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Neutrophil Recruitment to Lymph Nodes Limits Local Humoral Response to Staphylococcus aureus
Neutrophils form the first line of host defense against bacterial pathogens. They are rapidly mobilized to sites of infection where they help marshal host defenses and remove bacteria by phagocytosis. While splenic neutrophils promote marginal zone B cell antibody production in response to administe...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401519/ https://www.ncbi.nlm.nih.gov/pubmed/25884622 http://dx.doi.org/10.1371/journal.ppat.1004827 |
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author | Kamenyeva, Olena Boularan, Cedric Kabat, Juraj Cheung, Gordon Y. C. Cicala, Claudia Yeh, Anthony J. Chan, June L. Periasamy, Saravanan Otto, Michael Kehrl, John H. |
author_facet | Kamenyeva, Olena Boularan, Cedric Kabat, Juraj Cheung, Gordon Y. C. Cicala, Claudia Yeh, Anthony J. Chan, June L. Periasamy, Saravanan Otto, Michael Kehrl, John H. |
author_sort | Kamenyeva, Olena |
collection | PubMed |
description | Neutrophils form the first line of host defense against bacterial pathogens. They are rapidly mobilized to sites of infection where they help marshal host defenses and remove bacteria by phagocytosis. While splenic neutrophils promote marginal zone B cell antibody production in response to administered T cell independent antigens, whether neutrophils shape humoral immunity in other lymphoid organs is controversial. Here we investigate the neutrophil influx following the local injection of Staphylococcus aureus adjacent to the inguinal lymph node and determine neutrophil impact on the lymph node humoral response. Using intravital microscopy we show that local immunization or infection recruits neutrophils from the blood to lymph nodes in waves. The second wave occurs temporally with neutrophils mobilized from the bone marrow. Within lymph nodes neutrophils infiltrate the medulla and interfollicular areas, but avoid crossing follicle borders. In vivo neutrophils form transient and long-lived interactions with B cells and plasma cells, and their depletion augments production of antigen-specific IgG and IgM in the lymph node. In vitro activated neutrophils establish synapse- and nanotube-like interactions with B cells and reduce B cell IgM production in a TGF- β1 dependent manner. Our data reveal that neutrophils mobilized from the bone marrow in response to a local bacterial challenge dampen the early humoral response in the lymph node. |
format | Online Article Text |
id | pubmed-4401519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44015192015-04-21 Neutrophil Recruitment to Lymph Nodes Limits Local Humoral Response to Staphylococcus aureus Kamenyeva, Olena Boularan, Cedric Kabat, Juraj Cheung, Gordon Y. C. Cicala, Claudia Yeh, Anthony J. Chan, June L. Periasamy, Saravanan Otto, Michael Kehrl, John H. PLoS Pathog Research Article Neutrophils form the first line of host defense against bacterial pathogens. They are rapidly mobilized to sites of infection where they help marshal host defenses and remove bacteria by phagocytosis. While splenic neutrophils promote marginal zone B cell antibody production in response to administered T cell independent antigens, whether neutrophils shape humoral immunity in other lymphoid organs is controversial. Here we investigate the neutrophil influx following the local injection of Staphylococcus aureus adjacent to the inguinal lymph node and determine neutrophil impact on the lymph node humoral response. Using intravital microscopy we show that local immunization or infection recruits neutrophils from the blood to lymph nodes in waves. The second wave occurs temporally with neutrophils mobilized from the bone marrow. Within lymph nodes neutrophils infiltrate the medulla and interfollicular areas, but avoid crossing follicle borders. In vivo neutrophils form transient and long-lived interactions with B cells and plasma cells, and their depletion augments production of antigen-specific IgG and IgM in the lymph node. In vitro activated neutrophils establish synapse- and nanotube-like interactions with B cells and reduce B cell IgM production in a TGF- β1 dependent manner. Our data reveal that neutrophils mobilized from the bone marrow in response to a local bacterial challenge dampen the early humoral response in the lymph node. Public Library of Science 2015-04-17 /pmc/articles/PMC4401519/ /pubmed/25884622 http://dx.doi.org/10.1371/journal.ppat.1004827 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Kamenyeva, Olena Boularan, Cedric Kabat, Juraj Cheung, Gordon Y. C. Cicala, Claudia Yeh, Anthony J. Chan, June L. Periasamy, Saravanan Otto, Michael Kehrl, John H. Neutrophil Recruitment to Lymph Nodes Limits Local Humoral Response to Staphylococcus aureus |
title | Neutrophil Recruitment to Lymph Nodes Limits Local Humoral Response to Staphylococcus aureus
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title_full | Neutrophil Recruitment to Lymph Nodes Limits Local Humoral Response to Staphylococcus aureus
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title_fullStr | Neutrophil Recruitment to Lymph Nodes Limits Local Humoral Response to Staphylococcus aureus
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title_full_unstemmed | Neutrophil Recruitment to Lymph Nodes Limits Local Humoral Response to Staphylococcus aureus
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title_short | Neutrophil Recruitment to Lymph Nodes Limits Local Humoral Response to Staphylococcus aureus
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title_sort | neutrophil recruitment to lymph nodes limits local humoral response to staphylococcus aureus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401519/ https://www.ncbi.nlm.nih.gov/pubmed/25884622 http://dx.doi.org/10.1371/journal.ppat.1004827 |
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