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Natural Killer Cell Presence in Antibody-Mediated Rejection.
Diebold, Matthias; Farkash, Evan A; Barnes, Jenna; Regele, Heinz; Kozakowski, Nicolas; Schatzl, Martina; Mayer, Katharina A; Haindl, Susanne; Vietzen, Hannes; Hidalgo, Luis G; Halloran, Philip F; Eskandary, Farsad; Böhmig, Georg A.
Afiliación
  • Diebold M; Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
  • Farkash EA; Clinic for Transplantation Immunology and Nephrology, University Hospital Basel, Basel, Switzerland.
  • Barnes J; Department of Pathology, University of Michigan, Ann Arbor, MI, United States.
  • Regele H; Department of Pathology, University of Michigan, Ann Arbor, MI, United States.
  • Kozakowski N; Department of Pathology, Medical University of Vienna, Vienna, Austria.
  • Schatzl M; Department of Pathology, Medical University of Vienna, Vienna, Austria.
  • Mayer KA; Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
  • Haindl S; Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
  • Vietzen H; Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
  • Hidalgo LG; Center for Virology, Medical University of Vienna, Vienna, Austria.
  • Halloran PF; Department of Surgery, University of Wisconsin, Madison, WI, United States.
  • Eskandary F; Alberta Transplant Applied Genomics Centre, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.
  • Böhmig GA; Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
Transpl Int ; 37: 13209, 2024.
Article en En | MEDLINE | ID: mdl-38979120
ABSTRACT
Transcript analyses highlight an important contribution of natural killer (NK) cells to microvascular inflammation (MVI) in antibody-mediated rejection (ABMR), but only few immunohistologic studies have quantified their spatial distribution within graft tissue. This study included 86 kidney transplant recipients who underwent allograft biopsies for a positive donor-specific antibody (DSA) result. NK cells were visualized and quantified within glomeruli and peritubular capillaries (PTC), using immunohistochemistry for CD34 alongside CD16/T-bet double-staining. Staining results were analyzed in relation to histomorphology, microarray analysis utilizing the Molecular Microscope Diagnostic System, functional NK cell genetics, and clinical outcomes. The number of NK cells in glomeruli per mm2 glomerular area (NKglom) and PTC per mm2 cortical area (NKPTC) was substantially higher in biopsies with ABMR compared to those without rejection, and correlated with MVI scores (NKglom Spearman's correlation coefficient [SCC] = 0.55, p < 0.001, NKPTC 0.69, p < 0.001). In parallel, NK cell counts correlated with molecular classifiers reflecting ABMR activity (ABMRprob NKglom 0.59, NKPTC 0.75) and showed a trend towards higher levels in association with high functional FCGR3A and KLRC2 gene variants. Only NKPTC showed a marginally significant association with allograft function and survival. Our immunohistochemical results support the abundance of NK cells in DSA-positive ABMR.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Asesinas Naturales / Trasplante de Riñón / Rechazo de Injerto Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Transpl Int Asunto de la revista: TRANSPLANTE Año: 2024 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Asesinas Naturales / Trasplante de Riñón / Rechazo de Injerto Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Transpl Int Asunto de la revista: TRANSPLANTE Año: 2024 Tipo del documento: Article País de afiliación: Austria