Immunizations in solid organ and hematopoeitic stem cell transplant patients: A comprehensive review

被引:19
作者
L'Huillier, Arnaud G. [1 ,2 ]
Kumar, Deepali [3 ]
机构
[1] Univ Hosp Geneva, Dept Pediat, Pediat Infect Dis Unit, Geneva, Switzerland
[2] Geneva Sch Med, Geneva, Switzerland
[3] Univ Hlth Network, Transplant Infect Dis & Multiorgan Transplant Pro, Toronto, ON, Canada
关键词
graft versus host disease; Haematopoietic stem cell transplantation; immunogenicity; immunosuppression; safety; serology; solid organ transplantation; vaccine; VARICELLA-ZOSTER-VIRUS; BONE-MARROW-TRANSPLANTATION; PNEUMOCOCCAL CONJUGATE VACCINE; HEPATITIS-B-VACCINE; ORTHOTOPIC LIVER-TRANSPLANTATION; HIV-INFECTED ADULTS; INACTIVATED INFLUENZA VACCINE; CYTOMEGALOVIRUS DNA VACCINE; NATIONAL REFERENCE CENTER; PLACEBO-CONTROLLED TRIAL;
D O I
10.1080/21645515.2015.1078043
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The Solid Organ Transplantation (SOT) and Haematopoietic Stem Cell Transplantation (HSCT) population is continuously increasing as a result of broader indications for transplant and improved survival. Infectious diseases, including vaccine-preventable diseases, are a significant threat for this population, primarily after but also prior to transplantation. As a consequence, clinicians must ensure that patients are optimally immunized before transplantation, to provide the best protection during the early post-transplantation period, when immunosuppression is the strongest and vaccine responses are poor. After 3-6months, inactivated vaccines immunization can be resumed. By contrast, live-attenuated vaccines are lifelong contraindicated in SOT patients, but can be considered in HSCT patients at least 2years after transplantation, if there is no immunosuppression or graft-versus-host-disease. However, because of the advantages of live-attenuated over inactivated vaccines - and also sometimes the absence of an inactivated alternative - an increasing number of prospective studies on live vaccine immunization after transplantation are performed and give new insights about safety and immunogenicity in this population.
引用
收藏
页码:2852 / 2863
页数:12
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