Publication | Open Access
Upregulation of Membrane‐Bound <scp>CD</scp>40L on <scp>CD</scp>4<sup>+</sup> T cells in Women with Primary Sjögren's Syndrome
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Citations
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References
2013
Year
ImmunologyImmune RegulationEpigenetic DeregulationCd4 T Cell ResponsesImmune SystemImmunotherapyEpigeneticsImmune DysregulationDemethylation PatternsImmunopathologyCell SignalingPrimary SjögrenRegulatory T Cell BiologyAutoimmune DiseaseAllergyAutoimmunityHumoral ImmunityImmunologic DiseaseImmune FunctionEpigenetic RegulationCell BiologySjögren’s SyndromeLupusMethylation ProfilesCellular Immune ResponseMedicine
Epigenetic deregulation of genes encoded on the X chromosome as reported for CD40L in lupus could explain the female predominance of autoimmune diseases. We compared CD40L expression on CD4(+) T cells from primary Sjögren's syndrome (pSS) women and healthy controls and investigated DNA methylation patterns of the promoter and enhancer regions of CD40L. The expression of CD40L on activated CD4(+) T cells was higher in patients with pSS than controls after phorbolmyristate acetate and ionomycin activation (P = 0.02). CD40L mRNA level in CD4(+) T cells did not differ between patients with pSS and controls and was similar in both groups in cultures treated with the demethylating agent 5-azacytidine C. Pyrosequencing analysis revealed no significant differences in methylation profiles between patients and controls. Inducible membrane-bound CD40L on CD4(+) T cells is increased in patients with pSS but was not related to epigenetic deregulation by demethylation patterns of the regulatory regions of CD40L.
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