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Immunological Markers of Lung Disease Due to Non-Tuberculous Mycobacteria
Author(s) -
Andrew Lim,
Caris Allison,
Dino B.A. Tan,
Ben Oliver,
Patricia Price,
Grant Waterer
Publication year - 2010
Publication title -
disease markers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 66
eISSN - 1875-8630
pISSN - 0278-0240
DOI - 10.1155/2010/347142
Subject(s) - offspring , cxcl10 , medicine , immunology , cd8 , disease , lung , chemokine , immune system , biology , pregnancy , genetics
Lung disease due to nontuberculous mycobacteria (NTM) is a poorly understood condition that is difficult to treat. Treatment remains problematic as few tools are available to help clinicians monitor disease progression or predict treatment outcome. In this study, plasma levels of several inflammatory molecules and the frequency of circulating T cell subsets were measured in patients with NTM lung disease and known treatment status, and compared with their adult offspring and with unrelated healthy controls. Plasma levels of the chemokine CXCL10 and IL18 were assessed for associations with treatment efficacy. CXCL10 was higher in patients than adult offspring (p < 0.001) and unrelated controls ( p < 0.001). Plasma CXCL10 was also lower in patients who responded well to therapy or who controlled their infection without requiring therapy, when compared to patients who did not respond to therapy ( p = 0.03). Frequencies of activated (HLADR + ) CD4 + T cells were higher in patients than adult offspring ( p < 0.001) and unrelated controls ( p < 0.05), with the highest frequencies in individuals who had completed at least 6 months of treatment. Frequencies of activated (CD38 + ) CD8 + T cells in most treatment responders were similar to unrelated controls. Low plasma levels of CXCL10 may reflect successful control of NTM lung disease with or without therapy. Compared with responders, patients who responded poorly to treatment generally had higher plasma levels of CXCL10 and IL18, and higher frequencies of activated CD8 + T cells.

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