Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Respiratory Diseases Branch, Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Curr Opin Organ Transplant. 2023 Apr 1;28(2):76-84. doi: 10.1097/MOT.0000000000001056. Epub 2023 Feb 15.
SARS-CoV-2 resulted in a global pandemic that had a chilling effect on transplantation early in the pandemic and continues to result in significant morbidity and mortality of transplant recipients. Over the past 2.5 years, our understanding of the clinical utility of vaccination and mAbs to prevent COVID-19 in solid organ transplant (SOT) recipients has been studied. Likewise, approach to donors and candidates with SARS-CoV-2 has been better understood. This review will attempt to summarize our current understanding of these important COVID-19 topics.
Vaccination against SARS-CoV-2 is effective in reducing the risk of severe disease and death among transplant patients. Unfortunately, humoral and, to a lesser extent, cellular immune response to existing COVID-19 vaccines is reduced in SOT recipients compared with healthy controls. Additional doses of vaccine are required to optimize protection of this population and still may be insufficient in those who are highly immunosuppressed, those receiving belatacept, rituximab and other B-cell active mAbs. Until recently, mAbs were options for the prevention of SARS-CoV-2 but are markedly less effective with recent omicron variants. SARS-CoV-2-infected donors can generally be used for nonlung, nonsmall bowel transplants unless they have died of acute severe COVID-19 or COVID-19-associated clotting disorders.
Our transplant recipients require a three-dose mRNA or adenovirus-vector and one dose of mRNA vaccine to be optimally protected initially; they then need to receive a bivalent booster 2+ months after completing their initial series. Most nonlung, nonsmall bowel donors with SARS-CoV-2 can be utilized as organ donors.
SARS-CoV-2 引发了全球大流行,这在大流行早期对移植造成了寒蝉效应,并且继续导致移植受者发病率和死亡率显著增加。在过去的 2.5 年中,人们一直在研究疫苗和单抗在预防实体器官移植 (SOT) 受者 COVID-19 中的临床应用。同样,人们对 SARS-CoV-2 供者和候选者的处理方式也有了更好的理解。这篇综述将尝试总结我们目前对这些重要 COVID-19 主题的理解。
SARS-CoV-2 疫苗接种可有效降低移植患者发生重症疾病和死亡的风险。不幸的是,与健康对照者相比,SOT 受者对现有 COVID-19 疫苗的体液和(在较小程度上)细胞免疫反应降低。需要额外剂量的疫苗来优化该人群的保护效果,但对于那些免疫抑制程度较高、接受贝利尤单抗、利妥昔单抗和其他 B 细胞活性单抗的患者,疫苗接种可能仍然不够。直到最近,单抗还是预防 SARS-CoV-2 的选择,但最近的 omicron 变体使其效果明显降低。除非死于急性重症 COVID-19 或 COVID-19 相关凝血障碍,否则一般可使用感染 SARS-CoV-2 的供者进行非肺、非小肠移植。
我们的移植受者最初需要接受三剂 mRNA 或腺病毒载体疫苗和一剂 mRNA 疫苗才能得到最佳保护;然后,他们需要在完成初始系列疫苗接种后 2 个月以上接种二价加强针。大多数感染 SARS-CoV-2 的非肺、非小肠供者可作为器官供者。