Cancer vaccine technology aims to train or enhance the body's own immune system (primarily T cells and B cells) using specific formulations or cells, enabling it to specifically recognize, attack, and eliminate tumor cells. This is an innovative strategy that leverages immunological memory to provide durable protection or therapeutic effect. Successful cancer vaccines can not only induce potent cellular immune responses but also establish long-term immune surveillance in research models, opening new directions for cancer treatment.
Key Issues to Consider in Research
Identifying tumor antigens (such as neoantigens) that elicit a powerful and specific immune response while avoiding autoimmunity is the primary challenge in vaccine design. This requires combining high-precision sequencing and bioinformatics prediction models to identify optimal immunogenic targets.
The TME is often highly immunosuppressive, rich in regulatory T cells (Tregs), myeloid-derived suppressor cells (MDSCs), and tumor-associated macrophages (TAMs). Designing vaccines that can break through TME defenses and reverse the immunosuppressive state is a key factor affecting efficacy.
Ensuring that the vaccine payload (e.g., peptides, DNA, RNA, or cells) is efficiently and stably taken up and activated by antigen-presenting cells (APCs) and effectively reaches the lymph nodes is the technical core for achieving an effective immune response. The choice of delivery vehicle (e.g., liposomes, nanoparticles) is critical.
Precise and sensitive monitoring methods are needed to quantify the type (e.g., cytotoxic T cell activity, cytokine secretion profile) and strength of the immune response induced by the vaccine to guide subsequent optimization efforts. A lack of reliable biomarkers can hinder research progress.
Utilizing advanced adjuvants and delivery strategies to maximize T cell activation, we design cancer vaccines with enhanced immunogenicity, laying a solid foundation for effective anti-tumor immune responses.
With novel adjuvants and targeted strategies, we aim to reverse immune tolerance in the tumor microenvironment (TME), helping to break the immune suppression state and restore the body's anti-tumor immune function.
We provide an in-depth cellular and molecular functional data monitoring platform, enabling accurate quantification and analysis of the immune response induced by cancer vaccines, and providing reliable data support for vaccine optimization.
Guided by 'omics' technologies, we accelerate the discovery of potential therapeutic targets and biomarkers related to cancer vaccines, providing clear research directions for personalized cancer vaccine development.
Tumor-APC Fusion Technology: A cell vaccine strategy to enhance antigen cross-presentation. We fuse tumor cells with antigen-presenting cells (APCs) to present a more comprehensive tumor antigen profile.
Immune Monitoring Assay: High-throughput, multi-parameter immune response functional and cellular analysis. Provides precise flow cytometry and multiplex cytokine detection to quantify vaccine-induced immune responses.
Cytokine Development: Discovery, engineering, and production of key immune-modulating cytokines. Focused on developing and evaluating recombinant cytokines that enhance immune activation and T cell proliferation.
Anti-Treg Technology: Innovative targeting and inhibitory strategies for regulatory T cells (Treg). Aims to reduce immune suppression in the TME to improve vaccine efficacy.
Vaccine Combination Immunotherapy: Assessment of vaccines in combination with other immunotherapies (e.g., checkpoint inhibitors). Provides in vitro and in vivo combination study models to find potential synergistic effects.
Biomarker Discovery Technology: 'Omics'-based technology for discovering biomarkers of efficacy prediction and disease progression. Utilizes high-throughput screening and data analysis to identify molecular markers related to vaccine response.
Microfluidic Cell Squeezing Technology: A high-efficiency intracellular delivery platform. Gently introduces macromolecules (e.g., mRNA) into immune cells via mechanical deformation to increase transfection efficiency.
Antibody-Antigen Fusion Technology: Fusion protein design for targeted antigen delivery to APCs. Achieves high-specificity delivery of antigens to the surface of immune cells by linking antibodies and antigens.
MHC Class II associated li Protein Suppression Technology: Molecular technology for modulating antigen presentation processes to enhance immunogenicity. Optimizes the presentation efficiency of antigens by MHC Class II molecules by regulating the expression or function of the li protein.
Toll-Like Receptor 9 Agonist Development Technology: Develops CpG oligonucleotides to activate TLR9, inducing Th1-type immune responses and enhancing vaccine adjuvancy.
We offer complete integrated solutions from target discovery and vector construction to immune assessment, ensuring seamless transitions between different modules and greatly enhancing R&D efficiency and data consistency.
We continuously invest in cutting-edge technologies, including advanced microfluidic delivery systems, high-affinity fusion protein design, and novel immune checkpoint modulation strategies, ensuring client research remains at the forefront of the industry.
Our services are not "one-size-fits-all" standard products. We provide flexible adjustments and deeply customized experimental protocols and reports based on clients' specific tumor antigens, genetic backgrounds, and research objectives.
Through optimized project management processes and dedicated project managers, we ensure efficient project progression and the high-quality delivery of data and experimental materials within the agreed-upon timeframe.
Background
This study aimed to evaluate the immunogenicity of an SVA inactivated vaccine (CH-GX-01-2019 strain) with different adjuvants, addressing SVA’s threat of causing swine vesicular disease (clinically indistinguishable from FMDV) and the lack of approved vaccines to protect pig herds.
Solution
SVA was inactivated with binary ethylenimine. Mice (C57BL/6) were grouped (PBS, SVA alone, SVA+aluminum adjuvant, SVA+oil-in-water adjuvant) and pigs (post-weaned) into 4 groups (PBS, SVA-L:50μg+oil-in-water adjuvant, SVA-H:200μg+oil-in-water adjuvant). All were immunized twice (0/21 dpv). Immunogenicity was assessed via VNT (neutralizing antibodies), ELISA (total IgG, IgG subtypes, IL-4/IFN-γ).
Result
In mice, SVA+oil-in-water adjuvant induced higher neutralizing antibodies (21-35 dpv) and IL-4/IFN-γ than SVA+aluminum adjuvant; both adjuvant groups had higher IgG/IgG subtypes than SVA alone. In pigs, SVA-L/SVA-H induced high neutralizing antibodies (peaking at 35 dpv) and total IgG (7 dpv detectable); SVA-H had higher IFN-γ, confirming robust immunogenicity.

We support the development and research of various vaccine types, including those based on synthetic peptides, recombinant proteins, nucleic acids (DNA/mRNA), engineered viral vectors, and various forms of cell vaccines. Our services cover customized needs from early antigen design to late-stage in vitro functional validation.
We provide quantitative data on immune cell phenotype analysis (e.g., CD4+/CD8+ T cell ratios), cytokine release profiles, antibody titers, and Cytotoxic T Lymphocyte (CTL) killing activity. This data is used for a comprehensive assessment of the strength and nature of the immune response induced by the vaccine.
We offer Anti-treg technology and vaccine combination immunotherapy strategies. These services aim to enhance immune activation by targeting or inhibiting the function of immunosuppressive cells, or by evaluating the synergistic effects of combining vaccines with novel immune modulators.
We employ multi-step purification protocols and a strict quality control system for antigen preparation. For peptides and recombinant proteins, high-performance liquid chromatography (HPLC) is used for fine separation, and qualitative/quantitative verification is performed via SDS-PAGE and mass spectrometry, ensuring high purity and activity of the delivered antigens to support reliable downstream research.
This technology is mainly applied in cell engineering, particularly in non-viral vector systems. It uses gentle mechanical squeezing through microfluidic channels to deliver large molecules (e.g., mRNA, proteins) efficiently and with low toxicity into primary immune cells (such as DC or T cells), making it an important tool for constructing engineered cell vaccines in vitro.
Creative Biolabs is more than just a service provider; we are a pioneer in innovative cancer vaccine technologies. We offer a suite of unique, highly specialized platforms designed to resolve challenges related to low immunogenicity, immune suppression, and delivery, ensuring your customized vaccine project achieves maximum potency.
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