Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

DNA activates human immune cells through a CpG sequence-dependent manner.

M Bauer1, K Heeg, H Wagner

  • 1Institute of Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Germany.

Immunology
|August 24, 1999
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Therapeutic vaccination with papillomavirus E6 and E7 long peptides results in the control of both established virus-induced lesions and latently infected sites in a pre-clinical cottontail rabbit papillomavirus model.

Vaccine·2005
Same author

Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition.

Proceedings of the National Academy of Sciences of the United States of America·2001
Same author

Bacterial CpG-DNA triggers activation and maturation of human CD11c-, CD123+ dendritic cells.

Journal of immunology (Baltimore, Md. : 1950)·2001
Same author

Bacterial CpG-DNA activates dendritic cells in vivo: T helper cell-independent cytotoxic T cell responses to soluble proteins.

European journal of immunology·2001
Same author

Poly-guanosine motifs costimulate antigen-reactive CD8 T cells while bacterial CpG-DNA affect T-cell activation via antigen-presenting cell-derived cytokines.

Immunology·2000
Same author

Immunostimulatory DNA sequences help to eradicate intracellular pathogens.

Springer seminars in immunopathology·2000

Bacterial DNA and CpG oligonucleotides (ODN) activate human B cells, but not T cells or monocytes. Monocytes are the primary source of cytokines like IL-6 and IL-12, and upregulate antigen-presenting molecules upon CpG ODN stimulation.

Area of Science:

  • Immunology
  • Molecular Biology

Background:

  • Bacterial DNA and CpG oligonucleotides (ODN) are known immune activators in mice.
  • Their effects on human immune cells remain unclear.

Purpose of the Study:

  • Investigate the impact of bacterial DNA and CpG ODN on human peripheral blood mononuclear cells (PBMC) and their subsets.
  • Determine which human immune cells respond to these stimuli and how.

Main Methods:

  • Studied human PBMC, purified monocytes, T cells, and B cells.
  • Stimulated cells with bacterial DNA and CpG ODN.
  • Analyzed cell proliferation, cytokine production (IL-6, IL-12, TNF-α), and expression of surface molecules (MHC class I/II, CD86, CD40).

Main Results:

  • Bacterial DNA and CpG ODN induced proliferation only in human B cells.

Related Experiment Videos

  • Monocytes produced IL-6, IL-12, and TNF-α with bacterial DNA, and IL-6, IL-12 with CpG ODN.
  • Monocytes upregulated antigen-presenting and MHC molecules; monocytes and B cells upregulated CD86 and CD40.
  • CpG ODN's immunostimulatory potential depended on the CG motif.
  • Conclusions:

    • Human monocytes are the main cytokine producers in response to bacterial DNA and CpG ODN.
    • CpG ODN activates human B cells and monocytes, upregulating key immune-related molecules.
    • The CG sequence motif is crucial for CpG ODN's immune activation in humans.