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1.
Arch Dis Child ; 92(6): 519-20, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16798784

RESUMO

We report a case of pneumonia in a 13 month old male child with partial DiGeorge syndrome who died after inadvertently receiving live viral vaccines. Although live viral vaccines have been used safely in some children with DiGeorge syndrome, there are insufficient data to recommend their routine use in those with severe immunodeficiency.


Assuntos
Síndrome de DiGeorge/complicações , Infecções Oportunistas/etiologia , Pneumonia Viral/etiologia , Vacinas Virais/efeitos adversos , Síndrome de DiGeorge/imunologia , Evolução Fatal , Humanos , Hospedeiro Imunocomprometido , Lactente , Masculino , Vacina contra Sarampo-Caxumba-Rubéola/efeitos adversos , Infecções Oportunistas/imunologia , Pneumonia Viral/imunologia
2.
J Immunol ; 166(4): 2878-86, 2001 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-11160357

RESUMO

The CD8 alphabetaT cell receptor repertoire in joint fluid of individuals with active psoriatic arthritis contained an average of 32 major oligoclonal expansions in many variable genes of the TCR beta chain (BV) families, as shown by beta-chain CDR3 length analysis. Interestingly, a small number of oligoclonal expansions were shared between simultaneous samples of joint fluid and blood; however, most expansions found in joint fluid were not identifiable in blood emphasizing the immunologic specificity of the clonal events for the inflamed joint at a given point of time. The CD4 T cell joint fluid repertoire contained fewer and smaller oligoclonal expansions also largely restricted to the joint, suggesting that CD4 T cells participate perhaps by interacting cognitively to generate the CD8 clones. The inferred amino acid sequence of a single CD8 oligoclonal expansion revealed that they usually are composed of one or a few structurally related clones at the amino acid sequence level with beta-chains that encode identical or highly homologous CDR3 motifs. These were not shared among patients. Moreover, several clones that encoded the same amino acid sequence were found to be structurally distinct at the nucleotide level, strongly implying clonal selection and expansion is operating at the level of specific TCR-peptide interactions. The findings support a model of psoriatic arthritis inflammation involving extensive and selective Ag, likely autoantigen, driven intra-articular CD4, and CD8 T cell clonal expansions.


Assuntos
Artrite Psoriásica/imunologia , Artrite Psoriásica/patologia , Autoantígenos/imunologia , Linfócitos T CD4-Positivos/imunologia , Linfócitos T CD8-Positivos/imunologia , Líquido Sinovial/imunologia , Sequência de Aminoácidos , Artrite Psoriásica/genética , Artrite Psoriásica/metabolismo , Sequência de Bases , Linfócitos T CD4-Positivos/metabolismo , Linfócitos T CD4-Positivos/patologia , Linfócitos T CD8-Positivos/metabolismo , Linfócitos T CD8-Positivos/patologia , Divisão Celular/genética , Divisão Celular/imunologia , Células Clonais , Clonagem Molecular , Humanos , Articulação do Joelho/imunologia , Articulação do Joelho/metabolismo , Articulação do Joelho/patologia , Dados de Sequência Molecular , Receptores de Antígenos de Linfócitos T alfa-beta/biossíntese , Receptores de Antígenos de Linfócitos T alfa-beta/sangue , Receptores de Antígenos de Linfócitos T alfa-beta/genética , Padrões de Referência , Valores de Referência , Líquido Sinovial/metabolismo
4.
Artigo em Inglês | MEDLINE | ID: mdl-2863077

RESUMO

Myoglobin has been identified in the heart tissue of three species of antarctic icefish, Chaenocephalus aceratus, Pseudochaenichthys georgianus and Chaenodraco wilsoni. Quantitative analysis shows myoglobin concentrations that are substantially lower than other teleost fish. A simple and accurate method for the direct measurement of myoglobin in tissue is described.


Assuntos
Peixes/metabolismo , Miocárdio/análise , Mioglobina/análise , Animais , Regiões Antárticas , Carpas/metabolismo , Bovinos , Ventrículos do Coração/análise , Hemoglobinas , Peso Molecular , Especificidade da Espécie , Truta/metabolismo
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