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Elevated cytokine levels can appear in patient serum within minutes to hours after infusion. Standard in vitro immunogenicity assays and animal studies often fail to predict these severe reactions, as seen in the TGN1412 clinical trial (Suntharalingam et al., 2006).
This cytokine screening assay strengthens early immunogenicity assay development by identifying molecules with a higher risk of immune activation.
Abzena has developed an enhanced in vitro immunogenicity assay, the Cytokine Screen™, to assess the risk of biopharmaceutical products causing cytokine release syndrome before clinical trials.
The cytokine screening assay is available in whole blood format to evaluate innate immune responses or PBMC format to study adaptive responses, using standard or custom cytokine panels.
The Cytokine Screen™ assay is an in vitro immunogenicity assay that evaluates whether a therapeutic protein could trigger cytokine release and immune-related toxicity.
Cytokine screening helps detect early immune activation, complementing Abzena’s broader immunogenicity assays to predict potential safety risks before clinical studies.
The cytokine screen is available as a whole blood or PBMC-based assay to measure innate and adaptive immune responses using standard or custom cytokine panels.
Our scientists integrate cytokine screening assays into broader immunogenicity assay development workflows to support reliable preclinical safety evaluation.
In vitro immunogenicity assays identify cytokine release risks that animal models often miss, improving safety assessment before first-in-human studies.