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      Mathematical Modeling Reveals Kinetics of Lymphocyte Recirculation in the Whole Organism

      research-article
      1 , 2 , * , 2
      PLoS Computational Biology
      Public Library of Science

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          Abstract

          The kinetics of recirculation of naive lymphocytes in the body has important implications for the speed at which local infections are detected and controlled by immune responses. With a help of a novel mathematical model, we analyze experimental data on migration of 51Cr-labeled thoracic duct lymphocytes (TDLs) via major lymphoid and nonlymphoid tissues of rats in the absence of systemic antigenic stimulation. We show that at any point of time, 95% of lymphocytes in the blood travel via capillaries in the lung or sinusoids of the liver and only 5% migrate to secondary lymphoid tissues such as lymph nodes, Peyer's patches, or the spleen. Interestingly, our analysis suggests that lymphocytes travel via lung capillaries and liver sinusoids at an extremely rapid rate with the average residence time in these tissues being less than 1 minute. The model also predicts a relatively short average residence time of TDLs in the spleen (2.5 hours) and a longer average residence time of TDLs in major lymph nodes and Peyer's patches (10 hours). Surprisingly, we find that the average residence time of lymphocytes is similar in lymph nodes draining the skin (subcutaneous LNs) or the gut (mesenteric LNs) or in Peyer's patches. Applying our model to an additional dataset on lymphocyte migration via resting and antigen-stimulated lymph nodes we find that enlargement of antigen-stimulated lymph nodes occurs mainly due to increased entrance rate of TDLs into the nodes and not due to decreased exit rate as has been suggested in some studies. Taken together, our analysis for the first time provides a comprehensive, systems view of recirculation kinetics of thoracic duct lymphocytes in the whole organism.

          Author Summary

          It is has been well established that lymphocytes, major cells of the adaptive immune system, continuously recirculate between secondary lymphoid tissues in the body such as lymph nodes, spleen, and Peyer's patches. Yet, the kinetics of lymphocyte entrance into and more importantly, residence times in these tissues still remain incompletely determined. Using previously published experimental data and a novel mathematical model we address this problem and estimate the rates of lymphocyte entrance into and exit from major secondary lymphoid tissues. We find that lymphocytes on average must pass via vasculature of the lung or liver 20 times before they migrate to one of the secondary lymphoid tissues. Despite small size of capillaries in the lung and liver, we predict that on average lymphocytes spend less than 1 minute in the vasculature of these organs. Furthermore, we estimate that lymphocytes spend on average 2.5 hours in the spleen and 10 hours in the lymph nodes or Peyer's patches. Our mathematical modeling for the first time provides a quantitative, systems view of lymphocyte recirculation in the whole organism.

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          Most cited references76

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          Sphingosine-1-phosphate and lymphocyte egress from lymphoid organs.

          Much has been learned about how cells enter lymphoid tissues. But how do they leave? Sphingosine-1-phosphate (S1P) has emerged over the past decade as a central mediator of lymphocyte egress. In this review, we summarize the current understanding of how S1P promotes exit from the secondary lymphoid organs and thymus. We review what is known about additional requirements for emigration and summarize the mostly distinct requirements for exit from the bone marrow. Egress from lymphoid organs is limited during immune responses, and we examine how this regulation works. There is accumulating evidence for roles of S1P in directing immune cell behavior within lymphoid tissues. How such actions can fit together with the egress-promoting role of S1P is discussed. Finally, we examine current understanding of how FTY720, a drug that targets S1P receptors and is approved for the treatment of multiple sclerosis, causes immune suppression.
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            The outs and the ins of sphingosine-1-phosphate in immunity.

            The potent lipid mediator sphingosine-1-phosphate (S1P) is produced inside cells by two closely related kinases, sphingosine kinase 1 (SPHK1) and SPHK2, and has emerged as a crucial regulator of immunity. Many of the actions of S1P in innate and adaptive immunity are mediated by its binding to five G protein-coupled receptors, designated S1PR1-5, but recent findings have also identified important roles for S1P as a second messenger during inflammation. In this Review, we discuss recent advances in our understanding of the roles of S1P receptors and describe the newly identified intracellular targets of S1P that are crucial for immune responses. Finally, we discuss the therapeutic potential of new drugs that target S1P signalling and functions.
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              Different patterns of peripheral migration by memory CD4+ and CD8+ T cells.

              Infections localized to peripheral tissues such as the skin result in the priming of T-cell responses that act to control pathogens. Activated T cells undergo migrational imprinting within the draining lymph nodes, resulting in memory T cells that provide local and systemic protection. Combinations of migrating and resident memory T cells have been implicated in long-term peripheral immunity, especially at the surfaces that form pathogen entry points into the body. However, T-cell immunity consists of separate CD4(+) helper T cells and CD8(+) killer T cells, with distinct effector and memory programming requirements. Whether these subsets also differ in their ability to form a migrating pool involved in peripheral immunosurveillance or a separate resident population responsible for local infection control has not been explored. Here, using mice, we show key differences in the migration and tissue localization of memory CD4(+) and CD8(+) T cells following infection of the skin by herpes simplex virus. On resolution of infection, the skin contained two distinct virus-specific memory subsets; a slow-moving population of sequestered CD8(+) T cells that were resident in the epidermis and confined largely to the original site of infection, and a dynamic population of CD4(+) T cells that trafficked rapidly through the dermis as part of a wider recirculation pattern. Unique homing-molecule expression by recirculating CD4(+) T effector-memory cells mirrored their preferential skin-migratory capacity. Overall, these results identify a complexity in memory T-cell migration, illuminating previously unappreciated differences between the CD4(+) and CD8(+) subsets.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Comput Biol
                PLoS Comput. Biol
                plos
                ploscomp
                PLoS Computational Biology
                Public Library of Science (San Francisco, USA )
                1553-734X
                1553-7358
                May 2014
                15 May 2014
                : 10
                : 5
                : e1003586
                Affiliations
                [1 ]Department of Microbiology, University of Tennessee, Knoxville, Tennessee, United States of America
                [2 ]Department of Mathematics, University of Tennessee, Knoxville, Tennessee, United States of America
                Emory University, United States of America
                Author notes

                The authors have declared that no competing interests exist.

                Conceived and designed the experiments: VVG. Performed the experiments: VVG JA. Analyzed the data: VVG. Contributed reagents/materials/analysis tools: VVG. Wrote the paper: VVG JA.

                Article
                PCOMPBIOL-D-13-01261
                10.1371/journal.pcbi.1003586
                4022467
                24830705
                3cbbf280-15a2-4c62-8f61-17c688588f1f
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 16 July 2013
                : 12 March 2014
                Page count
                Pages: 15
                Funding
                This work was supported by the start-up funds from the University of Tennessee and in part by the grant from the American Heart Association (to VVG). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Anatomy
                Lymphatic System
                Lymphoid Organs
                Cell Biology
                Cellular Types
                Animal Cells
                Immune Cells
                Computational Biology
                Immunology
                Immune System
                Physiology
                Immune Physiology
                Medicine and Health Sciences

                Quantitative & Systems biology
                Quantitative & Systems biology

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