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A Third Dose of SARS-CoV-2 Vaccine Increases Neutralizing Antibodies Against Variants of Concern in Solid Organ Transplant Recipients
Andrew H Karaba; Xianming Zhu; Tao Liang; Kristy H Wang; Alex G Rittenhouse; Olivia Akinde; Yolanda Eby; Jessica Ruff; Joel N Blankson; Aura Teles; Jennifer L Alejo; Andrea L Cox; Justin R Bailey; Elizabeth Thompson; Sabra L Klein; Dan Warren; Jacqueline M Garonzik-Wang; Brian J Boyarsky; Ioannis Sitaras; Andrew Pekosz; Dorry L Segev; Aaron AR Tobian; William A Werbel.
Affiliation
  • Andrew H Karaba; Johns Hopkins
  • Xianming Zhu; Johns Hopkins
  • Tao Liang; Johns Hopkins
  • Kristy H Wang; Johns Hopkins
  • Alex G Rittenhouse; Johns Hopkins
  • Olivia Akinde; Johns Hopkins
  • Yolanda Eby; Johns Hopkins
  • Jessica Ruff; Johns Hopkins University
  • Joel N Blankson; Johns Hopkins
  • Aura Teles; Johns Hopkins
  • Jennifer L Alejo; Johns Hopkins
  • Andrea L Cox; Johns Hopkins
  • Justin R Bailey; Johns Hopkins
  • Elizabeth Thompson; Johns Hopkins University
  • Sabra L Klein; Johns Hopkins
  • Dan Warren; Johns Hopkins University
  • Jacqueline M Garonzik-Wang; Johns Hopkins
  • Brian J Boyarsky; Johns Hopkins
  • Ioannis Sitaras; Johns Hopkins University School of Public Health
  • Andrew Pekosz; Johns Hopkins
  • Dorry L Segev; Johns Hopkins
  • Aaron AR Tobian; Johns Hopkins
  • William A Werbel; Johns Hopkins
Preprint in English | medRxiv | ID: ppmedrxiv-21261914
Journal article
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ABSTRACT
Vaccine-induced SARS-CoV-2 antibody responses are attenuated in solid organ transplant recipients (SOTRs) and breakthrough infections are more common. Additional SARS-CoV-2 vaccine doses increase anti-spike IgG in some SOTRs, but it is uncertain whether neutralization of variants of concern (VOCs) is enhanced. We tested 47 SOTRs for clinical and research anti-spike IgG, pseudoneutralization (ACE2 blocking), and live-virus neutralization (nAb) against VOCs before and after a third SARS-CoV-2 vaccine dose (70% mRNA, 30% Ad26.COV2.S) with comparison to 15 healthy controls after two mRNA vaccine doses. We used correlation analysis to compare anti-spike IgG assays and focused on thresholds associated with neutralizing activity. A third SARS-CoV-2 vaccine dose increased median anti-spike (1.6-fold) and receptor-binding domain (1.5-fold) IgG, as well as pseudoneutralization against VOCs (2.5-fold versus Delta). However, IgG and neutralization activity were significantly lower than healthy controls (p<0.001); 32% of SOTRs had zero detectable nAb against Delta after third vaccination. Correlation with nAb was seen at anti-spike IgG >4 AU on the clinical assay and >10^4 AU on the research assay. These findings highlight benefits of a third vaccine dose for some SOTRs and the need for alternative strategies to improve protection in a significant subset of this population.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Prognostic study Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Prognostic study Language: English Year: 2021 Document type: Preprint
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