PT - JOURNAL ARTICLE AU - EMMANOUIL SIFNAIOS AU - GEORGE MASTORAKOS AU - KATERINA PSARRA AU - NIKOLAOS-DIMITRIOS PANAGOPOULOS AU - KONSTANTINOS PANOULIS AU - NIKOLAOS VITORATOS AU - DEMETRIOS RIZOS AU - GEORGE CREATSAS TI - Gestational Diabetes and T-cell (Th1/Th2/Th17/Treg) Immune Profile AID - 10.21873/invivo.11435 DP - 2019 Jan 01 TA - In Vivo PG - 31--40 VI - 33 IP - 1 4099 - http://iv.iiarjournals.org/content/33/1/31.short 4100 - http://iv.iiarjournals.org/content/33/1/31.full SO - In Vivo2019 Jan 01; 33 AB - Background/Aim: Gestational diabetes mellitus (GDM) is a common pregnancy complication, characterized by insulin resistance and low-grade systemic inflammation with a pro-inflammatory immune system response. Our objective was to study the peripheral Th1, Th2, Th17 and Treg response in GDM compared to normal pregnancy. Materials and Methods: Th1, Th2, Th17 and Treg subsets was determined by flow cytometry based on staining for specific intracellular cytokines, as well as C-reactive protein (CRP) and total IgE circulating levels. The health status of all offspring was also assessed 6 months post-delivery. Results: A total of 49 Caucasian adult pregnant women were enrolled into a GDM (n=26) and Control (n=23) group. At the third trimester of pregnancy, the GDM group had a higher proportion of Th2, Th17 and Treg cells compared to control. Contrary to the control group, the GDM group exhibited no significant change in the Th1/Th2/Th17/Treg profile postpartum. Furthermore, higher circulating CRP and total IgE levels were noted in the GDM group compared to controls. At the 6-month post-delivery assessment, 30.8% of the offspring from the GDM group were found to have developed atopic dermatitis, food allergy or allergic proctocolitis compared to none from the control group. Conclusion: Compared to an uncomplicated pregnancy, GDM exhibits a significantly different peripheral T-cell profile at the third pregnancy trimester characterized by higher proportion of Th2, Th17 and Treg cells which persist six months post-delivery, while the increased high sensitivity CRP (hsCRP) levels stressed the low-grade inflammatory profile of this disease.