TNFRSF9: Enhancing Immune Cell Activity Against Tumors

In addition to its effects on T cells, TNFRSF9 also enhances the activity of natural killer (NK) cells, which play a vital role in innate immune responses against tumors. TNFRSF9 signaling in NK cells leads to:

• Increased cytotoxicity: TNFRSF9 activation boosts the cytotoxic potential of NK cells, enhancing their ability to recognize and destroy cancer cells.
• Improved cytokine secretion: Like T cells, NK cells activated through TNFRSF9 produce higher levels of IFN-γ, which promotes anti-tumor immunity and supports T cell function.
• Enhanced survival: TNFRSF9 signaling supports the survival and persistence of NK cells, allowing them to continuously patrol and attack tumor cells.

Through its effects on both T cells and NK cells, TNFRSF9 is a critical checkpoint in the immune response to cancer, capable of amplifying the body’s natural defense mechanisms against tumors.

In the tumor microenvironment (TME), cancer cells and tumor-associated immune cells often exploit immune checkpoints to suppress T cell and NK cell function. Although TNFRSF9 signaling can boost immune activation, its expression is tightly regulated and often only occurs upon T cell and NK cell activation. Tumors may produce immunosuppressive cytokines and recruit regulatory T cells (Tregs) and myeloid-derived suppressor cells (MDSCs), which inhibit TNFRSF9 signaling pathways, dampening the immune response.

The immunosuppressive nature of the TME, combined with the limited and regulated expression of TNFRSF9, underscores the need for therapeutic interventions that can selectively activate TNFRSF9 to overcome immune evasion.

Therapies targeting TNFRSF9 aim to activate T cells and NK cells within the TME, enhancing their anti-tumor activity despite the immunosuppressive signals present. By engaging TNFRSF9 with agonistic antibodies like B3113, these therapies can deliver a targeted co-stimulatory signal to boost immune cell function without the systemic effects seen with broader immune stimulants.

Potential benefits of TNFRSF9-targeting therapies include:

• Reinvigorating T cell responses: Targeting TNFRSF9 enhances the expansion and survival of T cells, particularly cytotoxic CD8+ T cells, which are essential for tumor clearance.
• Activating NK cells: TNFRSF9 signaling in NK cells boosts their cytotoxic function, increasing
  their ability to attack and kill tumor cells directly.

https://www.assaygenie.com/human-tnf-alpha-elisa-kit/B3113 is an agonistic monoclonal antibody that specifically binds to TNFRSF9, mimicking the natural ligand (4-1BBL) and activating the receptor. The mechanism of action of B3113 involves:

1. Direct activation of TNFRSF9: B3113 binds to TNFRSF9 on T cells and NK cells, delivering a co-stimulatory signal that enhances their proliferation, survival, and cytotoxic function.
2. Boosting cytokine production: By activating TNFRSF9, B3113 promotes the release of key cytokines such as IFN-γ and TNF-α, which support immune cell recruitment and function within the TME.
3. Enhancing T cell and NK cell cytotoxicity: B3113-activated immune cells show increased cytotoxicity against tumor cells, directly improving anti-tumor responses.

The therapeutic potential of B3113 is being explored in cancers with high levels of immune suppression in the TME, such as:

• Melanoma: Known for its immunosuppressive environment, melanoma can be effectively
  targeted by TNFRSF9 agonists to boost T cell and NK cell responses.
• Non-Small Cell Lung Cancer (NSCLC): High levels of Tregs and MDSCs in NSCLC can inhibit
  immune responses; targeting TNFRSF9 with B3113 may enhance immune cell activation and improve treatment outcomes.
• Hepatocellular Carcinoma (HCC): In HCC, TNFRSF9-targeting therapies can activate NK cells and T cells to counteract liver-specific immune suppression and attack tumor cells.

Checkpoint inhibitors like anti-PD-1 and anti-CTLA-4 are widely used in cancer treatment to remove inhibitory signals that limit T cell activation. Targeting TNFRSF9 with B3113 complements checkpoint inhibitors by directly enhancing T cell and NK cell activity, which can be especially beneficial in tumors resistant to checkpoint blockade alone.

• Enhanced T cell activation: B3113 boosts T cell activity and survival, making these cells more responsive to checkpoint inhibition.
• Overcoming resistance: In tumors where checkpoint inhibitors alone are insufficient, TNFRSF9 activation provides an additional layer of immune enhancement, helping to overcome immune evasion mechanisms in the TME.

Chimeric Antigen Receptor T cell (CAR-T) therapy involves engineering T cells to express specific receptors that target tumor cells. However, CAR-T cell efficacy is often limited in solid tumors due to the immunosuppressive TME. Targeting TNFRSF9 with B3113 can enhance CAR-T cell function by increasing their survival and activity within the TME, potentially improving outcomes in CAR-T cell-treated patients.

As with other immune-stimulating therapies, activating TNFRSF9 with B3113 could lead to immune-related adverse events (irAEs), such as excessive inflammation or cytokine release syndrome (CRS). Careful patient monitoring, dose optimization, and selective activation of TNFRSF9 will be critical to maximize therapeutic efficacy while minimizing risks.

Future studies will likely explore the broader application of TNFRSF9-targeting therapies in other cancers with high levels of immune suppression. Biomarker studies to identify patients most likely to benefit from TNFRSF9 agonists will also be essential, allowing for more personalized approaches in cancer immunotherapy.

TNFRSF9 (4-1BB) is a powerful immune co-stimulatory receptor that enhances T cell and NK cell function, making it an important target in cancer immunotherapy. By targeting TNFRSF9 with therapies like B3113, researchers aim to amplify immune cell responses, overcome tumor-induced immune suppression, and enhance the effectiveness of existing cancer treatments, such as checkpoint inhibitors and CAR-T therapies. As research advances, TNFRSF9-targeted therapies hold great potential for expanding the cancer immunotherapy landscape and improving outcomes for patients with immune-resistant tumors.

1. Chester, C., et al., 2018. 4-1BB agonists in cancer immunotherapy. Journal for Immunotherapy of Cancer, 6(1), pp.39-52.
2. Vinay, D.S., Kwon, B.S., 2014. Therapeutic potential of 4-1BB (CD137) in cancer. Seminars in Oncology, 41(5), pp.532-538. 
3. Liu, L., et al., 2016. TNFRSF9 signaling: A key pathway in cancer immunotherapy. Trends in Immunology, 37(6), pp. 407-417.
4. Melero, I., et al., 2015. Therapeutic strategies to enhance anti-tumor immunity by targeting CD137 (4-1BB) signaling. Cytokine & Growth Factor Reviews, 26(2), pp.137-145.
5. Guo, Z., et al., 2014. Targeting CD137 for T cell cancer immunotherapy. Journal of Hematology & Oncology, 7(1), pp.18-26.
6. Sharma, P., Allison, J.P., 2015. The future of immune checkpoint therapy. Science, 348(6230), pp.56-61.
7. Choi, B.K., Lee, D.Y., Lee, D.G., et al., 2011. 4-1BB-based immunotherapy in solid tumors. Current Opinion in Immunology, 23(2), pp.203-209.
8. Pardoll, D.M., 2012. The blockade of immune checkpoints in cancer immunotherapy. Nature Reviews Cancer, 12(4), pp.252-264.