TY - JOUR
T1 - Identification of potent biodegradable adjuvants that efficiently break self-tolerance--a key issue in the development of therapeutic vaccines
AU - Ringvall, Maria
AU - Huijbers, Elisabeth J M
AU - Ahooghalandari, Parvin
AU - Alekseeva, Ludmila
AU - Andronova, Tatyana
AU - Olsson, Anna-Karin
AU - Hellman, Lars
PY - 2009/12/10
Y1 - 2009/12/10
N2 - Monoclonal antibodies are used successfully in the treatment of many human disorders. However, these antibodies are expensive and have in many countries put a major strain on the health care economy. Therapeutic vaccines, directed against the same target molecules, may offer a solution to this problem. Vaccines usually involve lower amount of recombinant protein, approximately 10,000-20,000 times less, which is significantly more cost effective. Attempts to develop such therapeutic vaccines have also been made. However, their efficacy has been limited by the lack of potent immunostimulatory compounds, adjuvants, for human use. To address this problem we have conducted a broad screening for adjuvants that can enhance the efficacy of therapeutic vaccines, whilst at the same time being non-toxic and biodegradable. We have now identified adjuvants that show these desired characteristics. A combination of Montanide ISA720 and phosphorothioate stabilized CpG stimulatory DNA, induced similar or even higher anti-self-antibody titers compared to Freund's adjuvant, currently the most potent, but also toxic, adjuvant available. This finding removes one of the major limiting factors in the field and facilitates the development of a broad range of novel therapeutic vaccines.
AB - Monoclonal antibodies are used successfully in the treatment of many human disorders. However, these antibodies are expensive and have in many countries put a major strain on the health care economy. Therapeutic vaccines, directed against the same target molecules, may offer a solution to this problem. Vaccines usually involve lower amount of recombinant protein, approximately 10,000-20,000 times less, which is significantly more cost effective. Attempts to develop such therapeutic vaccines have also been made. However, their efficacy has been limited by the lack of potent immunostimulatory compounds, adjuvants, for human use. To address this problem we have conducted a broad screening for adjuvants that can enhance the efficacy of therapeutic vaccines, whilst at the same time being non-toxic and biodegradable. We have now identified adjuvants that show these desired characteristics. A combination of Montanide ISA720 and phosphorothioate stabilized CpG stimulatory DNA, induced similar or even higher anti-self-antibody titers compared to Freund's adjuvant, currently the most potent, but also toxic, adjuvant available. This finding removes one of the major limiting factors in the field and facilitates the development of a broad range of novel therapeutic vaccines.
KW - Adjuvants, Immunologic/pharmacology
KW - Animals
KW - Antibody Formation
KW - Autoantibodies/blood
KW - DNA/immunology
KW - Enzyme-Linked Immunosorbent Assay
KW - Female
KW - Freund's Adjuvant/immunology
KW - Immunoglobulin E/immunology
KW - Immunoglobulin Heavy Chains/immunology
KW - Mannitol/analogs & derivatives
KW - Oleic Acids/immunology
KW - Oligodeoxyribonucleotides
KW - RNA, Double-Stranded/immunology
KW - Rats
KW - Rats, Wistar
KW - Self Tolerance/immunology
KW - Vaccines/immunology
U2 - 10.1016/j.vaccine.2009.09.122
DO - 10.1016/j.vaccine.2009.09.122
M3 - Article
C2 - 19835827
SN - 0264-410X
VL - 28
SP - 48
EP - 52
JO - Vaccine
JF - Vaccine
IS - 1
ER -