Search Results - "Pettigrew, Gavin"

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    T cell Allorecognition Pathways in Solid Organ Transplantation by Siu, Jacqueline H Y, Surendrakumar, Veena, Richards, James A, Pettigrew, Gavin J

    Published in Frontiers in immunology (05-11-2018)
    “…Transplantation is unusual in that T cells can recognize alloantigen by at least two distinct pathways: as intact MHC alloantigen on the surface of donor cells…”
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    Journal Article
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    Kidney donation after circulatory death (DCD): state of the art by Summers, Dominic M, Watson, Christopher J E, Pettigrew, Gavin J, Johnson, Rachel J, Collett, David, Neuberger, James M, Bradley, J Andrew

    Published in Kidney international (01-08-2015)
    “…The use of kidneys from controlled donation after circulatory death (DCD) donors has the potential to markedly increase kidney transplants performed. However,…”
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    Defining Delayed Graft Function after Renal Transplantation: Simplest Is Best by Mallon, Dermot H, Summers, Dominic M, Bradley, J Andrew, Pettigrew, Gavin J

    Published in Transplantation (27-11-2013)
    “…BACKGROUNDDelayed graft function (DGF) after renal transplantation can be diagnosed according to several different definitions, complicating comparison between…”
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    Allorecognition Unveiled: Integrating Recent Breakthroughs Into the Current Paradigm by Charmetant, Xavier, Pettigrew, Gavin J., Thaunat, Olivier

    Published in Transplant international (11-11-2024)
    “…In transplantation, genetic differences between donor and recipient trigger immune responses that cause graft rejection. Allorecognition, the process by which…”
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    Survival advantage for patients accepting the offer of a circulatory death liver transplant by Taylor, Rhiannon, Allen, Elisa, Richards, James A., Goh, Mingzheng A., Neuberger, James, Collett, David, Pettigrew, Gavin J.

    Published in Journal of hepatology (01-05-2019)
    “…[Display omitted] •Outcomes for DCD are inferior to DBD liver transplantation in the UK experience.•There is a survival advantage in accepting a DCD offer…”
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    A Systematic Review of Opt-out Versus Opt-in Consent on Deceased Organ Donation and Transplantation (2006–2016) by Ahmad, M. Usman, Hanna, Afif, Mohamed, Ahmed-Zayn, Schlindwein, Alex, Pley, Caitlin, Bahner, Ingrid, Mhaskar, Rahul, Pettigrew, Gavin J., Jarmi, Tambi

    Published in World journal of surgery (01-12-2019)
    “…Background Significant numbers of patients in the USA and UK die while waiting for solid organ transplant. Only 1–2% of deaths are eligible as donors with a…”
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    Preoperative Assessment of the Deceased-Donor Kidney: From Macroscopic Appearance to Molecular Biomarkers by Dare, Anna J, Pettigrew, Gavin J, Saeb-Parsy, Kourosh

    Published in Transplantation (27-04-2014)
    “…Variation in deceased-donor kidney quality can significantly affect outcomes after kidney transplantation. Suboptimal organ selection for a given recipient can…”
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    Passenger donor lymphocytes: To affinity and beyond by Manook, Miriam, Motallebzadeh, Reza, Pettigrew, Gavin J

    Published in Science translational medicine (21-09-2022)
    “…Graft-versus-host recognition by passenger donor lymphocytes within organ transplants can trigger host alloantibody production (Charmetant .)…”
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    Spoiling for a Fight: B Lymphocytes As Initiator and Effector Populations within Tertiary Lymphoid Organs in Autoimmunity and Transplantation by Alsughayyir, Jawaher, Pettigrew, Gavin J, Motallebzadeh, Reza

    Published in Frontiers in immunology (23-11-2017)
    “…Tertiary lymphoid organs (TLOs) develop at ectopic sites within chronically inflamed tissues, such as in autoimmunity and rejecting organ allografts. TLOs…”
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    Allorecognition Pathways in Transplant Rejection and Tolerance by Ali, Jason M, Bolton, Eleanor M, Bradley, J Andrew, Pettigrew, Gavin J

    Published in Transplantation (27-10-2013)
    “…With the advent of cellular therapies, it has become clear that the success of future therapies in prolonging allograft survival will require an intimate…”
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    Protection against renal ischemia-reperfusion injury in vivo by the mitochondria targeted antioxidant MitoQ by Dare, Anna J, Bolton, Eleanor A, Pettigrew, Gavin J, Bradley, J Andrew, Saeb-Parsy, Kourosh, Murphy, Michael P

    Published in Redox biology (01-08-2015)
    “…Ischemia-reperfusion (IR) injury to the kidney occurs in a range of clinically important scenarios including hypotension, sepsis and in surgical procedures…”
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    Kidney transplantation following uncontrolled donation after circulatory death by Summers, Dominic M., Pettigrew, Gavin J.

    Published in Current opinion in organ transplantation (01-04-2020)
    “…The identification and utilization of kidneys from uncontrolled donation after circulatory death (uDCD) donors for transplantation may increase transplantation…”
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    Analysis of ischemia/reperfusion injury in time‐zero biopsies predicts liver allograft outcomes by Ali, Jason M., Davies, Susan E., Brais, Rebecca J., Randle, Lucy V., Klinck, John R., Allison, Michael E. D., Chen, Yining, Pasea, Laura, Harper, Simon F. J., Pettigrew, Gavin J.

    Published in Liver transplantation (01-04-2015)
    “…Ischemia/reperfusion injury (IRI) that develops after liver implantation may prejudice long‐term graft survival, but it remains poorly understood. Here we…”
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    Humoral autoimmunity after solid organ transplantation: Germinal ideas may not be natural by Siu, Jacqueline H.Y., Motallebzadeh, Reza, Pettigrew, Gavin J.

    Published in Cellular immunology (01-08-2020)
    “…Non-HLA antibody responses following solid organ transplantation have become increasingly emphasised, with several large clinical series suggesting that such…”
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    CD8 T-cell recognition of acquired alloantigen promotes acute allograft rejection by Harper, Simon J. F., Ali, Jason M., Wlodek, Elizabeth, Negus, Marg C., Harper, Ines G., Chhabra, Manu, Qureshi, M. Saeed, Mallik, Mekhola, Bolton, Eleanor, Bradley, J. Andrew, Pettigrew, Gavin J.

    “…Adaptive CD8 T-cell immunity is the principal arm of the cellular alloimmune response, but its development requires help. This can be provided by CD4 T cells…”
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