Sp. Atamas et al., Production of type 2 cytokines by CD8+lung cells is associated with greater decline in pulmonary function in patients with systemic sclerosis, ARTH RHEUM, 42(6), 1999, pp. 1168-1178
Objective. This study addresses the hypothesis that a profibrotic pattern o
f cytokines is produced in the lungs of patients with systemic sclerosis (S
Sc) and causes fibrosis,
Methods, Using a reverse transcriptase-polymerase chain reaction technique,
interleukin-4 (IL-4), IL-5, and interferon-gamma (IFN gamma) messenger RNA
(mRNA) were measured in unseparated CD8+ and CD4+ bronchoalveolar lavage (
BAL) cells from SSc patients and healthy controls. To confirm the results,
CD8+ T cells were cloned from BAL fluids, and the pattern of cytokine mRNA
made by these cells was determined. Serial pulmonary function tests were do
ne.
Results, BAL cells from healthy controls made IFN gamma mRNA, with no or li
ttle IL-4 or IL-5 mRNA, In contrast, BAL cells from the majority of SSc pat
ients made IL-4 and/or IL-5 mRNA, with or without approximately equal amoun
ts of IFN gamma mRNA. This pattern of cytokines was made by CD8+ T cells, w
hich were increased in the lungs of these SSc patients. Patients whose BAL
cells made this type 2 pattern of cytokine mRNA had a significant decline i
n forced vital capacity over time after the BAL, whereas patients whose BAL
cells made lFN gamma mRNA alone did not, Both wild-type and an alternative
splice variant of IL-4 mRNA were increased in BAL cells from SSc patients.
Both forms of IL-4 stimulated alpha 2(I) collagen mRNA in human dermal and
lung fibroblasts.
Conclusion. The type 2 pattern of cytokine mRNA produced by BAL cells from
SSc patients differs from unopposed IFN gamma production found in healthy B
AL cells. This production of type 2 cytokine mRNA by CD8+ T cells is associ
ated with a significant decline in lung function over time, which suggests
a pathologic role for these T cells in interstitial fibrosis in SSc.