Therapeutic Potential of Anti-Interferon α Vaccination on SjS-Related Features in the MRL/lpr Autoimmune Mouse Model.
Animals
Antibodies, Neutralizing
/ blood
Autoantibodies
/ blood
Autoimmunity
B-Lymphocytes
/ immunology
Disease Models, Animal
Female
Gene Expression Profiling
Hemocyanins
/ administration & dosage
Humans
Immunoconjugates
/ administration & dosage
Immunotherapy, Active
Interferon-alpha
/ administration & dosage
Interferons
/ biosynthesis
Lacrimal Apparatus
/ immunology
Mice
Mice, Inbred MRL lpr
Salivary Glands
/ immunology
Sjogren's Syndrome
/ genetics
Sjögren’s syndrome
adjuvant
interferon a (IFN-a)
kinoid
vaccination
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
09
02
2021
accepted:
21
10
2021
entrez:
6
12
2021
pubmed:
7
12
2021
medline:
24
12
2021
Statut:
epublish
Résumé
Sjögren's syndrome (SjS) is a frequent systemic autoimmune disease responsible for a major decrease in patients' quality of life, potentially leading to life-threatening conditions while facing an unmet therapeutic need. Hence, we assessed the immunogenicity, efficacy, and tolerance of IFN-Kinoid (IFN-K), an anti-IFNα vaccination strategy, in a well-known mouse model of systemic autoimmunity with SjS-like features: MRL/MpJ-Faslpr/lpr (MRL/lpr) mice. Two cohorts (with ISA51 or SWE01 as adjuvants) of 26 female MRL/lpr were divided in parallel groups, "controls" (not treated, PBS and Keyhole Limpet Hemocyanin [KLH] groups) or "IFN-K" and followed up for 122 days. Eight-week-old mice received intra-muscular injections (days 0, 7, 28, 56 and 84) of PBS, KLH or IFN-K, emulsified in the appropriate adjuvant, and blood samples were serially collected. At sacrifice, surviving mice were euthanized and their organs were harvested for histopathological analysis (focus score in salivary/lacrimal glands) and IFN signature evaluation. SjS-like features were monitored. IFN-K induced a disease-modifying polyclonal anti-IFNα antibody response in all treated mice with high IFNα neutralization capacities, type 1 IFN signature's reduction and disease features' (ocular and oral sicca syndrome, neuropathy, focus score, glandular production of BAFF) improvement, as reflected by the decrease in Murine Sjögren's Syndrome Disease Activity Index (MuSSDAI) modelled on EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI). No adverse effects were observed. We herein report on the strong efficacy of an innovative anti-IFNα vaccination strategy in a mouse model of SjS, paving the way for further clinical development (a phase IIb trial has just been completed in systemic lupus erythematosus with promising results).
Identifiants
pubmed: 34867938
doi: 10.3389/fimmu.2021.666134
pmc: PMC8635808
doi:
Substances chimiques
Antibodies, Neutralizing
0
Autoantibodies
0
Immunoconjugates
0
Interferon-alpha
0
Interferons
9008-11-1
Hemocyanins
9013-72-3
keyhole-limpet hemocyanin
FV4Y0JO2CX
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
666134Informations de copyright
Copyright © 2021 Killian, Colaone, Haumont, Nicco, Cerles, Chouzenoux, Cathébras, Rochereau, Chanut, Thomas, Laroche, Forest, Grouard-Vogel, Batteux and Paul.
Déclaration de conflit d'intérêts
Authors FC, PH and GG-V were employed by company NEOVACS S.A. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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