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1.
Am J Kidney Dis ; 74(6): 849-852, 2019 12.
Artículo en Inglés | MEDLINE | ID: mdl-31451329

RESUMEN

Antibodies against THSD7A (thrombospondin type 1 domain-containing protein 7A) have been proposed to play a causal role in the development of nephrotic syndrome in patients with THSD7A antibody-positive membranous nephropathy. We hypothesized that removal of these antibodies from plasma could lead to a rapid reduction in proteinuria. Using immunoadsorption to reduce THSD7A antibodies led to a rapid reduction in proteinuria in 2 patients with THSD7A antibody-positive membranous nephropathy. Moreover, our findings support and strengthen the pathogenic role of the antibodies in the development of nephrotic syndrome in patients with THSD7A antibody-positive membranous nephropathy. Taken together, these 2 cases suggest that immunoadsorption could be a useful tool in the treatment of patients with THSD7A antibody-positive membranous nephropathy.


Asunto(s)
Autoanticuerpos/inmunología , Glomerulonefritis Membranosa/inmunología , Glomerulonefritis Membranosa/terapia , Síndrome Nefrótico/patología , Trombospondinas/inmunología , Adulto , Anciano , Biopsia con Aguja , Progresión de la Enfermedad , Glomerulonefritis Membranosa/patología , Humanos , Inmunohistoquímica , Masculino , Síndrome Nefrótico/fisiopatología , Plasmaféresis , Pronóstico , Proteinuria/inmunología , Proteinuria/fisiopatología , Medición de Riesgo , Muestreo , Resultado del Tratamiento
2.
Ann Transplant ; 23: 775-781, 2018 Nov 06.
Artículo en Inglés | MEDLINE | ID: mdl-30397188

RESUMEN

BACKGROUND We evaluated the Kidney Donor Risk Index (KDRI) scoring system for kidney transplantation in the Eurotransplant Senior Program (ESP) that allocates kidneys from older donors to older recipients (≥65 years). MATERIAL AND METHODS We retrospectively analyzed data of 37 kidney transplant recipients and 36 kidney donors who participated in kidney transplantation program according to the ESP at our center from January 2004 until December 2013. RESULTS Mean recipient and donor age was 67.9±2.6 and 70.5±4.0 years respectively. The mean KDRI score was 1.7±0.27. Uncensored graft survival after 1 year and 5 years was 64.2% and 53.7% respectively. Subgroup analysis showed that in kidney transplantation with KDRI >1.83, graft survival was significantly reduced compared to lower KDRI subgroups. KDRI was significantly correlated with serum creatinine level at discharge (r=0.4). CONCLUSIONS ESP kidneys represent a group of high-risk grafts with high KDRI scores. Higher KDRI scores in ESP kidneys was associated with reduced postoperative short-term and long-term graft outcomes. KDRI might be useful in decision-making for selecting donors for ESP kidney transplantation.


Asunto(s)
Trasplante de Riñón/métodos , Donantes de Tejidos , Obtención de Tejidos y Órganos/métodos , Anciano , Femenino , Supervivencia de Injerto , Humanos , Masculino , Estudios Retrospectivos , Resultado del Tratamiento
3.
Curr Opin Organ Transplant ; 19(4): 395-400, 2014 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-24905021

RESUMEN

PURPOSE OF REVIEW: Ischemia/reperfusion injury is an unavoidable companion after kidney transplantation and influences short-term as well as long-term graft outcome. Clinically ischemia/reperfusion injury is associated with delayed graft function, graft rejection, and chronic graft dysfunction. Ischemia/reperfusion affects many regulatory systems at the cellular level as well as in the renal tissue that eventually result in a distinct inflammatory reaction of the kidney graft. RECENT FINDINGS: Underlying factors include energy metabolism, cellular changes of the mitochondria and cellular membranes, initiation of different forms of cell death-like apoptosis and necrosis together with a recently discovered mixed form termed necroptosis. Chemokines and cytokines together with other factors promote the inflammatory response leading to activation of the innate immune system as well as the adaptive immune system. If the inflammatory reaction continues within the graft tissue, a progressive interstitial fibrosis develops that impacts long-term graft outcome. SUMMARY: It is of particular importance in kidney transplantation to understand the underlying mechanisms and effects of ischemia/reperfusion on the graft as this knowledge also opens strategies to prevent or treat ischemia/reperfusion injury after transplantation in order to improve graft outcome.


Asunto(s)
Trasplante de Riñón , Daño por Reperfusión/inmunología , Animales , Rechazo de Injerto/inmunología , Humanos , Inmunidad Innata , Daño por Reperfusión/fisiopatología , Linfocitos T/inmunología
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