Annexin1 regulates DC efferocytosis and cross-presentation during Mycobacterium tuberculosis infection

The phagocytosis of apoptotic cells and associated vesicles (efferocytosis) by DCs is an important mechanism for both self tolerance and host defense. Although some of the engulfment ligands involved in efferocytosis have been identified and studied in vitro, the contributions of these ligands in vi...

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Veröffentlicht in:The Journal of clinical investigation 2015-02, Vol.125 (2), p.752-768
Hauptverfasser: Tzelepis, Fanny, Verway, Mark, Daoud, Jamal, Gillard, Joshua, Hassani-Ardakani, Kimya, Dunn, Jonathan, Downey, Jeffrey, Gentile, Marilena Elena, Jaworska, Joanna, Sanchez, Anthony Michel Jean, Nédélec, Yohann, Vali, Hojatollah, Tabrizian, Maryam, Kristof, Arnold Scott, King, Irah Luther, Barreiro, Luis Bruno, Divangahi, Maziar
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container_issue 2
container_start_page 752
container_title The Journal of clinical investigation
container_volume 125
creator Tzelepis, Fanny
Verway, Mark
Daoud, Jamal
Gillard, Joshua
Hassani-Ardakani, Kimya
Dunn, Jonathan
Downey, Jeffrey
Gentile, Marilena Elena
Jaworska, Joanna
Sanchez, Anthony Michel Jean
Nédélec, Yohann
Vali, Hojatollah
Tabrizian, Maryam
Kristof, Arnold Scott
King, Irah Luther
Barreiro, Luis Bruno
Divangahi, Maziar
description The phagocytosis of apoptotic cells and associated vesicles (efferocytosis) by DCs is an important mechanism for both self tolerance and host defense. Although some of the engulfment ligands involved in efferocytosis have been identified and studied in vitro, the contributions of these ligands in vivo remain ill defined. Here, we determined that during Mycobacterium tuberculosis (Mtb) infection, the engulfment ligand annexin1 is an important mediator in DC cross-presentation that increases efferocytosis in DCs and intrinsically enhances the capacity of the DC antigen-presenting machinery. Annexin1-deficient mice were highly susceptible to Mtb infection and showed an impaired Mtb antigen-specific CD8+ T cell response. Importantly, annexin1 expression was greatly downregulated in Mtb-infected human blood monocyte-derived DCs, indicating that reduction of annexin1 is a critical mechanism for immune evasion by Mtb. Collectively, these data indicate that annexin1 is essential in immunity to Mtb infection and mediates the power of DC efferocytosis and cross-presentation.
doi_str_mv 10.1172/JCI77014
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Although some of the engulfment ligands involved in efferocytosis have been identified and studied in vitro, the contributions of these ligands in vivo remain ill defined. Here, we determined that during Mycobacterium tuberculosis (Mtb) infection, the engulfment ligand annexin1 is an important mediator in DC cross-presentation that increases efferocytosis in DCs and intrinsically enhances the capacity of the DC antigen-presenting machinery. Annexin1-deficient mice were highly susceptible to Mtb infection and showed an impaired Mtb antigen-specific CD8+ T cell response. Importantly, annexin1 expression was greatly downregulated in Mtb-infected human blood monocyte-derived DCs, indicating that reduction of annexin1 is a critical mechanism for immune evasion by Mtb. 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Verway, Mark ; Daoud, Jamal ; Gillard, Joshua ; Hassani-Ardakani, Kimya ; Dunn, Jonathan ; Downey, Jeffrey ; Gentile, Marilena Elena ; Jaworska, Joanna ; Sanchez, Anthony Michel Jean ; Nédélec, Yohann ; Vali, Hojatollah ; Tabrizian, Maryam ; Kristof, Arnold Scott ; King, Irah Luther ; Barreiro, Luis Bruno ; Divangahi, Maziar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c737t-9e84ad20bc43b5494097355095a8aba15c49786b9231cf2d10329fd408a00c893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Annexin A1 - genetics</topic><topic>Annexin A1 - immunology</topic><topic>Antigens</topic><topic>Apoptosis</topic><topic>Apoptotic proteins</topic><topic>Autophagy</topic><topic>Biomedical research</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - pathology</topic><topic>Cross-Priming</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - pathology</topic><topic>Distribution</topic><topic>Drug dosages</topic><topic>Gene expression</topic><topic>Genomes</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Immunity, Cellular</topic><topic>Infection</topic><topic>Infections</topic><topic>Life Sciences</topic><topic>Ligands</topic><topic>Lymphocytes</topic><topic>Medical research</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Monocytes - immunology</topic><topic>Monocytes - pathology</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - immunology</topic><topic>Phagocytosis</topic><topic>Physiological aspects</topic><topic>Properties</topic><topic>Studies</topic><topic>Tuberculosis</topic><topic>Tuberculosis - genetics</topic><topic>Tuberculosis - immunology</topic><topic>Tuberculosis - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tzelepis, Fanny</creatorcontrib><creatorcontrib>Verway, Mark</creatorcontrib><creatorcontrib>Daoud, Jamal</creatorcontrib><creatorcontrib>Gillard, Joshua</creatorcontrib><creatorcontrib>Hassani-Ardakani, Kimya</creatorcontrib><creatorcontrib>Dunn, Jonathan</creatorcontrib><creatorcontrib>Downey, Jeffrey</creatorcontrib><creatorcontrib>Gentile, Marilena Elena</creatorcontrib><creatorcontrib>Jaworska, Joanna</creatorcontrib><creatorcontrib>Sanchez, Anthony Michel Jean</creatorcontrib><creatorcontrib>Nédélec, Yohann</creatorcontrib><creatorcontrib>Vali, Hojatollah</creatorcontrib><creatorcontrib>Tabrizian, Maryam</creatorcontrib><creatorcontrib>Kristof, Arnold Scott</creatorcontrib><creatorcontrib>King, Irah Luther</creatorcontrib><creatorcontrib>Barreiro, Luis Bruno</creatorcontrib><creatorcontrib>Divangahi, Maziar</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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subjects Animals
Annexin A1 - genetics
Annexin A1 - immunology
Antigens
Apoptosis
Apoptotic proteins
Autophagy
Biomedical research
CD8-Positive T-Lymphocytes - immunology
CD8-Positive T-Lymphocytes - pathology
Cross-Priming
Dendritic Cells - immunology
Dendritic Cells - pathology
Distribution
Drug dosages
Gene expression
Genomes
Human health and pathology
Humans
Immunity, Cellular
Infection
Infections
Life Sciences
Ligands
Lymphocytes
Medical research
Mice
Mice, Knockout
Monocytes - immunology
Monocytes - pathology
Mycobacterium tuberculosis
Mycobacterium tuberculosis - immunology
Phagocytosis
Physiological aspects
Properties
Studies
Tuberculosis
Tuberculosis - genetics
Tuberculosis - immunology
Tuberculosis - pathology
title Annexin1 regulates DC efferocytosis and cross-presentation during Mycobacterium tuberculosis infection
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