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1.
Transplant Proc ; 49(7): 1587-1590, 2017 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-28838446

RESUMEN

In 2015, an outbreak involving a highly virulent zoonotic outbreak strain of Streptococcus agalactiae serotype III, multilocus sequence type 283 occurred in Singapore with increased neurologic complications, septic arthritis, and spinal infections in healthier patients. We report a case of a successful dual kidney transplant from a deceased donor with infective endocarditis and disseminated infection with the same strain of S agalactiae and we review the current literature.


Asunto(s)
Profilaxis Antibiótica/métodos , Endocarditis Bacteriana/prevención & control , Trasplante de Riñón/efectos adversos , Complicaciones Posoperatorias/prevención & control , Infecciones Estreptocócicas/prevención & control , Streptococcus agalactiae/genética , Anciano , Antibacterianos/uso terapéutico , Brotes de Enfermedades , Endocarditis Bacteriana/microbiología , Endocarditis Bacteriana/transmisión , Femenino , Humanos , Trasplante de Riñón/métodos , Masculino , Persona de Mediana Edad , Tipificación de Secuencias Multilocus , Complicaciones Posoperatorias/microbiología , Serogrupo , Infecciones Estreptocócicas/microbiología , Infecciones Estreptocócicas/transmisión , Donantes de Tejidos , Resultado del Tratamiento
3.
Leukemia ; 30(6): 1311-9, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-26854024

RESUMEN

Epitheliotropic intestinal T-cell lymphoma (EITL, also known as type II enteropathy-associated T-cell lymphoma) is an aggressive intestinal disease with poor prognosis and its molecular alterations have not been comprehensively characterized. We aimed to identify actionable easy-to-screen alterations that would allow better diagnostics and/or treatment of this deadly disease. By performing whole-exome sequencing of four EITL tumor-normal pairs, followed by amplicon deep sequencing of 42 tumor samples, frequent alterations of the JAK-STAT and G-protein-coupled receptor (GPCR) signaling pathways were discovered in a large portion of samples. Specifically, STAT5B was mutated in a remarkable 63% of cases, JAK3 in 35% and GNAI2 in 24%, with the majority occurring at known activating hotspots in key functional domains. Moreover, STAT5B locus carried copy-neutral loss of heterozygosity resulting in the duplication of the mutant copy, suggesting the importance of mutant STAT5B dosage for the development of EITL. Dysregulation of the JAK-STAT and GPCR pathways was also supported by gene expression profiling and further verified in patient tumor samples. In vitro overexpression of GNAI2 mutants led to the upregulation of pERK1/2, a member of MEK-ERK pathway. Notably, inhibitors of both JAK-STAT and MEK-ERK pathways effectively reduced viability of patient-derived primary EITL cells, indicating potential therapeutic strategies for this neoplasm with no effective treatment currently available.


Asunto(s)
Linfoma de Células T Asociado a Enteropatía/metabolismo , Quinasas Janus/metabolismo , Receptores Acoplados a Proteínas G/metabolismo , Factores de Transcripción STAT/metabolismo , Transducción de Señal , Adulto , Anciano , Anciano de 80 o más Años , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Linfoma de Células T Asociado a Enteropatía/patología , Femenino , Subunidad alfa de la Proteína de Unión al GTP Gi2/genética , Perfilación de la Expresión Génica , Humanos , Janus Quinasa 3/genética , Masculino , Persona de Mediana Edad , Mutación , Inhibidores de Proteínas Quinasas/farmacología , Factor de Transcripción STAT5/genética , Transducción de Señal/efectos de los fármacos , Adulto Joven
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