| Literature DB >> 20599279 |
Lili Cui1, Xuemei Huang, Jiapeng Wang, Yingjiu Zhang.
Abstract
To reduce the risk of an adverse T cell-mediated immune response to Aβ42, three (Aβ9)16-based recombinant immunogens were designed to immunize mice. Compared with Aβ42, they elicited significantly stronger anti-Aβ42 antibody responses and mainly resulted in IgG1 and IgG2b anti-Aβ42 antibodies. These (Aβ9)16-induced antibodies exhibited stronger abilities not only to inhibit Aβ42 aggregation and to disassemble Aβ42 aggregation, but also to inhibit and neutralize Aβ42-induced cytotoxicity in vitro though they showed higher specificities to Aβ42 monomers and Aβ42 oligomers. These results suggested that (Aβ9)16 was a promising candidate for the safe and effective primary immunogen against Aβ42.Entities:
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Year: 2010 PMID: 20599279 DOI: 10.1016/j.jneuroim.2010.06.004
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478