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      Neutrophil phenotypes in bronchial airways differentiate single from dual responding allergic asthmatics

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          Abstract

          Introduction

          Allergic asthmatics with both an early (EAR) and a late allergic reaction (LAR) following allergen exposure are termed ‘dual responders’ (DR), while ‘single responders’ (SR) only have an EAR. Mechanisms that differentiate DR from SR are largely unknown, particularly regarding the role and phenotypes of neutrophils. Therefore, we aimed to study neutrophils in DR and SR asthmatics.

          Methods

          Thirty‐four allergic asthmatics underwent an inhaled allergen challenge, samples were collected before and up to 24 h post‐challenge. Cell differentials were counted from bronchial lavage, alveolar lavage and blood; and tissue neutrophils were quantified in immune‐stained bronchial biopsies. Lavage neutrophil nuclei lobe segmentation was used to classify active (1–4 lobes) from suppressive neutrophils (≥5 lobes). Levels of transmigration markers: soluble (s)CD62L and interleukin‐1Ra, and activity markers: neutrophil elastase (NE), DNA‐histone complex and dsDNA were measured in lavage fluid and plasma.

          Results

          Compared with SR at baseline, DR had more neutrophils in their bronchial airways at baseline, both in the lavage ( = .0031) and biopsies ( p = .026) and elevated bronchial neutrophils correlated with less antitransmigratory IL‐1Ra levels ( r = −0.64). DR airways had less suppressive neutrophils and more 3‐lobed (active) neutrophils ( = .029) that correlated with more bronchial lavage histone ( = .020) and more plasma NE ( = .0016). Post‐challenge, DR released neutrophil extracellular trap factors in the blood earlier and had less pro‐transmigratory sCD62L during the late phase ( = .0076) than in SR.

          Conclusion

          DR have a more active airway neutrophil phenotype at baseline and a distinct neutrophil response to allergen challenge that may contribute to the development of an LAR. Therefore, neutrophil activity should be considered during targeted diagnosis and bio‐therapeutic development for DR.

          Abstract

          Allergic asthmatics underwent an inhaled allergen challenge with samples taken from the airway and blood at baseline and after the challenge. Dual responding allergic asthmatics (DR) had more 2‐ to 3‐lobed (known as ‘active’) and less ≥5‐lobed (‘suppressive’) airway neutrophils correlating with less circulating IL‐1Ra than single responders (SR) at baseline. Following an inhaled allergen challenge, DR had more circulating NETosis factors than SR during the early allergic reaction phase (EAR).

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          Most cited references50

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          Neutrophil recruitment and function in health and inflammation.

          Neutrophils have traditionally been thought of as simple foot soldiers of the innate immune system with a restricted set of pro-inflammatory functions. More recently, it has become apparent that neutrophils are, in fact, complex cells capable of a vast array of specialized functions. Although neutrophils are undoubtedly major effectors of acute inflammation, several lines of evidence indicate that they also contribute to chronic inflammatory conditions and adaptive immune responses. Here, we discuss the key features of the life of a neutrophil, from its release from bone marrow to its death. We discuss the possible existence of different neutrophil subsets and their putative anti-inflammatory roles. We focus on how neutrophils are recruited to infected or injured tissues and describe differences in neutrophil recruitment between different tissues. Finally, we explain the mechanisms that are used by neutrophils to promote protective or pathological immune responses at different sites.
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            Sputum neutrophil counts are associated with more severe asthma phenotypes using cluster analysis.

            Clinical cluster analysis from the Severe Asthma Research Program (SARP) identified 5 asthma subphenotypes that represent the severity spectrum of early-onset allergic asthma, late-onset severe asthma, and severe asthma with chronic obstructive pulmonary disease characteristics. Analysis of induced sputum from a subset of SARP subjects showed 4 sputum inflammatory cellular patterns. Subjects with concurrent increases in eosinophil (≥2%) and neutrophil (≥40%) percentages had characteristics of very severe asthma.
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              A subset of neutrophils in human systemic inflammation inhibits T cell responses through Mac-1.

              Suppression of immune responses is necessary to limit damage to host tissue during inflammation, but it can be detrimental in specific immune responses, such as sepsis and antitumor immunity. Recently, immature myeloid cells have been implicated in the suppression of immune responses in mouse models of cancer, infectious disease, bone marrow transplantation, and autoimmune disease. Here, we report the identification of a subset of mature human neutrophils (CD11cbright/CD62Ldim/CD11bbright/CD16bright) as what we believe to be a unique circulating population of myeloid cells, capable of suppressing human T cell proliferation. These cells were observed in humans in vivo during acute systemic inflammation induced by endotoxin challenge or by severe injury. Local release of hydrogen peroxide from the neutrophils into the immunological synapse between the neutrophils and T cells mediated the suppression of T cell proliferation and required neutrophil expression of the integrin Mac-1 (αMβ2). Our data demonstrate that suppression of T cell function can be accomplished by a subset of human neutrophils that can be systemically induced in response to acute inflammation. Identification of the pivotal role of neutrophil Mac-1 and ROS in this process provides a potential target for modulating immune responses in humans.
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                Author and article information

                Contributors
                nicole.van_der_burg@med.lu.se
                Journal
                Clin Exp Allergy
                Clin Exp Allergy
                10.1111/(ISSN)1365-2222
                CEA
                Clinical and Experimental Allergy
                John Wiley and Sons Inc. (Hoboken )
                0954-7894
                1365-2222
                28 April 2022
                January 2023
                : 53
                : 1 ( doiID: 10.1111/cea.v53.1 )
                : 65-77
                Affiliations
                [ 1 ] Department of Clinical Sciences Lund, Respiratory Medicine and Allergology Lund University Lund Sweden
                [ 2 ] Center for Primary Health Care Research Department of Clinical Sciences Malmö Lund University Lund Sweden
                [ 3 ] Division of ENT Diseases Department of Clinical Science, Intervention and Technology Karolinska Institutet Stockholm Sweden
                [ 4 ] Department of Microbiology Immunology & Transplantation KU Leuven Catholic University of Leuven Leuven Belgium
                [ 5 ] Department of Respiratory Medicine First Faculty of Medicine Charles University and Thomayer Hospital Prague Czech Republic
                [ 6 ] Department of Experimental Medical Science, Cell and Tissue biology Lund University Lund Sweden
                [ 7 ] Department of Otorhinolaryngology Head & Neck Surgery Institute of Clinical Sciences Skane University Hospital Lund Sweden
                Author notes
                [*] [* ] Correspondence

                Nicole van der Burg, Department of Clinical Sciences Lund, Respiratory Medicine and Allergology, Lund University, Lund, Sweden.

                Email: nicole.van_der_burg@ 123456med.lu.se

                Author information
                https://orcid.org/0000-0002-3369-6425
                https://orcid.org/0000-0003-0133-0100
                https://orcid.org/0000-0003-0538-9580
                https://orcid.org/0000-0002-6716-3010
                https://orcid.org/0000-0002-4941-332X
                Article
                CEA14149
                10.1111/cea.14149
                10083921
                35437872
                8028fb0c-a43d-47f5-9509-88970156dc6d
                © 2022 The Authors. Clinical & Experimental Allergy published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 18 March 2022
                : 09 December 2021
                : 11 April 2022
                Page count
                Figures: 8, Tables: 1, Pages: 13, Words: 7151
                Funding
                Funded by: Swedish Asthma and Allergy Association’s Research Foundation
                Funded by: Crafoord Foundation , doi 10.13039/501100003173;
                Funded by: Alfred Österlund Foundation , doi 10.13039/501100005390;
                Funded by: Hjärt‐Lungfonden , doi 10.13039/501100003793;
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                January 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.7 mode:remove_FC converted:10.04.2023

                Immunology
                allergic asthma,cd62l,il‐1ra,inhaled allergen challenge,late allergic reaction,netosis,neutrophils

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