The diagnosis of pulmonary sarcoidosis relies in part on the observation of
alveolar CD4(+) lymphocytosis. However, this criterion is not fully discri
minative because this anomaly is also found in other types of lung diseases
. Among other possible distinctive criteria, we investigated the expression
of lymphocyte-addressing molecules, which could differ according to the pa
thophysiology of lung diseases. We investigated CD103 (alpha(E)beta 7 integ
rin, CD103-beta 7), reported to be both expressed on intra-epithelial lymph
ocytes in mucosal areas, including bronchi, and possibly involved in the re
cruitment of alveolar lymphocytes. The expression of CD103 was examined on
bronchoalveolar lavage lymphocytes from 93 consecutive patients, including
34 patients with CD4(+) lymphocytosis. For all patients, the expression of
CD19, CD3, CD4, CD8, CD57, LFA1, DR, and CD103 was assessed by flow cytomet
ry. Sarcoidosis seemed remarkably characterized by the lack of CD103 expres
sion on the predominant CD4(+) subset. Statistically significant difference
s were found between patients with sarcoidosis, with other types of CD4(+)
lymphocytosis, and with other lung disorders in the CD103(+) cell levels an
d in the CD103/CD4 ratio. Combined use of the CD4/CD8 ratio (> 2.5) and the
CD103/CD4 ratio (< 0.31) to assess bronchoalveolar lavage lymphocytes is a
promising new tool for the diagnosis of sarcoidosis.