Immunophenotyping and extracellular matrix remodeling in pulmonary and extrapulmonary sarcoidosis


Autoria(s): Ramos Quintino da Silva, Pedro Henrique; Parra, Edwin Roger; Zocolaro, William Sanches; Narde, Ivy; Rodrigues, Fabiola; Kairalla, Ronaldo Adib; Ribeiro Carvalho, Carlos Roberto; Capelozzi, Vera Luiza
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

05/11/2013

05/11/2013

2012

Resumo

Objective: To investigate the significance of cellular immune markers, as well as that of collagen and elastic components of the extracellular matrix, within granulomatous structures in biopsies of patients with pulmonary or extrapulmonary sarcoidosis. Methods: We carried out qualitative and quantitative evaluations of inflammatory cells, collagen fibers, and elastic fibers in granulomatous structures in surgical biopsies of 40 patients with pulmonary and extrapulmonary sarcoidosis using histomorphometry, immunohistochemistry, picrosirius red staining, and Weigert's resorcin-fuchsin staining. Results: The extrapulmonary tissue biopsies presented significantly higher densities of lymphocytes, macrophages, and neutrophils than did the lung tissue biopsies. Pulmonary granulomas showed a significantly higher number of collagen fibers and a lower density of elastic fibers than did extrapulmonary granulomas. The amount of macrophages in the lung samples correlated with FVC (p < 0.05), whereas the amount of CD3+, CD4+, and CD8+ lymphocytes correlated with the FEV1/FVC ratio and VC. There were inverse correlations between TLC and the CD1a+ cell count (p < 0.05), as well as between DLCO and collagen/elastic fiber density (r = -0.90; p = 0.04). Conclusions: Immunophenotyping and remodeling both showed differences between pulmonary and extrapulmonary sarcoidosis in terms of the characteristics of the biopsy samples. These differences correlated with the clinical and spirometric data obtained for the patients, suggesting that two different pathways are involved in the mechanism of antigen clearance, which was more effective in the lungs and lymph nodes.

Brazilian Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq, National Council for Scientific and Technological Development)

Brazilian Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq, National Council for Scientific and Technological Development)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP, Sao Paulo Research Foundation) [2007/56617-5]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP, Sao Paulo Research Foundation)

Identificador

JORNAL BRASILEIRO DE PNEUMOLOGIA, BRASILIA DF, v. 38, n. 3, supl. 1, Part 2, pp. 321-330, MAY-JUN, 2012

1806-3713

http://www.producao.usp.br/handle/BDPI/41061

10.1590/S1806-37132012000300007 

http://dx.doi.org/10.1590/S1806-37132012000300007 

Idioma(s)

eng

Publicador

SOC BRASILEIRA PNEUMOLOGIA TISIOLOGIA

BRASILIA DF

Relação

JORNAL BRASILEIRO DE PNEUMOLOGIA

Direitos

openAccess

Copyright SOC BRASILEIRA PNEUMOLOGIA TISIOLOGIA

Palavras-Chave #SARCOIDOSIS #GRANULOMATOUS DISEASE, CHRONIC #EXTRACELLULAR MATRIX #IMMUNOPHENOTYPING #RESPIRATORY FUNCTION TESTS #IDIOPATHIC INTERSTITIAL PNEUMONIAS #PROGNOSTIC-SIGNIFICANCE #FIBROSIS #FIBERS #STATEMENT #SECONDARY #COLLAGEN #SYSTEM #RESPIRATORY SYSTEM
Tipo

article

original article

publishedVersion