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Omicron BA.1 and BA.2 Neutralizing Activity Following Pre-Exposure Prophylaxis with Tixagevimab plus Cilgavimab in Vaccinated Solid Organ Transplant Recipients
Andrew H Karaba; Jake Kim; Teresa Po-Yu Chiang; Jennifer L Alejo; Aura T Abedon; Jonathan Mitchell; Amy Chang; Yolanda Eby; Trevor Scott Johnston; Tihitina Y Aytenfisu; Casey Hussey; Alexa Jefferis; Nicole Fortune; Rivka Abedon; Letitia Thomas; Daniel S Warren; Ioannis Sitaras; Andrew Pekosz; Robin K Avery; Allan B Massie; William Clarke; Aaron AR Tobian; Dorry Segev; William A Werbel.
Affiliation
  • Andrew H Karaba; Johns Hopkins
  • Jake Kim; Johns Hopkins
  • Teresa Po-Yu Chiang; Johns Hopkins
  • Jennifer L Alejo; Johns Hopkins
  • Aura T Abedon; Johns Hopkins
  • Jonathan Mitchell; Johns Hopkins
  • Amy Chang; Johns Hopkins
  • Yolanda Eby; Johns Hopkins
  • Trevor Scott Johnston; Johns Hopkins
  • Tihitina Y Aytenfisu; Johns Hopkins
  • Casey Hussey; Johns Hopkins
  • Alexa Jefferis; Johns Hopkins
  • Nicole Fortune; Johns Hopkins
  • Rivka Abedon; Johns Hopkins
  • Letitia Thomas; Johns Hopkins
  • Daniel S Warren; Johns Hopkins
  • Ioannis Sitaras; Johns Hopkins
  • Andrew Pekosz; Johns Hopkin
  • Robin K Avery; Johns Hopkins
  • Allan B Massie; NYU
  • William Clarke; Johns Hopkins
  • Aaron AR Tobian; Johns Hopkin
  • Dorry Segev; NYU
  • William A Werbel; Johns Hopkins
Preprint in English | medRxiv | ID: ppmedrxiv-22275467
ABSTRACT
Neutralizing antibody responses are attenuated in many solid organ transplant recipients (SOTRs) despite SARS-CoV-2 vaccination. Pre-exposure prophylaxis (PrEP) with the monoclonal antibody combination Tixagevimab and Cilgavimab (T+C) might augment immunoprotection, yet activity against Omicron sublineages in vaccinated SOTRs is unknown. Vaccinated SOTRs who received 300+300mg T+C (either single dose or two 150+150mg doses) within a prospective observational cohort submitted pre- and post-injection samples between 1/10/2022-4/4/2022. Binding antibody (anti-receptor binding domain [RBD], Roche) and surrogate neutralization (%ACE2 inhibition; [≥]20% connoting neutralizing inhibition, Meso Scale Discovery) were measured against variants including Omicron sublineages BA.1 and BA.2. Data were analyzed using the Wilcoxon matched-pairs signed-rank test and McNemars test. Among 61 participants, median (IQR) anti-RBD increased from 424 (IQR <0.8-2322.5) to 3394.5 (IQR 1403.9-7002.5) U/ml post T+C (p<0.001). The proportion demonstrating vaccine strain neutralizing inhibition increased from 46% to 100% post-T+C (p<0.001). BA.1 neutralization was low and did not increase (8% to 16% of participants post-T+C, p=0.06). In contrast, BA.2 neutralization increased from 7% to 72% of participants post-T+C (p<0.001). T+C increased anti-RBD levels, yet BA.1 neutralizing activity was minimal. Encouragingly, BA.2 neutralization was augmented and in the current variant climate T+C PrEP may serve as a useful complement to vaccination in high-risk SOTRs.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Experimental_studies / Observational study / Prognostic study Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Experimental_studies / Observational study / Prognostic study Language: English Year: 2022 Document type: Preprint
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