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Novel codon-optimized GM-CSF gene as an adjuvant to enhance the immunity of a DNA vaccine against HIV-1 Gag
被引:27
|作者:
Qiu, Jian-Tai
Chang, Ting- Chang
Lin, Cheng-Tao
Chen, Yi-Ming
Li, Frank Q.
Soong, Yung-Kuei
Lai, Chyong-Huey
机构:
[1] Chang Gung Mem Hosp, Dept Obstet & Gynecol, Tao Yuan 333, Taiwan
[2] Chang Gung Univ, Coll Med, Dept Life Sci, Tao Yuan 333, Taiwan
[3] Natl Yang Ming Univ, AIDs Prevent & Res Ctr, Taipei 112, Taiwan
[4] Vaxim Inc, Rockville, MD 20850 USA
来源:
关键词:
GM-CSF;
DNA vaccine;
HIV-1;
T-lymphocytes;
immunity;
COLONY-STIMULATING FACTOR;
T-CELL RESPONSES;
VIRUS TYPE-1 GAG;
DENDRITIC CELLS;
PLASMID DNA;
FUSION PROTEIN;
PHASE-I;
EXPRESSION;
IMMUNOGENICITY;
ANTIGEN;
D O I:
10.1016/j.vaccine.2006.07.034
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a potent immunomodulatory cytokine. Here we generated a novel codon-optimized murine GM-CSF gene as an adjuvant. The codon-optimized GM-CSF gene significantly increased protein expression levels in all cells tested. Although injection of the wild-type GM-CSF plasmids adjuvanted HIV-1 Gag DNA vaccine induced detectable immune responses. co-administration of plasmids encoding the codon-optimized GM-CSF sequence with the DNA vaccine resulted in a strong antibody and CTL responses and a protective immune response against infection with recombinant vaccinia virus expressing HIV-1 Gag. This novel codon-optimized GM-CSF gene offers a practical molecular strategy for potentiating immune responses to vaccines as well as other immunotherapeutic strategies. (c) 2006 Elsevier Ltd. All rights reserved.
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页码:253 / 263
页数:11
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