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Updated: Jul 3, 2026

Tumor Transplantation for Assessing the Dynamics of Tumor-Infiltrating CD8+ T Cells in Mice
Published on: June 12, 2021
Cancer immunotherapeutic effects of novel CpG ODN in murine tumor model
Hyeon Cheol Cho1, Bo Hwan Kim, Kyunghoon Kim
1Department of Microbiology, Wonju College of Medicine, Yonsei University, Wonju 220-701, South Korea.
Abstract:
While CpG oligodeoxynucleotides (ODN) are excellent candidates for cancer immunotherapeutics, the numbers of usable CpG ODNs are limited in current clinical settings. To resolve this, we investigated whether novel CpG ODN (KSK-CpG) would be an effective immunotherapeutic in a murine tumor model by affecting in vivo and in vitro parameters, such as survival span, the number of tumor nodules, natural killer (NK) cell and cytotoxic T lymphocyte (CTL) activity and interleukin (IL)-6 or IL-12 cytokine release in splenocytes. We found that KSK-CpG was effective in the murine cancer model by way of prolonging survival span, reducing the number of tumor nodules, augmenting NK cell and CTL cytotoxicity, as well as evoking IL-6 and IL-12 cytokine release in splenocytes. Collectively, these data demonstrate that KSK-CpG is active against the highly malignant B16BL6 and EL4 tumor mouse model via innate immune augmentation.
Insights
A novel CpG oligodeoxynucleotide (ODN), KSK-CpG, effectively boosts anti-tumor immunity. This cancer immunotherapeutic prolongs survival and reduces tumor nodules by enhancing natural killer (NK) and cytotoxic T lymphocyte (CTL) responses.
Area of Science:
- Immunology
- Oncology
- Pharmacology
Background:
- CpG oligodeoxynucleotides (ODN) show promise as cancer immunotherapeutics.
- Limited availability of clinically usable CpG ODNs hinders their application.
- Novel CpG ODN development is crucial for advancing cancer immunotherapy.
Purpose of the Study:
- To evaluate the efficacy of a novel CpG ODN, KSK-CpG, as a cancer immunotherapeutic.
- To assess KSK-CpG's impact on in vivo and in vitro anti-tumor parameters.
- To investigate KSK-CpG's effects on immune cell activity and cytokine release.
Main Methods:
- Utilized a murine tumor model (B16BL6 and EL4).
- Administered novel CpG ODN (KSK-CpG) to tumor-bearing mice.
- Monitored survival span, tumor nodule count, natural killer (NK) cell activity, cytotoxic T lymphocyte (CTL) activity, and cytokine (IL-6, IL-12) release from splenocytes.
Main Results:
- KSK-CpG significantly prolonged survival span in the murine cancer model.
- Reduced the number of tumor nodules in treated mice.
- Augmented NK cell and CTL cytotoxicity.
- Evoked increased release of IL-6 and IL-12 cytokines from splenocytes.
Conclusions:
- KSK-CpG demonstrates significant anti-tumor activity in a murine model.
- The efficacy of KSK-CpG is mediated through innate immune augmentation.
- KSK-CpG represents a promising novel candidate for cancer immunotherapy.
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