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PMID: 15246624 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

CpG oligonucleotides improve the protective immune response induced by the anthrax vaccination of rhesus macaques.

Vaccine ·Vol. 22 ·No. 21-22 ·2004-07-29 ·Pages 2881-6

Klinman DM, Xie H, Little SF, Currie D, Ivins BE

Abstract

Synthetic oligodeoxynucleotides (ODN) containing unmethylated CpG motifs act as immune adjuvants, improving the immune response elicited by co-administered vaccines. Combining CpG ODN with anthrax vaccine adsorbed (AVA, the licensed human vaccine) increased the speed, magnitude and avidity of the resultant anti-anthrax response. The protective activity of these Abs was established by passive transfer to anthrax-challenged mice. The ability of CpG ODN to accelerate and magnify the immune response to AVA suggests this strategy may contribute to the development of prophylactic and therapeutic vaccines against biothreat pathogens.

MeSH Terms
Animals Anthrax/immunology,prevention & control Anthrax Vaccines/immunology Antigens, Bacterial/immunology Enzyme-Linked Immunosorbent Assay Humans Immune Sera/immunology Immunoglobulin G/analysis,biosynthesis Indicators and Reagents Macaca mulatta Neutralization Tests Oligonucleotides/pharmacology Vaccines, Synthetic/immunology
Chemicals
Anthrax Vaccines Antigens, Bacterial Immune Sera Immunoglobulin G Indicators and Reagents Oligonucleotides Vaccines, Synthetic
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Klinman Dennis M
Section of Retroviral Immunology, Center for Biologics Evaluation and Research, Food and Drug Administration, Bldg. 29A, Rm. 3 D 10, Bethesda, MD 20892, USA. klinman@cber.fda.gov
Xie Hang
Little Stephen F
Currie Debra
Ivins Bruce E
Article Info
Journal
Vaccine
Abbr.
Vaccine
ISSN
0264-410X
Published
2004-07-29
Pages
2881-6
Language
English
Region
Netherlands
NLM ID
8406899
Subset
IM
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