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      Biologics and airway remodeling in severe asthma

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          Abstract

          Asthma is a chronic inflammatory airway disease resulting in airflow obstruction, which in part can become irreversible to conventional therapies, defining the concept of airway remodeling. The introduction of biologics in severe asthma has led in some patients to the complete normalization of previously considered irreversible airflow obstruction. This highlights the need to distinguish a “fixed” airflow obstruction due to structural changes unresponsive to current therapies, from a “reversible” one as demonstrated by lung function normalization during biological therapies not previously obtained even with high‐dose systemic glucocorticoids. The mechanisms by which exposure to environmental factors initiates the inflammatory responses that trigger airway remodeling are still incompletely understood. Alarmins represent epithelial‐derived cytokines that initiate immunologic events leading to inflammatory airway remodeling. Biological therapies can improve airflow obstruction by addressing these airway inflammatory changes. In addition, biologics might prevent and possibly even revert “fixed” remodeling due to structural changes. Hence, it appears clinically important to separate the therapeutic effects (early and late) of biologics as a new paradigm to evaluate the effects of these drugs and future treatments on airway remodeling in severe asthma.

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          Most cited references255

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          Reference-based analysis of lung single-cell sequencing reveals a transitional profibrotic macrophage

          Tissue fibrosis is a major cause of mortality that results from the deposition of matrix proteins by an activated mesenchyme. Macrophages accumulate in fibrosis, but the role of specific subgroups in supporting fibrogenesis has not been investigated in vivo. Here we used single-cell RNA sequencing (scRNA-seq) to characterize the heterogeneity of macrophages in bleomycin-induced lung fibrosis in mice. A novel computational framework for the annotation of scRNA-seq by reference to bulk transcriptomes (SingleR) enabled the subclustering of macrophages and revealed a disease-associated subgroup with a transitional gene expression profile intermediate between monocyte-derived and alveolar macrophages. These CX3CR1+SiglecF+ transitional macrophages localized to the fibrotic niche and had a profibrotic effect in vivo. Human orthologues of genes expressed by the transitional macrophages were upregulated in samples from patients with idiopathic pulmonary fibrosis. Thus, we have identified a pathological subgroup of transitional macrophages that are required for the fibrotic response to injury.
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            International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma.

            Severe or therapy-resistant asthma is increasingly recognised as a major unmet need. A Task Force, supported by the European Respiratory Society and American Thoracic Society, reviewed the definition and provided recommendations and guidelines on the evaluation and treatment of severe asthma in children and adults. A literature review was performed, followed by discussion by an expert committee according to the GRADE (Grading of Recommendations, Assessment, Development and Evaluation) approach for development of specific clinical recommendations. When the diagnosis of asthma is confirmed and comorbidities addressed, severe asthma is defined as asthma that requires treatment with high dose inhaled corticosteroids plus a second controller and/or systemic corticosteroids to prevent it from becoming "uncontrolled" or that remains "uncontrolled" despite this therapy. Severe asthma is a heterogeneous condition consisting of phenotypes such as eosinophilic asthma. Specific recommendations on the use of sputum eosinophil count and exhaled nitric oxide to guide therapy, as well as treatment with anti-IgE antibody, methotrexate, macrolide antibiotics, antifungal agents and bronchial thermoplasty are provided. Coordinated research efforts for improved phenotyping will provide safe and effective biomarker-driven approaches to severe asthma therapy.
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              Single-cell RNA-seq reveals new types of human blood dendritic cells, monocytes, and progenitors

              Dendritic cells (DCs) and monocytes play a central role in pathogen sensing, phagocytosis, and antigen presentation and consist of multiple specialized subtypes. However, their identities and interrelationships are not fully understood. Using unbiased single-cell RNA sequencing (RNA-seq) of ~2400 cells, we identified six human DCs and four monocyte subtypes in human blood. Our study reveals a new DC subset that shares properties with plasmacytoid DCs (pDCs) but potently activates T cells, thus redefining pDCs; a new subdivision within the CD1C+ subset of DCs; the relationship between blastic plasmacytoid DC neoplasia cells and healthy DCs; and circulating progenitor of conventional DCs (cDCs). Our revised taxonomy will enable more accurate functional and developmental analyses as well as immune monitoring in health and disease.
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                Author and article information

                Contributors
                gildanet@gmail.com
                Journal
                Allergy
                Allergy
                10.1111/(ISSN)1398-9995
                ALL
                Allergy
                John Wiley and Sons Inc. (Hoboken )
                0105-4538
                1398-9995
                23 August 2022
                December 2022
                : 77
                : 12 ( doiID: 10.1111/all.v77.12 )
                : 3538-3552
                Affiliations
                [ 1 ] Department of Translational Medical Sciences University of Naples Federico II Naples Italy
                [ 2 ] Center for Basic and Clinical Immunology Research (CISI) University of Naples Federico II Naples Italy
                [ 3 ] World Allergy Organization (WAO) Center of Excellence Naples Italy
                [ 4 ] Institute of Experimental Endocrinology and Oncology (IEOS) National Research Council Naples Italy
                [ 5 ] Personalized Medicine Asthma and Allergy Unit ‐ IRCCS Humanitas Research Hospital Milan Italy
                [ 6 ] Department of Biomedical Sciences Humanitas University Milan Italy
                [ 7 ] Departments of Pneumology and Critical Care Medicine University of Rostock Rostock Germany
                Author notes
                [*] [* ] Correspondence

                Gilda Varricchi, Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, 80131 Naples, Italy.

                Email: gildanet@ 123456gmail.com

                Author information
                https://orcid.org/0000-0002-9285-4657
                https://orcid.org/0000-0002-1831-9672
                https://orcid.org/0000-0002-1441-0145
                https://orcid.org/0000-0002-4723-0167
                https://orcid.org/0000-0001-7889-425X
                https://orcid.org/0000-0003-1458-4863
                https://orcid.org/0000-0003-3953-9225
                https://orcid.org/0000-0003-4291-1956
                https://orcid.org/0000-0002-0492-5663
                https://orcid.org/0000-0001-8467-2557
                Article
                ALL15473 ALL-2022-00415.R2
                10.1111/all.15473
                10087445
                35950646
                d288fba9-21ce-4c0d-ae4d-532595f24a42
                © 2022 The Authors. Allergy published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 03 August 2022
                : 22 April 2022
                : 05 August 2022
                Page count
                Figures: 1, Tables: 1, Pages: 15, Words: 12776
                Funding
                Funded by: Regione Campania , doi 10.13039/501100003852;
                Funded by: TIMING Project
                Funded by: University of Naples Federico II , doi 10.13039/100007195;
                Categories
                Review Article
                Review Articles
                Custom metadata
                2.0
                December 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.7 mode:remove_FC converted:11.04.2023

                Immunology
                airway remodeling,biologics,biomarkers,immunotherapies,severe asthma
                Immunology
                airway remodeling, biologics, biomarkers, immunotherapies, severe asthma

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