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Herpes simplex virus-2 transmission following solid organ transplantation: Donor-derived infection and transplantation from prior organ recipients
被引:11
作者:
Macesic, Nenad
[1
,2
]
Abbott, Iain J.
[3
]
Kaye, Matthew
[3
]
Druce, Julian
[3
]
Glanville, Allan R.
[4
]
Gow, Paul J.
[5
,6
]
Hughes, Peter D.
[7
]
Korman, Tony M.
[8
]
Mulley, William R.
[9
,10
]
O'Connell, Phillip J.
[11
]
Opdam, Helen
[12
]
Paraskeva, Miranda
[13
]
Pitman, Matthew C.
[14
]
Setyapranata, Stella
[7
]
Rawlinson, William D.
[15
]
Johnson, Paul D. R.
[1
,6
]
机构:
[1] Austin Hlth, Dept Infect Dis, Melbourne, Vic, Australia
[2] Columbia Univ, Med Ctr, Div Infect Dis, New York, NY USA
[3] Doherty Inst, Victorian Infect Dis Reference Lab, Melbourne, Vic, Australia
[4] St Vincents Hosp, Dept Thorac Med, Sydney, NSW, Australia
[5] Austin Hlth, Liver Transplant Unit, Melbourne, Vic, Australia
[6] Univ Melbourne, Dept Med, Melbourne, Vic, Australia
[7] Royal Melbourne Hosp, Dept Nephrol, Melbourne, Vic, Australia
[8] Monash Univ, Monash Infect Dis, Monash Hlth, Melbourne, Vic, Australia
[9] Monash Univ, Dept Med, Melbourne, Vic, Australia
[10] Monash Hlth, Dept Nephrol, Melbourne, Vic, Australia
[11] Westmead Hosp, Natl Pancreas Transplant Unit, Sydney, NSW, Australia
[12] DonateLife, Melbourne, Vic, Australia
[13] Alfred Hosp, Dept Allergy Immunol & Resp Med, Melbourne, Vic, Australia
[14] Royal Melbourne Hosp, Victorian Infect Dis Serv, Melbourne, Vic, Australia
[15] Univ NSW, South Eastern Area Lab Serv, Serol & Virol Div SAVID, Sydney, NSW, Australia
关键词:
allograft re-use;
donor-derived infection;
herpes simplex virus hepatitis;
transplantation;
TYPE-2;
REUSE;
HEPATITIS;
D O I:
10.1111/tid.12739
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Background: Owing to limited availability of donor organs, previous solid organ transplant (SOT) recipients are increasingly considered as potential organ donors. We report donor-derived transmission of herpes simplex virus type-2 (HSV-2) to two clusters of SOT recipients with transmission from the original donor and an HSV-2-infected recipient who subsequently became a donor. Methods: We reviewed medical records of the donors and recipients in both clusters. Pre-transplant serology and virological features of HSV-2 were characterized. Genotyping of HSV-2 isolates to determine potential for donor transmission of HSV-2 through transplantation of organs from prior organ recipients was performed. Results: A kidney-pancreas recipient died day 9 post transplant. Following confirmation of brain death, the lungs and recently transplanted kidney were donated to two further recipients. The liver was not retrieved, but biopsy confirmed HSV-2 infection. Testing on the original donor showed negative HSV-2 polymerase chain reaction and HSV immunoglobulin (Ig) M, but positive HSV-2 IgG. The liver recipient from the original donor developed HSV-2 hepatitis and cutaneous infection that responded to treatment with intravenous acyclovir. In the second cluster, lung and kidney recipients both developed HSV-2 viremia that was successfully treated with antiviral therapy. Genotyping of all HSV-2-positive samples showed 100% sequence homology for three recipients. Conclusions: Donor-derived HSV infection affected two clusters of recipients because of transplantation of organs from a prior organ recipient. HSV should be considered as a possible cause of illness in febrile SOT recipients in the immediate post-transplant period and may cause disseminated disease and re-infection in HSV-2-seropositive recipients. Testing of HSV serology and prophylaxis may be considered in SOT recipients not receiving cytomegalovirus prophylaxis.
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