Related Experiment Video
Updated: Aug 15, 2026

Overlapping Peptide Library to Map Qa-1 Epitopes in a Protein
Published on: December 20, 2017
Multiple administrations of oligodeoxynucleotides containing CpG motifs influence Ig isotype production
1Center for Neuropathology and Prion Research, Ludwig-Maximilians Universität München, München, Germany.
Abstract:
Oligodeoxynucleotides containing CpG motifs (CpG-ODN) activate cells of the innate immune system. Recent studies have shown that sole CpG-ODN administration induces resistance against infection and tumors. Effects of CpG-ODN administration are rapidly induced, and regarding infections only short-term protection was seen. One conceivable strategy to prolong protective effects is multiple administrations of CpG-ODN. However, inappropriate immune activation via CpG motifs has been implicated in septic shock and autoimmunity. To investigate effects of multiple CpG-ODN administrations, we analyzed Th1- and Th-2-associated Ig antibody levels, during and after multiple treatment with CpG-ODN. Our results show that multiple administrations of CpG-ODN lead to an increase in total IgG2c levels in CpG-ODN-treated mice in comparison to controls with distinct time and frequency correlation, in the absence of additional stimuli. This indicates a humoral Th1 bias based on stimulation of Th1-Ig isotype-producing B cells. These effects could account for observed anti-infection and anti-tumor properties of multiple CpG-ODN administrations; on the other hand, they might cause autoimmune disease.
Insights
Multiple administrations of CpG-ODN boost IgG2c antibody levels, indicating a Th1 immune bias. This repeated immune activation may enhance anti-infection and anti-tumor effects but carries risks of autoimmunity.
Area of Science:
- Immunology
- Innate Immunity
- Humoral Immunity
Background:
- CpG-ODN activate innate immune cells, offering short-term resistance against infections and tumors.
- Prolonging CpG-ODN effects requires multiple administrations, but carries risks of immune overactivation, like septic shock and autoimmunity.
Purpose of the Study:
- To investigate the effects of multiple CpG-ODN administrations on immune responses.
- To analyze Th1- and Th-2-associated immunoglobulin (Ig) antibody levels following repeated CpG-ODN treatment.
Main Methods:
- Mice were administered CpG-ODN multiple times.
- Levels of Th1- and Th-2-associated Ig antibodies were measured during and after treatment.
Main Results:
- Multiple CpG-ODN administrations significantly increased total IgG2c levels in treated mice compared to controls.
- This increase in IgG2c showed a distinct time and frequency correlation, even without additional stimuli.
- Results indicate a humoral Th1 bias due to stimulation of Th1-Ig isotype-producing B cells.
Conclusions:
- Repeated CpG-ODN administration induces a Th1-biased humoral immune response, evidenced by elevated IgG2c levels.
- This Th1 bias may explain the observed anti-infection and anti-tumor properties of multiple CpG-ODN treatments.
- Potential risks include the induction of autoimmune diseases due to inappropriate immune activation.
More Related Videos
06:15Characterization of Thymus-dependent and Thymus-independent Immunoglobulin Isotype Responses in Mice Using Enzyme-linked Immunosorbent Assay
Published on: September 7, 2018
07:13Induction of Maternal Immune Activation in Mice at Mid-gestation Stage with Viral Mimic Poly(I:C)
Published on: March 25, 2016