| Literature DB >> 29603613 |
Anat R Tambur1, Patricia Campbell2, Frans H Claas3, Sandy Feng4, Howard M Gebel5, Annette M Jackson6, Roslyn B Mannon7, Elaine F Reed8, Kathryn Tinckam9, Medhat Askar10, Anil Chandraker11, Patricia P Chang12, Monica Colvin13, Anthony-Jake Demetris14, Joshua M Diamond15, Anne I Dipchand9, Robert L Fairchild16, Mandy L Ford5, John Friedewald1, Ronald G Gill17, Denis Glotz18, Hilary Goldberg11, Ramsey Hachem19, Stuart Knechtle20, Jon Kobashigawa21, Deborah J Levine22, Joshua Levitsky1, Michael Mengel2, Edgar Milford11, Kenneth A Newell5, Jacqueline G O'Leary23, Scott Palmer20, Parmjeet Randhawa14, John Smith24, Laurie Snyder20, Randall C Starling16, Stuart Sweet19, Timucin Taner25, Craig J Taylor26, Steve Woodle27, Adriana Zeevi14, Peter Nickerson28.
Abstract
The presence of preexisting (memory) or de novo donor-specific HLA antibodies (DSAs) is a known barrier to successful long-term organ transplantation. Yet, despite the fact that laboratory tools and our understanding of histocompatibility have advanced significantly in recent years, the criteria to define presence of a DSA and assign a level of risk for a given DSA vary markedly between centers. A collaborative effort between the American Society for Histocompatibility and Immunogenetics and the American Society of Transplantation provided the logistical support for generating a dedicated multidisciplinary working group, which included experts in histocompatibility as well as kidney, liver, heart, and lung transplantation. The goals were to perform a critical review of biologically driven, state-of-the-art, clinical diagnostics literature and to provide clinical practice recommendations based on expert assessment of quality and strength of evidence. The results of the Sensitization in Transplantation: Assessment of Risk (STAR) meeting are summarized here, providing recommendations on the definition and utilization of HLA diagnostic testing, and a framework for clinical assessment of risk for a memory or a primary alloimmune response. The definitions, recommendations, risk framework, and highlighted gaps in knowledge are intended to spur research that will inform the next STAR Working Group meeting in 2019.Entities:
Keywords: alloantibody; clinical research/practice; clinical trial design; guidelines; histocompatibility; immunobiology; monitoring: immune; sensitization
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Year: 2018 PMID: 29603613 DOI: 10.1111/ajt.14752
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086