Clinical correlations of human cytomegalovirus strains and viral load in kidney transplant recipients


Autoria(s): NOGUEIRA, Eliana; OZAKI, Kikumi Suzete; TOMIYAMA, Helena; CAMARA, Niels Olsen Saraiva; GRANATO, Celso Francisco Hernandes
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

Little is known about clinical differences associated with cytomegalovirus (CMV) infection by distinct strains in renal transplant patients. Different clinical pictures may be associated with specific viral genotypes. viral load, as well as host factors. The objective of this study was to identify CMV strains to determine viral load (antigenemia), and their correlation with clinical data in renal transplant recipients. Seventy-one patients were enrolled, comprising 91 samples. After selection, polymorphonuclear cells were used to amplify and sequence the gB region of CMV DNA. The sequences were analyzed to ascertain the frequency of different genotypes. Additionally, the results of this Study showed that the gB coding gene presents a great variability, revealing a variety of patterns: classical gB (1.4%), gB1V (46.4%), classical gB2 (35.2%), gB2V (2.8%), gB3 (1.4%), classical gB4 (4.9%) and gB4V (4.9%). The mean viral load in kidney transplant patient was 75.1 positive cells (1-1000). A higher viral load was observed in patients with genotype 4 infection. Statistically significant differences were detected between gB1 and gB4 (p=0.010), and between gB2 and gB4 (p=0.021). The average numbers of positive cells in relation to clinical presentation were: 34.5 in asymptomatic, 49.5 in CMV associated syndrome and 120.7 in patients with invasive disease (p=0.048). As a group, gB1 was the most frequent strain and revealed a potential risk for developing invasive disease. Viral load also seemed to be important as a marker associated with clinical presentation of the disease. (C) 2008 Elsevier B.V. All rights reserved.

Identificador

INTERNATIONAL IMMUNOPHARMACOLOGY, v.9, n.1, p.26-31, 2009

1567-5769

http://producao.usp.br/handle/BDPI/28315

10.1016/j.intimp.2008.08.020

http://dx.doi.org/10.1016/j.intimp.2008.08.020

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

Relação

International Immunopharmacology

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #Renal transplantation #Cytomegalovirus #Genotyping #pp65 antigenemia #GLYCOPROTEIN B GENOTYPES #HUMAN-IMMUNODEFICIENCY-VIRUS #ENVELOPE GLYCOPROTEIN #ALLOGRAFT RECIPIENTS #INFECTED PATIENTS #AIDS PATIENTS #CMV DISEASE #BONE-MARROW #RETINITIS #BLOOD #Immunology #Pharmacology & Pharmacy
Tipo

article

original article

publishedVersion