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1.
Biomédica (Bogotá) ; 39(supl.2): 26-31, ago. 2019. graf
Artículo en Español | LILACS | ID: biblio-1038825

RESUMEN

Resumen Los pacientes con lepra lepromatosa que han recibido tratamiento durante años, usualmente requieren seguimiento con biopsias de piel para detectar lesiones persistentes o si la baciloscopia es positiva, incluso si los valores son menores que los iniciales. Se presenta el caso de una mujer de 48 años de edad con lepra lepromatosa de 15 años de evolución, índice bacilar de 4 en el extendido directo y en la biopsia, que recibió tratamiento con múltiples medicamentos durante 32 meses, aunque lo recomendado por la Organización Mundial de la Salud (OMS) es una duración de 12 meses. Se tomó una biopsia de piel para determinar si la enfermedad estaba activa. Se observó inflamación dérmica difusa con numerosas células gigantes de tipo cuerpo extraño y macrófagos vacuolados (células de Virchow). Estas células, CD68 positivas, contenían material granular ácido-alcohol resistente positivo con inmunohistoquímica para BCG. Se encontraron bacilos fragmentados y el índice bacilar fue de 2. Se interpretó como una forma residual de lepra lepromatosa y se concluyó que la paciente no requería prolongar el tratamiento con múltiples medicamentos. Este perfil histológico se ha observado en casos similares, pero sin datos clínicos estas biopsias representan un reto diagnóstico. La acumulación de lípidos en estas células gigantes se debe a la destrucción bacilar y a la fusión de macrófagos vacuolados. Se revisó el papel de los lípidos del bacilo y del huésped en la patogenia de la lepra lepromatosa. En estos casos, no es necesario extender los 12 meses de tratamiento con múltiples medicamentos recomendados por la OMS. En el seguimiento de los pacientes, se recomienda contar con los hallazgos clínicos, la baciloscopia, la biopsia anual de piel y los títulos IgM antiglucolípido fenólico.


Abstract Patients with lepromatous leprosy that have received treatment for many years usually get follow up biopsies for persistent skin lesions or positive bacilloscopy even if the values are lower than in the initial bacilloscopy. We report the case of a 48-year old woman with long-standing lepromatous leprosy of 15 years of evolution, with a bacterial index of 4 in the direct smear and the initial skin biopsy. The patient was treated with multidrug therapy for 32 months although the treatment recommended by the World Health Organization (WHO) is only for 12 months. A skin biopsy was taken to determine if there was an active disease. We observed a diffuse dermal inflammation with numerous foreign body giant cells and vacuolated macrophages (Virchow´s cells). These cells contained granular acid-fast material that was also positive with immunohistochemistry for BCG. There were fragmented bacilli and the BI was 2. These cells were also strongly positive for CD68. The biopsy was interpreted as a residual form of lepromatous leprosy that did not require further multidrug therapy. We have observed similar histological profiles in several cases. The lack of clinical data makes it a histological challenge. The accumulation of lipids in these giant cells is due to bacillary destruction and fusion of vacuolated macrophages. We discuss here the role of bacillary and host lipids in the pathogenesis of lepromatous leprosy. We concluded that there was no need to extend the 12-month multidrug therapy recommended by WHO. Clinical findings, bacilloscopy, annual skin biopsy, and anti-phenolic glycolipid-I IgM titers are recommended procedures for the follow-up of these patients.


Asunto(s)
Femenino , Humanos , Persona de Mediana Edad , Piel/patología , Lepra Lepromatosa/patología , Células Gigantes de Cuerpo Extraño/patología , Células Espumosas/patología , Piel/microbiología , Vacuolas , Biopsia , Antígenos de Diferenciación Mielomonocítica/análisis , Lepra Lepromatosa/tratamiento farmacológico , Antígenos CD/análisis , Células Gigantes de Cuerpo Extraño/microbiología , Células Gigantes de Cuerpo Extraño/química , Pared Celular/química , Quimioterapia Combinada , Interacciones Huésped-Patógeno , Células Espumosas/microbiología , Células Espumosas/química , Leprostáticos/uso terapéutico , Lípidos/análisis , Mycobacterium leprae/aislamiento & purificación , Mycobacterium leprae/química
2.
J Biosci ; 2007 Aug; 32(5): 937-45
Artículo en Inglés | IMSEAR | ID: sea-110634

RESUMEN

Functional classification of proteins is central to comparative genomics. The need for algorithms tuned to enable integrative interpretation of analytical data is felt globally. The availability of a general,automated software with built-in flexibility will significantly aid this activity. We have prepared ARC (Automated Resource Classifier), which is an open source software meeting the user requirements of flexibility. The default classification scheme based on keyword match is agglomerative and directs entries into any of the 7 basic non-overlapping functional classes: Cell wall, Cell membrane and Transporters (C), Cell division (D), Information (I), Translocation (L), Metabolism (M), Stress(R), Signal and communication (S) and 2 ancillary classes: Others (O) and Hypothetical (H).The keyword library of ARC was built serially by first drawing keywords from Bacillus subtilis and Escherichia coli K12. In subsequent steps,this library was further enriched by collecting terms from archaeal representative Archaeoglobus fulgidus, Gene Ontology, and Gene Symbols. ARC is 94.04% successful on 6,75,663 annotated proteins from 348 prokaryotes. Three examples are provided to illuminate the current perspectives on mycobacterial physiology and costs of proteins in 333 prokaryotes. ARC is available at http://arc.igib.res.in.


Asunto(s)
Algoritmos , Proteínas Arqueales/clasificación , Archaeoglobus fulgidus/química , Bacillus subtilis/química , Proteínas Bacterianas/clasificación , Biología Computacional , Escherichia coli K12/química , Proteínas de Escherichia coli/clasificación , Mycobacterium bovis/química , Mycobacterium leprae/química , Mycobacterium tuberculosis/química , Análisis por Matrices de Proteínas
3.
Belem; s.n; 2004. 126 p. ilus, tab, graf.
Tesis en Portugués | LILACS, SES-SP, HANSEN, HANSENIASE, SESSP-ILSLACERVO, SES-SP | ID: biblio-1241929

RESUMEN

Analisou-se a prevalencia de anticoepos IgM utilizando teste sorologico e antigeno especifico Glicolipidio Fenolico I (PGL-I) do Mycobacterium leprae, por meio do teste rapido ML Dipstick em 1611 individuos sadios categorizados em contatos de pacientes hansenicos intradomiciliares e comunitarios, residentes em cinco municipios endemicos para hanseniase. Realizou-se estudo tranversal pela analise do banco de dados do laboratorio de hanseniase, Instituto Evandro Chagas. O estudo estendeu-se de março a dezembro de 1998, com reavaliaçoes anuais ate dezembro de 2002, no qual, os municipios selecionados-Curinopolis, Eldorado do Carajas, Xinguara, Rondon do Para e Dom Eliseu - apresentaram taxas de prevalencia em hanseniase maiores que 20 em cada 10.000 hab. e detecçao de casos novos maiores que quatro em cada 10.000 hab. A idade variou de 2 a 90 anos, devido ao fato de que a doença em areas de alta endemicidade possibilita o diagnostico de crianças. Estudou-se 957 mulheres (957/1611-59.4 por cento), 654 homens (654/1611-40.6 por cento) e observou-se predominancia de soropositividade entre as mulheres na faixa etaria entre 21 e 50 anos, 62.81 por cento contra 53.97 por cento nos homens. A analise foi realizada nos bancos de dados D-BASE, EPI-INFO 6.4 e 2002, BIOESTAT 3.0 e SINAM, existentes no Instituto Evandro Chagas e Secretaria Estadual de Saude do Para...


Asunto(s)
Humanos , Lepra/epidemiología , Lepra/fisiopatología , Lepra/inmunología , Lepra/rehabilitación , Mycobacterium leprae/citología , Mycobacterium leprae/fisiología , Mycobacterium leprae/genética , Mycobacterium leprae/inmunología , Mycobacterium leprae/patogenicidad , Mycobacterium leprae/química , Inmunoglobulina M , Inmunoglobulina M/análisis , Inmunoglobulina M/química
4.
Indian J Lepr ; 1999 Jan-Mar; 71(1): 1-10
Artículo en Inglés | IMSEAR | ID: sea-54775

RESUMEN

This study was undertaken under the assumption that antigenic mimicry plays a role in the pathogenesis of neuropathy in leprosy, a unique feature among mycobacterial diseases. The SWISS-PROT protein sequence databank was scanned using a computer programme based on an identity matrix algorithm, to identify common amino acid regions between human myelin and mycobacterial proteins. The highlighted motifs were back-tested against a database of MHC-binding peptides (MHCPEP). Of the 28 common sequences between mycobacterial and human myelin proteins, only two were found to yield some matches with MHC-presenting peptides. Both motifs were from M.leprae. The myelin proteolipid protein was the human protein containing the identified similarities. We believe that this theoretical approach can provide a way to predict potentially "mimetic" motifs by search for antigenic regions in protein sequence databases without screening a large number of synthetic peptides.


Asunto(s)
Secuencia de Aminoácidos , Proteínas Bacterianas/química , Bases de Datos Factuales , Humanos , Datos de Secuencia Molecular , Mycobacterium leprae/química , Proteína Proteolipídica de la Mielina/química , Análisis de Secuencia de Proteína/métodos , Homología de Secuencia de Aminoácido , Programas Informáticos
5.
Indian J Lepr ; 1992 Oct-Dec; 64(4): 529-35
Artículo en Inglés | IMSEAR | ID: sea-55578

RESUMEN

On the basis of thin layer chromatography and gas-chromatography-mass spectrometric studies, the lipid profiles of all the chemoautotrophic nocardioform (CAN) bacteria derived from human and animal leprosy tissues appear to be identical with each other, and closest to or identical with the most probable profile of M. leprae.


Asunto(s)
Actinomycetales/química , Lepra/microbiología , Lípidos/análisis , Mycobacterium leprae/química , Ácidos Esteáricos/análisis
6.
Indian J Exp Biol ; 1992 May; 30(5): 451-3
Artículo en Inglés | IMSEAR | ID: sea-56014

RESUMEN

Thirty nine untreated patients of bacilliferous leprosy with a mean bacteriological index of 4.8 and morphological index of 1.3% formed the study group. Adenosine triphosphate assay was carried out by (i) enzyme treatment method in 18 patients and (ii) percoll buoyant density gradient method in 21 patients. ATP content obtained by percoll buoyant density gradient method was significantly higher than that obtained by enzyme treatment method. Percoll buoyant density centrifugation for purification and isolation of bacilli from human leproma is simplier, quicker and can serve as an alternate method of enzyme treatment.


Asunto(s)
Adenosina Trifosfato/análisis , Centrifugación por Gradiente de Densidad , Humanos , Lepra Dimorfa/microbiología , Lepra Lepromatosa/microbiología , Mycobacterium leprae/química , Povidona , Dióxido de Silicio
7.
Indian J Lepr ; 1992 Jan-Mar; 64(1): 28-41
Artículo en Inglés | IMSEAR | ID: sea-54303

RESUMEN

The cell wall components of mycobacteria are said to be vitally linked with their pathogenicity. Peptidoglycan, one of the major cell wall component in most of the bacteria are multilayered in gram positive bacteria and it is diverse in nature for the Gram positive strain rather than gram negative. The cell wall of bacteria are primary targets for many drugs and antibiotics and conformation of the major cell wall components provide invaluable information and understanding at molecular level to medicinal chemists and drug designers. Mycobacterial peptidoglycan has been studied critically by computer modelling on various aspects. A plausible structure and conformation has been identified and glycan chain is found to have a pseudo two fold symmetry taking disaccharide unit as monomer with Knox & Murthy H-bond scheme. This paper attempts to clarify the understanding of organisation and possible interaction mode of peptidoglycan of organisation in complex mycobacterial cell wall structure.


Asunto(s)
Secuencia de Aminoácidos , Pared Celular/química , Simulación por Computador , Modelos Químicos , Datos de Secuencia Molecular , Estructura Molecular , Mycobacterium leprae/química , Peptidoglicano/química , Conformación Proteica
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