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Updated: Aug 17, 2026

Trans-vivo Delayed Type Hypersensitivity Assay for Antigen Specific Regulation
Published on: May 2, 2013
Cytotoxic T-lymphocyte antigen 4 gene polymorphisms and susceptibility to acute allograft rejection
E Slavcheva1, E Albanis, Q Jiao
1Division of Nephrology, Mount Sinai School of Medicine, 1 Gustave L. Levy Place, Box 1243, New York, NY 10029, USA.
Background:
Cytotoxic T-lymphocyte antigen 4 (CTLA4) has been shown to play a critical role in the down-regulation of the immune response. We retrospectively examined the association between acute rejection and two polymorphisms in the CTLA4 gene, the dinucleotide (AT)n repeat polymorphism in exon 3 and the single nucleotide polymorphism A/G at position 49 in exon 1, in a cohort of liver and kidney transplant recipients.
Methods And Results:
A total of 207 liver and 167 renal transplant recipients were analyzed. In the case of the (AT)n repeat polymorphism we found an increased incidence of acute rejection in association with allele 3 and 4 in both liver and kidney (P=0.002 and 0.05, respectively). In addition, in liver transplant recipients, allele 7 was associated with acute rejection independent of ethnicity (P<0.05). Allele 1 was less frequently observed in African American as compared with Caucasian liver and kidney transplant recipients, with a frequency of 33.8% and 69%, respectively (P<0.0001). Those patients with allele 1 had a tendency toward a lower rate of rejection at 42% versus 57.8% (P=0.058), suggesting a potential protective effect of allele 1. Analysis of the A/G single nucleotide polymorphism demonstrated no association between either allele and the incidence of acute rejection in the patients studied.
Conclusion:
These initial observations provide the necessary basis to further investigate the risk stratification of transplant recipients based on specific CTLA4 gene polymorphisms.
Insights
Specific Cytotoxic T-lymphocyte antigen 4 (CTLA4) gene polymorphisms, particularly the (AT)n repeat, are associated with acute transplant rejection. Alleles 3 and 4 of the (AT)n repeat increase rejection risk, while allele 1 may offer protection.
Area of Science:
- Immunogenetics
- Transplantation immunology
- Molecular biology
Background:
- Cytotoxic T-lymphocyte antigen 4 (CTLA4) is crucial in regulating immune responses.
- CTLA4 gene polymorphisms are investigated for their role in transplant outcomes.
Purpose of the Study:
- To examine the association between CTLA4 gene polymorphisms and acute rejection in liver and kidney transplant recipients.
- To identify specific CTLA4 variants that may predict rejection risk.
Main Methods:
- Retrospective analysis of 207 liver and 167 kidney transplant recipients.
- Genotyping for two CTLA4 polymorphisms: (AT)n repeat in exon 3 and A/G SNP in exon 1.
- Statistical analysis to correlate genotypes with acute rejection incidence.
Main Results:
- The (AT)n repeat polymorphism showed increased acute rejection with alleles 3 and 4 in both liver and kidney transplants (P=0.002 and 0.05).
- In liver recipients, allele 7 was linked to rejection (P<0.05), and allele 1 showed a potential protective effect (P=0.058).
- The CTLA4 A/G single nucleotide polymorphism did not correlate with acute rejection incidence.
Conclusions:
- Specific CTLA4 (AT)n repeat polymorphisms are associated with acute rejection risk in transplant recipients.
- Further research into CTLA4 gene variants can aid in risk stratification for transplantation.
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