Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
1.
J Pathol ; 209(1): 56-66, 2006 May.
Artículo en Inglés | MEDLINE | ID: mdl-16508918

RESUMEN

The origin and function of monocytoid B cells (MBCs) are poorly understood. Taking advantage of their strong expression of IRTA1 (a receptor that is also associated with MALT marginal zone B cells), we have comprehensively analysed MBCs in 25 cases of lymphadenitis of different aetiologies, shedding new light on the topographical distribution, immunophenotype and IgV(H) gene usage and mutational profile of this B cell subset. IRTA1(+) MBCs, although predominantly located in the subcapsular and intermediary sinuses, were also observed scattered within germinal centres (GCs) in all lymphadenitis cases examined. The molecular characterization of IgV(H) genes revealed that IRTA1(+) MBCs residing in different areas of the lymph node (subcapsular sinus, intermediary sinuses and GCs) can be clonally related (with intraclonal variation), and that those located in GCs are consistently more mutated and selected for expression of a functional antigen receptor than those located in the sinuses. Moreover, by contrast, IRTA1(+) MBCs in GCs express the memory B cell marker CD27. Finally, in toxoplasmic lymphadenitis, the IRTA1(+) MBC population shows a highly preferential usage of the V(H) genes 3-7 and 3-30 (without any obvious peculiarity in their CDR3s), possibly suggesting that a superantigen expressed by Toxoplasma gondii may be involved in the early activation of this B cell subset.


Asunto(s)
Subgrupos de Linfocitos B/inmunología , Genes de Inmunoglobulinas , Linfadenitis/inmunología , Receptores de Superficie Celular/análisis , Receptores Fc/análisis , Análisis Mutacional de ADN/métodos , Reordenamiento Génico de Cadena Pesada de Linfocito B , Centro Germinal/inmunología , Humanos , Cadenas Pesadas de Inmunoglobulina/genética , Región Variable de Inmunoglobulina/genética , Inmunofenotipificación , Linfadenitis/etiología , Linfadenitis/genética , Microdisección/métodos , Reacción en Cadena de la Polimerasa/métodos , Superantígenos/inmunología , Toxoplasmosis/inmunología , Miembro 7 de la Superfamilia de Receptores de Factores de Necrosis Tumoral/análisis
2.
Histopathology ; 43(5): 491-4, 2003 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-14636276

RESUMEN

AIMS: Tumours of dendritic/accessory cell origin are rare neoplasms arising in lymph nodes. Among these, tumours derived from cytokeratin-positive interstitial reticulum cells (CIRCs), a subset of fibroblastic reticulum cells, are reported even less frequently. The International Lymphoma Study Group (ILSG) has recently proposed a classification for tumours of histiocytes and accessory dendritic cells in which CIRC tumours are not included. We report a case of a CIRC tumour arising in a submandibular lymph node of a 66-year-old male. METHODS AND RESULTS: The neoplasm was composed of spindle cells with elongated or round nuclei, prominent nucleoli and abundant cytoplasm. These cells were arranged in a diffuse fascicular and vaguely whorled pattern. The tumour cells stained diffusely for S100, vimentin, desmin, lysozyme, and focally for CD68 and cytokeratins 7, 8, 18, CK-AE1 and CK-pool. Electron microscopy was performed for further evaluation on samples taken from the paraffin block; this revealed cytoplasmic projections and rudimentary cell junctions. CONCLUSIONS: Histopathologist should be aware of the existence of tumours deriving from CIRCs, as these cases may be misdiagnosed as metastatic carcinoma. Careful clinical and pathological evaluation is necessary to exclude this possibility.


Asunto(s)
Células Dendríticas/patología , Queratinas/metabolismo , Ganglios Linfáticos/patología , Linfoma/patología , Neoplasias de la Glándula Submandibular/patología , Anciano , Células Dendríticas/diagnóstico por imagen , Células Dendríticas/metabolismo , Diagnóstico Diferencial , Humanos , Ganglios Linfáticos/metabolismo , Ganglios Linfáticos/ultraestructura , Linfoma/clasificación , Linfoma/metabolismo , Masculino , Microscopía Electrónica , Neoplasias de la Glándula Submandibular/clasificación , Neoplasias de la Glándula Submandibular/metabolismo , Ultrasonografía
4.
Oncogene ; 20(56): 8148-53, 2001 Dec 06.
Artículo en Inglés | MEDLINE | ID: mdl-11781829

RESUMEN

Human Papillomavirus type 16 (HPV-16) is the cause of both benign lesions and ano-genital cancers. In HPV-associated cancers the transforming properties of the expressed viral E6 and E7 proteins have been revealed by a number of different assays. We have generated transgenic mice expressing HPV-16 E6/E7 genes under the control of the murine keratin 5 gene promoter, which should confer cell-type specific expression in the basal cells of squamous stratified epithelia. Transgenic mice developed thymic hyperplasia and lung neoplasia with 100% frequency, the thymus showing a size increase at 2 months and reaching the maximum dimension at 6 months, when lung carcinomas appeared. After this time the size of hyperplastic thymi decreased, while malignant formations invaded the mediastinal area. Hepatic metastasis could be also observed in some of the animals at the autopsy and death invariably occurred around 10-11 months of age.


Asunto(s)
Carcinoma/virología , Queratinas/genética , Neoplasias Pulmonares/virología , Proteínas Oncogénicas Virales/farmacología , Infecciones por Papillomavirus/patología , Proteínas Represoras , Hiperplasia del Timo/virología , Infecciones Tumorales por Virus/patología , Animales , Carcinoma/complicaciones , Carcinoma/patología , Queratina-15 , Queratina-5 , Neoplasias Hepáticas/complicaciones , Neoplasias Hepáticas/patología , Neoplasias Hepáticas/secundario , Neoplasias Pulmonares/complicaciones , Neoplasias Pulmonares/patología , Ratones , Ratones Transgénicos , Proteínas Oncogénicas Virales/genética , Tamaño de los Órganos , Proteínas E7 de Papillomavirus , Infecciones por Papillomavirus/complicaciones , Regiones Promotoras Genéticas , Proteínas Recombinantes de Fusión/farmacología , Timo/patología , Hiperplasia del Timo/complicaciones , Hiperplasia del Timo/patología , Infecciones Tumorales por Virus/complicaciones
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA