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1.
J Leukoc Biol ; 108(4): 1129-1137, 2020 10.
Artigo em Inglês | MEDLINE | ID: mdl-32779279

RESUMO

Multiple sclerosis is a chronic and demyelinating disease of the central nervous system (CNS), most prevalent in women, and with an important social and economic cost worldwide. It is triggered by self-reacting lymphocytes that infiltrate the CNS and initiate neuroinflammation. Further, axonal loss and neuronal death takes place, leading to neurodegeneration and brain atrophy. The murine model for studying MS, experimental autoimmune encephalomyelitis (EAE), consists in immunizing mice with myelin-derived epitopes. APCs activate encephalitogenic T CD4 and CD8 lymphocytes that migrate mainly to the spinal cord resulting in neuroinflammation. Most of the knowledge on the pathophysiology and treatment of MS was obtained from EAE experiments, as Th17 cells, anti-alpha4 blocking Abs and the role of microbiota. Conversely, recent technology breakthroughs, such as CyTOF and single-cell RNA-seq, promise to revolutionize our understanding on the mechanisms involved both in MS and EAE. In fact, the importance of specific cellular populations and key molecules in MS/EAE is a constant matter of debate. It is well accepted that both Th1 and Th17 T CD4 lymphocytes play a relevant role in disease initiation after re-activation in situ. What is still under constant investigation, however, is the plasticity of the lymphocyte population, and the individual contribution of both resident and inflammatory cells for the progression or recovery of the disease. Thus, in this review, new findings obtained after single-cell analysis of blood and central nervous system infiltrating cells from MS/EAE and how they have contributed to a better knowledge on the cellular and molecular mechanisms of neuroinflammation are discussed.


Assuntos
Linfócitos T CD8-Positivos/imunologia , Encefalomielite Autoimune Experimental/imunologia , Esclerose Múltipla/imunologia , Análise de Célula Única , Células Th1/imunologia , Células Th17/imunologia , Animais , Linfócitos T CD8-Positivos/patologia , Modelos Animais de Doenças , Encefalomielite Autoimune Experimental/microbiologia , Encefalomielite Autoimune Experimental/patologia , Encefalomielite Autoimune Experimental/terapia , Humanos , Camundongos , Esclerose Múltipla/microbiologia , Esclerose Múltipla/patologia , Esclerose Múltipla/terapia , Células Th1/patologia , Células Th17/patologia
2.
Vet Microbiol ; 162(2-4): 866-872, 2013 Mar 23.
Artigo em Inglês | MEDLINE | ID: mdl-23206410

RESUMO

Escherichia coli Vacuolating Factor (ECVF) is a heat-labile, vacuolating cytotoxin produced by avian pathogenic E. coli (APEC) isolated from avian cellulitis lesions. In this report, we intend to demonstrate that purified ECVF induces the inflammatory process of cellulitis. Our group is the first to demonstrate the effect of ECVF in a histological analysis by in situ inoculation of broiler chickens with purified ECVF. The animals were inoculated with the APEC AC53 and with purified ECVF subcutaneously on their ventral surface (in the sternum region). The histological analysis showed different grades of an acute inflammatory response in the epidermis, dermis and panniculus. An increase in mRNA expression of the proinflammatory cytokine TNF-α was also demonstrated in the inflamed tissue. When ECVF was systemically administered, increased levels of TNF-α and IL-10 were observed in the serum. These results suggest that ECVF plays a key role in the inflammatory process associated with cellulitis that is mainly mediated by TNF-α. In addition, this inflammation can be downregulated by the anti-inflammatory cytokine IL-10.


Assuntos
Toxinas Bacterianas/biossíntese , Toxinas Bacterianas/toxicidade , Celulite (Flegmão)/veterinária , Infecções por Escherichia coli/veterinária , Escherichia coli/metabolismo , Doenças das Aves Domésticas/induzido quimicamente , Doenças das Aves Domésticas/microbiologia , Animais , Celulite (Flegmão)/sangue , Celulite (Flegmão)/induzido quimicamente , Celulite (Flegmão)/microbiologia , Embrião de Galinha , Galinhas , Escherichia coli/genética , Infecções por Escherichia coli/sangue , Infecções por Escherichia coli/induzido quimicamente , Infecções por Escherichia coli/microbiologia , Interleucina-10/biossíntese , Interleucina-10/sangue , Interleucina-10/genética , Masculino , Doenças das Aves Domésticas/sangue , RNA Mensageiro/biossíntese , RNA Mensageiro/genética , Fator de Necrose Tumoral alfa/biossíntese , Fator de Necrose Tumoral alfa/sangue , Fator de Necrose Tumoral alfa/genética
3.
Rev. bras. anestesiol ; 32(6): 363-6, 1982.
Artigo em Português | LILACS | ID: lil-13184

RESUMO

Os autores estudaram 30 pacientes de sexo feminino que foram anestesiadas com alfatesin e fentanil para serem submetidas a mamaplastia redutora, em posicao sentada.A associacao destes agentes possibilitou uma anestesia de excelente qualidade e facil execucao, com boa cardioestabilidade, pequeno sangramento per-anestesico e despertar isento de excitacao, nauseas ou vomitos. Por estas vantagens e por ser uma tecnica venosa total, nao poluente e de baixo custo, os autores a consideram uma opcao segura para pacientes que tenham que ser operados na posicao sentada, desde que respeitadas as contra-indicacoes inerentes aos agentes utilizados


Assuntos
Humanos , Feminino , Mistura de Alfaxalona Alfadolona , Anestesia Intravenosa , Mama , Fentanila , Cirurgia Plástica
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