Chronic rhinoviral infection in lung transplant recipients

被引:155
作者
Kaiser, Laurent
Aubert, John-David
Pache, Jean-Claude
Deffernez, Christelle
Rochat, Thierry
Garbino, Jorge
Wunderli, Werner
Meylan, Pascal
Yerly, Sabine
Perrin, Luc
Letovanec, Igor
Nicod, Laurent
Tapparel, Caroline
Soccal, Paola M.
机构
[1] Univ Hosp Geneva, Cent Lab Virol, Div Infect Dis, Dept Internal Med, CH-1211 Geneva 14, Switzerland
[2] Univ Hosp Geneva, Clin Thorac Surg, Dept Surg, CH-1211 Geneva, Switzerland
[3] Univ Hosp Geneva, Dept Internal Med, Div Pulm Med, CH-1211 Geneva 14, Switzerland
[4] Univ Lausanne Hosp, Dept Med, Div Pulm Med, Lausanne, Switzerland
[5] Univ Lausanne Hosp, Inst Microbiol, Lausanne, Switzerland
[6] Univ Lausanne Hosp, Dept Pathol, Div Infect Dis, Lausanne, Switzerland
[7] Univ Hosp Bern, Div Pulm Med, CH-3010 Bern, Switzerland
关键词
lung transplantation; picornavirus; respiratory virus; rhinovirus; VP1;
D O I
10.1164/rccm.200604-489OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Lung transplant recipients are particularly at risk of complications from rhinovirus, the most frequent respiratory virus circulating in the community. Objectives: To determine whether lung transplant recipients can be chronically infected by rhinovirus and the potential clinical impact. Methods: We first identified an index case, in which rhinovirus was isolated repeatedly, and conducted detailed molecular analysis to determine whether this was related to a unique strain or to reinfection episodes. Transbronchial biopsies were used to assess the presence of rhinovirus in the lung parenchyma. The incidence of chronic rhinoviral infections and potential clinical impact was assessed prospectively in a cohort of 68 lung transplant recipients during 19 mo by screening of bronchoalveolar lavages. Measurements and Main Results: We describe 3 lung transplant recipients with graft dysfunctions in whom rhinovirus was identified by reverse transcriptase-polymerase chain reaction in upper and lower respiratory specimens over a 12-mo period. In two cases, rhinovirus was repeatedly isolated in culture. The persistence of a unique strain in each case was confirmed by sequence analysis of the 5'NCR and VP1 gene. In the index case, rhinovirus was detected in the lower respiratory parenchyma. In the cohort of lung transplant recipients, rhinoviral infections were documented in bronchoalveolar lavage specimens of 10 recipients, and 2 presented with a persistent infection. Conclusions: Rhinoviral infection can be persistent in lung transplant recipients with graft dysfunction, and the virus can be detected in the lung parenchyma. Given the potential clinical impact, chronic rhinoviral infection needs to be considered in lung transplant recipients.
引用
收藏
页码:1392 / 1399
页数:8
相关论文
共 56 条
  • [51] Influenza and parainfluenza respiratory viral infection requiring admission in adult lung transplant recipients
    Vilchez, R
    McCurry, K
    Dauber, J
    Iacono, A
    Keenan, R
    Griffith, B
    Kusne, S
    [J]. TRANSPLANTATION, 2002, 73 (07) : 1075 - 1078
  • [52] A RHINOVIRUS OUTBREAK AMONG RESIDENTS OF A LONG-TERM-CARE FACILITY
    WALD, TG
    SHULT, P
    KRAUSE, P
    MILLER, BA
    DRINKA, P
    GRAVENSTEIN, S
    [J]. ANNALS OF INTERNAL MEDICINE, 1995, 123 (08) : 588 - 593
  • [53] Asthmatic bronchial epithelial cells have a deficient innate immune response to infection with rhinovirus
    Wark, PAB
    Johnston, SL
    Bucchieri, F
    Powell, R
    Puddicombe, S
    Laza-Stanca, V
    Holgate, ST
    Davies, DE
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (06) : 937 - 947
  • [54] Picornavirus infections in children diagnosed by RT-PCR during longitudinal surveillance with weekly sampling: Association with symptomatic illness and effect of season
    Winther, B
    Hayden, FG
    Hendley, JO
    [J]. JOURNAL OF MEDICAL VIROLOGY, 2006, 78 (05) : 644 - 650
  • [55] Yousem SA, 1996, J HEART LUNG TRANSPL, V15, P1
  • [56] Molecular epidemiology of two consecutive outbreaks of parainfluenza 3 in a bone marrow transplant unit
    Zambon, M
    Bull, T
    Sadler, CJ
    Goldman, JM
    Ward, KN
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (08) : 2289 - 2293