Changes in Cytokine Production During Pregnancy in Patients with Graves' Disease

In order to investigate the role of type 1 and type 2 cytokines in the remission of Graves' disease (GD) during pregnancy, spontaneous and mitogen-stimulated production of interleukin (IL)-4, IL-6, IL-10, IL-12, interferon-γ (IFN-γ), and tumour necrosis factor-α (TNF-α) were measured by enzyme-...

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Veröffentlicht in:Thyroid (New York, N.Y.) N.Y.), 2000-08, Vol.10 (8), p.71-707
Hauptverfasser: Jones, Brian M., Kwok, Janette S. Y., Kung, Annie W. C.
Format: Artikel
Sprache:eng
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Zusammenfassung:In order to investigate the role of type 1 and type 2 cytokines in the remission of Graves' disease (GD) during pregnancy, spontaneous and mitogen-stimulated production of interleukin (IL)-4, IL-6, IL-10, IL-12, interferon-γ (IFN-γ), and tumour necrosis factor-α (TNF-α) were measured by enzyme-linked immunospot assay of peripheral blood mononuclear cells from 10 pregnant women with GD, 8 healthy pregnant women, and 10 healthy nonpregnant women. Tests were performed in the first, second, and third trimesters of pregnancy and 10-17 weeks after delivery. IL-4 production was not affected greatly by normal or GD pregnancy, whereas IFN-γ production was suppressed throughout pregnancy but returned to normal levels after delivery in both controls and patients. IL-6 and TNF-α tended to be higher in GD pregnancy than normal pregnancy, especially in the second and third trimesters. Controls had raised IL-10 in the first trimester with a return to normal levels by the third trimester, whereas patients had raised levels throughout pregnancy. IL-12 levels were suppressed to a greater extent in control than Graves' pregnancy, especially during the second and third trimesters. Ratios of IL10:IL12 in phytohemaglutinin (PHA)-stimulated cultures were much lower in GD than normal pregnancy and cross-regulation of IL-10 and IL-12 may be deficient in GD.
ISSN:1050-7256
1557-9077
DOI:10.1089/10507250050137798