Adenovirus infections in stem cell transplant recipients: Recent developments in understanding of pathogenesis, diagnosis and management

被引:68
作者
Chakrabarti, S [1 ]
Milligan, DW
Moss, PAH
Mautner, V
机构
[1] Univ Hosp Birmingham, Dept Haematol, Birmingham B15 2TH, W Midlands, England
[2] Univ Birmingham, Canc Res UK, Inst Canc Studies, Birmingham B15 2TT, W Midlands, England
[3] Heartlands Hosp, Dept Haematol, Birmingham, W Midlands, England
基金
英国医学研究理事会;
关键词
adenovirus; stem cell transplantation; PCR; preemptive therapy;
D O I
10.1080/10428190310001628176
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adenovirus is increasingly recognized as an important pathogen in stem cell transplant recipients, reflecting increased awareness about the virus, together with changes in transplant practice such as the performance of more high-risk transplants, and improvements in diagnostic methods. In retrospective studies, the reported incidence of adenovirus infections ranged between 4 - 20% with a similar variation in the proportion of patients developing invasive disease. In contrast, the incidence of adenovirus infection varies between 20 - 30% in recent prospective studies on T-cell depleted or mismatched allografts and about 30 - 40% of these patients develop invasive disease. These prospective studies have established a relationship between the risk of invasive adenovirus disease and a number of factors such as the extent of T-cell depletion, the intensity of immunosuppressive therapy and the kinetics of lymphocyte recovery post-transplant. Polymerase chain reaction (PCR) assays to detect adenovirus DNA in peripheral blood have shown a strong correlation between viremia and the risk of disseminated adenovirus disease. These developments have led to the possibility of a preemptive antiviral treatment strategy for asymptomatic adenovirus infections. In addition, a better understanding of the interactions between adenovirus and host immune system in the post-transplant setting might enable development of effective immunotherapeutic strategies against adenovirus infections.
引用
收藏
页码:873 / 885
页数:13
相关论文
共 100 条
  • [1] ABKEN H, 1987, ANTICANCER RES, V7, P553
  • [2] DNA RESTRICTION ANALYSIS OF ADENOVIRUS PROTOTYPE-1 TO PROTOTYPE-41
    ADRIAN, T
    WADELL, G
    HIERHOLZER, JC
    WIGAND, R
    [J]. ARCHIVES OF VIROLOGY, 1986, 91 (3-4) : 277 - 290
  • [3] Adenovirus is a key pathogen in hemorrhagic cystitis associated with bone marrow transplantation
    Akiyama, H
    Kurosu, T
    Sakashita, C
    Inoue, T
    Mori, S
    Ohashi, K
    Tanikawa, S
    Sakamaki, H
    Onozawa, Y
    Chen, Q
    Zheng, HY
    Kitamura, T
    [J]. CLINICAL INFECTIOUS DISEASES, 2001, 32 (09) : 1325 - 1330
  • [4] POLYMERASE CHAIN-REACTION FOR DETECTION OF ADENOVIRUSES IN STOOL SAMPLES
    ALLARD, A
    GIRONES, R
    JUTO, P
    WADELL, G
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (12) : 2659 - 2667
  • [5] Rapid typing of human adenoviruses by a general PCR combined with restriction endonuclease analysis
    Allard, A
    Albinsson, B
    Wadell, G
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (02) : 498 - 505
  • [6] Selective depletion of donor alloreactive T cells without loss of antiviral or antileukernic responses
    Amrolia, PJ
    Muccioli-Casadei, G
    Yvon, E
    Huls, H
    Sili, U
    Wieder, ED
    Bollard, C
    Heslop, HE
    Molldrem, JJ
    Rooney, CM
    Brenner, MK
    [J]. BLOOD, 2003, 102 (06) : 2292 - 2299
  • [7] Outcome and clinical course of 100 patients with adenovirus infection following bone marrow transplantation
    Baldwin, A
    Kingman, H
    Darville, M
    Foot, ABM
    Grier, D
    Cornish, JM
    Goulden, N
    Oakhill, A
    Pamphilon, DH
    Steward, CG
    Marks, DI
    [J]. BONE MARROW TRANSPLANTATION, 2000, 26 (12) : 1333 - 1338
  • [8] CYTOMEGALOVIRUS (CMV) IN COMPROMISED HOST(S)
    BETTS, RF
    HANSHAW, JB
    [J]. ANNUAL REVIEW OF MEDICINE, 1977, 28 : 103 - 110
  • [9] BLANKE C, 1995, AM J MED, V99, P326, DOI 10.1016/S0002-9343(99)80169-7
  • [10] Bordigoni Pierre, 2001, Clinical Infectious Diseases, V32, P1290, DOI 10.1086/319984