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Analysis of CC chemokine receptor 5 and 2 polymorphisms and renal transplant survival. | LitMetric

AI Article Synopsis

  • Chronic rejection leads to graft failure, and chemokines may play a role in acute renal rejection, increasing the risk of chronic rejection.
  • This study focused on genetic variants of chemokine receptors in 85 Turkish renal transplant patients to explore their correlation with acute rejection.
  • Results showed no impact from CCR5-Delta32 but significant differences in allele distribution related to acute rejection for CCR2V641 and CCR5-59029, suggesting these genetic variations could be targets for preventing renal transplant loss.

Article Abstract

Chronic rejection is an immune process leading to graft failure. By regulating the trafficking of leukocytes, chemokines and chemokine receptors are thought to be one of the reasons causing acute renal rejection (ARE), which increases the possibility of chronic rejection and organ destruction. This study was designed to investigate, in the Turkish population, an association of chemokine receptor genetic variants, CCR2V641, CCR5-59029-A/G, CCR5-Delta32 and acute renal rejection after renal transplant surgery. We carried out our study in 85 Turkish renal transplant patients (45 men, 40 women; mean age 39 +/- 2 years) by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) techniques. We found no significant difference in the incidence of rejection among patients possessing or lacking CCR5-Delta32. For the groups with and without acute renal rejection, we found a significant difference between the groups in A and G allele distribution in both CCR2V641and CCR559029 gene variants (p = 0.003 and p = 0.003, respectively). According to our findings, the risk of acute rejection in renal transplantation may be associated with genetic variation in the chemokine receptor genes CCR5-59029 and CCR2V641 in Turkey, and studies on these gene polymorphisms could be an ideal target for future interventions intended to prevent renal transplant loss.

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Source
http://dx.doi.org/10.1002/cbf.1322DOI Listing

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