Latent viral infections in young patients with inflammatory diseases treated with biological agents: Prevalence of JC virus genotype 2

被引:17
作者
Comar, Manola [1 ,2 ]
Delbue, Serena [3 ]
Lepore, Loredana [2 ]
Martelossi, Stefano [2 ]
Radillo, Oriano [2 ]
Ronfani, Luca [2 ]
D'Agaro, Pierlanfranco [1 ,2 ]
Ferrante, Pasquale [4 ,5 ]
机构
[1] Univ Trieste, Dept Reprod Dev & Publ Hlth Sci, I-34137 Trieste, Italy
[2] Inst Maternal & Child Hlth IRCCS Burlo Garofolo, Trieste, Italy
[3] Hlth Sci Fdn Ettore Sansavini, Lugo, RA, Italy
[4] Univ Milan, Dept Publ Hlth, Milan, Italy
[5] Clin Inst Citta Studi, Milan, Italy
关键词
JC virus; infliximab; inflammatory bowel diseases; children; human herpesviruses; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; CROHNS-DISEASE; INFLIXIMAB; POLYOMAVIRUS; REACTIVATION; URINE; NATALIZUMAB; THERAPY; BLOOD; RISK;
D O I
10.1002/jmv.23525
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Treatment with biological drugs is associated with increased susceptibility to viral infections. Reactivation of JC virus (JCV) and human cytomegalovirus (HCMV) in adults after therapy has been documented. The long-term effects of biological and conventional therapy on human herpesviruses and polyomaviruses infections in young patients were assessed. One hundred eighty-six samples [urine, serum, and blood cells (PBMCs)] from 62 patients (15.8 +/- 6.2 years old) with Crohn's disease, ulcerative rectocolitis or juvenile rheumatoid arthritis treated with immunotherapy or conventional therapy for over 12 months were tested by real time PCR. One hundred twenty-four samples (urine and blood) from 62 matched healthy volunteers (13.8 +/- 8.6 years old) were included as controls. Sequencing of the JCV viral protein 1 (VP1) and transcriptional control region (TCR) was performed. Herpes simplex virus 1/2 and varicella zoster virus genomes were not detected in any patients, whereas EpsteinBarr virus, HCMV, and human herpesvirus-6 genomes were detected in 4.8%, 3.2%, and 1.6% of the patients, respectively. JCV was detected in 22.6% (14/62) of urine samples from patients and in 8% (5/62) from controls, in 50% (7/14) of sera from patients shedding JCV, and in 71.4% (5/7) of matched PBMCs. There was a significant association between infliximab treatment and excretion of JCV genotype 2. Subclinical infection/reactivation of JCV genotype 2 in young patients during infliximab therapy was demonstrated. Conversely, increased susceptibility to herpesviruses infection was not shown. Future studies are warranted to investigate the effects of JCV reactivation on the health of young patients treated with infliximab. J. Med. Virol. 85:716722, 2013. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:716 / 722
页数:7
相关论文
共 34 条
[1]
Genotype profile of human polyomavirus JC excreted in urine of immunocompetent individuals [J].
Agostini, HT ;
Ryschkewitsch, CF ;
Stoner, GL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (01) :159-164
[2]
BKV-DNA and JCV-DNA in CSF of patients with suspected meningitis or encephalitis [J].
Behzad-Behbahani, A ;
Klapper, PE ;
Vallely, PJ ;
Cleator, GM ;
Bonington, A .
INFECTION, 2003, 31 (06) :374-378
[3]
Polyomavirus JC reactivation and noncoding control region sequence analysis in pediatric Crohn's disease patients treated with infliximab [J].
Bellizzi, Anna ;
Anzivino, Elena ;
Ferrari, Federica ;
Di Nardo, Giovanni ;
Colosimo, Maria Teresa ;
Fioriti, Daniela ;
Mischitelli, Monica ;
Chiarini, Fernanda ;
Cucchiara, Salvatore ;
Pietropaolo, Valeria .
JOURNAL OF NEUROVIROLOGY, 2011, 17 (04) :303-313
[4]
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY IN HIV-1-INFECTED CHILDREN [J].
BERGER, JR ;
SCOTT, G ;
ALBRECHT, J ;
BELMAN, AL ;
TORNATORE, C ;
MAJOR, EO .
AIDS, 1992, 6 (08) :837-841
[5]
Asymptomatic Reactivation of JC Virus in Patients Treated with Natalizumab [J].
Chen, Yiping ;
Bord, Evelyn ;
Tompkins, Troy ;
Miller, Janice ;
Tan, Chen S. ;
Kinkel, R. Philip ;
Stein, Marion C. ;
Viscidi, Raphael P. ;
Ngo, Long H. ;
Koralnik, Igor J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (11) :1067-1074
[6]
de Chambrun GP, 2008, GUT, V57, P1633
[7]
A case of a progressive multifocal leukoencephalopathy patient with four different JC virus transcriptional control region rearrangements in cerebrospinal fluid, blood, serum, and urine [J].
Delbue, S ;
Sotgiu, G ;
Fumagalli, D ;
Valli, M ;
Borghi, E ;
Mancuso, R ;
Marchioni, E ;
Maserati, R ;
Ferrante, P .
JOURNAL OF NEUROVIROLOGY, 2005, 11 (01) :51-57
[8]
JC virus genotypes in France: Molecular epidemiology and potential significance for progressive multifocal leukoencephalopathy [J].
Dubois, V ;
Moret, H ;
Lafon, ME ;
Brodard, V ;
Icart, J ;
Ruffault, A ;
Guist'hau, O ;
Buffet-Janvresse, C ;
Abbed, K ;
Dussaix, E ;
Ingrand, D .
JOURNAL OF INFECTIOUS DISEASES, 2001, 183 (02) :213-217
[9]
EVIDENCE OF HUMAN POLYOMAVIRUS-BK AND POLYOMAVIRUS-JC INFECTION IN NORMAL BRAIN-TISSUE [J].
ELSNER, C ;
DORRIES, K .
VIROLOGY, 1992, 191 (01) :72-80
[10]
Ferrante P, 2001, J NEUROVIROL, V7, P35