Normal expression of IFNgR in four patients with uncommon mycobacterial infection phenotypes
ABSTRACT: Several primary immunodeficiency diseases affecting the interleukin 12/interferon gamma (IFN-g) pathway have been identified, most of them characterized by recurrent and protracted infections produced by intracellular microorganisms, particularly by several species of mycobacteria. In the...
- Autores:
-
Rugeles López, María Teresa
Rincón Orozco, Bladimiro
Rugeles López, Claudia
Montoya Guarín, Carlos Julio
Hernández, Mariluz
Estrada, Carlos
Olivares Gómez, María Margarita
Patiño Grajales, Pablo Javier
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2004
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/25682
- Acceso en línea:
- http://hdl.handle.net/10495/25682
- Palabra clave:
- Mycobacterial disease
IFN-γ
IFN-γ receptor
STAT-1
SSCP-PCR
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/2.5/co/
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| dc.title.spa.fl_str_mv |
Normal expression of IFNgR in four patients with uncommon mycobacterial infection phenotypes |
| title |
Normal expression of IFNgR in four patients with uncommon mycobacterial infection phenotypes |
| spellingShingle |
Normal expression of IFNgR in four patients with uncommon mycobacterial infection phenotypes Mycobacterial disease IFN-γ IFN-γ receptor STAT-1 SSCP-PCR |
| title_short |
Normal expression of IFNgR in four patients with uncommon mycobacterial infection phenotypes |
| title_full |
Normal expression of IFNgR in four patients with uncommon mycobacterial infection phenotypes |
| title_fullStr |
Normal expression of IFNgR in four patients with uncommon mycobacterial infection phenotypes |
| title_full_unstemmed |
Normal expression of IFNgR in four patients with uncommon mycobacterial infection phenotypes |
| title_sort |
Normal expression of IFNgR in four patients with uncommon mycobacterial infection phenotypes |
| dc.creator.fl_str_mv |
Rugeles López, María Teresa Rincón Orozco, Bladimiro Rugeles López, Claudia Montoya Guarín, Carlos Julio Hernández, Mariluz Estrada, Carlos Olivares Gómez, María Margarita Patiño Grajales, Pablo Javier |
| dc.contributor.author.none.fl_str_mv |
Rugeles López, María Teresa Rincón Orozco, Bladimiro Rugeles López, Claudia Montoya Guarín, Carlos Julio Hernández, Mariluz Estrada, Carlos Olivares Gómez, María Margarita Patiño Grajales, Pablo Javier |
| dc.contributor.researchgroup.spa.fl_str_mv |
Inmunodeficiencias Primarias Inmunovirología |
| dc.subject.proposal.spa.fl_str_mv |
Mycobacterial disease IFN-γ IFN-γ receptor STAT-1 SSCP-PCR |
| topic |
Mycobacterial disease IFN-γ IFN-γ receptor STAT-1 SSCP-PCR |
| description |
ABSTRACT: Several primary immunodeficiency diseases affecting the interleukin 12/interferon gamma (IFN-g) pathway have been identified, most of them characterized by recurrent and protracted infections produced by intracellular microorganisms, particularly by several species of mycobacteria. In the present study we analyzed the expression of IFN-g receptor (IFN-gR) and signal transducer and activator of transcription 1 (STAT-1) in 4 children with Mycobacterium tuberculosis infection of uncommon clinical presentation. These molecules were evaluated by flow cytometry and Western blotting in B cells transformed with Epstein-Barr virus and mutations were scanned by single-strand conformational polymorphisms and DNA sequencing. The expression of IFN-gR1 was normal in all 4 patients. The genetic analysis of IFN-gR1 and IFN-gR2 coding sequences did not reveal any mutation. The expression of the STAT-1 molecule was similar in patients and healthy controls; however, when the phosphorylation of this transcription factor in response to IFN-g activation was evaluated by Western blot, a significant lower signal was evident in one patient. These data indicate that there are no alterations in the expression or function of the IFN-gR chains in these patients. However, the low level of STAT-1 phosphorylation found in one of these patients might be explained by a defect in one of the molecules involved in the signal transduction pathway after IFN-g interacts with its receptor. In the other three patients the inability to eliminate the mycobacteria may be due to a defect in another effector mechanism of the mononuclear phagocytes. |
| publishDate |
2004 |
| dc.date.issued.none.fl_str_mv |
2004 |
| dc.date.accessioned.none.fl_str_mv |
2022-01-28T16:50:10Z |
| dc.date.available.none.fl_str_mv |
2022-01-28T16:50:10Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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0100-879X |
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http://hdl.handle.net/10495/25682 |
| dc.identifier.doi.none.fl_str_mv |
10.1590/S0100-879X2004000900010 |
| dc.identifier.eissn.none.fl_str_mv |
1414-431X |
| identifier_str_mv |
0100-879X 10.1590/S0100-879X2004000900010 1414-431X |
| url |
http://hdl.handle.net/10495/25682 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Braz. J. Med. Biol. Res. |
| dc.relation.citationendpage.spa.fl_str_mv |
1363 |
| dc.relation.citationissue.spa.fl_str_mv |
9 |
| dc.relation.citationstartpage.spa.fl_str_mv |
1353 |
| dc.relation.citationvolume.spa.fl_str_mv |
37 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Brazilian Journal of Medical and Biological Research |
| dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by/2.5/co/ |
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https://creativecommons.org/licenses/by/4.0/ |
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Associação Brasileira de Divulgação Científica |
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São Paulo, Brasil |
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Universidad de Antioquia |
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Rugeles López, María TeresaRincón Orozco, BladimiroRugeles López, ClaudiaMontoya Guarín, Carlos JulioHernández, MariluzEstrada, CarlosOlivares Gómez, María MargaritaPatiño Grajales, Pablo JavierInmunodeficiencias PrimariasInmunovirología2022-01-28T16:50:10Z2022-01-28T16:50:10Z20040100-879Xhttp://hdl.handle.net/10495/2568210.1590/S0100-879X20040009000101414-431XABSTRACT: Several primary immunodeficiency diseases affecting the interleukin 12/interferon gamma (IFN-g) pathway have been identified, most of them characterized by recurrent and protracted infections produced by intracellular microorganisms, particularly by several species of mycobacteria. In the present study we analyzed the expression of IFN-g receptor (IFN-gR) and signal transducer and activator of transcription 1 (STAT-1) in 4 children with Mycobacterium tuberculosis infection of uncommon clinical presentation. These molecules were evaluated by flow cytometry and Western blotting in B cells transformed with Epstein-Barr virus and mutations were scanned by single-strand conformational polymorphisms and DNA sequencing. The expression of IFN-gR1 was normal in all 4 patients. The genetic analysis of IFN-gR1 and IFN-gR2 coding sequences did not reveal any mutation. The expression of the STAT-1 molecule was similar in patients and healthy controls; however, when the phosphorylation of this transcription factor in response to IFN-g activation was evaluated by Western blot, a significant lower signal was evident in one patient. These data indicate that there are no alterations in the expression or function of the IFN-gR chains in these patients. However, the low level of STAT-1 phosphorylation found in one of these patients might be explained by a defect in one of the molecules involved in the signal transduction pathway after IFN-g interacts with its receptor. In the other three patients the inability to eliminate the mycobacteria may be due to a defect in another effector mechanism of the mononuclear phagocytes.COL0012426COL001244411application/pdfengAssociação Brasileira de Divulgação CientíficaSão Paulo, Brasilhttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Normal expression of IFNgR in four patients with uncommon mycobacterial infection phenotypesArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionMycobacterial diseaseIFN-γIFN-γ receptorSTAT-1SSCP-PCRBraz. J. Med. Biol. 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