Precision transplant pathology
Transplant pathology contributes substantially to personalized treatment of organ allograft recipients. Rapidly advancing next-generation human leukocyte antigen (HLA) sequencing and pathology are enhancing the abilities to improve donor/recipient matching and allograft monitoring. The present revie...
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Published in: | Current opinion in organ transplantation Vol. 25; no. 4; pp. 412 - 419 |
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01-08-2020
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Abstract | Transplant pathology contributes substantially to personalized treatment of organ allograft recipients. Rapidly advancing next-generation human leukocyte antigen (HLA) sequencing and pathology are enhancing the abilities to improve donor/recipient matching and allograft monitoring.
The present review summarizes the workflow of a prototypical patient through a pathology practice, highlighting histocompatibility assessment and pathologic review of tissues as areas that are evolving to incorporate next-generation technologies while emphasizing critical needs of the field.
Successful organ transplantation starts with the most precise pratical donor-recipient histocompatibility matching. Next-generation sequencing provides the highest resolution donor-recipient matching and enables eplet mismatch scores and more precise monitoring of donor-specific antibodies (DSAs) that may arise after transplant. Multiplex labeling combined with hand-crafted machine learning is transforming traditional histopathology. The combination of traditional blood/body fluid laboratory tests, eplet and DSA analysis, traditional and next-generation histopathology, and -omics-based platforms enables risk stratification and identification of early subclinical molecular-based changes that precede a decline in allograft function. Needs include software integration of data derived from diverse platforms that can render the most accurate assessment of allograft health and needs for immunosuppression adjustments. |
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AbstractList | PURPOSE OF REVIEWTransplant pathology contributes substantially to personalized treatment of organ allograft recipients. Rapidly advancing next-generation human leukocyte antigen (HLA) sequencing and pathology are enhancing the abilities to improve donor/recipient matching and allograft monitoring.RECENT FINDINGSThe present review summarizes the workflow of a prototypical patient through a pathology practice, highlighting histocompatibility assessment and pathologic review of tissues as areas that are evolving to incorporate next-generation technologies while emphasizing critical needs of the field.SUMMARYSuccessful organ transplantation starts with the most precise pratical donor-recipient histocompatibility matching. Next-generation sequencing provides the highest resolution donor-recipient matching and enables eplet mismatch scores and more precise monitoring of donor-specific antibodies (DSAs) that may arise after transplant. Multiplex labeling combined with hand-crafted machine learning is transforming traditional histopathology. The combination of traditional blood/body fluid laboratory tests, eplet and DSA analysis, traditional and next-generation histopathology, and -omics-based platforms enables risk stratification and identification of early subclinical molecular-based changes that precede a decline in allograft function. Needs include software integration of data derived from diverse platforms that can render the most accurate assessment of allograft health and needs for immunosuppression adjustments. Transplant pathology contributes substantially to personalized treatment of organ allograft recipients. Rapidly advancing next-generation human leukocyte antigen (HLA) sequencing and pathology are enhancing the abilities to improve donor/recipient matching and allograft monitoring. The present review summarizes the workflow of a prototypical patient through a pathology practice, highlighting histocompatibility assessment and pathologic review of tissues as areas that are evolving to incorporate next-generation technologies while emphasizing critical needs of the field. Successful organ transplantation starts with the most precise pratical donor-recipient histocompatibility matching. Next-generation sequencing provides the highest resolution donor-recipient matching and enables eplet mismatch scores and more precise monitoring of donor-specific antibodies (DSAs) that may arise after transplant. Multiplex labeling combined with hand-crafted machine learning is transforming traditional histopathology. The combination of traditional blood/body fluid laboratory tests, eplet and DSA analysis, traditional and next-generation histopathology, and -omics-based platforms enables risk stratification and identification of early subclinical molecular-based changes that precede a decline in allograft function. Needs include software integration of data derived from diverse platforms that can render the most accurate assessment of allograft health and needs for immunosuppression adjustments. |
Author | Wood-Trageser, Michelle A. Demetris, Anthony J. Randhawa, Parmjeet Zeevi, Adriana Lesniak, Drew Xu, Qinyong |
AuthorAffiliation | 2 Division of Liver and Transplantation Pathology, Department of Pathology, University of Pittsburgh, PA 15213, USA 1 Thomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, PA 15213 USA |
AuthorAffiliation_xml | – name: 2 Division of Liver and Transplantation Pathology, Department of Pathology, University of Pittsburgh, PA 15213, USA – name: 1 Thomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, PA 15213 USA |
Author_xml | – sequence: 1 givenname: Michelle A. surname: Wood-Trageser fullname: Wood-Trageser, Michelle A. organization: Thomas E. Starzl Transplantation Institute, University of Pittsburgh – sequence: 2 givenname: Qinyong surname: Xu fullname: Xu, Qinyong organization: Thomas E. Starzl Transplantation Institute, University of Pittsburgh – sequence: 3 givenname: Adriana surname: Zeevi fullname: Zeevi, Adriana organization: Thomas E. Starzl Transplantation Institute, University of Pittsburgh – sequence: 4 givenname: Parmjeet surname: Randhawa fullname: Randhawa, Parmjeet organization: Thomas E. Starzl Transplantation Institute, University of Pittsburgh – sequence: 5 givenname: Drew surname: Lesniak fullname: Lesniak, Drew organization: Thomas E. Starzl Transplantation Institute, University of Pittsburgh – sequence: 6 givenname: Anthony J. surname: Demetris fullname: Demetris, Anthony J. organization: Thomas E. Starzl Transplantation Institute, University of Pittsburgh |
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Snippet | Transplant pathology contributes substantially to personalized treatment of organ allograft recipients. Rapidly advancing next-generation human leukocyte... PURPOSE OF REVIEWTransplant pathology contributes substantially to personalized treatment of organ allograft recipients. Rapidly advancing next-generation... |
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SubjectTerms | Histocompatibility Testing HLA Antigens - immunology Humans Organ Transplantation - methods Precision Medicine - methods Tissue Donors Transplantation Immunology Transplantation, Homologous Transplants - immunology Transplants - pathology |
Title | Precision transplant pathology |
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