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The Immunological Character of Polypeptide B Cell Epitopes Vaccines of Alzheimer's Disease in Different Adjuvants |
CHEN Ao1,2, YU Yun-zhou1, WANG Wen-bin1, PANG Xiao-bin2, WANG Shuang1, YU Wei-yuan1, SUN Zhi-wei1 |
1. Institute of Biotechnology,Academy of Military Medical Sciences,Beijing 100071,China;
2. Pharmaceutical College of Henan University,Kaifeng 475001,China |
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Abstract Objective:To evaluate the immune response of polypeptide vaccines Aβ1-15-PADRE(Aβ-T)against Alzheimer's disease containing the immunodominant B cell epitope from β-amyloid and pan-DR helper T cell epitopes and determine whether various adjuvants could boost the efficacy or performance of the vaccine in mouse model. Methods:The polypeptides of 2Aβ1-15-PADRE containing two B cell epitopes Aβ1-15 and one pan-DR helper T cell epitope PADRE was be artificially synthesized as polypeptide vaccines Aβ1-15-PADRE. Compared to the PBS control or untreated control,the immunogenicity of polypeptide vaccines without adjuvant and with four different adjuvants(Aluminum,Freund's adjuvant,MF59 adjuvant and Abisco adjuvant respectively)were evaluated in Balb/C mouse model. Results:All groups produced the specific antibody IgG against Aβ. But the four adjuvant groups were better to generate immune response than Mock group or negative control. Of these,the titer of antibodies produced by the Freund's adjuvant group was highest. The results of dot blotting showed that the sera antibodies could bind to the oligomer of Aβ better than the monomer form. But the antibodies have not binding reaction to the fiber form. Conclusion:All of these adjuvants could enhance the effect of polypeptide vaccine against Alzheimer's disease in mouse model. All of the sera antibodies bind to the oligomer form of Aβ. The immunological character shows that the polypeptide vaccine is potential in clinical trial.
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Received: 31 December 2010
Published: 25 August 2011
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