Cargando…

Analysis of the autoimmune response against BP180 in patients with Alzheimer’s disease

BACKGROUND: Current epidemiological studies suggest a significant correlation between Alzheimer’s disease (AD) and bullous pemphigoid (BP). However, the autoimmune response against BP180 in patients with AD has not been fully understood. investigated. METHODS: We randomly enrolled 48 patients with A...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Ya-Nan, Hammers, Christoph M., Mao, Xuming, Jin, Hong-Zhong, Yuan, Jing, Li, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867912/
https://www.ncbi.nlm.nih.gov/pubmed/33569409
http://dx.doi.org/10.21037/atm-20-5343
Descripción
Sumario:BACKGROUND: Current epidemiological studies suggest a significant correlation between Alzheimer’s disease (AD) and bullous pemphigoid (BP). However, the autoimmune response against BP180 in patients with AD has not been fully understood. investigated. METHODS: We randomly enrolled 48 patients with AD and 50 sex- and age-matched healthy controls. We detected the presence/absence and the level of anti-BP180/BP230 immunoglobulin G (IgG) autoantibodies in the patients’ serum to determine whether said antibodies possess reactivity against the BP180 protein in the human brain and skin. RESULTS: The enzyme-linked immunosorbent assay (ELISA) results revealed that the positive rate of anti-BP180 autoantibodies in patients with AD (23/48, 47.9%) was significantly higher than that in controls (4/50, 8.0%; P<0.0001). These ELISA-positive patients were further examined through immunoblotting. Sera from nine patients with AD (9/23, 39.1%) and one control (1/4, 25.0%) reacted with human cutaneous recombinant full-length BP180 and BP180-noncollagenous 16A (NC16A). Sera from 11 (11/23, 47.8%) patients with AD reacted with a 180-kDa protein from the human brain extract, but none of the controls’ sera recognized the corresponding protein band. The majority of the patients in the anti-BP180-positive AD group were men (14/23, 60.9%) who were older (74.0 years) compared with those in the control group (6/25, 24.0%; P<0.05) (72.2 years; P<0.01). CONCLUSIONS: Anti-BP180 autoantibodies are present in AD and recognize human recombinant full-length BP180 and a 180-kDa protein from the human brain extract, suggesting that BP180 is a shared autoantigen in AD and BP and may help clarify the mechanism to explain why a high risk of BP exists in AD. Elderly male patients with AD are significantly more likely to develop BP180 serum autoreactivity compared with other patients with AD.