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Amyloid-beta reduction by memapsin 2 (beta-secretase) immunization
被引:34
|作者:
Chang, Wan-Pin
Downs, Deborah
Huang, Xiang-Ping
Da, Huining
Fung, Kar-Ming
Tang, Jordan
机构:
[1] Oklahoma Med Res Fdn, Prot Studies Program, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Pathol, Oklahoma City, OK USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Biochem & Mol Biol, Oklahoma City, OK 73190 USA
来源:
关键词:
immunotherapy;
Alzheimer's disease;
BACE1;
D O I:
10.1096/fj.06-7993com
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Memapsin 2 (beta-secretase, BACE1) is the protease that initiates cleavage of beta-amyloid precursor protein leading to the production of amyloid-beta (A beta) and the onset of Alzheimer's disease (AD). Reducing A beta by targeting memapsin 2 is a major strategy in developing new AD therapy. Here, in a proof-of-concept study, we show that immunization of transgenic AD mice (Tg2576) with memapsin 2 resulted in A beta reduction and cognitive improvement. To study the basis of this therapy, we demonstrated that anti-memapsin 2 (anti-M2) antibodies were rapidly internalized and reduced A beta production in cultured cells. These antibodies also effectively crossed the blood-brain barrier to reach the brain. Two-and 10-month Tg2576 mice were immunized and monitored over 10 and 6 months, respectively. We observed a significant decrease of plasma and brain A beta(40) and A beta(42) (similar to 35%) in the immunized mice as compared to controls. Immunized mice also showed better cognitive performance than controls in both cohorts. Brain histological analyses found no evidence of T cell/microglia/astrocyte activation in the immunized mice, suggesting the absence of inflammatory responses. These results suggest that memapsin 2 immunization in Tg2576 was effective in reducing A beta production and improving cognitive function and that the current approach warrants further investigation as a therapy for AD.
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页码:3184 / 3196
页数:13
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