med, Rotterdam, Netherlands
[4] Univ Med Ctr Rotterdam, Erasmus MC, Dept Hosp Pharm, Rotterdam, Netherlands
[5] Heidelberg Univ, Univ Hosp Heidelberg & Mannheim, Dept Nephrol, Heidelberg, Germany
[6] Charite Univ Med Berlin, Med Klin Schwerpunkt Nephrol, Berlin, Germany
[7] Catholic Univ Louvain, Louvain Ctr Toxicol & Appl Pharmacol, Inst Rech Expt & Clin, Clin Univ St Luc, B-1200 Brussels, Belgium
[8] Catholic Univ Louvain, Clin Univ St Luc, Dept Clin Chem, B-1200 Brussels, Belgium
[9] Univ Colorado, Dept Anesthesiol, Clin Res & Dev C42, Aurora, CO USA
[10] Hosp Univ Marques de Valdecilla IDIVAL, Immunol Lab, Santander, Spain
[11] Univ Heart Ctr Hamburg, Dept Cardiovasc Surg, Hamburg, Germany
[12] Oslo Univ Hosp, Dept Pharmacol, Oslo, Norway
[13] Univ Limoges, CHU Limoges, INSERM U850, F-87065 Limoges, France
[14] Univ Med Ctr Rotterdam, Erasmus MC, Dept Internal Med, Div Nephrol & Renal Transplantat, Rotterdam, Netherlands
[15] Hosp Cent Fuerzas Armadas, Natl Ctr Liver Transplantat, Liver Dis Dept, Montevideo, Uruguay
[16] Med Univ Warsaw, Fac Pharm, Dept Drug Chem, Warsaw, Poland
[17] Univ Gottingen, Univ Med Ctr Gottingen, Dept Clin Pharmacol, D-37073 Gottingen, Germany
关键词
biomarkers of immunosuppression; immunologic biomarkers; consensus; assessment of acute rejection; graft outcome; graft injury; pharmacogenetics; pharmacokinetics; pharmacodynamics; personalized immunosuppression; solid organ transplantation; REGULATORY T-CELLS; BLOOD MONONUCLEAR-CELLS; 5'-MONOPHOSPHATE DEHYDROGENASE-ACTIVITY; TACROLIMUS TROUGH CONCENTRATIONS; CALCINEURIN PHOSPHATASE-ACTIVITY; IMPDH1 GENE POLYMORPHISMS; MESSENGER-RNA EXPRESSION; PREDICTS ACUTE REJECTION; TERM GRAFT-SURVIVAL; RENAL-TRANSPLANT;
D O I
10.1097/FTD.0000000000000287
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
With current treatment regimens, a relatively high proportion of transplant recipients experience underimmunosuppression or overimmunosuppression. Recently, several promising biomarkers have been identified for determining patient alloreactivity, which help in assessing the risk of rejection and personal response to the drug; others correlate with graft dysfunction and clinical outcome, offering a realistic opportunity for personalized immunosuppression. This consensus document aims to help tailor immunosuppression to the needs of the individual patient. It examines current knowledge on biomarkers associated with patient risk stratification and immunosuppression requirements that have been generally accepted as promising. It is based on a comprehensive review of the literature and the expert opinion of the Biomarker Working Group of the International Association of Therapeutic Drug Monitoring and Clinical Toxicology. The quality of evidence was systematically weighted, and the strength of recommendations was rated according to the GRADE system. Three types of biomarkers are discussed: (1) those associated with the risk of rejection (alloreactivity/tolerance), (2) those reflecting individual response to immunosuppressants, and (3) those associated with graft dysfunction. Analytical aspects of biomarker measurement and novel pharmacokinetic-pharmacodynamic models accessible to the transplant community are also addressed. Conventional pharmacokinetic biomarkers may be used in combination with those discussed in this article to achieve better outcomes and improve long-term graft survival. Our group of experts has made recommendations for the most appropriate analysis of a proposed panel of preliminary biomarkers, most of which are currently under clinical evaluation in ongoing multicentre clinical trials. A section of Next Steps was also included, in which the Expert Committee is committed to sharing this knowledge with the Transplant Community in the form of triennial updates.
引用
收藏
页码:S1 / S20
页数:20
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