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Co-stimulation with TNF receptor superfamily 4/25 antibodies enhances in-vivo expansion of CD4+CD25+Foxp3+T cells (Tregs) in a mouse study for active DNA Aβ42 immunotherapy
被引:16
|作者:
Lambracht-Washington, Doris
[1
]
Rosenberg, Roger N.
[1
]
机构:
[1] Univ Texas SW Med Ctr Dallas, Alzheimers Dis Ctr, Dept Neurol & Neurotherapeut, Dallas, TX 75390 USA
关键词:
TNFRSF4/25 antibody co-stimulation;
DNA A beta 42 immunization;
Alzheimer disease;
Th2/Treg differentiation;
Skin immunity;
REGULATORY T-CELLS;
BETA IMMUNIZATION AN1792;
ALZHEIMERS-DISEASE;
IL-4;
COSTIMULATION;
ACTIVATION;
EXPRESSION;
INDUCTION;
RESPONSES;
TNFRSF25;
D O I:
10.1016/j.jneuroim.2014.12.007
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The study was designed to test DNA A beta 42 immunization in mice as alternative approach for possible active immunotherapy in Alzheimer patients. As results, we found polarized Th2 immune responses, efficient A beta 42 antibody levels, and disappearance of antigen specific T cells. In-vivo TNFRSF4/25 antibody co-stimulation enhanced A beta 42 specific T cell responses with initial Th2 expansion and subsequent development of A beta 42 specific CD4 + CD25 + Foxp3 + cells. It showed that Th2 biased responses due to gene gun immunizations propagate the development of regulatory T cells. In conclusion, full-length DNA A beta 42 immunization into skin results in a regulatory response with minimal risk of inflammation and autoimmunity. (C) 2014 Elsevier B.V. All rights reserved.
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页码:90 / 99
页数:10
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