Clinical Outcomes of SARS-CoV-2 Breakthrough Infections in Liver Transplant Recipients during the Omicron Wave

Viruses. 2023 Jan 20;15(2):297. doi: 10.3390/v15020297.

Abstract

At the start of the pandemic, liver transplant recipients (LTR) were at high risk of developing severe COVID-19. Here, the outcomes of breakthrough infections in fully vaccinated LTR (n = 98) during the Omicron wave were assessed. In most patients, a mild disease course was observed, but 11 LTR (11.2%) required hospitalization for COVID-19-related complications. All patients survived. The LTR requiring hospitalization were older (67 years vs. 54 years; p < 0.001), had a higher Charlson comorbidity index (9 vs. 5; p < 0.001), and a lower anti-S RBD titer (Roche Elecsys) prior to infection (508.3 AU/mL vs. 2044 AU/mL; p = 0.03). Long-lasting symptoms for ≥4 weeks were reported by 37.5% of LTR (30/80). Risk factors in LTR included female sex (p = 0.01; Odds Ratio (OR) = 4.92 (95% confidence interval (CI) (1.5-16.5)) and dyspnea (p = 0.009; OR = 7.2 (95% CI (1.6-31.6)) during infection. Post-infection high anti-S RBD antibody levels were observed in LTR, and healthy controls (HC), while the cellular immune response, assessed by interferon-gamma release assay (EUROIMMUN), was significantly lower in LTR compared with HC (p < 0.001). In summary, in fully vaccinated LTR, SARS-CoV-2 breakthrough infections during the Omicron wave led to mild disease courses in the majority of patients and further boosted the humoral and cellular hybrid anti-SARS-CoV-2-directed immune response. While all patients survived, older and multimorbid LTR with low baseline antibody titers after vaccination still had a substantial risk for a disease course requiring hospitalization due to COVID-19-related complications.

Keywords: COVID-19; SARS-CoV-2; VOC Omicron; liver transplant recipients; post-acute COVID-19 syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies
  • Breakthrough Infections
  • COVID-19*
  • Disease Progression
  • Female
  • Humans
  • Liver Transplantation* / adverse effects
  • SARS-CoV-2

Substances

  • Antibodies

Supplementary concepts

  • COVID-19 breakthrough infections

Grants and funding

Julian Schulze zur Wiesch received research funding from SFB1328, project A12; Golda Meline Schaub was supported by a German Center for Infection Research (DZIF) MD Stipend through the DZIF Academy. Marylyn Martina Addo reported funding from the DZIFTTU 01709. No further funding was used for the research reported.