A1 Refereed original research article in a scientific journal
B cell immune response to human bocaviruses
Authors: Karaaslan Cagatay, Wirz Oliver, Tan Ge, Globinska Anna, Boonpiyathad Tadech, Hedman Klaus, Vaselek Slavica, Söderlund-Venermo Maria, Jartti Tuomas, Akdis Mubeccel, Akdis Cezmi A.
Publisher: Wiley-Blackwell
Publishing place: HOBOKEN
Publication year: 2024
Journal: Clinical and Experimental Allergy
Journal name in source: CLINICAL AND EXPERIMENTAL ALLERGY
Journal acronym: CLIN EXP ALLERGY
Volume: 54
Issue: 6
First page : 388
Last page: 401
Number of pages: 14
ISSN: 0954-7894
eISSN: 1365-2222
DOI: https://doi.org/10.1111/cea.14453
Web address : https://doi.org/10.1111/cea.14453
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/387342662
Background: Human bocaviruses (HBoVs) have been demonstrated in respiratory and gastrointestinal infections; however, the immune response to them has not been studied in detail. In this study, we investigated the B cell immune responses to HBoV1 and HBoV2, representing two different species of bocaviruses in humans.
Methods: We analyzed the effects of stimulations with HBoV1 and 2 virus-like particles (VLPs) and of co-stimulation with HBoV1-rhinovirus (RV) on cells of the immune system by flow cytometry, transcriptomics, and luminometric immune assays.
Results: Human B cells, and particularly B regulatory cells (Breg cells), showed an increased immune response to HBoV1-VLPs stimulation. These immune responses were also supported by increased IL-1RA and PDL1 expressions in IL-10+ B cells from peripheral blood mononuclear cells (PBMCs) stimulated with HBoV1-VLPs. In addition, increased levels of IL-10 and IL-1RA were determined in the supernatants of PBMCs following HBoV1-VLPs stimulation. HBoV1-VLPs and RV co-stimulation increased the IL-10+ B cell population. Transcriptome analysis by next-generation RNA sequencing showed an increased expression of IL-10 signalling and Breg cell markers in PBMCs stimulated with HBoV1-VLPs. Furthermore, TGF-β and chemoattractants MIP-1α, MIP-1β and IP10 protein levels were high in the supernatants of PBMCs stimulated with HBoV1-VLPs.
Conclusions: The findings demonstrate that in Breg cells, IL-10 signalling pathways, and anti-inflammatory activity are induced by HBoV1, which can explain the often mild nature of the disease. In addition, the immune regulatory response induced by HBoV1-VLPs may indicate a potential immunomodulatory role of HBoV1 on the immune system and may represent an immune regulatory strategy.
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