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December 09-10, 2019 | Barcelona, Spain

Volume 02

Journal of Immune Disorders & Therapy

J Immune Disord Ther, Volume 02

World Immunology 2019 & Cancer Summit 2019

December 09-10, 2019

9

th

WORLD CONGRESS ON

IMMUNOLOGY AND CANCER

Human CD8

+

CD25

+

CD127

low

regulatory T cells: MicroRNA signature and impact on

TGF-β and IL-10 expression

R

egulatory T cells (Tregs) are central for maintaining immune balance and their dysfunction drives the expansion of critical

immunologic disorders. During the past decade, microRNAs (miRNAs) have emerged as potent regulators of gene

expression among which immune related genes and their immunomodulatory properties have been associated with different

immune-based diseases. The miRNA signature of human peripheral blood (PB) CD8

+

CD2

5

+ CD127

low

Tregs has not been

described yet. We thus identified, using TaqMan Low-DensityArray (TLDA) technique followed by individual quantitative real-

time PCR (qRT-PCR) confirmation, fourteen miRNAs, among which twelve were downregulated whilst two were upregulated

in CD8

+

CD2

5

+ CD127

low

Tregs in comparison to CD8

+

CD25

-

T cells. In a next step, microRNAData Integration Portal (mirDIP)

was used to identify potential miRNA target sites in the 3’UTR of key Treg cell-immunomodulatory genes with special focus

on IL-10 and TGF-β. Having identified potential miR target sites in the 3’UTR of IL-10 (miR-27b-3p, miR-340-5p) and TGF-β

(miR-330-3p), we showed following transfection, and transduction assays that overexpression of two under-expressed miRNAs,

miR-27b-3p and miR-340-5p, downregulates IL-10 expression upon targeting its 3’UTR. Similarly, overexpression of miR-

330-3p negatively regulates TGF-β expression. These results highlight an important impact of the CD8

+

Treg mirnome on the

expression of genes with significant implication in immunosuppression. These observations could help in better understanding

the mechanism orchestrating Treg immunosuppressive function towards unravelling new targets for treating auto- immune

pathologies and cancer.

Biography

Hussein Fayyad-Kazan is a full time professor at the Lebanese University-Faculty of Science. He got his Bachelor degree in Biochemistry in

2005 from the Lebanese University-Faculty of Science. Later on, he continued his studies in the Free University of Brussels (ULB) where got

his Master’s Degree in Molecular Biology and Biotechnology in 2007 and then a PhD in December 2010. Thereafter, He did a postdoc in the

Laboratory of Experimental Hematology-Jules Bordet Institute-ULB till September 2018 where he worked on several Molecular Immunology

topics. He have about sixty scientific papers being published in high impact factor journals. His research work is focused on Cancer Biology

and Molecular Immunology.

hfayyadk@gmail.com

Hussein Fayyad-Kazan

Lebanese University, Lebanon