Chronic Obstructive Pulmonary Disease Clinical Trial
Official title:
Phenotype and Number of Regulatory T Cells Present in Peripheral Blood of COPD Patients Versus Healthy Controls
Lymphoid follicles, consisting of T-and B cells, are involved in the chronic inflammatory
response in COPD. Foxp3 positive regulatory T cells (Tregs) are present in these follicles
and may be involved in the suppression of this chronic inflammatory response.
We hypothesise that a dysfunction of Tregs underlies the development of the inflammatory
response in COPD. This could be either due to a decreased presence of Tregs in COPD, or to
an altered function of Tregs possibly caused by a decreased HO-1 expression and/or an
altered TGFβ regulation.
COPD is a leading cause of death worldwide and its morbidity and mortality are still
rising.So far, no effective treatment is available To find better treatment methods more
insight is needed in the nature/origin of the chronic inflammation that underlies the
development of COPD.
The important role of neutrophils, macrophages and cytotoxic T cells is well established in
this respect, yet the role of CD4 T cells and B cells has only recently (re)attracted
attention. We detected the presence of lymphoid follicles in lung tissue of COPD patients,
consisting of B cells surrounded by T cells. Recently, we have found the presence of Foxp3
positive T cells as a component of these lymphoid follicles in COPD. Since Foxp3 is a
distinctive marker of regulatory T cells (Tregs), this finding suggests that Tregs are
involved in the inflammatory response in COPD.
Tregs are important in controlling immunological tolerance and preventing auto-immune
responses by inhibiting T-cell responses. Dysfunction of Tregs can lead to auto-immune
diseases, allergy and chronic inflammatory diseases. However, nothing is known so far about
their contribution to the chronic inflammatory response in COPD. Recent studies show that,
next to direct inhibition by cell-cell contact, the inhibitory effects of Tregs are mediated
by heme oxygenase-1 (HO-1) expression and membrane bound TGFβ.
We hypothesise that a dysfunction of regulatory T cells underlies the development of the
inflammatory response in COPD. This could be due to a decreased presence of Tregs in COPD,
or to an altered function of Tregs. The latter may be due to a decreased HO-1 expression, as
we have shown in macrophages of COPD patients compared to those in healthy controls, and/or
an altered TGFβ regulation, a cytokine that plays a prime role in COPD.
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