Relationships of circulating CD4(+) T cell subsets and cytokines with the risk of relapse in patients with Crohn's disease

Background and aimsWe aimed to analyze circulating CD4(+) T cell subsets and cytokines during the course of Crohn's disease (CD). Methods and resultsCD4(+) T cell subsets, ultrasensitive C-reactive protein (usCRP), and various serum cytokines (IL-6, IL-8, IL-10, IL-13, IL-17A, IL-23, TNF alpha, IFN gamma, and TGF beta) were prospectively monitored every 3 months for 1 year, using multicolor flow cytometry and an ultrasensitive Erenna method in CD patients in remission at inclusion. Relapse occurred in 35 out of the 113 consecutive patients (31%). For patients in remission within 4 months prior to relapse and at the time of relapse, there was no significant difference in Th1, Th17, Treg, and double-positive CD4(+) T cell subsets co-expressing either IFN gamma and FOXP3, IL-17A and FOXP3, or IFN gamma and IL-17A. On the contrary, in patients who remained in remission, the mean frequency and number of double-positive IL-17A(+)FOXP3(+) CD4(+) T cells and the level of usCRP were significantly higher (p <= 0.01) 1 to 4 months prior to relapse. At the time of relapse, only the IL-6 and usCRP levels were significantly higher (p <= 0.001) compared with those patients in remission. On multivariate analysis, a high number of double-positive IL-17A(+)FOXP3(+) CD4(+) T cells (>= 1.4 cells/mm3) and elevated serum usCRP (>= 3.44 mg/L) were two independent factors associated with risk of relapse. ConclusionsDetection of circulating double-positive FOXP3(+)IL-17A(+) CD4(+) T cell subsets supports that T cell plasticity may reflect the inflammatory context of Crohn's disease. Whether this subset contributes to the pathogenesis of CD relapse needs further studies.