Am. J. Respir. Crit. Care Med., Vol 154, No. 3, 09 1996, 713-719.
Anti-inflammatory cytokine release by alveolar macrophages in pulmonary sarcoidosis
G Zissel, J Homolka, J Schlaak, M Schlaak and J Muller-Quernheim
Research Institute Borstel, Medical Hospital, Germany.
Sarcoidosis is a systemic, granulomatous disorder with a high rate of
spontaneous remission indicating the presence of antiinflammatory
mechanisms. Antiinflammatory mediators such as interleukin-10 (IL-10) and
transforming growth factor-beta (TGF-beta) should be able to induce
spontaneous remission of sarcoidosis. By measuring the release of both
mediators in culture supernatants of bronchoalveolar lavage (BAL) cells, we
investigated their relevance in the spontaneous remission of sarcoidosis.
No spontaneous IL-10 release was observed by BAL cells of sarcoid patients.
In supernatants of BAL cells of seven patients found retrospectively to be
free of any interstitial lung disease, we found 612 +/- 261.2 pg/ml (mean
+/- SEM) TGF-beta. TGF-beta release was recorded in 20 of 39 patients with
active disease. Patients with active disease without TGF-beta release in
BAL cell culture either required therapy (n = 21; 677 +/- 159 pg/ml) or
showed evidence of persisting disease (n = 6; 762 +/- 419 pg/ml). Patients
with active disease without indications for therapy and with significantly
increased TGF- beta release (n = 12; 1,422 +/- 215 pg/ml; p < 0.004 in
all comparisons) had a spontaneous remission within 6 mo. Increased TGF-
beta release (1,560 +/- 353 pg/ml) was observed in five of five patients
receiving therapy. We conclude that TGF-beta is a regulator of the
inflammatory process in sarcoidosis.
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Copyright © 1996 American Thoracic Society
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