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      Immunophenotyping and activation status of maternal peripheral blood leukocytes during pregnancy and labour, both term and preterm

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          Abstract

          The onset of labour in rodents and in humans is associated with physiological inflammation which is manifested by infiltration of activated maternal peripheral leukocytes (mPLs) into uterine tissues. Here, we used flow cytometry to immunophenotype mPLs throughout gestation and labour, both term and preterm. Peripheral blood was collected from non‐pregnant women and pregnant women in the 1st, 2nd and 3rd trimesters. Samples were also collected from women in active labour at term (TL) or preterm (PTL) and compared with women term not‐in‐labour (TNIL) and preterm not‐in‐labour (PTNIL). Different leukocyte populations were identified by surface markers such as CD45, CD14, CD15, CD3, CD4, CD8, CD19 and CD56. Their activation status was measured by the expression levels of CD11b, CD44, CD55, CD181 and CD192 proteins. Of all circulating CD45+ leukocytes, we detected significant increases in CD15+ granulocytes ( i) in pregnant women versus non‐pregnant; ( ii) in TL women versus TNIL and versus pregnant women in the 1st/2nd/3rd trimester; ( iii) in PTL women versus PTNIL. TL was characterized by ( iv) increased expressions of CD11b, CD55 and CD192 on granulocytes; ( v) increased mean fluorescent intensity (MFI) of CD55 and CD192 on monocytes; ( vi) increased CD44 MFI on CD3+ lymphocytes as compared to late gestation. In summary, we have identified sub‐populations of mPLs that are specifically activated in association with gestation (granulocytes) or with the onset of labour (granulocytes, monocytes and lymphocytes). Additionally, beta regression analysis created a set of reference values to rank this association between immune markers of pregnancy and to identify activation status with potential prognostic and diagnostic capability.

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          Most cited references52

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          Granules of the human neutrophilic polymorphonuclear leukocyte.

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            Neutrophils cascading their way to inflammation.

            Neutrophils are pivotal effector cells of innate immunity. Their recruitment into peripheral tissues is indispensable for host defense. Given their destructive potential, neutrophil entry into tissue must be tightly regulated in vivo to avoid damage to the host. An array of chemically diverse chemoattractants is active on neutrophils and participates in recruitment. Neutrophil chemoattractants were thought redundant in the control of neutrophil recruitment into peripheral tissue, based on their often indistinguishable effects on neutrophils in vitro and their frequently overlapping patterns of expression at inflammatory sites in vivo. Recent data, however, suggest that neutrophil chemoattractants have unique functions in the recruitment of neutrophils into inflammatory sites in vivo, dictated by their distinct patterns of temporal and spatial expression. Copyright © 2011 Elsevier Ltd. All rights reserved.
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              Inflammation in preterm and term labour and delivery.

              Inflammation has been implicated in the mechanisms responsible for preterm and term parturition, as well as fetal injury. Out of all of the suspected causes of preterm labour and delivery, infection and/or inflammation is the only pathological process for which both a firm causal link with preterm birth has been established and a molecular pathophysiology defined. Inflammation has also been implicated in the mechanism of spontaneous parturition at term. Most cases of histopathological inflammation and histological chorioamnionitis, both in preterm and term labour, are sub-clinical in nature. The isolation of bacteria in the amniotic fluid, known as microbial invasion of the amniotic cavity, is a pathological finding; the frequency of which is dependent upon the clinical presentation and gestational age. There is a window of time during which it may be possible to detect a 'molecular signature of inflammation' by analysis of the transcriptome before histological evidence is observed. This article reviews the role of inflammation in preterm and term parturition. It is possible that modulation of inflammation using anti-inflammatory cytokines, corticoids, antioxidants and/or other factors may complement antibiotic therapy and limit fetal injury.
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                Author and article information

                Contributors
                shynlova@lunenfeld.ca
                Journal
                J Cell Mol Med
                J. Cell. Mol. Med
                10.1111/(ISSN)1582-4934
                JCMM
                Journal of Cellular and Molecular Medicine
                John Wiley and Sons Inc. (Hoboken )
                1582-1838
                1582-4934
                21 April 2017
                October 2017
                : 21
                : 10 ( doiID: 10.1111/jcmm.2017.21.issue-10 )
                : 2386-2402
                Affiliations
                [ 1 ] Lunenfeld‐Tanenbaum Research Institute Mount Sinai Hospital Toronto ON Canada
                [ 2 ] Department of Obstetrics & Gynecology University of Toronto Toronto ON Canada
                [ 3 ] Department of Physiology University of Toronto Toronto ON Canada
                Author notes
                [*] [* ] Correspondence to: Dr. Oksana SHYNLOVA

                E‐mail: shynlova@ 123456lunenfeld.ca

                Author information
                http://orcid.org/0000-0002-6084-8156
                Article
                JCMM13160
                10.1111/jcmm.13160
                5618694
                28429508
                3e04402e-86a8-4b38-991c-fae4323f3ad7
                © 2017 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 24 November 2016
                : 14 February 2017
                Page count
                Figures: 6, Tables: 4, Pages: 17, Words: 8490
                Funding
                Funded by: Burroughs Wellcome Fund
                Award ID: 1013759
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                jcmm13160
                October 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.2.0 mode:remove_FC converted:28.09.2017

                Molecular medicine
                pregnancy,peripheral leukocytes,term labour,preterm labour,immune activation
                Molecular medicine
                pregnancy, peripheral leukocytes, term labour, preterm labour, immune activation

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