Immune responses and exacerbations in severe asthma.
Allergens
/ immunology
Animals
Asthma
/ diagnosis
Cytokines
/ metabolism
Disease Progression
Disease Susceptibility
/ immunology
Eosinophils
/ immunology
Host-Pathogen Interactions
/ genetics
Humans
Immunity
Immunization
Neutrophils
/ immunology
Organ Specificity
/ immunology
Severity of Illness Index
T-Lymphocyte Subsets
/ immunology
Journal
Current opinion in immunology
ISSN: 1879-0372
Titre abrégé: Curr Opin Immunol
Pays: England
ID NLM: 8900118
Informations de publication
Date de publication:
10 2021
10 2021
Historique:
received:
11
02
2021
accepted:
05
03
2021
pubmed:
28
3
2021
medline:
11
3
2022
entrez:
27
3
2021
Statut:
ppublish
Résumé
Asthma as a clinical entity manifests with a broad spectrum of disease severity. Unlike milder asthma, severe disease is poorly controlled by inhaled corticosteroids, the current standard of care. Transcriptomic data, along with patient characteristics and response to biologics show that though Type 2 (T2) immune response remains an integral feature of asthma, additional molecular and immunologic factors may play important roles in pathogenesis. Mechanisms of T2 development, cellular sources of T2 cytokines and their relationship to additional immune pathways concurrently activated may distinguish several different subphenotypes, and perhaps endotypes of asthma, with differential response to non-specific and targeted anti-inflammatory therapies. Recent data have also associated non-T2 cytokines derived from T cells, particularly IFN-γ, and epithelial mediators with severe asthma. These topics and their relationships to acute asthma exacerbations are discussed in this review.
Identifiants
pubmed: 33773471
pii: S0952-7915(21)00024-8
doi: 10.1016/j.coi.2021.03.004
pmc: PMC8460694
mid: NIHMS1687505
pii:
doi:
Substances chimiques
Allergens
0
Cytokines
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
34-42Subventions
Organisme : NHLBI NIH HHS
ID : F32 HL147415
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL113956
Pays : United States
Organisme : NIAID NIH HHS
ID : P01 AI106684
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI048927
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL007563
Pays : United States
Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.
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