H. Garn et al., T-LYMPHOCYTE ACTIVATION IN THE ENLARGED THORACIC LYMPH-NODES OF RATS WITH SILICOSIS, American journal of respiratory cell and molecular biology, 16(3), 1997, pp. 309-316
Silicosis is primarily a mononuclear cell inflammatory and fibrotic di
sease of the pulmonary parenchyma. It is known that lung-associated ly
mph nodes are also affected. To study the involvement of lymphocytes i
n silicosis, we examined lymph nodes of rats 12 months after an 8-day
silica aerosol exposure. We found that 2 thoracic lymph nodes close to
the thymus were enormously enlarged in silicotic rats and contained a
49-fold higher cell number than control lymph nodes. The higher cell
number was caused by parallel increases in T- and B-lymphocytes, natur
al killer (NK) cells, and macrophages without change in the relative p
roportions when compared with control thoracic lymph nodes. By examini
ng interleukin-2 (IL-2) receptor and intercellular adhesion molecule-1
expression, we detected a significantly higher percentage of activate
d CD8(+) T cells and, to a lower degree, of CD4(+) T cells in thoracic
lymph nodes of silicotic animals. In contrast, no differences in the
activation state were found in T cells obtained from cervical or mesen
teric lymph nodes of silicotic and control rats. The occurrence of act
ivated T cells in thoracic lymph nodes of silicotic rats was documente
d further by selectively enhanced interferon-gamma (IFN-gamma) mRNA ex
pression in the absence of IL-2 and IL-4 mRNA changes. These data show
that T-lymphocytes of thoracic lymph nodes have become activated with
an enhanced IFN-gamma gene transcription which may be an important ca
use of macrophage activation during silicosis.