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1.
BMC Immunol ; 15: 42, 2014 Oct 08.
Artigo em Inglês | MEDLINE | ID: mdl-25293512

RESUMO

BACKGROUND: The spleen is thought to be central in regulating the immune system, a metabolic asset involved in endocrine function. Overwhelming postsplenectomy infection leads to a mortality rate of up to 50%. However, there is still controversy on performing subtotal splenectomy as treatment of splenomegaly due to portal hypertension in cirrhotic patients. In the present study, immunocytes and the indexes of splenic size, hemodynamics, hematology and immunology in the residual spleen were analyzed to support subtotal splenectomy due to splenomegaly. RESULTS: In residual spleen, T lymphocytes mainly were focal aggregation in the periarterial lymphatic sheath. While B lymphocytes densely distributed in splenic corpuscle. In red pulp, macrophages were equally distributed in the xsplenic cord and adhered to the wall of splenic sinus with high density. The number of unit area T and B lymphocytes of splenic corpuscle and marginal zone as well as macrophages of red pulp were obviously increased in the residual spleen, while the number of macrophages didn't be changed among the three groups in white pulp. While there were some beneficial changes (i.e., Counts of platelet and leucocyte as well as serum proportion of CD3+ T cells, CD4+ T cells, CD8+ T cells were increased markedly; serum levels of M-CSF and GM-CSF were decreased significantly; The proportion of granulocyte, erythrocyte, megakaryocyte in bone marrow were changed obviously; But serum IgA, IgM, IgG, Tuftsin level, there was no significant difference; splenic artery flow volume, portal venous diameter and portal venous flow volume, a significant difference was observed in residual spleen) in the clinical indices. CONCLUSION: After subtotal splenectomy with splenomegaly due to portal hypertension in cirrhotic patients, the number of unit area T and B lymphocytes, and MØ in red pulp of residual spleen increased significantly. However, whether increase of T, B lymphocytes and MØs in residual splenic tissue can enhance the immune function of the spleen, still need further research to confirm.


Assuntos
Cirrose Hepática , Linfócitos , Monócitos , Baço , Esplenectomia , Esplenomegalia , Adulto , Feminino , Fator Estimulador de Colônias de Granulócitos e Macrófagos/sangue , Fator Estimulador de Colônias de Granulócitos e Macrófagos/imunologia , Humanos , Imunoglobulinas/sangue , Imunoglobulinas/imunologia , Contagem de Leucócitos , Cirrose Hepática/sangue , Cirrose Hepática/imunologia , Cirrose Hepática/patologia , Cirrose Hepática/cirurgia , Linfócitos/imunologia , Linfócitos/metabolismo , Linfócitos/patologia , Fator Estimulador de Colônias de Macrófagos/sangue , Fator Estimulador de Colônias de Macrófagos/imunologia , Masculino , Monócitos/imunologia , Monócitos/metabolismo , Monócitos/patologia , Estudos Retrospectivos , Baço/imunologia , Baço/metabolismo , Baço/patologia , Baço/cirurgia , Esplenomegalia/sangue , Esplenomegalia/imunologia , Esplenomegalia/patologia , Esplenomegalia/cirurgia
3.
Oncology ; 57(3): 211-5, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10545789

RESUMO

The aim of this study was to simultaneously determine IL-6, M-CSF and IAP levels in 61 serum samples of previously untreated ovarian cancer patients. A direct correlation between IL-6 and M-CSF has been found in our patient population (r = +0.41, p = 0.013), while IAP serum levels failed to correlate with M-CSF (r = +0.15, p = 0. 24) and IL-6 (r = +0.17, p = 0.18) levels. Since IL-6 and M-CSF have been demonstrated to be both induced in response to the same agents, it is conceivable that a mechanism of coregulation in the production of these cytokines by tumor cells and macrophages might occur. The direct correlation between IL-6 and M-CSF also suggests that tumor-derived cytokines can potentially lead to a self-maintaining cytokine network by recruiting cytokine-producing host cells and by perpetuating cytokine production.


Assuntos
Biomarcadores Tumorais/sangue , Interleucina-6/sangue , Fator Estimulador de Colônias de Macrófagos/sangue , Proteínas de Neoplasias/sangue , Neoplasias Ovarianas/sangue , Feminino , Humanos , Pessoa de Meia-Idade
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