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Renal Transplantation With Final Allocation Based on the Virtual Crossmatch
C P Johnson1, J J Schiller2, Y R Zhu1
1Department of Surgery (Division of Transplantation), Medical College of Wisconsin, Milwaukee, WI.
Solid phase immunoassays (SPI) are effective for detecting HLA antibodies in kidney transplants. This study shows SPI can replace flow cytometric crossmatch (FCXM) for donor-recipient compatibility, ensuring successful long-term graft survival.
Area of Science:
- Transplantation immunology
- Nephrology
- Clinical diagnostics
Background:
- Solid phase immunoassays (SPI) are standard for detecting HLA antibodies.
- Flow cytometric crossmatch (FCXM) is the traditional method for assessing donor-recipient compatibility in renal transplantation.
- A shift in protocol has occurred, prioritizing SPI over FCXM for final allocation decisions since 2005.
Purpose of the Study:
- To evaluate long-term graft outcomes in kidney transplant recipients.
- To compare outcomes between FCXM-positive (FCXM+) and FCXM-negative (FCXM-) recipients under a protocol using SPI for allocation.
- To determine if crossmatch status impacts graft survival and acute rejection rates.
Main Methods:
- Analysis of 508 consecutive kidney transplants where allocation was based on SPI.
- Categorization of recipients into FCXM+ (n=54) and FCXM- (n=454) groups.
- Assessment of primary outcomes: graft survival and acute rejection within 1 year, with a median follow-up of 7.1 years.
Main Results:
- FCXM+ recipients had higher rates of sensitization and specific risk factors (e.g., longer dialysis duration, retransplants).
- Despite risk factor differences, 5-year actual graft survival was comparable (87% FCXM+ vs. 84% FCXM-).
- Acute rejection within 1 year was similar between groups (13% FCXM+ vs. 12% FCXM-); crossmatch status did not predict outcomes.
Conclusions:
- Renal transplantation can be successfully performed using SPI as the definitive test for donor-recipient compatibility.
- The study supports the use of SPI, potentially simplifying the pre-transplant compatibility assessment process.
- Long-term graft survival is not adversely affected by relying on SPI over FCXM for allocation decisions.
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