Interleukin-12- and Gamma Interferon-Dependent Protection against Malaria Conferred by CpG Oligodeoxynucleotide in Mice

Author:

Gramzinski Robert A.1,Doolan Denise L.12,Sedegah Martha13,Davis Heather L.45,Krieg Arthur M.6,Hoffman Stephen L.1

Affiliation:

1. Malaria Program, Naval Medical Research Center, Silver Spring, Maryland 20910-75001;

2. Department of Molecular Microbiology and Immunology, School of Hygiene and Public Health, Johns Hopkins University, Baltimore, Maryland 21205-21792;

3. Department of Microbiology, University of Maryland School of Medicine, Baltimore, Maryland 212013;

4. Loeb Research Institute, Ottawa Civic Hospital,4and

5. Faculties of Health Sciences and Medicine, University of Ottawa,5 Ottawa, Canada K1Y 4E9; and

6. Department of Internal Medicine, University of Iowa, Iowa City, Iowa 522426

Abstract

ABSTRACT Unmethylated CpG dinucleotides in bacterial DNA or synthetic oligodeoxynucleotides (ODNs) cause B-cell proliferation and immunoglobulin secretion, monocyte cytokine secretion, and activation of natural killer (NK) cell lytic activity and gamma interferon (IFN-γ) secretion in vivo and in vitro. The potent Th1-like immune activation by CpG ODNs suggests a possible utility for enhancing innate immunity against infectious pathogens. We therefore investigated whether the innate immune response could protect against malaria. Treatment of mice with CpG ODN 1826 (TCCATGA CG TTCCTGA CG TT, with the CpG dinucleotides underlined) or 1585 (ggGGTCAA CG TTGAgggggG, with g representing diester linkages and phosphorothioate linkages being to the right of lowercase letters) in the absence of antigen 1 to 2 days prior to challenge with Plasmodium yoelii sporozoites conferred sterile protection against infection. A higher level of protection was consistently induced by CpG ODN 1826 compared with CpG ODN 1585. The protective effects of both CpG ODNs were dependent on interleukin-12, as well as IFN-γ. Moreover, CD8 + T cells (but not CD4 + T cells), NK cells, and nitric oxide were implicated in the CpG ODN 1585-induced protection. These data establish that the protective mechanism induced by administration of CpG ODN 1585 in the absence of parasite antigen is similar in nature to the mechanism induced by immunization with radiation-attenuated P. yoelii sporozoites or with plasmid DNA encoding preerythrocytic-stage P. yoelii antigens. We were unable to confirm whether CD8 + T cells, NK cells, or nitric oxide were required for the CpG ODN 1826-induced protection, but this may reflect differences in the potency of the ODNs rather than a real difference in the mechanism of action of the two ODNs. This is the first report that stimulation of the innate immune system by CpG immunostimulatory motifs can confer sterile protection against malaria.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference39 articles.

1. Functional diversity of helper T lymphocytes;Abbas A. K.;Nature,1996

2. Induction of natural killer activity in murine and human cells by CpG motifs in oligodeoxynucleotides and bacterial DNA;Ballas Z. K.;J. Immunol.,1996

3. CpG islands as gene markers in the vertebrate nucleus;Bird A. P.;Trends Genet.,1987

4. Two types of mouse helper T cell clone. III. Further differences in lymphocyte synthesis between Th1 and Th2 clones revealed by RNA hybridization, functionally monospecific bioassays, and monoclonal antibodies;Cherwinski H. M.;J. Exp. Med.,1987

5. CpG oligodeoxynucleotides act as adjuvants that switch on T helper (Th1) immunity;Chu R. S.;J. Exp. Med.,1997

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3