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Glycolysis Modulation based CD8⁺ T Cell Activation Service

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Creative Biolabs offers a glycolysis modulation-based CD8+ T cell activation service to help you overcome challenges in enhancing T cell activation and optimizing metabolic pathways for improved effector functions in your adoptive cell therapy projects, thereby advancing your research.

The Critical Role of Glycolysis in CD8+ T Cell Activation

Glycolysis plays a crucial role in CD8+ T cell activation and effector function. Activated T cells undergo metabolic reprogramming, shifting towards increased glycolysis to meet the bioenergetic and biosynthetic demands of rapid proliferation and cytokine production. This metabolic shift is essential for mounting an effective immune response. Research has shown that modulating glycolysis can enhance T cell activation and improve their therapeutic efficacy in various contexts. The development of glycolysis modulation strategies is crucial for optimizing cell therapies, particularly in cancer immunotherapy, where enhancing T cell function is paramount.

Fig.1 The metabolic communication and competition between tumor cells and T cell. (OA Literature)Fig.1 Tumor cells and T cell communicate and compete metabolically.1,3

Glycolysis Modulation based CD8+ T Cell Activation Service at Creative Biolabs

Glycolysis modulation can increase ATP production, provide essential metabolic intermediates, and support the biosynthetic demands of activated T cells, leading to enhanced effector functions. Creative Biolabs offers a comprehensive glycolysis modulation based CD8+ T cell activation service designed to optimize your cell therapy development. Our service provides tailored solutions to enhance CD8+ T cell activation and effector function through precise glycolysis metabolic interventions.

How to Work: End-to-End Service Process

Step 1. T Cell Isolation and Preparation

CD8+ T cell populations are isolated from clinical or research specimens through standardized enrichment protocols, achieving stringent thresholds for purity (>95%) and viability (>90%) via fluorescence-activated cell sorting.

Step 2. Glycolytic Pathway Modulation (Optional)

For projects requiring metabolic reprogramming, tailored intervention protocols are developed using pharmacological agents, genetic modification techniques, or environmental parameter optimization to fine-tune glycolytic flux in CD8+ T cells.

Step 3. Activation and Expansion Protocols

Isolated T cells are activated through investigator-defined stimuli under standardized culture parameters (37°C, 5% CO2), integrating customer-specified metabolic regulators. Cellular responses are tracked through longitudinal assessment of viability metrics, proliferative capacity, and surface activation markers (CD25/CD69).

Step 4. Functional Characterization

Post-modulation T cell functionality is systematically evaluated through multiplexed assays quantifying cytotoxic potential (granzyme B/perforin secretion), cytokine production profiles (IFN-γ, TNF-α), and metabolic flux analyses.

Step 5. Analytical Deliverables

Experimental outcomes undergo quantitative analysis employing statistical frameworks, with results synthesized into technical documentation detailing experimental parameters, analytical workflows, empirical findings, and evidence-based interpretations.

Adjustable CD8+ T cell samples

We can work with a wide variety of CD8+ T cell samples, including:

  • Primary T cells from peripheral blood and tumor-infiltrating lymphocytes (TILs)
  • Established cell lines
  • Engineered T cells

Attractive Advantages

  • Experienced research team
  • Enhanced T cell effector functions
  • Improved therapeutic efficacy
  • Customizable strategies
  • Comprehensive data package

Case Study

  • Background:
The tumor microenvironment (TME) often presents metabolic challenges for CD8+ T cells, impairing their anti-tumor functions. This study explores how targeting glycolysis in CD8+ T cells can improve their efficacy in cancer immunotherapy.
  • Method:
Researchers investigated the effects of modulating glycolysis in CD8+ T cells within the TME. They used a combination of genetic and pharmacological approaches to modulate glycolytic activity in these cells. The impact on T cell function, tumor control, and overall survival was assessed in preclinical models.
  • Results:
Disrupting glycolysis through MCT1 deficiency hinders proliferation and memory formation, while enhancing glycolytic metabolism via genetic modifications can accelerate memory cell differentiation and improve responses to secondary infections. Furthermore, pharmacological interventions like GSK3 inhibition offer a promising avenue to reprogram CD8+ T cells, enhancing their functionality and promoting a memory-like state.

Fig.2 Interfering with glycolysis boosts the anti-tumor effect of local ablation in a CD8+T cell-dependent manner. (OA Literature)Fig.2 Targeting glycolysis enhances local cancer therapy by empowering CD8+ T cells.2,3

FAQs

Q1: Can I combine glycolysis modulation with other T cell activation strategies?

A1: Yes, glycolysis modulation can be integrated with other activation methods, such as co-stimulatory signals and cytokine stimulation, to achieve synergistic effects.

Q2: What are the key applications of glycolysis modulation in cell therapy?

A2: Glycolysis modulation can be applied to enhance the efficacy of CAR-T cell therapy, TCR-T cell therapy, and other adoptive cell therapies, particularly in cancer immunotherapy and infectious disease.

Associated Services

Creative Biolabs offers a comprehensive portfolio of related services to support your cell therapy development needs. In addition to glycolysis modulation, we also provide other metabolic pathway-targeted modulation services to enhance CD8+ T cell-based immunotherapy, including:

Work with Creative Biolabs

By leveraging our expertise in CD8+ T cell metabolism and cutting-edge technologies, Creative Biolabs is dedicated to helping you achieve your research and cell therapy development goals. We are confident that our glycolysis modulation based CD8+ T cell activation service will provide you with the tools and support necessary to accelerate your progress and achieve meaningful results. Please click the link to get in touch with us for more details.

References

  1. Chen, Chen et al. "Manipulating T-cell metabolism to enhance immunotherapy in solid tumor." Frontiers in immunology vol. 13 1090429. 22 Dec. 2022, doi:10.3389/fimmu.2022.1090429
  2. Tang, Xinyu et al. "Glycolysis inhibition induces anti-tumor central memory CD8+T cell differentiation upon combination with microwave ablation therapy." Nature communications vol. 15,1 4665. 31 May. 2024, doi:10.1038/s41467-024-49059-6
  3. Distributed under Open Access License CC BY 4.0, without modification.
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