AI-based analysis of label-free live cell imaging of T-cell mediated tumor killing assay enables competitive and

Josefa Chuh1, Daniel Siegismund2, John Moffat1

  • 1Genentech Inc., South San Francisco, CA, USA.

Insights

A new AI workflow analyzes brightfield images for immune cell killing assays, eliminating fluorescent labels. This approach simplifies T-cell mediated killing assays and improves efficiency for personalized cancer treatment discovery.

Area of Science:

  • Immunology
  • Biotechnology
  • Computational Biology

Background:

  • Personalized cancer treatments like T-cell receptor (TCR-T) therapy and bispecific antibodies (BsAbs) require robust functional validation.
  • Current immune-mediated killing assays rely on fluorescent labeling and classical image analysis, which are prone to artifacts and require extensive parameter adjustments.

Purpose of the Study:

  • To develop and validate a novel, marker-free artificial intelligence (AI)-based analysis workflow for immune-mediated killing assays.
  • To improve the efficiency and consistency of analyzing T-cell mediated killing assays.

Main Methods:

  • Utilized brightfield microscopy images instead of fluorescent markers.
  • Developed a hands-free, scalable AI-based analysis workflow.
  • Applied and benchmarked the AI workflow against traditional cell segmentation-based analysis of fluorescent images in a T-cell mediated killing assay.

Main Results:

  • The AI workflow successfully analyzed phenotypically diverse cancer cells without fluorescent labeling.
  • Achieved greater efficiency by eliminating manual adjustment steps common in traditional methods.
  • Produced results of equivalent consistency compared to conventional fluorescent image analysis.

Conclusions:

  • The AI-based brightfield image analysis workflow offers a substantial simplification of T-cell mediated live cell killing assays.
  • Eliminates the need for fluorescent labeling and time-consuming analysis of labeled images.
  • Enables efficient and consistent functional activity confirmation for immune cell therapeutics discovery.

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