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Tipo do documento: Artigo
Título: The use of Mycobacterium tuberculosis HspX and GlcB proteins to identify latent tuberculosis in rheumatoid arthritis patients
Autor: Silva, Bruna Daniella Souza
Silva, Daniela Graner Schuwartz Tannus
Rabahi, Marcelo Fouad
Kipnis, Andre
Junqueira-Kipnis, Ana Paula
Abstract: Rheumatoid arthritis (RA) is an autoimmune disease characterised by the destruction of articular cartilage and bone damage. The chronic treatment of RA patients causes a higher susceptibility to infectious diseases such as tuberculosis (TB); one-third of the world’s population is latently infected (LTBI) with Mycobacterium tuberculosis (Mtb). The tuberculin skin test is used to identify individuals LTBI, but many studies have shown that this test is not suitable for RA patients. The goal of this work was to test the specific cellular immune responses to the Mtb malate synthase (GlcB) and heat shock protein X (HspX) antigens of RA patients and to correlate those responses with LTBI status. The T-helper (Th)1, Th17 and Treg-specific immune responses to the GlcB and HspX Mtb antigens were analysed in RA patients candidates for tumour necrosis factor-α blocker treatment. Our results demonstrated that LTBI RA patients had Th1-specific immune responses to GlcB and HspX. Patients were followed up over two years and 14.3% developed active TB. After the development of active TB, RA patients had increased numbers of Th17 and Treg cells, similar to TB patients. These results demonstrate that a GlcB and HspX antigen assay can be used as a diagnostic test to identify LTBI RA patients.
Palavras-chave: Th cells
Latent infected tuberculosis
País: Brasil
Unidade acadêmica: Instituto de Patologia Tropical e Saúde Pública - IPTSP (RG)
Citação: SILVA, Bruna Daniella Souza et. al. The use of Mycobacterium tuberculosis HspX and GlcB proteins to identify latent tuberculosis in rheumatoid arthritis patients. Memórias do Instituto Oswaldo Cruz, Rio de Janeiro, v. 109, n. 1, p. 29-37, Feb. 2014.
Tipo de acesso: Acesso Aberto
Identificador do documento: 10.1590/0074-02760140140
Identificador do documento: 10.1590/0074-02760140140
Data de publicação: Fev-2014
Aparece nas coleções:IPTSP - Artigos publicados em periódicos

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