AI Article Synopsis

  • The study investigates the role of genetic polymorphisms in the innate immune system that may increase the risk of cytomegalovirus (CMV) infection in transplant patients, particularly those receiving organs from CMV-positive donors.
  • A total of 116 CMV-seronegative transplant recipients were monitored for CMV infection post-surgery, with notable findings that 53% experienced some level of infection, including asymptomatic and symptomatic cases.
  • A polygenic score based on specific genetic markers was developed to predict the risk of CMV disease, showing moderate effectiveness (AUC of 0.68), emphasizing the need for additional validation studies to enhance predictive models for at-risk transplant recipients.

Article Abstract

Several genetic polymorphisms of the innate immune system have been described to increase the risk of cytomegalovirus (CMV) infection in transplant patients. The aim of this study was to assess the impact of a polygenic score to predict CMV infection and disease in high risk CMV transplant recipients (heart, liver, kidney or pancreas). On hundred and sixteen CMV-seronegative recipients of grafts from CMV-seropositive donors undergoing heart, liver, and kidney or pancreas transplantation from 7 centres were prospectively included for this purpose during a 2-year period. All recipients received 100-day prophylaxis with valganciclovir. CMV infection occurred in 61 patients (53%) at 163 median days from transplant, 33 asymptomatic replication (28%) and 28 CMV disease (24%). Eleven patients (9%) had recurrent CMV infection. Clinically and/or functionally relevant single nucleotide polymorphisms (SNPs) from , , , , , , , , IFI16, , and were assessed by real time polymerase chain reaction (RT-PCR) or sequence-based typing (PCR-SBT). A polygenic score including the (rs4986790/rs4986791), (rs3775291), (rs3775296), (rs855873), (rs179008), (OO/OA/XAO), (rs12979860) and (rs6940) SNPs was built based on the risk of CMV infection and disease. The CMV score predicted the risk of CMV disease with an AUC of the model of 0.68, with sensitivity and specificity of 64.3 and 71.6%, respectively. Even though further studies are needed to validate this score, its use would represent an effective model to develop more robust scores predicting the risk of CMV disease in donor/recipient mismatch (D+/R-) transplant recipients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9397545PMC
http://dx.doi.org/10.3389/fimmu.2022.897912DOI Listing

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