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      Frequency distribution of IL- 17A G197A (rs2275913) and IL- 17F A7488G (rs763780) polymorphisms among healthy Sudanese population

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          Abstract

          Objectives

          IL- 17A G197A and IL- 17F A7488G polymorphisms has been identified to be associated with the susceptibility to many diseases. This study aimed to investigate the frequency distribution of IL-17A G197A and IL-17F A7488G polymorphisms among healthy Sudanese population. A descriptive cross-sectional hospital-based molecular study conducted in different sites throughout Sudan. Two ml blood samples were collected from 717 healthy participants. Demographic data and the medical history of the participants were collected.

          Results

          Of the 717 participants, 355 (49.5%) were males and 362 (50.5%) were females, their mean age was 30.2 ± 17.2 and 32.2 ± 16.5, respectively. For IL- 17A, the most frequent genotype detected among males and females was IL- 17A heterozygote allele (AG); 215 (60.6%) and 194 (53.6%), respectively. Whereas, for IL- 17F, the most frequent allele among males and females was the homozygote allele (AA); 298 (83.9%) for males and 322 (89.0%) for females. HWE for genotype distributions of IL- 17A was showing statistical insignificance for IL- 17A among males and females, P value 0.614. While HWE for IL- 17F reached the equilibrium level, P value 0.048. The most frequent age group was those aged between 21 to 40 years; 281 (39.2%). Arab constituted the major ethnicity of the study participants; 418 (58.3%), P value 0.034.

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          Most cited references25

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          A distinct lineage of CD4 T cells regulates tissue inflammation by producing interleukin 17.

          Interleukin 17 (IL-17) has been linked to autoimmune diseases, although its regulation and function have remained unclear. Here we have evaluated in vitro and in vivo the requirements for the differentiation of naive CD4 T cells into effector T helper cells that produce IL-17. This process required the costimulatory molecules CD28 and ICOS but was independent of the cytokines and transcription factors required for T helper type 1 or type 2 differentiation. Furthermore, both IL-4 and interferon-gamma negatively regulated T helper cell production of IL-17 in the effector phase. In vivo, antibody to IL-17 inhibited chemokine expression in the brain during experimental autoimmune encephalomyelitis, whereas overexpression of IL-17 in lung epithelium caused chemokine production and leukocyte infiltration. Thus, IL-17 expression characterizes a unique T helper lineage that regulates tissue inflammation.
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            Development, cytokine profile and function of human interleukin 17-producing helper T cells.

            T(H)-17 cells are a distinct lineage of proinflammatory T helper cells that are essential for autoimmune disease. In mice, commitment to the T(H)-17 lineage is dependent on transforming growth factor-beta and interleukin 6 (IL-6). Here we demonstrate that IL-23 and IL-1beta induced the development of human T(H)-17 cells expressing IL-17A, IL-17F, IL-22, IL-26, interferon-gamma, the chemokine CCL20 and transcription factor RORgammat. In situ, T(H)-17 cells were identified by expression of the IL-23 receptor and the memory T cell marker CD45RO. Psoriatic skin lesions contained IL-23-producing dendritic cells and were enriched in the cytokines produced by human T(H)-17 cells that promote the production of antimicrobial peptides in human keratinocytes. Our data collectively indicate that human and mouse T(H)-17 cells require distinct factors during differentiation and that human T(H)-17 cells may regulate innate immunity in epithelial cells.
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              The biological functions of T helper 17 cell effector cytokines in inflammation.

              T helper 17 (Th17) cells belong to a recently identified T helper subset, in addition to the traditional Th1 and Th2 subsets. These cells are characterized as preferential producers of interleukin-17A (IL-17A), IL-17F, IL-21, and IL-22. Th17 cells and their effector cytokines mediate host defensive mechanisms to various infections, especially extracellular bacteria infections, and are involved in the pathogenesis of many autoimmune diseases. The receptors for IL-17 and IL-22 are broadly expressed on various epithelial tissues. The effector cytokines of Th17 cells, therefore, mediate the crucial crosstalk between immune system and tissues, and play indispensable roles in tissue immunity.
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                Author and article information

                Contributors
                nouh_saad@outlook.com
                Emanwell-eds3@hotmail.com
                abdallah_elseer@yahoo.com
                musabali39@yahoo.com
                hanadi3814@gmail.com
                eman2taha@gmail.com
                anadilalsubki@gmail.com
                sabahalhaj1991@gmail.com
                mado93344@gmail.com
                mohamedsideeg@yahoo.com
                hussomco@gmail.com
                maha_mahgoub2008@yahoo.com
                alkhatimali@gmail.com
                aedris@ub.edu.sa
                ayman.ame.ahmed@gmail.com
                rihab.omer@yahoo.com
                Journal
                BMC Res Notes
                BMC Res Notes
                BMC Research Notes
                BioMed Central (London )
                1756-0500
                2 July 2020
                2 July 2020
                2020
                : 13
                : 317
                Affiliations
                [1 ]Department of Parasitology and Medical Entomology, Faculty of Medical Laboratory Sciences, Nile University, Khartoum, Sudan
                [2 ]Alfarrabi College for Science and Technology, Khartoum, Sudan
                [3 ]GRID grid.442429.d, ISNI 0000 0004 0447 7471, Department of Parasitology and Medical Entomology, Faculty of Medicine, , Sinnar University, ; Sinnar, Sudan
                [4 ]School of Medicine, Nile University, Khartoum, Sudan
                [5 ]GRID grid.9763.b, ISNI 0000 0001 0674 6207, Mycetoma Research Center, , University of Khartoum, ; Khartoum, Sudan
                [6 ]GRID grid.442415.2, ISNI 0000 0001 0164 5423, Department of Biotechnology, School of Pharmacy, , Ahfad University for Women, ; Omdurman, Sudan
                [7 ]GRID grid.9763.b, ISNI 0000 0001 0674 6207, Department of Histopathology and Cytology, Faculty of Medical Laboratory Sciences, , University of Khartoum, ; Khartoum, Sudan
                [8 ]GRID grid.417467.7, ISNI 0000 0004 0443 9942, Department of Neurology, , Mayo Clinic, ; Jacksonville, FL USA
                [9 ]GRID grid.417467.7, ISNI 0000 0004 0443 9942, Department of Radiology, , Mayo Clinic, ; Jacksonville, FL USA
                [10 ]GRID grid.9763.b, ISNI 0000 0001 0674 6207, Department of Internal Medicine, Faculty of Medicine, , University of Khartoum, ; Khartoum, Sudan
                [11 ]GRID grid.440839.2, Faculty of Medicine, , Neelain University, ; Khartoum, Sudan
                [12 ]GRID grid.494608.7, ISNI 0000 0004 6027 4126, Department of Histopathology and Cytology, Faculty of Applied Medical Sciences, , University of Bisha, ; Bisha, Kingdom of Saudi Arabia
                [13 ]GRID grid.9763.b, ISNI 0000 0001 0674 6207, Institute of Endemic Diseases, University of Khartoum, ; Khartoum, Sudan
                [14 ]GRID grid.9647.c, ISNI 0000 0004 7669 9786, Department of Molecular Biology, , Institute of Parasitology, University of Leipzig, ; Leipzig, Germany
                Author information
                http://orcid.org/0000-0001-6843-3361
                Article
                5165
                10.1186/s13104-020-05165-4
                7330939
                c20bef85-26bc-4b18-82c5-08d4b768b968
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 25 May 2020
                : 29 June 2020
                Categories
                Research Note
                Custom metadata
                © The Author(s) 2020

                Medicine
                interleukin 17a,interleukin 17f,polymorphism,healthy population,sudan
                Medicine
                interleukin 17a, interleukin 17f, polymorphism, healthy population, sudan

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