Am. J. Respir. Cell Mol. Biol., Vol 12, No. 5, 05 1995, 567-578.
Peripheral blood CD4 but not CD8 t-lymphocytes in patients with exacerbation of asthma transcribe and translate messenger RNA encoding cytokines which prolong eosinophil survival in the context of a Th2- type pattern: effect of glucocorticoid therapy
CJ Corrigan, Q Hamid, J North, J Barkans, R Moqbel, S Durham, V Gemou-Engesaeth and AB Kay
Department of Allergy and Clinical Immunology, National Heart and Lung Institute, London, United Kingdom.
T-lymphocyte (T-LC)-derived cytokines have been implicated in asthma
pathogenesis. Activation of peripheral blood CD4 but not CD8 T-LC and a
Th2-type pattern of elevated cytokine mRNA expression in BAL fluid T-LC
have been observed in asthmatics, but the principal source (CD4 or CD8
T-LC) of these cytokines is unknown. Our objective was to measure
expression of Th1- and Th2-type cytokine mRNA and spontaneous secretion of
IL-3, IL-5, and GM-CSF by peripheral blood CD4 and CD8 T-LC from asthmatics
before and after oral glucocorticoid therapy and non- asthmatic controls.
We used in situ hybridization to detect mRNA expression in isolated CD4 and
CD8 T-LC, and an in vitro eosinophil survival assay to detect secretion of
IL-3, IL-5, and GM-CSF in T-LC culture supernatants. Comparing the
asthmatics with the controls, elevated percentages of CD4 T-LC expressed
mRNA encoding IL-5, IL-4, and GM-CSF (P < 0.02) but not IL-3, IL-2, or
IFN-gamma. In CD8 T-LC, mRNA expression was generally low with no
significant differences between the groups. In the asthmatics, the
percentages of CD4 T-LC expressing IL-5 mRNA correlated with disease
severity and the numbers of peripheral blood eosinophils (P < 0.01).
Culture supernatants of asthmatic CD4 but not CD8 T-LC exhibited
significantly higher (P = 0.0003) eosinophil survival-prolonging activity
compared with controls, in which low activity was detected. Inhibition with
anti-cytokine antibodies suggested that GM-CSF, and to a lesser extent IL-5
and IL-3, could account for this activity. After oral glucocorticoid
therapy of the asthmatics, lung function improved and the percentages of
CD4 T-LC expressing mRNA encoding IL-3, IL-5, and GM-CSF but not IL-2,
IL-4, or IFN-gamma were reduced (P < 0.04). Secretion of eosinophil
survival- prolonging activity by the CD4 T-LC was also reduced (P = 0.004).
We conclude that peripheral blood CD4 but not CD8 T-LC from asthmatics
express cytokine mRNA in a Th2-type pattern and show elevated secretion of
cytokines prolonging eosinophil survival. Glucocorticoid therapy of
asthmatics is associated with a reduction in the percentages of CD4 T- LC
expressing IL-3, IL-5, and GM-CSF mRNA and secretion of the corresponding
proteins.
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Copyright © 1995 American Thoracic Society.
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