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1.
Am J Transplant ; 24(9): 1698-1702, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-38734417

RESUMEN

The strategy for progressive multifocal leukoencephalopathy (PML) in solid organ transplant recipients primarily focuses on reducing immunosuppressive therapy. However, this approach offers limited efficacy and carries a high risk of graft loss. Here, we present the case of a 64-year-old male kidney transplant recipient with a high degree of immunosuppression who developed PML in October 2022. Despite the standard reduction of immunosuppressive therapy, the patient's condition continued to deteriorate, as evidenced by worsening neurological symptoms and increasing JC virus (JCV) DNA levels in cerebrospinal fluid. This prompted the innovative use of BKPyV-virus-specific T cell (BKPyV-VST) therapy, given the genetic similarities between BK and JCVs. Infusion of third-party donor BKPyV-VST resulted in clinical stabilization, a significant reduction in JCV-DNA levels, and the emergence of a JCV-specific T cell response, as observed in enzyme-linked immunospot assays and TCRß sequencing. This represents the first case report of successful third-party BKPyV-VST therapy in a kidney recipient presenting PML, without graft-versus-host disease or graft dysfunction.


Asunto(s)
Virus BK , Trasplante de Riñón , Leucoencefalopatía Multifocal Progresiva , Infecciones por Polyomavirus , Linfocitos T , Humanos , Leucoencefalopatía Multifocal Progresiva/terapia , Leucoencefalopatía Multifocal Progresiva/inmunología , Leucoencefalopatía Multifocal Progresiva/etiología , Trasplante de Riñón/efectos adversos , Masculino , Persona de Mediana Edad , Linfocitos T/inmunología , Infecciones por Polyomavirus/inmunología , Infecciones por Polyomavirus/terapia , Pronóstico , Virus JC/inmunología , Receptores de Trasplantes , Tratamiento Basado en Trasplante de Células y Tejidos/métodos
2.
J Nephrol ; 16(1): 116-20, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12649542

RESUMEN

BACKGROUND: Bsml vitamin D receptor (VDR) gene polymorphism has been reported to influence the progression of secondary hyperparathyroidism but it is not known how much the genetic background contributes to the need for parathyroidectomy (PTx). We investigated the influence of VDR gene polymorphism on PTx in patients with different dialysis vintage. METHODS: We studied 121 parathyroidectomized HD patients ("PTx " group). Patients who had required early parathyroidectomy ("early PTx" group) or late parathyroidectomy ("late PTx" group) were analyzed separately. The cut-off point between these two groups was 89 months (mean time on hemodialysis (HD) before parathyroidectomy). Serum intact parathyroid hormone, calcium, phosphorus and alkaline phosphatase were measured. Bsml genotypes were analyzed by polymerase chain reaction. Statistical analysis was done with univariant analysis of variance (ANOVA) to compare the genotype groups and general factorial ANOVA, entering time on HD as the dependent variable, with genotype, sex, age and chronic renal failure (CRF) etiology as factors. As a control group for the association studies we determined genotypic frequencies in 162 HD patients ("total HD" group), and in a healthy control population of 120 individuals ("healthy" group), tested by contingency table analysis and the chi-square test. RESULTS: No significant differences were found between the genotypes except for the time on HD. General factorial ANOVA showed that the adjusted means of the time on HD were significantly different for the various genotypes (p = 0.015). The BB genotype was significantly less frequent in the "early PTx " group than in the "total HD" and "late PTx" groups. CONCLUSIONS: Individuals with the BB genotype can remain longer on HD before they need parathyroidectomy.


Asunto(s)
Hiperparatiroidismo Secundario/genética , Hiperparatiroidismo Secundario/cirugía , Fallo Renal Crónico/terapia , Polimorfismo Genético , Receptores de Calcitriol/genética , Diálisis Renal/efectos adversos , Adulto , Análisis de Varianza , Estudios de Cohortes , Femenino , Marcadores Genéticos/genética , Genotipo , Humanos , Hiperparatiroidismo Secundario/diagnóstico , Masculino , Persona de Mediana Edad , Probabilidad , Pronóstico , Diálisis Renal/métodos , Medición de Riesgo , Sensibilidad y Especificidad , Índice de Severidad de la Enfermedad , Factores de Tiempo
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