COVID-19 Outcomes in Lung Transplant Recipients Following Pre-Exposure Prophylaxis With Tixagevimab-Cilgavimab During the Omicron BA.5 Surge: A Single Center Analysis

Transpl Int. 2024 Jan 24:37:12061. doi: 10.3389/ti.2024.12061. eCollection 2024.

Abstract

Lung transplant (LTx) recipients are at high risk for COVID-19 related morbidity and mortality. Data regarding pre-exposure prophylaxis (PrEP) with tixagevimab-cilgavimab in this population are scarce. We therefore evaluated COVID-19 breakthrough infections and COVID-19 related complications after PrEP in a retrospective single-center study, including 264 LTx recipients who received PrEP between June 2022 and December 2022, when Omicron BA.5 was the dominant circulating SARS-CoV-2 variant. PrEP was indicated for fully vaccinated patients with poor seroconversion (anti-S <260 BAU/mL). COVID-19 breakthrough infection after PrEP occurred in 11.0% within the first 3 months, increasing to 17.4% within 6 months. Hospitalization rate rose from 27.6% to 52.9% (p = 0.046), while ICU admissions and COVID-19 mortality remained low, respectively occurring in 6.5% and 4.3% of patients with breakthrough infection within 6 months. COVID-19 breakthrough infection and associated hospitalization remained an important problem during the Omicron BA.5 surge in fully vaccinated LTx recipients with deficient seroconversion, despite PrEP with tixagevimab-cilgavimab. However, ICU admissions and COVID-19 mortality were low. Waning of neutralizing effects of PrEP and changing circulating SARS-CoV-2 variants may explain increases in COVID-19 infections and hospitalizations over time after PrEP, highlighting the need for novel, long-term effective PrEP strategies in these high-risk patients.

Keywords: COVID-19; lung transplantation; outcome predictors; pre-exposure prophylaxis; tixagevimab-cilgavimab.

MeSH terms

  • Antibodies, Monoclonal*
  • Breakthrough Infections*
  • COVID-19* / prevention & control
  • Humans
  • Lung
  • Pre-Exposure Prophylaxis*
  • Retrospective Studies
  • SARS-CoV-2
  • Transplant Recipients

Substances

  • tixagevimab
  • cilgavimab
  • Antibodies, Monoclonal

Supplementary concepts

  • COVID-19 breakthrough infections
  • SARS-CoV-2 variants

Grants and funding

RV is supported by the Research Foundation-Flanders (FWO) as senior clinical researcher (1803521N) and by a research grant (G060322N). RV is supported by an academic research grant from AstraZeneca, but the study was conducted without Industry sponsorship.