Cytokine and LL-37 gene expression levels in Bartonella spp. seropositive and seronegative patients of a rheumatology clinic.


Journal

Advances in medical sciences
ISSN: 1898-4002
Titre abrégé: Adv Med Sci
Pays: Netherlands
ID NLM: 101276222

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 25 09 2021
revised: 07 02 2022
accepted: 24 02 2022
pubmed: 14 3 2022
medline: 6 4 2022
entrez: 13 3 2022
Statut: ppublish

Résumé

The variation in the immune response to Bartonella spp. infection in humans remains unclear. The present study compares the expression of selected interleukins, cytokines and cathelicidin (LL-37) in rheumatology clinic patients suffering from musculoskeletal symptoms with healthy blood donors. The patients had previously been tested for the presence of Bartonella henselae antibodies. Gene expression of LL-37, interleukin (IL)-2, IL-4, IL-6, IL-12, interferon-(IFN)-γ, and tumor necrosis factor (TNF-α)-α was determined in blood samples using quantitative Polymerase Chain Reaction (qPCR). Statistical analysis was prepared with STATISTICA. Statistically significant differences in the mRNA levels of the tested cytokines (IFN-γ, TNF-α, IL-2, IL-4, IL-6, IL-12; p<0.0001) were observed between the healthy controls and patients; however, no difference was observed for LL37 mRNA (p ​= ​0.1974). No significant differences in mRNA expression were observed between IgG in anti-Bartonella seropositive and seronegative individuals (p>0.05). The only significant differences between the Bartonella spp. DNA positive and negative patients, indicated by PCR, were observed for TNF-α and IL-12 mRNA (p ​= ​0.0045 and p ​= ​0.0255, respectively). A broadly similar immune response to the tested cytokines was observed among the participants irrespective of anti-Bartonella spp. IgG seropositivity. However, the Bartonella DNA-positive participants demonstrated significantly lower expression of IL-12 and TNF-α mRNA; this may indicate that these bacteria have a suppressive influence on the immune system.

Identifiants

pubmed: 35279619
pii: S1896-1126(22)00011-6
doi: 10.1016/j.advms.2022.02.007
pii:
doi:

Substances chimiques

Antimicrobial Cationic Peptides 0
Cytokines 0
Cathelicidins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

163-169

Informations de copyright

Copyright © 2022 Medical University of Bialystok. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Monika E Łysakowska (ME)

Department of Microbiology and Medical Laboratory Immunology, Medical University of Lodz, Lodz, Poland. Electronic address: monika.lysakowska@umed.lodz.pl.

Małgorzata Szybka (M)

Department of Microbiology and Medical Laboratory Immunology, Medical University of Lodz, Lodz, Poland.

Brzezińska Olga (B)

Department of Rheumatology, Medical University of Lodz, Lodz, Poland.

Sylwia Moskwa (S)

Department of Microbiology and Medical Laboratory Immunology, Medical University of Lodz, Lodz, Poland.

Magdalena Konieczka (M)

Department of Microbiology and Medical Laboratory Immunology, Medical University of Lodz, Lodz, Poland.

Joanna Makowska (J)

Department of Rheumatology, Medical University of Lodz, Lodz, Poland.

Dorota Pastuszak-Lewandoska (D)

Department of Microbiology and Medical Laboratory Immunology, Medical University of Lodz, Lodz, Poland.

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Classifications MeSH