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      Decidual leukocytes respond to African lineage Zika virus infection with mild anti-inflammatory changes during acute infection in rhesus macaques

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          Abstract

          Zika virus (ZIKV) can be vertically transmitted during pregnancy resulting in a range of adverse pregnancy outcomes. The decidua is commonly found to be infected by ZIKV, yet the acute immune response to infection remains understudied in vivo. We hypothesized that in vivo African-lineage ZIKV infection induces a pro-inflammatory response in the decidua. To test this hypothesis, we evaluated the decidua in pregnant rhesus macaques within the first two weeks following infection with an African-lineage ZIKV and compared our findings to gestationally aged-matched controls. Decidual leukocytes were phenotypically evaluated using spectral flow cytometry, and cytokines and chemokines were measured in tissue homogenates from the decidua, placenta, and fetal membranes. The results of this study did not support our hypothesis. Although ZIKV RNA was detected in the decidual tissue samples from all ZIKV infected dams, phenotypic changes in decidual leukocytes and differences in cytokine profiles suggest that the decidua undergoes mild anti-inflammatory changes in response to that infection. Our findings emphasize the immunological state of the gravid uterus as a relatively immune privileged site that prioritizes tolerance of the fetus over mounting a pro-inflammatory response to clear infection.

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          Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes.

          Mononuclear phagocytes are versatile cells that can express different functional programs in response to microenvironmental signals. Fully polarized M1 and M2 (or alternatively activated) macrophages are the extremes of a continuum of functional states. Macrophages that infiltrate tumor tissues are driven by tumor-derived and T cell-derived cytokines to acquire a polarized M2 phenotype. These functionally polarized cells, and similarly oriented or immature dendritic cells present in tumors, have a key role in subversion of adaptive immunity and in inflammatory circuits that promote tumor growth and progression.
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            • Record: found
            • Abstract: not found
            • Article: not found

            Single-cell reconstruction of the early maternal–fetal interface in humans

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              FlowSOM: Using self-organizing maps for visualization and interpretation of cytometry data.

              The number of markers measured in both flow and mass cytometry keeps increasing steadily. Although this provides a wealth of information, it becomes infeasible to analyze these datasets manually. When using 2D scatter plots, the number of possible plots increases exponentially with the number of markers and therefore, relevant information that is present in the data might be missed. In this article, we introduce a new visualization technique, called FlowSOM, which analyzes Flow or mass cytometry data using a Self-Organizing Map. Using a two-level clustering and star charts, our algorithm helps to obtain a clear overview of how all markers are behaving on all cells, and to detect subsets that might be missed otherwise. R code is available at https://github.com/SofieVG/FlowSOM and will be made available at Bioconductor.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2617177Role: Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/564805Role: Role: Role:
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                URI : https://loop.frontiersin.org/people/497616Role: Role: Role:
                URI : https://loop.frontiersin.org/people/636876Role: Role: Role: Role: Role: Role:
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                07 March 2024
                2024
                : 15
                : 1363169
                Affiliations
                [1] 1Department of Comparative Biosciences, University of Wisconsin-Madison , Madison, WI, United States
                [2] 2Department of Obstetrics and Gynecology, University of Wisconsin-Madison , Madison, WI, United States
                [3] 3Wisconsin National Primate Research Center, University of Wisconsin-Madison , Madison, WI, United States
                Author notes

                Edited by: Gil Mor, Wayne State University, United States

                Reviewed by: Jiahui Ding, Wayne State University, United States

                Alexandre Urban Borbely, Federal University of Alagoas, Brazil

                *Correspondence: Thaddeus G. Golos, golos@ 123456primate.wisc.edu
                Article
                10.3389/fimmu.2024.1363169
                10954895
                38515747
                823ed3d1-6d1d-418f-a35c-8b00e02e47f2
                Copyright © 2024 Koenig, Vazquez, Leyva Jaimes, Mitzey, Stanic and Golos

                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
                : 29 December 2023
                : 23 February 2024
                Page count
                Figures: 9, Tables: 2, Equations: 0, References: 106, Pages: 20, Words: 9532
                Funding
                Funded by: National Institutes of Health , doi 10.13039/100000002;
                Award ID: T32 GM007133
                Funded by: National Institute of Allergy and Infectious Diseases , doi 10.13039/100000060;
                Award ID: R01 AI132519
                Funded by: Office of Research Infrastructure Programs, National Institutes of Health , doi 10.13039/100016958;
                Award ID: P51 OD011106
                The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This research was supported by NIH grants T32 GM007133 to MK, R01 AI132519 to TG, and P51 OD011106 to the Wisconsin National Primate Research Center. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
                Categories
                Immunology
                Original Research
                Custom metadata
                Immunological Tolerance and Regulation

                Immunology
                zika virus,decidua,inflammation,immunome,rhesus macaque,pregnancy
                Immunology
                zika virus, decidua, inflammation, immunome, rhesus macaque, pregnancy

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