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Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 A Fungal Protease Model to Interrogate Allergic Lung Immunity
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    Chapter 4 A Mouse Model of Peanut Allergy Induced by Sensitization Through the Gastrointestinal Tract
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    Chapter 5 Induction and Characterization of the Allergic Eye Disease Mouse Model
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    Chapter 6 Isolation and Purification of Epithelial and Endothelial Cells from Mouse Lung
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    Chapter 10 Determination of the Fate and Function of Innate Lymphoid Cells Following Adoptive Transfer of Innate Lymphoid Cell Precursors
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    Chapter 11 Characterization of Thymic Development of Natural Killer T Cell Subsets by Multiparameter Flow Cytometry
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    Chapter 12 Characterization of Mouse γδ T Cell Subsets in the Setting of Type-2 Immunity
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    Chapter 14 Generation of Allergen-Specific Tetramers for a Murine Model of Airway Inflammation
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    Chapter 15 The Generation and Use of Allergen-Specific TCR Transgenic Animals
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    Chapter 18 Imaging Precision-Cut Lung Slices to Visualize Leukocyte Localization and Trafficking
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    Chapter 19 Study of IgE-Producing B Cells Using the Verigem Fluorescent Reporter Mouse
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    Chapter 24 Identification of Functionally Relevant microRNAs in the Regulation of Allergic Inflammation
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    Chapter 25 The Use of Biodegradable Nanoparticles for Tolerogenic Therapy of Allergic Inflammation
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    Chapter 26 Assessing the Mouse Intestinal Microbiota in Settings of Type-2 Immune Responses
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    Chapter 28 A Consistent Method to Identify and Isolate Mononuclear Phagocytes from Human Lung and Lymph Nodes
  17. Altmetric Badge
    Chapter 30 Utilization of Air–Liquid Interface Cultures as an In Vitro Model to Assess Primary Airway Epithelial Cell Responses to the Type 2 Cytokine Interleukin-13
Attention for Chapter 28: A Consistent Method to Identify and Isolate Mononuclear Phagocytes from Human Lung and Lymph Nodes
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Chapter title
A Consistent Method to Identify and Isolate Mononuclear Phagocytes from Human Lung and Lymph Nodes
Chapter number 28
Book title
Type 2 Immunity
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7896-0_28
Pubmed ID
Book ISBNs
978-1-4939-7895-3, 978-1-4939-7896-0
Authors

Sophie L. Gibbings, Claudia V. Jakubzick, Gibbings, Sophie L., Jakubzick, Claudia V.

Abstract

Mononuclear phagocytes (MP) consist of macrophages, dendritic cells (DCs), and monocytes. In all organs, including the lung, there are multiple subtypes within these categories. The existence of all these cell types suggest that there is a clear division of labor and delicate balance between the MPs under steady state and inflammatory conditions. Although great strides have been made to understand MPs in the mouse lung, and human blood, little is known about the MPs that exist in the human lung and lung-draining lymph nodes (LNs), and even less is known about their functional roles, studies of which will require a large number of sorted cells. We have comprehensively examined cell surface markers previously used in a variety of organs to identify human pulmonary MPs. In the lung, we consistently identify five extravascular pulmonary MPs and three LN MPs. These MPs were present in over 100 lungs regardless of age or gender. Notably, the human blood CD141+ DCs, as described in the literature, were not observed in non-diseased lungs or their draining LNs. In the lung and draining LNs, expression of CD141 was only observed on HLADR+ CD11c+ CD14+ extravascular monocytes (often confused in the LN as resident DCs based on the level of HLADR expression and mouse LN data). In the human lung and LNs there are at least two DC subtypes expressing HLADR, DEC205 and CD1c, along with circulating monocytes that behave as either antigen-presenting cells or macrophages. Furthermore, we demonstrate how to distinguish between alveolar macrophages and interstitial macrophage subtypes. It still remains unclear how the human pulmonary MPs identified here align with mouse MPs. Clearly, we are now past the stage of cell surface marker characterization, and future studies will need to move toward understanding what these cell types are and how they function. Our hope is that the strategy described here can help the pulmonary community take this next step.

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The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 21 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 21 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 7 33%
Researcher 3 14%
Student > Postgraduate 2 10%
Student > Master 1 5%
Student > Bachelor 1 5%
Other 2 10%
Unknown 5 24%
Readers by discipline Count As %
Immunology and Microbiology 8 38%
Biochemistry, Genetics and Molecular Biology 2 10%
Medicine and Dentistry 2 10%
Agricultural and Biological Sciences 2 10%
Pharmacology, Toxicology and Pharmaceutical Science 1 5%
Other 2 10%
Unknown 4 19%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 30 June 2018.
All research outputs
#15,538,060
of 23,092,602 outputs
Outputs from Methods in molecular biology
#5,411
of 13,207 outputs
Outputs of similar age
#270,127
of 442,643 outputs
Outputs of similar age from Methods in molecular biology
#596
of 1,499 outputs
Altmetric has tracked 23,092,602 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,207 research outputs from this source. They receive a mean Attention Score of 3.4. This one is in the 44th percentile – i.e., 44% of its peers scored the same or lower than it.
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We're also able to compare this research output to 1,499 others from the same source and published within six weeks on either side of this one. This one is in the 42nd percentile – i.e., 42% of its contemporaries scored the same or lower than it.