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Experimental Studies |
Department of Medicine, University of Sheffield, Clinical Sciences Centre, Northern General Hospital, Sheffield S5 7AU, United Kingdom
IL-12, IL-13, and IL-15 are important cytokines that have not been
studied previously in human autoimmune thyroid diseases. By applying
RT-PCR on RNA extracted from tissue samples, we have investigated
in vivo gene expression of these cytokines in
multinodular goiter (MNG), Graves disease (GD), and Hashimotos
thyroiditis (HT). In addition, in vitro studies were
carried out using the transformed human thyroid cell line, HT-ori3, and
primary thyroid cell cultures derived from patients with GD. These
cells were used either unstimulated or stimulated for 12 h with
TSH, IL-1, or interferon-
(IFN-
). IL-12 p40 gene expression was
identified in 2 of 10 MNG samples, 6 of 12 GD, and 3 of 4 HT. HT-ori3
and primary thyroid cell cultures were positive for IL-12 p40 messenger
RNA (mRNA) expression in both unstimulated and stimulated cell
cultures. IL-13 mRNA was expressed in 2 MNG, 9 GD, and 1 HT sample.
Both HT-ori3 and primary thyroid cultures expressed IL-13 after TSH,
IL-1, or IFN-
stimulation; unstimulated primary cultures of thyroid
cells, however, did not express IL-13. IL-15 gene expression was
detected in 8 MNG, 8 GD, and 4 HT samples. HT-ori3 and primary thyroid
cell cultures, stimulated with TSH, IL-1, or IFN-
, showed expression
of this cytokine. Unstimulated cells showed only a weak expression. Our
results indicate that the cytokine patterns in the various diseases
studied are heterogeneous; that thyroid cells can express IL-12, IL-13,
and IL-15 mRNA in culture, particularly after TSH, IL-1, or IFN-
stimulation; and that IL-15 is expressed in most of the tissue samples
studied.
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