Immunotherapy in Alzheimer's Disease: Where Do We Stand? Where Should We Go?

被引:22
|
作者
von Bernhardi, Rommy [1 ]
机构
[1] Pontificia Univ Catolica Chile, Neurosci Lab, Dept Neurol, Fac Med, Santiago, Chile
关键词
Alzheimer's disease; amyloid-beta; amyloid clearance; cognitive impairment; glial cells; immunization; microglia; neuroinflammation; senile plaques; AMYLOID-BETA-PEPTIDE; BLOOD-BRAIN-BARRIER; REDUCES BEHAVIORAL IMPAIRMENT; HUMAN MONOCLONAL-ANTIBODIES; DEPOSITING TRANSGENIC MICE; MILD COGNITIVE IMPAIRMENT; UNFOLDED PROTEIN RESPONSE; EFRH-PHAGE IMMUNIZATION; SINGLE-CHAIN ANTIBODY; A-BETA;
D O I
10.3233/JAD-2010-1248
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is a highly prevalent neurodegenerative disease. In addition to its enormous personal and socioeconomic costs, the situation is worsened by the lack of an effective prevention and treatment. Anti-amyloid-beta (A beta) immunization strategies showed excellent results when tested on AD transgenic models. However, clinical studies with active and passive immunotherapy have been disappointing in several aspects, especially lately, when reports analyzing long term result of immunization protocols failed to show improvement in cognitive function and disease progression. Furthermore, some of the active immunotherapy protocols appear to be associated with severe side effects, including brain inflammation and amyloid angiopathy mediated hemorrhage. However, even through detailed information on the mechanism for A beta clearance is still missing, results are valuable for the understanding of the disease. The focus of this review is to discuss the current experience with the various types of immunotherapy tested in animal models and AD patients, and the information they provide regarding disease mechanisms. In light of those results, alternatives or conditions that could improve immunotherapy utility are analyzed. Regardless of the setbacks, immunotherapy as a combination therapy, including humoral and cell-based approaches, still holds a promise for the treatment of AD.
引用
收藏
页码:405 / 421
页数:17
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