Increased IgA Expression in Lung Lymphoid Follicles in Severe Chronic Obstructive Pulmonary Disease.
Acute Disease
Animals
B-Lymphocytes
/ immunology
Case-Control Studies
Disease Models, Animal
Enzyme-Linked Immunosorbent Assay
Female
Fluorescent Antibody Technique
Humans
Immunoglobulin A
/ metabolism
Interleukin-6
/ metabolism
Interleukins
/ metabolism
Lung
/ immunology
Male
Mice, Inbred C57BL
Middle Aged
Pulmonary Disease, Chronic Obstructive
/ immunology
Real-Time Polymerase Chain Reaction
Smoking
/ adverse effects
Tertiary Lymphoid Structures
/ immunology
B lymphocytes
COPD
IgA
lymphoid follicles
Journal
American journal of respiratory and critical care medicine
ISSN: 1535-4970
Titre abrégé: Am J Respir Crit Care Med
Pays: United States
ID NLM: 9421642
Informations de publication
Date de publication:
01 03 2019
01 03 2019
Historique:
pubmed:
20
10
2018
medline:
7
1
2020
entrez:
20
10
2018
Statut:
ppublish
Résumé
Accumulation of B cells and lymphoid follicles (LFs) has been described in chronic obstructive pulmonary disease (COPD) airways, but the functional status of lung B cells remains poorly known. To characterize LFs for expression of IgA, the main mucosal antibody. The presence of B cells and LFs, including intrafollicular IgA expression, were determined in the lung from patients with COPD (n = 37) versus control subjects (n = 34) by immunohistochemistry. We also evaluated follicular IgA responses in the lungs from mice infected with Pseudomonas aeruginosa (PAO1) (n = 10 per group) and in smoking mice. Whereas in smokers B-cell numbers slightly increased, robust increases in B-cell and LF numbers (mainly in distal airways) were only observed in severe COPD. Most follicular B cells were IgM This study shows that IgA production occurs in peribronchiolar LFs from severe COPD, where IL-21-producing T cells are present, and presumably represents a feature of exacerbated mucosal adaptive immune responses against microbial and/or self-antigens.
Identifiants
pubmed: 30339768
doi: 10.1164/rccm.201802-0352OC
doi:
Substances chimiques
Immunoglobulin A
0
Interleukin-6
0
Interleukins
0
interleukin-21
MKM3CA6LT1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
592-602Commentaires et corrections
Type : CommentIn
Type : CommentIn
Type : CommentIn