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Updated: Jun 5, 2026

18:48
In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
[Immunologic study of the donor-receptor couple]
M Guadalupe Ercilla1, Jaume Martorell
1Servico de Inmunología (CDB), Hospital Clinic de Bacelona. gercilla@clinic.ub.es
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia
|December 25, 2010
Summary
Identifying donor-specific antibodies and HLA incompatibilities is crucial for assessing graft failure risk. Various pre- and post-transplant methods, including virtual crossmatch, aid in predicting and managing rejection, optimizing transplant outcomes.
Area of Science:
- Transplantation immunology
- Immunogenetics
- Clinical diagnostics
Context:
- Donor-specific antibodies and HLA incompatibilities are key factors in graft failure.
- Pre-transplant assessment involves HLA typing, alloantibody screening (PRA-CDC, Solid Phase), and virtual crossmatch.
- Post-transplant monitoring is essential for diagnosing rejection and predicting long-term graft survival.
Purpose:
- To evaluate the risk of graft failure by identifying donor-specific antibodies and HLA incompatibilities.
- To compare the sensitivity and prognostic value of different alloantibody detection methods.
- To assess the utility of various crossmatch techniques (Cytotoxicity, Flow-Cytometry, Virtual) in predicting transplant outcomes.
Summary:
- Pre-transplant evaluation includes HLA typing, alloantibody screening (PRA-CDC, Solid Phase), and virtual crossmatch for sensitized recipients.
- Crossmatch methods like Cytotoxicity (CM-CDC) and Flow-Cytometry (FCCM) are used pre-transplant, with FCCM particularly useful for re-transplants.
- Post-transplant, alloantibody identification aids in diagnosing humoral rejection and serves as a marker for long-term graft survival.
Impact:
- Cytotoxicity crossmatch identifies high risk for hyperacute rejection, serving as a contraindication.
- Flow Cytometry crossmatch predicts increased graft loss risk in the first year, especially for re-transplants (>30%).
- Virtual crossmatch indicates a higher probability of antibody-mediated rejection (5-55%) but may not always contraindicate transplantation.
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