Programmable White Blood Cells: A Two-Marker Specificity-Logic Design for Engineered T Cells

Design paper (SIMULATED, NOT MEASURED) specifying a two-marker AND-gate specificity logic for engineered T cells: a priming receptor for one disease marker induces a killing receptor for a second, so firing requires both markers on the same target cell. Occupancy modelling gives a discrimination ratio of 25.0 versus 2.5 for a single-receptor design, with computed dose, expansion, cytokine-risk, persistence, and antigen-escape budgets, failure modes, and quantitative stopping conditions. All numbers are outputs of the accompanying computation script. Nothing is described as built or tested.

Authors

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-11-10
DOI
https://doi.org/10.5281/zenodo.24108794
Primary Topic
CAR-T cell therapy research
Type
preprint
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preprint

Programmable White Blood Cells: A Two-Marker Specificity-Logic Design for Engineered T Cells

William Alexander Aldred
Zenodo (CERN European Organization for Nuclear Research)
CAR-T cell therapy research
preprint

Programmable White Blood Cells: A Two-Marker Specificity-Logic Design for Engineered T Cells

William Alexander Aldred
preprint en

Abstract

Design paper (SIMULATED, NOT MEASURED) specifying a two-marker AND-gate specificity logic for engineered T cells: a priming receptor for one disease marker induces a killing receptor for a second, so firing requires both markers on the same target cell. Occupancy modelling gives a discrimination ratio of 25.0 versus 2.5 for a single-receptor design, with computed dose, expansion, cytokine-risk, persistence, and antigen-escape budgets, failure modes, and quantitative stopping conditions. All numbers are outputs of the accompanying computation script. Nothing is described as built or tested.

Zenodo (CERN European Organization for Nuclear Research)
CAR-T cell therapy research
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