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Cell Avidity

Revolutionize binding for the future of cell & antibody therapeutics

Imagine measuring the combined strength of cell-cell / cell-protein binding, generating direct, physiologically relevant measurements of binding in its full, dynamic complexity. To supportprogress in immunotherapy, we need to measure binding the way it happens—in real life, in real cells. This is Cell Avidity.

Select potent candidates, faster

Balance efficacy and safety

Accelerate your path to clinic

The challenge

There are no simple answers to immuno-oncology’s greatest challenges

Many immunotherapies adapt to solve the field’s most pressing issues (an intricate balance between persistence, potency, and safety) by integrating multiple signaling mechanisms and engaging with more than one target in parallel. With that trend, the binding mechanisms between binder and target also complexify. Yet, most binding assays haven’t kept up.

A solution for tomorrow

Cell Avidity, the missing link

By measuring the combined strength of cell-cell / cell-protein binding with controlled forces, Cell Avidity generates direct, physiologically relevant measurements of binding in its full, dynamic complexity. It reveals the mechanisms of action, facilitates rational design choices and selects the right candidates fast and early, ultimately improving therapeutic outcomes.

Our users

Dynamic Single-Molecule is being adopted by pioneers across the globe.

Simon is studying how our cells repair damage to their DNA, and how failures in this process lead to cancer and other diseases

It is truly transformative for our understanding. The [C-Trap's Dynamic Single-Molecule] technology allows us to see the real-time dynamic aspects of what the molecules are doing.

Simon Boulton, PhD
Principal Group Leader
The Francis Crick Institute
Simon is studying how our cells repair damage to their DNA, and how failures in this process lead to cancer and other diseases

It is truly transformative for our understanding. The [C-Trap's Dynamic Single-Molecule] technology allows us to see the real-time dynamic aspects of what the molecules are doing.

Simon Boulton, PhD
Principal Group Leader

The Francis Crick Institute

Simon is studying how our cells repair damage to their DNA, and how failures in this process lead to cancer and other diseases

Hopefully most universities and microscope facilities around the world will be able to procure a LUMICKS C-Trap. Once one person is trained by the great staff, running the instrument is not any more difficult than a confocal microscope.

Ben Van Houten, PhD
Professor of Molecular Oncology
University of Pittsburgh
Simon is studying how our cells repair damage to their DNA, and how failures in this process lead to cancer and other diseases

Hopefully most universities and microscope facilities around the world will be able to procure a LUMICKS C-Trap. Once one person is trained by the great staff, running the instrument is not any more difficult than a confocal microscope.

Ben Van Houten, PhD
Professor of Molecular Oncology

University of Pittsburgh

Workflow

Intuitive, from start to finish

Measure the overall strength of interaction between cells, or between proteins and cells.

Seed your target cells

Target cells (adherent or non-adherent) are generally of two types:

Tumor cells to assess potency or antigen sensitivity 

Healthy cells to assess on-target off-tumor toxicity 

Introduce your effector cells or molecules

Introduction of labeled binders to the uniform monolayer. These can include:

Therapeutic effector cell products like CAR T, TCR T, NK. 

Effector cells with compound drugs such as cell engagers, small molecule inhibitors or modified environmental factors.

Fluorescent beads coated with antibodies or other proteins.

Controlled force application & fluorescent imaging

Controlled force applied to the bound cells probes the strength of interactions between labeled and target populations. Fluorescence microscopy captures the number of bound cells before and after force application. The percentage of bound cells after force application indicates the population’s Cell Avidity.

Instant data acquisition

Cell Avidity quantifies cell binding with hundreds of cells per measurement, revealing percentage (%) of cells bound, or percentage (%) of antibody-coated beads bound.

Applications

Screen cell lines, cell engagers, and antibodies, faster and better.

A Swiss army knife for next generation binding, Cell Avidity can be used to tackle a wide variety of challenges.

Cell Therapy

Steer receptor binding to overcome cell therapy exhaustion, improve potency, minimize OTOT, and refine binding sensitivity to overcome immune escape.

Featuring case studies from:

Yufei Wang, PhD
Lydia Lee, PhD
Mark Leick, MD
Cell Therapy

Cell Engagers

Determine avidity EC50 and binding kinetics of T cell engagers to quantify trimer formation across multiple dimensions in the cell-cell context.

Featuring case studies from:

David B. Weiner, PhD
Cell Engagers

Antibody Therapy

Elucidate binding effects of antibodies within the 2D membrane-constrained cellular environment, taking into account the effects of epitope, steric hindrance, and multivalency.

Featuring case studies from:

William Sellers, MD
Antibody Therapy

Tackle more than affinity ever can

Utilize Cell Avidity in a wide variety of applications.

Binding potency

Avidity ranking & cell characterization

Binding sensitivity

Titration assay for CE, Peptide or Ab

Binding specificity

Monolayer safety screening

Applicable to a variety of use-cases

Utilize Cell Avidity in a wide variety of applications.

Binder screening and optimization

Optimize binding to overcome exhaustion, improve potency, minimize OTOT and refine sensitivity to overcome immune escape.

Understand the impact of different antibody formats and fine-tune Cell Avidity to select candidates based on multi-domain binding measured in a single assay.

Effector functional modification

Measure how functional modifications in effector cells impact binding. Intracellularly driven differences in Cell Avidity can inform on potency and persistence.

Reveal the mechanism of action in therapy designs that change signaling sensitivity, activate cytokine or chemokine receptors, or reduce checkpoint receptors.

Tumor microenvironment response

Measure the tumor microenvironment’s impact on binding by measuring Cell Avidity in the presence of tumor or TME modifying compounds.

Get insights into immune trafficking, effects of environment-modulating compounds, hypoxia effects and more.

Donor selection and quality control

Measure the combined effect of donor/host interactome or assess the combined effect of cell fitness, receptor expression, and population purity.

Quantify the degree of (mis)matching between donor and host or assess product quality across multiple key product attributes.

Industry

Unlock faster R&D cycles

Integrating Cell Avidity in the drug development workflow leads to faster identification of the most potent, safe and sensitive drug candidate by reducing the required number of design iterations or eliminating candidates from in vivo preclinical studies which ultimately bind ineffectively in a cellular context.

Early in the pipeline - Select the right candidates fast

Quickly rank hundreds to thousands of therapeutic candidates to get insights into sensitivity and safety. Incorporate Cell Avidity early in the discovery workflow helps ensure that only candidates with the most promising binding characteristics progress.

Late-stage - Deep candidate characterization to drive clinical selection

Carry out deep functional characterization of select final candidates. Reveal differences in binding dynamics and target engagement to confidently select the optimal therapeutics for clinical development.

Solutions

Avidion

The next generation Cell Avidity platform

Ideal for cell therapy candidate screening and large characterization studies. Run up to 4 disposable 48-well cartridges a day for a total of 192 measurements with <80 min. hands-on time.
Discover Avidion

Avidigo

White glove Cell Avidity services

Full-service contract research from experimental design to data report based on Cell Avidity measurements at high throughput.
Discover Avidigo

z-Movi

For small sized Cell Avidity studies

A fast and simple solution for single-sample Cell Avidity experiments. Run up to 20 measurements per day.
Discover z-Movi
Key content

Download the brochure

Get the complete picture and specifications

Cell Avidity Technology Brochure
Cell Avidity Technology Brochure
Brochure
The latest all-in-one overview of our Cell Avidity technology.
Brochure

Publications

Understand the key insights by reading up on our latest publications

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Technical note:
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Tandem CAR-T cells targeting mesothelin and MUC16 overcome tumor heterogeneity by targeting one antigen at a time
Tandem CAR-T cells targeting mesothelin and MUC16 overcome tumor heterogeneity by targeting one antigen at a time
Salas-Benito, D. et al.
2025
JITC
Cell Therapy
Text Link
Bicistronic CAR T Cell against BCMA and CD229 Effectively Controls Myeloma Even When BCMA Expression Is Limited
Bicistronic CAR T Cell against BCMA and CD229 Effectively Controls Myeloma Even When BCMA Expression Is Limited
Rodríguez-Lobato, L. G. et al.
2025
Cancer Immunology Research
Cell Therapy
Text Link
EZH1/EZH2 inhibition enhances adoptive T cell immunotherapy against multiple cancer models
EZH1/EZH2 inhibition enhances adoptive T cell immunotherapy against multiple cancer models
Porazzi, P. et al.
2025
Cancer Cell
Cell Therapy
Text Link
Adopting Cell Avidity

Let’s begin your LUMICKS journey

Our experts are ready to learn about your research challenges and see where our technologies can bring value.

Contact us

Demonstrating value

Our application scientists can help create interest among potential users through organizing different events such as seminars, workshops, and demonstrations, as well as meet with stakeholders individually to understand and help solve their needs.

Avidigo services

At our Amsterdam headquarters, our internal Avidigo service team supports academic and industry clients looking to integrate Cell Avidity into their workflows and pipeline. From experimental design to data analysis and interpretation, we support you all the way.

Grant & tender support

Throughout our history we have supported multiple successful grants across a broad spectrum of funding and users involved. Our application scientists are experienced in highlighting the unique value of Cell Avidity and its solutions.