M. Raulf et al., INCREASED GAMMA DELTA-POSITIVE T-CELLS IN BLOOD AND BRONCHOALVEOLAR LAVAGE OF PATIENTS WITH SARCOIDOSIS AND HYPERSENSITIVITY PNEUMONITIS/, The European respiratory journal, 7(1), 1994, pp. 140-147
A small population of T cells does not express the conventional T-cell
receptor (TCR), characterized by the alpha and beta polypeptide chain
s (alpha/beta TCR) but two polypeptides termed gamma and delta (gamma/
delta TCR). Changes in gamma/delta TCR expression may be relevant as t
he cause or consequence of several diseases. Our study was undertaken
to determine and compare the distribution of T-cells expressing gamma/
delta TCR in blood and bronchoalveolar lavage (BAL) of patients with s
arcoidosis, hypersensitivity pneumonitis (AP), idiopathic pulmonary fi
brosis (IPF), and of healthy controls. In addition, the association be
tween gamma/delta TCR of blood T-lymphocytes and accessory molecules w
as analysed. Using direct immunofluorescence with the anti-gamma/delta
TCR and anti-CD3 monoclonal antibodies (MoAbs) followed by now cytome
tric analysis, the blood of patients with pulmonary sarcoidosis, HP, I
PF and of healthy controls was analysed. To reveal the association bet
ween gamma/delta TCR of blood T lymphocytes and the accessory molecule
s, expression of CD4, CD8 and CD25 were determined. Calculating the pe
rcentage and the total number of CD3+ gamma/delta TCR cells hn blood,
the data indicated a significant increase of gamma/delta T-cells in in
dividuals with pulmonary sarcoidosis and HP, compared to healthy contr
ols and IPF patients. In sarcoidosis patients with elevated CD3+ gamma
/delta TCR levels, significantly lower CD4/CD8 ratios were observed. I
n addition, our data demonstrate a correlation between the decrease of
CD4+ cells in blood and the amplified appearance of gamma/delta TCR e
xpression in sarcoidosis patients, but not in HP patients. gamma/delta
TCR I cells were either CD8-positive (approximately 50%), or had a ''
double-negative phenotype'' (CD4-/CD8-) (remaining 50%). Circulating b
lood gamma/delta T-cells were CD25-negative, suggesting a lack of acti
vation. The total number of CD3+ gamma/delta TCR+-bearing lymphocytes
in BAL fluid was increased in sarcoidosis and HP, compared with IPF. A
corresponding increase of CD3+ gamma/delta TCR+ cells was observed in
blood and BAL of sarcoidosis patients. In conclusion, our data indica
te that levels of gamma/delta T-cells are increased in blood and BAL f
luid of patients with sarcoidosis and HP. Although this suggests a pat
hogenetic role for gamma/delta TCR, it is not clear whether its expres
sion is a causal factor, or a consequence, of these diseases.