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T cell response to amyloid-beta and to mitochondrial antigens in Alzheimer's disease.
Giubilei, Franco; Antonini, Giovanni; Montesperelli, Chiara; Sepe-Monti, Micaela; Cannoni, Stefania; Pichi, Alessandra; Tisei, Paolo; Casini, Anna Rosa; Buttinelli, Carla; Prencipe, Massimiliano; Salvetti, Marco; Ristori, Giovanni.
Afiliação
  • Giubilei F; Department of Neurological Sciences, University of Rome La Sapienza, Viale Dell'Università 30, I-00185 Rome, Italy. franco.giubilei@uniroma1.it
Dement Geriatr Cogn Disord ; 16(1): 35-8, 2003.
Article em En | MEDLINE | ID: mdl-12714798
Despite the vast amount of literature on non-specific immune mechanisms in Alzheimer's disease (AD), little is known about the role of antigen-specific immune responses. We investigated T cell reactivity to fragment 1-42 of amyloid-beta (Abeta) and to N-terminal peptides of human mitochondrial and control microbial proteins. Thirty subjects with a diagnosis of probable AD according to NINCDS-ADRDA criteria and 30 sex- and age-matched healthy controls were enrolled. T cell responses to Abeta fragment showed no significant differences between AD patients and controls. By contrast, the mean number of positive T cell responses to both human mitochondrial and microbial peptides was significantly decreased in AD patients compared to control subjects. No significant correlation was found between T cell responses and both the severity of cognitive impairment and duration of the disease. Our results suggest that antigen-specific immune responses are impaired in AD. Protective immune responses to harmful amyloidogenic substances may also be impaired, thus favoring their accumulation in the brain.
Assuntos
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Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Linfócitos T / Peptídeos beta-Amiloides / Doença de Alzheimer / Mitocôndrias Idioma: En Ano de publicação: 2003 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Linfócitos T / Peptídeos beta-Amiloides / Doença de Alzheimer / Mitocôndrias Idioma: En Ano de publicação: 2003 Tipo de documento: Article