Literature DB >> 25777542

Association between individual and combined SNPs in genes related to innate immunity and incidence of CMV infection in seropositive kidney transplant recipients.

M Fernández-Ruiz1, I Corrales, M Arias, J M Campistol, E Giménez, J Crespo, M O López-Oliva, I Beneyto, P L Martín-Moreno, F Llamas-Fuente, A Gutiérrez, T García-Álvarez, R Guerra-Rodríguez, N Calvo, A Fernández-Rodríguez, J M Tabernero-Romo, M D Navarro, A Ramos-Verde, J M Aguado, D Navarro.   

Abstract

In this study, we assessed the association between single-nucleotide polymorphisms (SNPs) in seven candidate genes involved in orchestrating the immune response against cytomegalovirus (CMV) and the 12-month incidence of CMV infection in 315 CMV-seropositive kidney transplant (KT) recipients. Patients were managed either by antiviral prophylaxis or preemptive therapy. CMV infection occurred in 140 patients (44.4%), including 13 episodes of disease. After adjusting for various clinical covariates, patients harboring T-allele genotypes of interleukin-28B (IL28B) (rs12979860) SNP had lower incidence of CMV infection (adjusted hazard ratio [aHR]: 0.66; 95% confidence interval [CI]: 0.46-0.96; p-value = 0.029). In the analysis restricted to patients not receiving prophylaxis, carriers of the TT genotype of toll-like receptor 9 (TLR9) (rs5743836) SNP had lower incidence of infection (aHR: 0.61; 95% CI: 0.38-0.96; p-value = 0.035), whereas the GG genotype of dendritic cell-specific ICAM 3-grabbing nonintegrin (DC-SIGN) (rs735240) SNP exerted the opposite effect (aHR: 1.86; 95% CI: 1.18-2.94; p-value = 0.008). An independent association was found between the number of unfavorable SNP genotypes carried by the patient and the incidence of CMV infection. In conclusion, specific SNPs in IL28B, TLR9 and DC-SIGN genes may play a role in modulating the susceptibility to CMV infection in CMV-seropositive KT recipients. © Copyright 2015 The American Society of Transplantation and the American Society of Transplant Surgeons.

Entities:  

Keywords:  clinical research / practice; immune regulation; infection and infectious agents; infectious disease; kidney disease: infectious; kidney transplantation / nephrology; molecular biology: single polynucleotide polymorphism; translational research / science; viral: Cytomegalovirus (CMV)

Mesh:

Substances:

Year:  2015        PMID: 25777542     DOI: 10.1111/ajt.13107

Source DB:  PubMed          Journal:  Am J Transplant        ISSN: 1600-6135            Impact factor:   8.086


  18 in total

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2.  Toll-like receptors genes polymorphisms and the occurrence of HCMV infection among pregnant women.

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4.  Association between single nucleotide polymorphisms (SNPs) of IL1, IL12, IL28 and TLR4 and symptoms of congenital cytomegalovirus infection.

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6.  Association of FOXP3 Single Nucleotide Polymorphisms With Clinical Outcomes After Allogenic Hematopoietic Stem Cell Transplantation.

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9.  Fine Mapping the Interaction Between Dendritic Cell-Specific Intercellular Adhesion Molecule (ICAM)-3-Grabbing Nonintegrin and the Cytomegalovirus Envelope Glycoprotein B.

Authors:  Coraline Chéneau; Flora Coulon; Vanessa Porkolab; Franck Fieschi; Stéphanie Laurant; Diane Razanajaona-Doll; Jean-Jacques Pin; Eva Maria Borst; Martin Messerle; Céline Bressollette-Bodin; Franck Halary
Journal:  J Infect Dis       Date:  2018-07-02       Impact factor: 5.226

10.  Impacts of Interleukin-18 Polymorphisms on the Incidence of Delayed-Onset Cytomegalovirus Infection in a Cohort of Kidney Transplant Recipients.

Authors:  Isabel Pérez-Flores; Jose Luis Santiago; Cristina Fernández-Pérez; Elena Urcelay; María Ángeles Moreno de la Higuera; Natividad Calvo Romero; Beatriz Rodríguez Cubillo; Ana Isabel Sánchez-Fructuoso
Journal:  Open Forum Infect Dis       Date:  2019-07-20       Impact factor: 3.835

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