Interferon signature in immunosuppressed patients with lower respiratory tract infections: dosage on bronchoalveolar lavage.


Journal

Minerva medica
ISSN: 1827-1669
Titre abrégé: Minerva Med
Pays: Italy
ID NLM: 0400732

Informations de publication

Date de publication:
Jun 2020
Historique:
pubmed: 23 11 2019
medline: 19 6 2020
entrez: 23 11 2019
Statut: ppublish

Résumé

Interferon signature (IS) is the measure of transcripts belonging to pathways of interferon activation. Viral infections can interfere with the interferon pathway, in particular herpesvirus present in immunocompromised hosts. The aim of our study was to evaluate if herpesvirus infections in immunocompromised patients with lower respiratory tract infections (LRTI) could lead to IS alterations. We measured IS transcription of six genes on bronchoalveolar lavage of immunocompromised patients with LRTI (IFI27, IFI44, IFIT1, ISG15, RSAD2, SIGLEC1). Patients were divided in three groups based on Epstein-Barr virus (EBV) and other herpesviruses coinfections. We included 56 patients, 10 without and 17 with only EBV reactivation (respectively N and E groups) and 29 with EBV and other herpesviruses (group C). IS was higher in group C (P=0.01) compared to other ones, but single gene expressions were different among groups: IFI27 was higher whereas IFIT1 and ISG15 were lower in group C (P<0.05). The continuous stimulation of interferon cascade by herpesviruses enhances IS. The analysis of IS in immunocompromised population is possible by limiting the use of IFI27, IFIT1, ISG15 genes. Our preliminary results seem to indicate that IS is a useful biomarker of cellular response to herpesvirus infection in immunocompromised patients.

Sections du résumé

BACKGROUND BACKGROUND
Interferon signature (IS) is the measure of transcripts belonging to pathways of interferon activation. Viral infections can interfere with the interferon pathway, in particular herpesvirus present in immunocompromised hosts. The aim of our study was to evaluate if herpesvirus infections in immunocompromised patients with lower respiratory tract infections (LRTI) could lead to IS alterations.
METHODS METHODS
We measured IS transcription of six genes on bronchoalveolar lavage of immunocompromised patients with LRTI (IFI27, IFI44, IFIT1, ISG15, RSAD2, SIGLEC1). Patients were divided in three groups based on Epstein-Barr virus (EBV) and other herpesviruses coinfections.
RESULTS RESULTS
We included 56 patients, 10 without and 17 with only EBV reactivation (respectively N and E groups) and 29 with EBV and other herpesviruses (group C). IS was higher in group C (P=0.01) compared to other ones, but single gene expressions were different among groups: IFI27 was higher whereas IFIT1 and ISG15 were lower in group C (P<0.05).
CONCLUSIONS CONCLUSIONS
The continuous stimulation of interferon cascade by herpesviruses enhances IS. The analysis of IS in immunocompromised population is possible by limiting the use of IFI27, IFIT1, ISG15 genes. Our preliminary results seem to indicate that IS is a useful biomarker of cellular response to herpesvirus infection in immunocompromised patients.

Identifiants

pubmed: 31755671
pii: S0026-4806.19.06334-1
doi: 10.23736/S0026-4806.19.06334-1
doi:

Substances chimiques

Adaptor Proteins, Signal Transducing 0
Antigens 0
Cytokines 0
Cytoskeletal Proteins 0
IFI27 protein, human 0
IFI44 protein, human 0
IFIT1 protein, human 0
Membrane Proteins 0
Proteins 0
RNA-Binding Proteins 0
SIGLEC1 protein, human 0
Sialic Acid Binding Ig-like Lectin 1 0
Ubiquitins 0
ISG15 protein, human 60267-61-0
Interferons 9008-11-1
Oxidoreductases Acting on CH-CH Group Donors EC 1.3.-
RSAD2 protein, human EC 1.3.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

245-253

Auteurs

Massimiliano Bergallo (M)

Department of Public Health and Pediatric Sciences, University of Turin Medical School, Turin, Italy.

Linda Ferrari (L)

Laboratory Medicine Department, Laboratory of Molecular Virology, Maggiore della Carità Hospital, Novara, Italy.

Giulia Faolotto (G)

Laboratory Medicine Department, Laboratory of Molecular Virology, Maggiore della Carità Hospital, Novara, Italy.

Piero E Balbo (PE)

Division of Respiratory Diseases, Medical Department, Maggiore della Carità Hospital, Novara, Italy.

Paola Montanari (P)

Department of Public Health and Pediatric Sciences, University of Turin Medical School, Turin, Italy.

Filippo Patrucco (F)

Division of Respiratory Diseases, Medical Department, Maggiore della Carità Hospital, Novara, Italy - filippo.patrucco@gmail.com.
Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.

Francesco Gavelli (F)

Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.

Matteo Daverio (M)

Division of Respiratory Diseases, Medical Department, Maggiore della Carità Hospital, Novara, Italy.

Mattia Bellan (M)

Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.
Center for Autoimmune and Allergic Diseases (CAAD), Novara, Italy.
Immunorheumatology Unit, Division of Internal Medicine, Medical Department, Maggiore della Carità Hospital, Novara, Italy.

Livia Salmi (L)

Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.

Luigi M Castello (LM)

Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.

Paolo Ravanini (P)

Laboratory Medicine Department, Laboratory of Molecular Virology, Maggiore della Carità Hospital, Novara, Italy.

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Classifications MeSH