Reduced frequency of T lymphocytes expressing CTLA-4 in frontotemporal dementia compared to Alzheimer's disease

被引:13
作者
Santos, Rodrigo Ribeiro [1 ]
Torres, Karen C. [2 ]
Lima, Giselle S. [2 ]
Fiamoncini, Carolina M. [2 ]
Mapa, Filipe C. [2 ]
Pereira, Patricia A. [2 ]
Rezende, Vitor B. [2 ]
Martins, Luiza C. [2 ]
Bicalho, Maria A. [1 ]
Moraes, Edgar N. [1 ]
Reis, Helton J. [3 ]
Teixeira, Antonio L. [1 ]
Romano-Silva, Marco A. [2 ]
机构
[1] Univ Fed Minas Gerais, Fac Med, Dept Clin Med, BR-30130100 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Fac Med, Dept Saude Mental, BR-30130100 Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Farmacol, BR-30130100 Belo Horizonte, MG, Brazil
关键词
Alzheimer; CTLA-4; Frontotemporal dementia; T lymphocytes; MILD COGNITIVE IMPAIRMENT; BLOOD MONONUCLEAR-CELLS; COSTIMULATORY MOLECULES; CD28; COSTIMULATION; SEMANTIC DEMENTIA; WORK GROUP; TNF-ALPHA; CYTOKINES; ACTIVATION; RECEPTORS;
D O I
10.1016/j.pnpbp.2013.06.019
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Studies suggest that inflammation is involved in the neurodegenerative cascade of dementias. Immunological mechanisms may be part of the pathophysiological process in frontotemporal dementia (FTD), but up till now only vague evidence of such mechanisms has been presented. The B7-CD28/CTLA-4 pathway is an important immunological signaling pathway involved in modulation of T cell activation. The aim of this study was to compare the expression of molecules associated with co-stimulatory signaling in peripheral blood mononuclear cells (PBMC) of FTD to Alzheimer disease (AD) and control groups. Our results confirm the previous demonstrated increased expression of CD80 in CD14+ Alzheimer patients T cells but show, for the first time, a reduction in the expression of CTLA-4 in CD4+ FTD cells. As CTLA-4 is the most potent negative regulators of T-cell activation we speculated that peripheral T lymphocytes in FTD are more activated and this could be involved in the neurodegeneration observed in this dementia. (C) 2013 Elsevier Inc. All rights reserved.
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页码:1 / 5
页数:5
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