Omicron infections profile and vaccination status among 1881 liver transplant recipients: a multi-centre retrospective cohort

Emerg Microbes Infect. 2022 Dec;11(1):2636-2644. doi: 10.1080/22221751.2022.2136535.

Abstract

ABSTRACTA wave of Omicron infections rapidly emerged in China in 2022, but large-scale data concerning the safety profile of vaccines and Coronavirus disease 2019 (COVID-19) infection features in liver transplant (LT) recipients have not been collected. Therefore, the aim of this study was to assess the protectiveness and safety profile of the inactivated vaccines in LT patients against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant infections. A multi-centre retrospective study was conducted in a cohort with a history of liver transplantation. A total of 1881 participants (487 vaccinated and 1394 unvaccinated patients) were enrolled from seven centres in China. Fourteen of the participants were infected by Omicron, and 50% patients had over 14 days of viral shedding duration. The protection rate of COVID-19 vaccinations to Omicron was 2.59%. The three breakthrough infections occurred more than 6 months after fully vaccinated. A total of 96 (19.7%) vaccinated patients had adverse events, including fatigue, myalgia, liver dysfunction, swelling, and scleroma. There were more Grade 3 adverse events in the preoperative vaccination group than those in the postoperative vaccination group. Inactivated whole-virion SARS-CoV-2 vaccines are safe in patients with post-liver transplantation. The efficacy of inactivated vaccines decreases after 6 months of vaccination, it is recommended that liver transplant patients get boosted vaccinations as early as possible even when they are fully vaccinated. Although clinical manifestations of Omicron infections were mild in LT patients, unvaccinated patients might have a higher risk of liver dysfunction during infections.

Keywords: Omicron; SARS-CoV-2; adverse events; inactivated vaccine; liver transplantation; protection rate.

Publication types

  • Multicenter Study

MeSH terms

  • COVID-19 Vaccines* / adverse effects
  • COVID-19* / prevention & control
  • Humans
  • Liver Transplantation*
  • Retrospective Studies
  • SARS-CoV-2
  • Vaccination
  • Vaccines, Inactivated / adverse effects

Substances

  • COVID-19 Vaccines
  • Vaccines, Inactivated

Supplementary concepts

  • SARS-CoV-2 variants

Grants and funding

This study was supported by grants from the Science and Technology Commission of Shanghai Municipality [grant number HS2021SHZX001], Shanghai Hospital Development Center [grant number SHDC2020CR2021B], National Natural Science Foundation of China [grant numbers 82071797, 81873874] and Shanghai Science and Technology Committee [grant numbers 20dz2260100, 21NL2600100, 20Z11901100, 20dz2210403].