COMMD8 changes expression during initial phase of wasp venom immunotherapy.


Journal

The journal of gene medicine
ISSN: 1521-2254
Titre abrégé: J Gene Med
Pays: England
ID NLM: 9815764

Informations de publication

Date de publication:
11 2020
Historique:
received: 17 01 2020
revised: 02 04 2020
accepted: 10 06 2020
pubmed: 20 6 2020
medline: 1 9 2021
entrez: 20 6 2020
Statut: ppublish

Résumé

Hymenoptera venom allergy (HVA) is of great concern because of the possibility of anaphylaxis, which may be fatal. Venom immunotherapy (VIT) is the only disease-modifying treatment in HVA and, although efficient, its mechanism remains partially unknown. Gene expression analysis may be helpful for establishing a proper model of tolerance induction during the build-up phase of VIT. The present study aimed to analyze how the start of VIT changes the expression of 15 selected genes. Forty-five patients starting VIT with a wasp venom allergy were enrolled. The diagnosis was established based on anaphylaxis history (third or fourth grade on the Mueller scale) and positive soluble immunoglobulin E and/or skin tests. Two blood collections were performed in the patient group: before and after 3 months of VIT. One sample was taken in the control group. Gene expression analysis was performed using a reverse transcriptase-polymerase chain reaction with microfluidic cards and normalized to the 18S housekeeping gene. Commd8 was the only gene that changed expression significantly after the start of VIT (p = 0.012). Its expression decreased towards the levels observed in the healthy controls. Twelve out of 15 genes (commd8, cldn1, cngb3, fads1, hes6, hla-drb5, htr3b, prlr, slc16a4, snx33, socs3 and twist2) revealed a significantly different expression compared to the healthy controls. The present study shows that commd8 changes significantly its expression during initial phase of VIT. This gene might be a candidate for VIT biomarker in future studies.

Sections du résumé

BACKGROUND
Hymenoptera venom allergy (HVA) is of great concern because of the possibility of anaphylaxis, which may be fatal. Venom immunotherapy (VIT) is the only disease-modifying treatment in HVA and, although efficient, its mechanism remains partially unknown. Gene expression analysis may be helpful for establishing a proper model of tolerance induction during the build-up phase of VIT. The present study aimed to analyze how the start of VIT changes the expression of 15 selected genes.
METHODS
Forty-five patients starting VIT with a wasp venom allergy were enrolled. The diagnosis was established based on anaphylaxis history (third or fourth grade on the Mueller scale) and positive soluble immunoglobulin E and/or skin tests. Two blood collections were performed in the patient group: before and after 3 months of VIT. One sample was taken in the control group. Gene expression analysis was performed using a reverse transcriptase-polymerase chain reaction with microfluidic cards and normalized to the 18S housekeeping gene.
RESULTS
Commd8 was the only gene that changed expression significantly after the start of VIT (p = 0.012). Its expression decreased towards the levels observed in the healthy controls. Twelve out of 15 genes (commd8, cldn1, cngb3, fads1, hes6, hla-drb5, htr3b, prlr, slc16a4, snx33, socs3 and twist2) revealed a significantly different expression compared to the healthy controls.
CONCLUSIONS
The present study shows that commd8 changes significantly its expression during initial phase of VIT. This gene might be a candidate for VIT biomarker in future studies.

Identifiants

pubmed: 32559011
doi: 10.1002/jgm.3243
doi:

Substances chimiques

Biomarkers 0
Delta-5 Fatty Acid Desaturase 0
Wasp Venoms 0
Immunoglobulin E 37341-29-0
FADS1 protein, human EC 1.14.19.3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e3243

Informations de copyright

© 2020 John Wiley & Sons, Ltd.

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Auteurs

Karol Kempiński (K)

Department of Allergology, Medical University of Gdańsk, Gdańsk, Poland.

Jan Romantowski (J)

Department of Allergology, Medical University of Gdańsk, Gdańsk, Poland.

Agnieszka Maciejewska (A)

Department of Forensic Medicine, Medical University of Gdansk, Gdańsk, Poland.

Ryszard Pawłowski (R)

Department of Forensic Medicine, Medical University of Gdansk, Gdańsk, Poland.

Marta Chełmińska (M)

Department of Allergology, Medical University of Gdańsk, Gdańsk, Poland.

Ewa Jassem (E)

Department of Allergology, Medical University of Gdańsk, Gdańsk, Poland.

Marek Niedoszytko (M)

Department of Allergology, Medical University of Gdańsk, Gdańsk, Poland.

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