Recent advances in DNA vaccines for autoimmune diseases

被引:11
|
作者
Silva, Celio L. [1 ,2 ]
Bonato, Vania L. D.
dos Santos-Junior, Rubens R. [3 ]
Zarate-Blades, Carlos R.
Sartori, Alexandrina [4 ]
机构
[1] Univ Sao Paulo, Dept Biochem & Immunol, Fac Med Ribeirao Preto, Med Sch Ribeirao Preto,Ctr TB Res, BR-14049900 Sao Paulo, Brazil
[2] Farmacore Biotechnol Ltd, Sao Paulo, Brazil
[3] Sao Paulo State Univ, Dept Clin Anal, Fac Pharmaceut Sci, BR-14801902 Sao Paulo, Brazil
[4] Sao Paulo State Univ, Dept Microbiol & Immunol, Biosci Inst, BR-18618000 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
autoimmunity; DNA vaccine; tolerance; Treg cell; REGULATORY T-CELLS; HEAT-SHOCK-PROTEIN; COLLAGEN-INDUCED ARTHRITIS; PRISTANE-INDUCED ARTHRITIS; ANTIGEN-SPECIFIC TOLERANCE; MYELIN BASIC-PROTEIN; PLASMID DNA; ADJUVANT ARTHRITIS; BACTERIAL-DNA; CPG MOTIFS;
D O I
10.1586/14760584.8.2.239
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vaccination is one of the most powerful health tools available owing to its ability to confer protection against various diseases. The long-term impact of such protection in terms of public-health savings is nearly incalculable and becomes even more evident when considering if the vaccination concept is extended to the therapeutic potential of a given molecule. In this sense, DNA vaccines are especially important tools with enormous potential owing to the molecular precision that they offer. The properties of the plasmid DNA molecule in terms of stability, cost-effectiveness and lack of cold-chain requirement are additional advantages over traditional vaccines and therapeutics. We focus on the current knowledge of autoimmune mechanisms, engineering of DNA vaccines and attempts that have already been made in order to intervene in autoimmune processes. Our experience with a genetic vaccine containing the heat-shock protein gene (hsp65) from mycobacteria is also described.
引用
收藏
页码:239 / 252
页数:14
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