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Eur Respir J 2005; 26:77-85
Copyright ©ERS Journals Ltd 2005

Characterisation of natural killer cells and CD56+ T-cells in sarcoidosis patients

K. Katchar1, K. Söderström2, J. Wahlstrom1, A. Eklund1 and J. Grunewald1

1 Dept of Medicine, Division of Respiratory Medicine, Karolinska Hospital, Stockholm, Sweden. 2 Dept of Pathology, Stanford Medical School, Stanford, CA, USA.

CORRESPONDENCE: K. Katchar, Beth Israel Deaconess Medical Center, Dana 601, 330 Brookline Avenue, Boston, MA 02215, USA. Fax: 1 6176678144. E-mail: kkatchar@bidmc.harvard.edu

Keywords: Bronchoalveolar lavage fluid, CD56+ T-cells, killer inhibitory receptors, natural killer cells, sarcoidosis

Received: March 15, 2005
Accepted April 1, 2005

The aim of the current study was to investigate the frequency, phenotype and functional activity of natural killer (NK) cells and CD56+ T-cells in the bronchoalveolar lavage fluid and peripheral blood of patients with pulmonary sarcoidosis when compared with healthy volunteers, using staining with a panel of monoclonal antibodies followed by flow cytometry.

The results revealed that the majority of the lung NK cell subpopulation expressed CD56bright. In contrast, there was a predominant CD56dim subset in the blood of both patients and healthy controls. Most lung NK cells expressed C-type lectin-like human leukocyte antigen (HLA)-E-specific inhibitory receptor (i.e. CD94/NKG2A), but only a few lung NK cells expressed killer cell immunoglobulin-like inhibitory receptors specific for HLA-A, -B or -C molecules. In addition, a significantly increased number of CD56+ T-cells were observed in the blood of patients when compared with controls. Upon in vitro stimulation, both lung NK and CD56+ T-cells produced considerable amounts of interferon-{gamma} and tumour necrosis factor-{alpha}.

Thus, in the lungs of patients with pulmonary sarcoidosis, a distinct phenotype of natural killer cells with the capacity to produce cytokines and actively participate in the T-helper 1-like inflammatory response associated with sarcoidosis was identified.




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