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Interleukin-25 initiates Th2 differentiation of human CD4(+) T cells and influences expression of its own receptor. | LitMetric

AI Article Synopsis

  • Human CRTh2(+) Th2 cells express the IL-25 receptor (IL-25R), and previous studies have shown that IL-25 enhances Th2 cytokine production, but how IL-25R is regulated and its role in Th2 differentiation were previously unclear.
  • Researchers investigated how IL-25 influences the differentiation of naïve human CD4(+) T cells into Th2 cells by activating them with IL-25, IL-4, or both, and assessed various markers related to Th2 response.
  • The results indicated that IL-25R expression increases early in Th2 differentiation, and IL-25 not only boosts the levels of its own receptor but also enhances the expression of Th2-related markers,

Article Abstract

Human CRTh2(+) Th2 cells express IL-25 receptor (IL-25R) and IL-25 has been shown to potentiate production of Th2 cytokines. However, regulation of IL-25R and whether it participates in Th2 differentiation of human cells have not been examined. We sought to characterize IL-25R expression on CD4(+) T cells and determine whether IL-25 plays a role in Th2 differentiation. Naïve human CD4(+) T cells were activated in the presence of IL-25, IL-4 (Th2 conditions) or both cytokines to assess their relative influence on Th2 differentiation. For experiments with differentiated Th2 cells, CRTh2-expressing cells were isolated from differentiating cultures. IL-25R, GATA3, CRTh2 and Th2 cytokine expression were assessed by flow cytometry, qRT-PCR and ELISA. Expression of surface IL-25R was induced early during Th2 differentiation (2 days). Addition of IL-25 to naïve CD4(+) T cells revealed that it induces expression of its own receptor, more strongly than IL-4. IL-25 also increased the proportions of IL-4-, GATA3- and CRTh2-expressing cells and expression of IL-5 and IL-13. Activation of differentiated CRTh2(+) Th2 cells through the TCR or by CRTh2 agonist increased surface expression of IL-25R, though re-expression of CRTh2 following TCR downregulation was impeded by IL-25. These data suggest that IL-25 may play various roles in Th2 mediated immunity. We establish here it regulates expression of its own receptor and can initiate Th2 differentiation, though not as strongly as IL-4.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693727PMC
http://dx.doi.org/10.1002/iid3.87DOI Listing

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