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Updated: Jul 3, 2026

Use of a Monocyte Monolayer Assay to Evaluate Fcγ Receptor-mediated Phagocytosis
Published on: January 2, 2017
The crossmatch may still be the most clinically relevant histocompatibility test performed
Ronald Kerman1, Jacqueline Lappin, Barry Kahan
1Department of Surgery, Division of Immunology and Organ Transplantation, University of Texas Medical School, Houston, TX, USA.
Insights
Performing a real-time crossmatch is crucial for predicting transplant outcomes. Virtual crossmatch evaluations are unreliable for determining positive or negative results, even with donor-specific antibodies present.
Area of Science:
- Transplantation immunology
- Clinical diagnostics
Background:
- Accurate prediction of transplant success is vital for patient outcomes.
- Current methods for antibody screening and crossmatching require careful evaluation.
Purpose of the Study:
- To evaluate the correlation between pre-transplant antibody screening methods and actual graft survival.
- To determine the reliability of virtual crossmatch predictions compared to real-time crossmatches.
Main Methods:
- Patient sera were analyzed using flowPRA (flow-cytometric panel reactive antibody), FCXM (flow cytometry crossmatch), and end-point donor-antigen titer.
- Results from these assays were correlated with clinical outcomes, specifically graft survival.
Main Results:
- A positive or negative FCXM result cannot be accurately predicted without performing the actual crossmatch.
- Even in the presence of donor-specific antigens, virtual evaluation is insufficient.
- Fluorescence intensity, used as a surrogate for antibody concentration, does not quantitatively correlate with crossmatch outcomes.
Conclusions:
- Real-time crossmatching is imperative for offering donor organs to recipients.
- Reliance on virtual evaluations alone is insufficient for accurate crossmatch prediction.
- Performing a direct crossmatch is essential for optimizing transplant eligibility and outcomes.
Abstract:
We evaluated patient sera for flow PRA, FCXM, and end-point donor-antigen titer, and we correlated the results with graft survival. You cannot accurately predict a positive or negative FCXM result-not even when the sera have donor-specific antigens-unless you actually perform a crossmatch. Using fluorescence intensity as a surrogate for antibody concentration does not correlate quantitatively with the occurrence of a positive or negative crossmatch. Therefore, it is imperative to give each recipient a chance at being offered a donor organ by performance of a real-time crossmatch and not rely on a virtual evaluation.
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