Preclinical and clinical safety studies on DNA vaccines

被引:96
作者
Schalk, Johanna A. C.
Mooi, Frits R.
Berbers, Guy A. M.
van Aerts, Leon A. G. J. M.
Ovelgonne, Hans
Kimman, Tieerd G.
机构
[1] Natl Inst Publ Hlth & Environm, Ctr Biol Med & Med Technol, NL-3720 BA Bilthoven, Netherlands
[2] Natl Inst Publ Hlth & Environm, Lab Vaccine Preventable Dis, NL-3720 BA Bilthoven, Netherlands
来源
HUMAN VACCINES | 2006年 / 2卷 / 02期
关键词
DNA vaccines; safety; integration; vertical transmission; auto-immunity; immunological tolerance; immunotoxicity; toxicity; environmental safety;
D O I
10.4161/hv.2.2.2620
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
DNA vaccines are based on the transfer of genetic material, encoding an antigen, to the cells of the vaccine recipient. Despite high expectations of DNA vaccines as a result of promising preclinical data their clinical utility remains unproven. However, much data is gathered in preclinical and clinical studies about the safety of DNA vaccines. Here we review current knowledge about the safety of DNA vaccines. Safety concerns of DNA vaccines relate to genetic, immunologic, toxic, and environmental effects. In this review we provide an overview of findings related to the safety of DNA vaccines, obtained so far. We conclude that the potential risks of DNA vaccines are minimal. However, their safety issues may differ case-by-case, and they should be treated accordingly.
引用
收藏
页码:45 / 53
页数:9
相关论文
共 90 条
[41]  
Kessis TD, 1996, ONCOGENE, V13, P427
[42]   Outbreak of poliomyelitis in Hispaniola associated with circulating type 1 vaccine-derived poliovirus [J].
Kew, O ;
Morris-Glasgow, V ;
Landaverde, M ;
Burns, C ;
Shaw, J ;
Garib, Z ;
André, J ;
Blackman, E ;
Freeman, CJ ;
Jorba, J ;
Sutter, R ;
Tambini, G ;
Venczel, L ;
Pedreira, C ;
Laender, F ;
Shimizu, H ;
Yoneyama, T ;
Miyamura, T ;
van der Avoort, H ;
Oberste, MS ;
Kilpatrick, D ;
Cochi, S ;
Pallansch, M ;
de Quadros, C .
SCIENCE, 2002, 296 (5566) :356-359
[43]   In vivo kinetics and biodistribution of a HIV-1 DNA vaccine after administration in mice [J].
Kim, BM ;
Lee, DS ;
Choi, JH ;
Kim, CY ;
Son, M ;
Suh, YS ;
Baek, KH ;
Park, KS ;
Sung, YC ;
Kim, WB .
ARCHIVES OF PHARMACAL RESEARCH, 2003, 26 (06) :493-498
[44]   RESPIRATORY SYNCYTIAL VIRUS DISEASE IN INFANTS DESPITE PRIOR ADMINISTRATION OF ANTIGENIC INACTIVATED VACCINE [J].
KIM, HW ;
CANCHOLA, JG ;
BRANDT, CD ;
PYLES, G ;
CHANOCK, RM ;
JENSEN, K ;
PARROTT, RH .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1969, 89 (04) :422-+
[45]   Enhancement of suicidal DNA vaccine potency by delaying suicidal DNA-induced cell death [J].
Kim, TW ;
Hung, CF ;
Juang, J ;
He, L ;
Hardwick, JM ;
Wu, TC .
GENE THERAPY, 2004, 11 (03) :336-342
[46]  
Klinman D M, 2000, Dev Biol (Basel), V104, P45
[47]   Semliki Forest virus-based DNA expression vector: transient protein production followed by cell death [J].
Kohno, A ;
Emi, N ;
Kasai, M ;
Tanimoto, M ;
Saito, H .
GENE THERAPY, 1998, 5 (03) :415-418
[48]   CpG motifs in bacterial DNA and their immune effects [J].
Krieg, AM .
ANNUAL REVIEW OF IMMUNOLOGY, 2002, 20 :709-760
[49]   Safety, tolerability and humoral immune responses after intramuscular administration of a malaria DNA vaccine to healthy adult volunteers [J].
Le, TP ;
Coonan, KM ;
Hedstrom, RC ;
Charoenvit, Y ;
Sedegah, M ;
Epstein, JE ;
Kumar, S ;
Wang, RB ;
Doolan, DL ;
Maguire, JD ;
Parker, SE ;
Hobart, P ;
Norman, J ;
Hoffman, SL .
VACCINE, 2000, 18 (18) :1893-1901
[50]   Plasmid DNA vaccines: Investigation of integration into host cellular DNA following intramuscular injection in mice [J].
Ledwith, BJ ;
Manam, S ;
Troilo, PJ ;
Barnum, AB ;
Pauley, CJ ;
Griffiths, TG ;
Harper, LB ;
Beare, CM ;
Bagdon, WJ ;
Nichols, WW .
INTERVIROLOGY, 2000, 43 (4-6) :258-272