Trimer IgG and neutralising antibody response to COVID-19 mRNA vaccination in individuals with sarcoidosis

Background Individuals with sarcoidosis are at higher risk for infection owing to underlying disease pathogenesis and need for immunosuppressive treatment. Current knowledge as to how subjects with sarcoidosis respond to different forms of vaccination is limited. We examined quantitative and functio...

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Main Authors: Christen L. Vagts, Yi-Shin Chang, Christian Ascoli, Jessica M. Lee, Kai Huang, Yue Huang, Ruth A. Cherian, Nandini Sarup, Samantha R. Warpecha, Russell Edafetanure-Ibeh, Md-Ruhul Amin, Tasmin Sultana, Mahmood Ghassemi, Nadera J. Sweiss, Richard Novak, David L. Perkins, Patricia W. Finn
Format: Article
Language:English
Published: European Respiratory Society 2023-01-01
Series:ERJ Open Research
Online Access:http://openres.ersjournals.com/content/9/1/00025-2022.full
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author Christen L. Vagts
Yi-Shin Chang
Christian Ascoli
Jessica M. Lee
Kai Huang
Yue Huang
Ruth A. Cherian
Nandini Sarup
Samantha R. Warpecha
Russell Edafetanure-Ibeh
Md-Ruhul Amin
Tasmin Sultana
Mahmood Ghassemi
Nadera J. Sweiss
Richard Novak
David L. Perkins
Patricia W. Finn
author_facet Christen L. Vagts
Yi-Shin Chang
Christian Ascoli
Jessica M. Lee
Kai Huang
Yue Huang
Ruth A. Cherian
Nandini Sarup
Samantha R. Warpecha
Russell Edafetanure-Ibeh
Md-Ruhul Amin
Tasmin Sultana
Mahmood Ghassemi
Nadera J. Sweiss
Richard Novak
David L. Perkins
Patricia W. Finn
author_sort Christen L. Vagts
collection DOAJ
description Background Individuals with sarcoidosis are at higher risk for infection owing to underlying disease pathogenesis and need for immunosuppressive treatment. Current knowledge as to how subjects with sarcoidosis respond to different forms of vaccination is limited. We examined quantitative and functional antibody response to COVID-19 vaccination in infection-naive subjects with and without sarcoidosis. Methods Our prospective cohort study recruited 14 subjects with biopsy-proven sarcoidosis and 27 age–sex matched controls who underwent a two-shot series of the BNT162b2 mRNA vaccine at the University of Illinois at Chicago. Baseline, 4-week and 6-month trimer spike protein IgG and neutralising antibody (nAb) titres were assessed. Correlation and multivariate regression analysis was conducted. Results Sarcoidosis subjects had a significant increase in short-term antibody production to a level comparable to controls; however, IgG titres significantly declined back to baseline levels by 6 months. Corresponding neutralising assays revealed robust nAb titres in sarcoidosis subjects that persisted at 6 months. A significant and strong correlation between IgG and nAb titres across all time points was observed in the control group. However within the sarcoidosis group, a significant but weak correlation between antibody levels was found. Overall, IgG levels were poor predictors of nAb titres at short- or long-term time points. Conclusions Sarcoidosis subjects exhibit nAb induced by the BNT162b2 mRNA SARS-CoV-2 vaccine at levels comparable to controls that persists at 6 months indicating conferred immunity. Trimer IgG levels are poor predictors of nAb in subjects with sarcoidosis. Studies of further antibody immunoglobulins and subtypes warrant investigation.
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spelling doaj.art-79fbfa4e161445099a271d51a0e709832023-06-07T13:30:43ZengEuropean Respiratory SocietyERJ Open Research2312-05412023-01-019110.1183/23120541.00025-202200025-2022Trimer IgG and neutralising antibody response to COVID-19 mRNA vaccination in individuals with sarcoidosisChristen L. Vagts0Yi-Shin Chang1Christian Ascoli2Jessica M. Lee3Kai Huang4Yue Huang5Ruth A. Cherian6Nandini Sarup7Samantha R. Warpecha8Russell Edafetanure-Ibeh9Md-Ruhul Amin10Tasmin Sultana11Mahmood Ghassemi12Nadera J. Sweiss13Richard Novak14David L. Perkins15Patricia W. Finn16 Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA Background Individuals with sarcoidosis are at higher risk for infection owing to underlying disease pathogenesis and need for immunosuppressive treatment. Current knowledge as to how subjects with sarcoidosis respond to different forms of vaccination is limited. We examined quantitative and functional antibody response to COVID-19 vaccination in infection-naive subjects with and without sarcoidosis. Methods Our prospective cohort study recruited 14 subjects with biopsy-proven sarcoidosis and 27 age–sex matched controls who underwent a two-shot series of the BNT162b2 mRNA vaccine at the University of Illinois at Chicago. Baseline, 4-week and 6-month trimer spike protein IgG and neutralising antibody (nAb) titres were assessed. Correlation and multivariate regression analysis was conducted. Results Sarcoidosis subjects had a significant increase in short-term antibody production to a level comparable to controls; however, IgG titres significantly declined back to baseline levels by 6 months. Corresponding neutralising assays revealed robust nAb titres in sarcoidosis subjects that persisted at 6 months. A significant and strong correlation between IgG and nAb titres across all time points was observed in the control group. However within the sarcoidosis group, a significant but weak correlation between antibody levels was found. Overall, IgG levels were poor predictors of nAb titres at short- or long-term time points. Conclusions Sarcoidosis subjects exhibit nAb induced by the BNT162b2 mRNA SARS-CoV-2 vaccine at levels comparable to controls that persists at 6 months indicating conferred immunity. Trimer IgG levels are poor predictors of nAb in subjects with sarcoidosis. Studies of further antibody immunoglobulins and subtypes warrant investigation.http://openres.ersjournals.com/content/9/1/00025-2022.full
spellingShingle Christen L. Vagts
Yi-Shin Chang
Christian Ascoli
Jessica M. Lee
Kai Huang
Yue Huang
Ruth A. Cherian
Nandini Sarup
Samantha R. Warpecha
Russell Edafetanure-Ibeh
Md-Ruhul Amin
Tasmin Sultana
Mahmood Ghassemi
Nadera J. Sweiss
Richard Novak
David L. Perkins
Patricia W. Finn
Trimer IgG and neutralising antibody response to COVID-19 mRNA vaccination in individuals with sarcoidosis
ERJ Open Research
title Trimer IgG and neutralising antibody response to COVID-19 mRNA vaccination in individuals with sarcoidosis
title_full Trimer IgG and neutralising antibody response to COVID-19 mRNA vaccination in individuals with sarcoidosis
title_fullStr Trimer IgG and neutralising antibody response to COVID-19 mRNA vaccination in individuals with sarcoidosis
title_full_unstemmed Trimer IgG and neutralising antibody response to COVID-19 mRNA vaccination in individuals with sarcoidosis
title_short Trimer IgG and neutralising antibody response to COVID-19 mRNA vaccination in individuals with sarcoidosis
title_sort trimer igg and neutralising antibody response to covid 19 mrna vaccination in individuals with sarcoidosis
url http://openres.ersjournals.com/content/9/1/00025-2022.full
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