Abstract

It is well established that TH17 lymphocytes are crucial in the pathogenesis of the chronic autoimmune disease multiple sclerosis (MS). However, the importance of IL-17 in MS is still under debate, and other TH17-associated cytokines are likely more crucial in the initiation and maintenance of neuroinflammation. In this study, we demonstrate that IL-26 is specifically produced by human TH17 lymphocytes and that it correlates strongly to other TH17-associated markers (IL-17, IL-22, IL-23R, RORc and MCAM).

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