Target intelligence / Profile preview

Autologous tumor lysate (ATL)

Target
ATL
Molecular classification
Complex biological mixture, Antigenic source, Tumor-associated antigens (TAAs), Neoantigens
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Overview

Autologous tumor lysate is a personalized therapeutic substrate derived from the lysis of a patient's own surgically resected tumor cells. Rather than targeting a single protein, it provides a comprehensive library of tumor-associated antigens (TAAs) and patient-specific neoantigens that reflect the unique molecular signature and heterogeneity of an individual's cancer (National Cancer Institute Drug Dictionary). This approach is primarily utilized in the production of personalized cancer vaccines, such as dendritic cell vaccines, where the lysate is used to 'train' the patient's immune system to recognize and attack malignant cells. By presenting a broad spectrum of antigens, autologous tumor lysate aims to overcome the challenge of 'antigen escape,' a common mechanism of resistance where tumors downregulate specific targets to evade immune detection (Srivatsan, S., et al. 2014, Methods in Molecular Biology). While highly specific to the patient, its use is limited by the requirement for sufficient high-quality tumor tissue and the logistical complexities of individualized manufacturing.

Other names
Patient-specific tumor lysateWhole tumor lysateAutologous tumor cell lysateTumor-derived lysate
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Mechanism of action

Autologous tumor lysate acts as a source of diverse antigens that are loaded into antigen-presenting cells (typically dendritic cells). These cells process the lysate and present tumor-specific peptides via MHC class I and II molecules to T-cells, inducing a polyclonal immune response against the patient's specific tumor profile (Liau, L. M., et al. 2023, JAMA Oncology).

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Biological functions

Immune responseAntigen presentationT-cell activationImmune system priming
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Disease associations

CancerGlioblastoma multiformeMelanomaRenal cell carcinomaOvarian cancer
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Safety considerations

Manufacturing failure due to insufficient tumor tissueAutoimmunity (theoretical risk of targeting healthy tissue)Injection site reactionsFlu-like symptomsTumor heterogeneity leading to incomplete antigen coverage
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Interacting drugs

Vaxidoretigene autotemcel (DCVax-L)

3 more in the full profile.

07

Biomarkers

Tumor mutational burden (TMB)Interferon-gamma (IFN-γ) productionMHC expression levelsDelayed-type hypersensitivity (DTH) skin test

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