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J Neuroimmunol ; 157(1-2): 71-80, 2004 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-15579283

RESUMO

HIV encephalopathy, one of the major complications of HIV infection, involves productive virus replication in macrophages in the brain in association with heightened expression of several host response factors. One or more of these factors are thought to be the cause of the degenerative changes in neurons in the brain. Macaques infected with SIV and SHIV viruses have provided excellent working models for studying mechanisms of the human disease. Although HIV encephalopathy is primarily associated with CCR5-utilizing viruses, our findings have shown that CXCR4-utilizing SHIVs were also capable of causing the syndrome in rhesus macaques. In SHIV-infected macaques, approximately 30% of the animals developed encephalitis. In order to understand the factors leading to end-stage encephalitis, we performed microarray analyses on brains of encephalitic and non-encephalitic-infected macaques, and found pronounced enhancement of expression of interleukin-4, platelet-derived growth factor-B chain, monocyte chemoattractant protein-1 and CXCL10 in the brains of the encephalitic animals. This review discusses the role of each of these factors in mediating SHIV encephalitis.


Assuntos
Encefalite/metabolismo , Síndrome de Imunodeficiência Adquirida dos Símios/metabolismo , Animais , Encéfalo/metabolismo , Encéfalo/virologia , Quimiocina CCL2/metabolismo , Quimiocina CXCL10 , Quimiocinas CXC/metabolismo , Modelos Animais de Doenças , Encefalite/etiologia , Humanos , Interleucina-4/metabolismo , Modelos Neurológicos , Proteínas Proto-Oncogênicas c-sis/metabolismo , Síndrome de Imunodeficiência Adquirida dos Símios/complicações
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