Natural antibodies targeting LPS in pleural effusions of various etiologies.

Anti-LPS Benign pleural effusions Infectious pleural effusions Malignant pleural effusions Natural antibodies

Journal

American journal of physiology. Lung cellular and molecular physiology
ISSN: 1522-1504
Titre abrégé: Am J Physiol Lung Cell Mol Physiol
Pays: United States
ID NLM: 100901229

Informations de publication

Date de publication:
09 Apr 2024
Historique:
medline: 9 4 2024
pubmed: 9 4 2024
entrez: 9 4 2024
Statut: aheadofprint

Résumé

Respiratory infection, cancer and heart failure can cause abnormal accumulation of fluid in the pleural cavity. The immune responses within the cavity are orchestrated by leucocytes that reside in the serosal associated lymphoid tissue. Natural antibodies (NAbs) are abundant in the serum having a major role in systemic and mucosal immunity, however their occurrence in pleural fluid remains an open question. Our aim herein was to detect and measure the levels of NAbs targeting LPS of M, G, and A class in both, the pleural fluid and the serum of 78 patients with pleural effusions (PEs) of various etiologies. The values of anti-LPS NAb activity were extracted through a normalization step regarding the total IgM, IgG and IgA levels and in addition the ratio of PF/S values were analyzed further with other critical biochemical parameters from biopsies. Anti-LPS NAbs of all Ig classes were detected in most of the samples, while a significant increase of anti-LPS activity was observed in infectious and non-infectious compared to malignant PEs. Multivariate linear regression confirmed a negative correlation of IgM and IgA anti-LPS PF/S ratio with malignancy. Moreover, anti-LPS NAbs PF/S measurements led to increased positive and negative predictive power in ROC curves generated for the discrimination between benign and malignant PEs. Our results highlight a potential role of anti-LPS NAbs in the pleural cavity that should be further explored.

Sections du résumé

BACKGROUND BACKGROUND
Respiratory infection, cancer and heart failure can cause abnormal accumulation of fluid in the pleural cavity. The immune responses within the cavity are orchestrated by leucocytes that reside in the serosal associated lymphoid tissue. Natural antibodies (NAbs) are abundant in the serum having a major role in systemic and mucosal immunity, however their occurrence in pleural fluid remains an open question. Our aim herein was to detect and measure the levels of NAbs targeting LPS of M, G, and A class in both, the pleural fluid and the serum of 78 patients with pleural effusions (PEs) of various etiologies.
METHODS METHODS
The values of anti-LPS NAb activity were extracted through a normalization step regarding the total IgM, IgG and IgA levels and in addition the ratio of PF/S values were analyzed further with other critical biochemical parameters from biopsies.
RESULTS RESULTS
Anti-LPS NAbs of all Ig classes were detected in most of the samples, while a significant increase of anti-LPS activity was observed in infectious and non-infectious compared to malignant PEs. Multivariate linear regression confirmed a negative correlation of IgM and IgA anti-LPS PF/S ratio with malignancy. Moreover, anti-LPS NAbs PF/S measurements led to increased positive and negative predictive power in ROC curves generated for the discrimination between benign and malignant PEs.
CONCLUSIONS CONCLUSIONS
Our results highlight a potential role of anti-LPS NAbs in the pleural cavity that should be further explored.

Identifiants

pubmed: 38591123
doi: 10.1152/ajplung.00377.2023
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Ioannis Sarrigeorgiou (I)

Department of Immunology, Hellenic Pasteur Institute, Greece.

Erasmia Rouka (E)

Faculty of Nursing, University of Thessaly, Larissa, Greece.

Ourania S Kotsiou (OS)

Department of Respiratory Medicine, University of Thessaly, Greece.

Garyfallia Perlepe (G)

Department of Respiratory Medicine, University of Thessaly, Greece.

Efrosini S Gerovasileiou (ES)

Department of Respiratory Medicine, University of Thessaly, Greece.

Konstantinos I Gourgoulianis (KI)

Department of Respiratory Medicine, University of Thessaly, Greece.

Peggy Lymberi (P)

Hellenic Pasteur Institute, Athens, Greece.

Sotirios G Zarogiannis (SG)

Department of Physiology, University Of Thessaly, Larissa, Greece.

Classifications MeSH