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1.
Allergol Int ; 58(3): 445-54, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19628980

RESUMO

BACKGROUND: Influenza A viral infection is concerned with induction of asthma. CD11c+ pulmonary antigen presenting cells (APCs) play a central role in sensitization with inhaled antigens during the acute phase of influenza A viral infection and also reside on bronchial epithelium for the long term after sensitization. To investigate the role of CD11c+ pulmonary APCs in the inhaled antigen sensitization during the acute phase of influenza A viral infection, we analyzed their function. METHODS: Mice were infected with influenza A virus and were sensitized intranasally with BSA/alum during the acute phase of influenza A viral infection. Expression of surface antigens on CD11c+ pulmonary APCs was analyzed by FACS. Cytokine production from CD11c+ pulmonary APCs, and interaction between CD11c+ pulmonary APCs and naïve CD4+ T cells was assessed by ELISA. Ability of antigen presentation by CD11c+ pulmonary APCs was measured by proliferation assay. RESULTS: BSA antigen sensitization during the acute phase of influenza A viral infection induced eosinophil recruitment into the lungs after BSA antigen challenge and moderately increased expression of MHC class II molecules on CD11c+ pulmonary APCs. The interaction between the CD11c+ pulmonary APCs and naïve CD4+ T cells secreted large amounts of IL-10. CONCLUSIONS: BSA antigen sensitization during the acute phase of influenza A viral infection enhanced IL-10 production from naïve CD4+ T cell interaction with CD11c+ pulmonary APCs. The IL-10 secretion evoked Th2 responses in the lungs with downregulation of Th1 responses and was important for the eosinophil recruitment into the lungs after BSA antigen challenge.


Assuntos
Células Apresentadoras de Antígenos/imunologia , Asma/imunologia , Antígeno CD11c/imunologia , Vírus da Influenza A Subtipo H1N1 , Influenza Humana/imunologia , Soroalbumina Bovina/imunologia , Doença Aguda , Animais , Antígenos/imunologia , Linfócitos T CD4-Positivos/imunologia , Linfócitos T CD4-Positivos/metabolismo , Modelos Animais de Doenças , Eosinófilos/metabolismo , Feminino , Genes MHC da Classe II/imunologia , Humanos , Imunização , Influenza Humana/complicações , Interleucina-10/biossíntese , Pulmão/imunologia , Camundongos , Camundongos Endogâmicos C57BL , Ovalbumina/imunologia
2.
J Biomed Mater Res A ; 68(1): 34-42, 2004 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-14661247

RESUMO

Cell separation from peripheral blood was investigated using surface-modified polyurethane (PU) membranes with different functional groups. Both red blood cells and platelets could pass through unmodified PU and PU-SO(3)H membranes, whereas the red blood cells preferentially passed through PU-N(C(2)H(5))(2) and PU-NHC(2)H(4)OH membranes. The permeation ratio of T and B cells was <25% for the surface-modified and unmodified PU membranes. CD34(+) cells have been recognized as various kinds of stem cells including hematopoietic and mesenchymal stem cells. The adhesiveness of CD34(+) cells on the PU membranes was found to be higher than that of red blood cells, platelets, T cells, or B cells. Overall, the adhesiveness of blood cells on the PU membranes increased in the following order: red blood cells

Assuntos
Citaferese/métodos , Poliuretanos , Antígenos CD/sangue , Antígenos CD34/sangue , Materiais Biocompatíveis , Células Sanguíneas/citologia , Células Sanguíneas/ultraestrutura , Hemofiltração/instrumentação , Hemofiltração/métodos , Humanos , Membranas Artificiais , Microscopia Eletrônica de Varredura
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