COVID-19 Vaccine: A Potential Risk Factor for Accelerating the Onset of Bullous Pemphigoid.

COVID-19 Vaccine: A Potential Risk Factor for Accelerating the Onset of Bullous Pemphigoid.

Publication date: Sep 05, 2024

Bullous pemphigoid (BP) is the most common autoimmune bullous disease, whose main autoantigens are hemidesmosomal components BP180 and BP230. Although recent studies found no association between COVID-19 vaccines and BP, since mass vaccinations started, more than 90 vaccine-associated BP cases have been reported. To find an agreement among real-life clinical observations and recent epidemiologic data, we further investigated this topic. A total of 64 patients with BP onset in 2021 were demographically, clinically, and serologically characterized: 14 (21. 9%) vaccine-associated patients (VA) developed BP within 5 weeks from the first/second vaccine dose. VA and vaccine-non-associated (VNA) patients had similar demographics and clinical and immunological characteristics. Noteworthy, the monthly distribution of BP onset during mass vaccinations paralleled vaccine administration to the elderly in the same catchment area. Additionally, in 2021, BP onsets in April-May and June-July significantly increased (p = 0. 004) and declined (p = 0. 027), respectively, compared to the three years before vaccination campaigns (2018-2020). Interestingly, VA and VNA patients showed statistically significant differences in the use of inhalers and diuretics. Our findings suggest that the COVID-19 vaccine may constitute an accelerating factor that, together with other triggering factors, could act in genetically predisposed individuals with possible sub-clinical autoreactivity against BP antigens, slightly accelerating BP onset.

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Concepts Keywords
Bp180 autoimmune bullous disease
Bullous bullous pemphigoid
June COVID-19
Vaccine pandemic
SARS-CoV-2
vaccine

Semantics

Type Source Name
disease MESH Bullous Pemphigoid
disease MESH Rare Diseases
disease MESH COVID 19
disease MESH blisters
disease MESH herpes zoster
disease MESH influenza
drug DRUGBANK Clostridium tetani toxoid antigen (formaldehyde inactivated)
drug DRUGBANK Coenzyme M
drug DRUGBANK Nonoxynol-9
pathway REACTOME Immune System
disease MESH autoimmune diseases
disease MESH psoriasis
disease MESH rheumatoid arthritis
pathway KEGG Rheumatoid arthritis
disease MESH autoimmunity
disease MESH relapse
disease MESH emergency
drug DRUGBANK Fluorescein
drug DRUGBANK Immune Globulin Human
drug DRUGBANK Pidolic Acid
disease IDO blood
drug DRUGBANK Clopidogrel
drug DRUGBANK Isoniazid
disease IDO production
drug DRUGBANK Hydrochlorothiazide
drug DRUGBANK Spironolactone
drug DRUGBANK Chlorthalidone
drug DRUGBANK Indapamide
drug DRUGBANK Acetylsalicylic acid
drug DRUGBANK Warfarin
disease MESH dementia
disease MESH Prostatitis
disease MESH urinary tract infection
drug DRUGBANK Allopurinol
disease MESH chronic renal insufficiency
disease MESH infection
drug DRUGBANK Medical air
disease MESH allergic reactions
disease MESH dermatoses
disease IDO susceptibility
disease MESH asthma
pathway KEGG Asthma
drug DRUGBANK Bismuth subgallate
disease MESH melanoma
pathway KEGG Melanoma
disease MESH pemphigus
disease MESH vitiligo
drug DRUGBANK Guanosine
disease MESH Alopecia areata
disease MESH Myocarditis
disease MESH Thrombocytopenia
disease MESH syndrome
disease MESH systemic lupus erythematosus
pathway KEGG Systemic lupus erythematosus
disease MESH antiphospholipid syndrome
disease MESH Autoimmune hepatitis
disease MESH Causality
disease MESH diabetes mellitus
disease MESH hemolytic anemia
drug DRUGBANK Rituximab
drug DRUGBANK Sodium Chloride
disease IDO history
disease MESH Atopic Dermatitis
disease MESH Allergic Rhinitis
disease MESH Dermatitis
drug DRUGBANK Aminosalicylic Acid
drug DRUGBANK Vildagliptin

Original Article

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