Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells

Ferreira, K. S. ; Lopes, J. D. ; Almeida, S. R.

Oxford, UK : Blackwell Science Ltd
Published 2003
ISSN:
1365-3083
Source:
Blackwell Publishing Journal Backfiles 1879-2005
Topics:
Medicine
Notes:
Paracoccidioidomycosis, endemic in Latin America, is a progressive systemic mycosis caused by Paracoccidioides brasiliensis. The infection can evolve into different clinical forms that are associated with various degrees of suppressed cell-mediated immunity. Assuming that the effector immune response is a consequence of the preferential activation of either Th1 or Th2 subsets, in the present work we evaluated whether the nature of antigen-presenting cells (APCs) can influence the Th1/Th2 balance in vivo. It was observed that the injection of mature dendritic cells (DCs), macrophages and B cells primed the mice and induced a proliferation of T cells in vitro. It was seen that DCs from resistant mice stimulated predominantly interleukin-2 (IL-2) and interferon-γ (IFN-γ), whereas macrophages activated IL-10, IL-4 and IFN-γ-secreting T cells and B cells IL-4 and IL-10 only. Results presented here clearly demonstrate that DC drives the development of cells secreting Th1-derived cytokines, whereas B cells induce the differentiation of a Th2 phenotype in vivo.
Type of Medium:
Electronic Resource
URL:
_version_ 1798290232001429505
autor Ferreira, K. S.
Lopes, J. D.
Almeida, S. R.
book_url http://dx.doi.org/10.1046/j.1365-3083.2003.01291.x
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLZ243699123
insertion_date 2012-04-27
issn 1365-3083
journal_name Scandinavian journal of immunology
materialart 1
notes Paracoccidioidomycosis, endemic in Latin America, is a progressive systemic mycosis caused by Paracoccidioides brasiliensis. The infection can evolve into different clinical forms that are associated with various degrees of suppressed cell-mediated immunity. Assuming that the effector immune response is a consequence of the preferential activation of either Th1 or Th2 subsets, in the present work we evaluated whether the nature of antigen-presenting cells (APCs) can influence the Th1/Th2 balance in vivo. It was observed that the injection of mature dendritic cells (DCs), macrophages and B cells primed the mice and induced a proliferation of T cells in vitro. It was seen that DCs from resistant mice stimulated predominantly interleukin-2 (IL-2) and interferon-γ (IFN-γ), whereas macrophages activated IL-10, IL-4 and IFN-γ-secreting T cells and B cells IL-4 and IL-10 only. Results presented here clearly demonstrate that DC drives the development of cells secreting Th1-derived cytokines, whereas B cells induce the differentiation of a Th2 phenotype in vivo.
package_name Blackwell Publishing
publikationsjahr_anzeige 2003
publikationsjahr_facette 2003
publikationsjahr_intervall 7999:2000-2004
publikationsjahr_sort 2003
publikationsort Oxford, UK
publisher Blackwell Science Ltd
reference 58 (2003), S. 0
search_space articles
shingle_author_1 Ferreira, K. S.
Lopes, J. D.
Almeida, S. R.
shingle_author_2 Ferreira, K. S.
Lopes, J. D.
Almeida, S. R.
shingle_author_3 Ferreira, K. S.
Lopes, J. D.
Almeida, S. R.
shingle_author_4 Ferreira, K. S.
Lopes, J. D.
Almeida, S. R.
shingle_catch_all_1 Ferreira, K. S.
Lopes, J. D.
Almeida, S. R.
Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells
Blackwell Science Ltd
Paracoccidioidomycosis, endemic in Latin America, is a progressive systemic mycosis caused by Paracoccidioides brasiliensis. The infection can evolve into different clinical forms that are associated with various degrees of suppressed cell-mediated immunity. Assuming that the effector immune response is a consequence of the preferential activation of either Th1 or Th2 subsets, in the present work we evaluated whether the nature of antigen-presenting cells (APCs) can influence the Th1/Th2 balance in vivo. It was observed that the injection of mature dendritic cells (DCs), macrophages and B cells primed the mice and induced a proliferation of T cells in vitro. It was seen that DCs from resistant mice stimulated predominantly interleukin-2 (IL-2) and interferon-γ (IFN-γ), whereas macrophages activated IL-10, IL-4 and IFN-γ-secreting T cells and B cells IL-4 and IL-10 only. Results presented here clearly demonstrate that DC drives the development of cells secreting Th1-derived cytokines, whereas B cells induce the differentiation of a Th2 phenotype in vivo.
1365-3083
13653083
shingle_catch_all_2 Ferreira, K. S.
Lopes, J. D.
Almeida, S. R.
Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells
Blackwell Science Ltd
Paracoccidioidomycosis, endemic in Latin America, is a progressive systemic mycosis caused by Paracoccidioides brasiliensis. The infection can evolve into different clinical forms that are associated with various degrees of suppressed cell-mediated immunity. Assuming that the effector immune response is a consequence of the preferential activation of either Th1 or Th2 subsets, in the present work we evaluated whether the nature of antigen-presenting cells (APCs) can influence the Th1/Th2 balance in vivo. It was observed that the injection of mature dendritic cells (DCs), macrophages and B cells primed the mice and induced a proliferation of T cells in vitro. It was seen that DCs from resistant mice stimulated predominantly interleukin-2 (IL-2) and interferon-γ (IFN-γ), whereas macrophages activated IL-10, IL-4 and IFN-γ-secreting T cells and B cells IL-4 and IL-10 only. Results presented here clearly demonstrate that DC drives the development of cells secreting Th1-derived cytokines, whereas B cells induce the differentiation of a Th2 phenotype in vivo.
1365-3083
13653083
shingle_catch_all_3 Ferreira, K. S.
Lopes, J. D.
Almeida, S. R.
Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells
Blackwell Science Ltd
Paracoccidioidomycosis, endemic in Latin America, is a progressive systemic mycosis caused by Paracoccidioides brasiliensis. The infection can evolve into different clinical forms that are associated with various degrees of suppressed cell-mediated immunity. Assuming that the effector immune response is a consequence of the preferential activation of either Th1 or Th2 subsets, in the present work we evaluated whether the nature of antigen-presenting cells (APCs) can influence the Th1/Th2 balance in vivo. It was observed that the injection of mature dendritic cells (DCs), macrophages and B cells primed the mice and induced a proliferation of T cells in vitro. It was seen that DCs from resistant mice stimulated predominantly interleukin-2 (IL-2) and interferon-γ (IFN-γ), whereas macrophages activated IL-10, IL-4 and IFN-γ-secreting T cells and B cells IL-4 and IL-10 only. Results presented here clearly demonstrate that DC drives the development of cells secreting Th1-derived cytokines, whereas B cells induce the differentiation of a Th2 phenotype in vivo.
1365-3083
13653083
shingle_catch_all_4 Ferreira, K. S.
Lopes, J. D.
Almeida, S. R.
Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells
Blackwell Science Ltd
Paracoccidioidomycosis, endemic in Latin America, is a progressive systemic mycosis caused by Paracoccidioides brasiliensis. The infection can evolve into different clinical forms that are associated with various degrees of suppressed cell-mediated immunity. Assuming that the effector immune response is a consequence of the preferential activation of either Th1 or Th2 subsets, in the present work we evaluated whether the nature of antigen-presenting cells (APCs) can influence the Th1/Th2 balance in vivo. It was observed that the injection of mature dendritic cells (DCs), macrophages and B cells primed the mice and induced a proliferation of T cells in vitro. It was seen that DCs from resistant mice stimulated predominantly interleukin-2 (IL-2) and interferon-γ (IFN-γ), whereas macrophages activated IL-10, IL-4 and IFN-γ-secreting T cells and B cells IL-4 and IL-10 only. Results presented here clearly demonstrate that DC drives the development of cells secreting Th1-derived cytokines, whereas B cells induce the differentiation of a Th2 phenotype in vivo.
1365-3083
13653083
shingle_title_1 Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells
shingle_title_2 Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells
shingle_title_3 Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells
shingle_title_4 Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells
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source_archive Blackwell Publishing Journal Backfiles 1879-2005
timestamp 2024-05-06T08:13:27.252Z
titel Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells
titel_suche Regulation of T Helper Cell Differentiation In Vivo by GP43 from Paracoccidioides brasiliensis Provided by Different Antigen-Presenting Cells
topic WW-YZ
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