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      Recombinant Human Thyroid-Stimulating Hormone Increases the Percentages of Natural Killer T Cells and B Lymphocytes in Human Peripheral Blood In Vivo

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          Abstract

          Multiple cellular and humoral components of the immune system play a significant role in the physiology and pathophysiology of various organs including the thyroid. On the other hand, both thyroid hormones and thyroid-stimulating hormone (TSH) have been shown to exert immunoregulatory activities, which are difficult to assess independently in vivo. In our study we employed a unique clinical model for the assessment of TSH biological function in humans. The structure of peripheral blood mononuclear cell populations was investigated, using flow cytometry, in athyroid patients (n = 109) after treatment because of the differentiated thyroid carcinoma (DTC) at two time-points: directly before and five days after recombinant human TSH (rhTSH) administration. The analysis revealed significant increase in the percentage of natural killer T cells and B lymphocytes in the peripheral blood of rhTSH treated patients, whereas, we did not observe any effects on investigated subpopulations of dendritic cells and monocytes, T cells and natural killer cells. The findings of the study indicate the immune regulatory role of TSH, directed specifically on selected cell subtypes.

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          Most cited references40

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          Mouse and human dendritic cell subtypes.

          Dendritic cells (DCs) collect and process antigens for presentation to T cells, but there are many variations on this basic theme. DCs differ in the regulatory signals they transmit, directing T cells to different types of immune response or to tolerance. Although many DC subtypes arise from separate developmental pathways, their development and function are modulated by exogenous factors. Therefore, we must study the dynamics of the DC network in response to microbial invasion. Despite the difficulty of comparing the DC systems of humans and mice, recent work has revealed much common ground.
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            Plasmacytoid Dendritic Cells: Development, Regulation, and Function

            Plasmacytoid dendritic cells (pDCs) are a unique sentinel cell type that can detect pathogen-derived nucleic acids and respond with rapid and massive production of type I interferon. This review summarizes our current understanding of pDC biology, including transcriptional regulation, heterogeneity, role in antiviral immune responses, and involvement in immune pathology, particularly in autoimmune diseases, immunodeficiency, and cancer. We also highlight the remaining gaps in our knowledge and important questions for the field, such as the molecular basis of unique interferon-producing capacity of pDCs. A better understanding of cell type-specific positive and negative control of pDC function should pave the way for translational applications focused on this immune cell type.
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              Dendritic cell maturation: functional specialization through signaling specificity and transcriptional programming.

              Dendritic cells (DC) are key regulators of both protective immune responses and tolerance to self-antigens. Soon after their discovery in lymphoid tissues by Steinman and Cohn, as cells with the unique ability to prime naïve antigen-specific T cells, it was realized that DC can exist in at least two distinctive states characterized by morphological, phenotypic and functional changes-this led to the description of DC maturation. It is now well appreciated that there are several subsets of DC in both lymphoid and non-lymphoid tissues of mammals, and these cells show remarkable functional specialization and specificity in their roles in tolerance and immunity. This review will focus on the specific characteristics of DC subsets and how their functional specialization may be regulated by distinctive gene expression programs and signaling responses in both steady-state and in the context of inflammation. In particular, we will highlight the common and distinctive genes and signaling pathways that are associated with the functional maturation of DC subsets. © 2014 The Authors.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/660538
                URI : https://loop.frontiersin.org/people/1014206
                URI : https://loop.frontiersin.org/people/1013733
                URI : https://loop.frontiersin.org/people/1014448
                URI : https://loop.frontiersin.org/people/199007
                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrinol.
                Frontiers in Endocrinology
                Frontiers Media S.A.
                1664-2392
                20 November 2020
                2020
                : 11
                : 543845
                Affiliations
                [1] 1 Department of Endocrinology and Metabolic Diseases, Medical University of Lodz , Lodz, Poland
                [2] 2 Department of Neurology, Medical University of Lodz , Lodz, Poland
                Author notes

                Edited by: Rauf Latif, Icahn School of Medicine at Mount Sinai, United States

                Reviewed by: Takao Ando, Nagasaki University Hospital, Japan; José C. Moreno, University of Zurich, Switzerland

                *Correspondence: Andrzej Lewiński, andrzej.lewinski@ 123456umed.lodz.pl

                †These authors have contributed equally to this work

                This article was submitted to Thyroid Endocrinology, a section of the journal Frontiers in Endocrinology

                Article
                10.3389/fendo.2020.543845
                7715015
                33329378
                56e7148f-6eff-42d3-95f0-604605780ae3
                Copyright © 2020 Adamczewski, Stasiołek, Zygmunt, Śliwka, Wieczorek-Szukała and Lewiński

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 18 March 2020
                : 16 October 2020
                Page count
                Figures: 4, Tables: 1, Equations: 0, References: 40, Pages: 8, Words: 4146
                Categories
                Endocrinology
                Original Research

                Endocrinology & Diabetes
                thyroid-stimulating hormone (tsh),dendritic cells,monocytes,thyroid,lymphocytes,natural killer (nk) cells,nkt cells

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