Department of Nephrology, Monash Medical Centre, Clayton, Victoria, Australia; Centre for Inflammatory Diseases, Department of Medicine, Monash University, Clayton, Victoria, Australia.
Centre for Inflammatory Diseases, Department of Medicine, Monash University, Clayton, Victoria, Australia; Monash Infectious Diseases, Monash Health, Clayton, Victoria, Australia.
J Heart Lung Transplant. 2018 Jul;37(7):844-852. doi: 10.1016/j.healun.2018.03.001. Epub 2018 Mar 10.
Clinical guidelines recommend vaccinations for solid-organ transplant recipients. However, concern exists that vaccination may stimulate adverse alloimmune responses.
We systematically reviewed the published literature regarding this aspect of vaccine safety. Electronic databases were searched for interventional and observational studies assessing de novo donor-specific antibodies (DSA) and rejection episodes after vaccination against infectious pathogens. Graft loss was also assessed. A meta-analysis was conducted for prospective, controlled studies. PRISMA reporting guidelines were followed.
Ninety studies (15,645 vaccinated patients and 42,924 control patients) were included. Twelve studies included control groups. The incidence of de novo DSA (14 studies) was 23 of 1,244 patients (1.85%) at 21 to 94 days. The incidence of rejection (83 studies) was 107 episodes in 5,116 patients (2.1%) at 0.7 to 6 months. Meta-analysis of prospective controlled studies (n = 8) showed no increased rejection risk with vaccination compared with no vaccination (RR 1.12, 95% CI 0.75 to 1.70). This finding was supported by data from 3 registry analyses.
Although the current evidence lacks high-quality, controlled studies, the currently available data provide reassurance that clinicians should recommend appropriate vaccination for their transplant patients as the risk of de novo DSA and rejection is relatively low.
临床指南建议为实体器官移植受者接种疫苗。然而,人们担心接种疫苗可能会刺激不良的同种异体免疫反应。
我们系统地回顾了关于疫苗安全性这一方面的已发表文献。检索电子数据库,以评估针对传染性病原体进行疫苗接种后新产生的供体特异性抗体(DSA)和排斥反应的干预性和观察性研究。还评估了移植物丢失。对前瞻性、对照研究进行了荟萃分析。遵循 PRISMA 报告准则。
共纳入 90 项研究(15645 例接种疫苗患者和 42924 例对照患者)。其中 12 项研究包括对照组。新产生的 DSA 的发生率(14 项研究)为 21 至 94 天内 1244 例患者中的 23 例(1.85%)。排斥反应的发生率(83 项研究)为 5116 例患者中 107 例(2.1%)在 0.7 至 6 个月。8 项前瞻性对照研究的荟萃分析显示,与未接种疫苗相比,接种疫苗并未增加排斥反应的风险(RR 1.12,95%CI 0.75 至 1.70)。这一发现得到了 3 项注册分析数据的支持。
尽管目前的证据缺乏高质量的对照研究,但现有的数据令人放心,临床医生应为其移植患者推荐适当的疫苗接种,因为新产生的 DSA 和排斥反应的风险相对较低。