Immunological Markers of Lung Disease Due to Non-Tuberculous Mycobacteria
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 inflammator...
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2010-01-01
|
Series: | Disease Markers |
Online Access: | http://dx.doi.org/10.3233/DMA-2010-0732 |
Summary: | 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. |
---|---|
ISSN: | 0278-0240 1875-8630 |