Cargando…
Poor immunogenicity upon SARS-CoV-2 mRNA vaccinations in autoimmune SLE patients is associated with pronounced EF-mediated responses and anti-BAFF/Belimumab treatment
Novel mRNA vaccines have resulted in a reduced number of SARS-CoV-2 infections and hospitalizations. Yet, there is a paucity of studies regarding their effectiveness on immunocompromised autoimmune subjects. In this study, we enrolled subjects naïve to SARS-CoV-2 infections from two cohorts of healt...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312827/ https://www.ncbi.nlm.nih.gov/pubmed/37398319 http://dx.doi.org/10.1101/2023.06.08.23291159 |
_version_ | 1785066994835390464 |
---|---|
author | Faliti, Caterina E. Anam, Fabliha A. Cheedarla, Narayanaiah Woodruff, Matthew C. Usman, Sabeena Y. Runnstrom, Martin C. Van, Trinh T.P. Kyu, Shuya Ahmed, Hasan Morrison-Porter, Andrea Quehl, Hannah Haddad, Natalie S. Chen, Weirong Cheedarla, Suneethamma Neish, Andrew S. Roback, John D. Antia, Rustom Khosroshahi, Arezou Lee, F. Eun-Hyung Sanz, Ignacio |
author_facet | Faliti, Caterina E. Anam, Fabliha A. Cheedarla, Narayanaiah Woodruff, Matthew C. Usman, Sabeena Y. Runnstrom, Martin C. Van, Trinh T.P. Kyu, Shuya Ahmed, Hasan Morrison-Porter, Andrea Quehl, Hannah Haddad, Natalie S. Chen, Weirong Cheedarla, Suneethamma Neish, Andrew S. Roback, John D. Antia, Rustom Khosroshahi, Arezou Lee, F. Eun-Hyung Sanz, Ignacio |
author_sort | Faliti, Caterina E. |
collection | PubMed |
description | Novel mRNA vaccines have resulted in a reduced number of SARS-CoV-2 infections and hospitalizations. Yet, there is a paucity of studies regarding their effectiveness on immunocompromised autoimmune subjects. In this study, we enrolled subjects naïve to SARS-CoV-2 infections from two cohorts of healthy donors (HD, n=56) and systemic lupus erythematosus (SLE, n=69). Serological assessments of their circulating antibodies revealed a significant reduction of potency and breadth of neutralization in the SLE group, only partially rescued by a 3(rd) booster dose. Immunological memory responses in the SLE cohort were characterized by a reduced magnitude of spike-reactive B and T cell responses that were strongly associated with poor seroconversion. Vaccinated SLE subjects were defined by a distinct expansion and persistence of a DN2 spike-reactive memory B cell pool and a contraction of spike-specific memory cTfh cells, contrasting with the sustained germinal center (GC)-driven activity mediated by mRNA vaccination in the healthy population. Among the SLE-associated factors that dampened the vaccine responses, treatment with the monoclonal antibody anti-BAFF/Belimumab (a lupus FDA-approved B cell targeting agent) profoundly affected the vaccine responsiveness by restricting the de novo B cell responses and promoting stronger extra-follicular (EF)-mediated responses that were associated with poor immunogenicity and impaired immunological memory. In summary, this study interrogates antigen-specific responses and characterized the immune cell landscape associated with mRNA vaccination in SLE. The identification of factors associated with reduced vaccine efficacy illustrates the impact of SLE B cell biology on mRNA vaccine responses and provides guidance for the management of boosters and recall vaccinations in SLE patients according to their disease endotype and modality of treatment. |
format | Online Article Text |
id | pubmed-10312827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-103128272023-07-01 Poor immunogenicity upon SARS-CoV-2 mRNA vaccinations in autoimmune SLE patients is associated with pronounced EF-mediated responses and anti-BAFF/Belimumab treatment Faliti, Caterina E. Anam, Fabliha A. Cheedarla, Narayanaiah Woodruff, Matthew C. Usman, Sabeena Y. Runnstrom, Martin C. Van, Trinh T.P. Kyu, Shuya Ahmed, Hasan Morrison-Porter, Andrea Quehl, Hannah Haddad, Natalie S. Chen, Weirong Cheedarla, Suneethamma Neish, Andrew S. Roback, John D. Antia, Rustom Khosroshahi, Arezou Lee, F. Eun-Hyung Sanz, Ignacio medRxiv Article Novel mRNA vaccines have resulted in a reduced number of SARS-CoV-2 infections and hospitalizations. Yet, there is a paucity of studies regarding their effectiveness on immunocompromised autoimmune subjects. In this study, we enrolled subjects naïve to SARS-CoV-2 infections from two cohorts of healthy donors (HD, n=56) and systemic lupus erythematosus (SLE, n=69). Serological assessments of their circulating antibodies revealed a significant reduction of potency and breadth of neutralization in the SLE group, only partially rescued by a 3(rd) booster dose. Immunological memory responses in the SLE cohort were characterized by a reduced magnitude of spike-reactive B and T cell responses that were strongly associated with poor seroconversion. Vaccinated SLE subjects were defined by a distinct expansion and persistence of a DN2 spike-reactive memory B cell pool and a contraction of spike-specific memory cTfh cells, contrasting with the sustained germinal center (GC)-driven activity mediated by mRNA vaccination in the healthy population. Among the SLE-associated factors that dampened the vaccine responses, treatment with the monoclonal antibody anti-BAFF/Belimumab (a lupus FDA-approved B cell targeting agent) profoundly affected the vaccine responsiveness by restricting the de novo B cell responses and promoting stronger extra-follicular (EF)-mediated responses that were associated with poor immunogenicity and impaired immunological memory. In summary, this study interrogates antigen-specific responses and characterized the immune cell landscape associated with mRNA vaccination in SLE. The identification of factors associated with reduced vaccine efficacy illustrates the impact of SLE B cell biology on mRNA vaccine responses and provides guidance for the management of boosters and recall vaccinations in SLE patients according to their disease endotype and modality of treatment. Cold Spring Harbor Laboratory 2023-06-12 /pmc/articles/PMC10312827/ /pubmed/37398319 http://dx.doi.org/10.1101/2023.06.08.23291159 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Faliti, Caterina E. Anam, Fabliha A. Cheedarla, Narayanaiah Woodruff, Matthew C. Usman, Sabeena Y. Runnstrom, Martin C. Van, Trinh T.P. Kyu, Shuya Ahmed, Hasan Morrison-Porter, Andrea Quehl, Hannah Haddad, Natalie S. Chen, Weirong Cheedarla, Suneethamma Neish, Andrew S. Roback, John D. Antia, Rustom Khosroshahi, Arezou Lee, F. Eun-Hyung Sanz, Ignacio Poor immunogenicity upon SARS-CoV-2 mRNA vaccinations in autoimmune SLE patients is associated with pronounced EF-mediated responses and anti-BAFF/Belimumab treatment |
title | Poor immunogenicity upon SARS-CoV-2 mRNA vaccinations in autoimmune SLE patients is associated with pronounced EF-mediated responses and anti-BAFF/Belimumab treatment |
title_full | Poor immunogenicity upon SARS-CoV-2 mRNA vaccinations in autoimmune SLE patients is associated with pronounced EF-mediated responses and anti-BAFF/Belimumab treatment |
title_fullStr | Poor immunogenicity upon SARS-CoV-2 mRNA vaccinations in autoimmune SLE patients is associated with pronounced EF-mediated responses and anti-BAFF/Belimumab treatment |
title_full_unstemmed | Poor immunogenicity upon SARS-CoV-2 mRNA vaccinations in autoimmune SLE patients is associated with pronounced EF-mediated responses and anti-BAFF/Belimumab treatment |
title_short | Poor immunogenicity upon SARS-CoV-2 mRNA vaccinations in autoimmune SLE patients is associated with pronounced EF-mediated responses and anti-BAFF/Belimumab treatment |
title_sort | poor immunogenicity upon sars-cov-2 mrna vaccinations in autoimmune sle patients is associated with pronounced ef-mediated responses and anti-baff/belimumab treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312827/ https://www.ncbi.nlm.nih.gov/pubmed/37398319 http://dx.doi.org/10.1101/2023.06.08.23291159 |
work_keys_str_mv | AT faliticaterinae poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT anamfablihaa poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT cheedarlanarayanaiah poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT woodruffmatthewc poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT usmansabeenay poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT runnstrommartinc poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT vantrinhtp poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT kyushuya poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT ahmedhasan poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT morrisonporterandrea poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT quehlhannah poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT haddadnatalies poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT chenweirong poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT cheedarlasuneethamma poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT neishandrews poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT robackjohnd poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT antiarustom poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT khosroshahiarezou poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT leefeunhyung poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment AT sanzignacio poorimmunogenicityuponsarscov2mrnavaccinationsinautoimmuneslepatientsisassociatedwithpronouncedefmediatedresponsesandantibaffbelimumabtreatment |