H. Yamasaki et al., Polarized type 1 cytokine profile in bronchoalveolar lavage T cells of patients with hypersensitivity pneumonitis, J IMMUNOL, 163(6), 1999, pp. 3516-3523
Hypersensitivity pneumonitis (HP) is characterized by an inflammatory lymph
ocytic alveolitis comprised of both CD8(+) and CD4(+) T cells, Animal model
s suggest that HP is facilitated by overproduction of IFN-gamma, and that I
L-10 ameliorates severity of the disease, indicating a Th1-type response. T
o determine whether a Th1 phenotype in HP also exists clinically, bronchoal
veolar lavage (BAL) and peripheral blood (PB) T cells were obtained from HP
individuals and analyzed for Th1 vs Th2 cytokine profiles. It was determin
ed that soluble OKT3-stimulated BAL T cells cocultured with alveolar macrop
hages produced more IFN-gamma and less IL-10 than PB T cells cocultured wit
h monocytes, but no difference was observed in IL-4 production. The monocyt
ic cells did not account for this difference, as CD80 and CD86 expressions
were similar, and coculturing PB T cells with alveolar macrophages resulted
in no difference in IFN-gamma production, Similarly, there was no differen
ce in IL-12 production between stimulated BAL or PB T Cells; however, addit
ion of rIL-12 significantly increased production of IFN-gamma by BAL T cell
s, but not by FB T cells. This effect was due to a difference in IL-12R exp
ression, High affinity IL-12R mere only present in association with BAL T c
ells, These studies indicate that clinical HP is characterized by a predomi
nance of IFN-gamma-producing T cells, perhaps resulting from a reduction in
IL-10 production and an increase in high affinity IL-12R compared with blo
od T cells.