Cargando…

Frailty impacts immune responses to Moderna COVID-19 mRNA vaccine in older adults

BACKGROUND: Immune responses to COVID-19 mRNA vaccines have not been well characterized in frail older adults. We postulated that frailty is associated with impaired antibody and cellular mRNA vaccine responses. METHODS: We followed older adults in a retirement facility with longitudinal clinical an...

Descripción completa

Detalles Bibliográficos
Autores principales: Semelka, Charles T., DeWitt, Michael E., Blevins, Maria W., Holbrook, Beth C., Sanders, John W., Alexander-Miller, Martha A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843107/
https://www.ncbi.nlm.nih.gov/pubmed/36650551
http://dx.doi.org/10.1186/s12979-023-00327-x
_version_ 1784870311022297088
author Semelka, Charles T.
DeWitt, Michael E.
Blevins, Maria W.
Holbrook, Beth C.
Sanders, John W.
Alexander-Miller, Martha A.
author_facet Semelka, Charles T.
DeWitt, Michael E.
Blevins, Maria W.
Holbrook, Beth C.
Sanders, John W.
Alexander-Miller, Martha A.
author_sort Semelka, Charles T.
collection PubMed
description BACKGROUND: Immune responses to COVID-19 mRNA vaccines have not been well characterized in frail older adults. We postulated that frailty is associated with impaired antibody and cellular mRNA vaccine responses. METHODS: We followed older adults in a retirement facility with longitudinal clinical and serological samples from the first Moderna mRNA-1273 vaccine dose starting in February 2021 through their 3rd (booster) vaccine dose. Outcomes were antibody titers, antibody avidity, and AIM+ T cell function and phenotype. Statistical analysis used linear regression with clustered error for antibody titers over multiple timepoints with clinical predictors including, age, sex, prior infection status, and clinical frailty scale (CFS) score. T cell function analysis used linear regression models with clinical predictors and cellular memory phenotype variables. RESULTS: Participants (n = 15) had median age of 90 years and mild, moderate, or severe frailty scores (n = 3, 7, or 5 respectively). Over the study time course, anti-spike antibody titers were 10-fold higher in individuals with lower frailty status (p = 0.001 and p = 0.005, unadjusted and adjusted for prior COVID-19 infection). Following the booster, titers to spike protein improved regardless of COVID-19 infection or degree of frailty (p = 0.82 and p = 0.29, respectively). Antibody avidity significantly declined over 6 months in all participants following 2 vaccine doses (p < 0.001), which was further impaired with higher frailty (p = 0.001). Notably, avidity increased to peak levels after the booster (p < 0.001). Overall antibody response was inversely correlated with a phenotype of immune-senescent T cells, CD8 + CD28- TEMRA cells (p = 0.036, adjusted for COVID-19 infection). Furthermore, there was increased detection of CD8 + CD28- TEMRA cells in individuals with greater frailty (p = 0.056, adjusted for COVID-19). CONCLUSIONS: We evaluated the immune responses to the Moderna COVID-19 mRNA vaccine in frail older adults in a retirement community. A higher degree of frailty was associated with diminished antibody quantity and quality. However, a booster vaccine dose at 6 months overcame these effects. Frailty was associated with an increased immune-senescence phenotype that may contribute to the observed changes in the vaccine response. While the strength of our conclusions was limited by a small cohort, these results are important for guiding further investigation of vaccine responses in frail older adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12979-023-00327-x.
format Online
Article
Text
id pubmed-9843107
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-98431072023-01-17 Frailty impacts immune responses to Moderna COVID-19 mRNA vaccine in older adults Semelka, Charles T. DeWitt, Michael E. Blevins, Maria W. Holbrook, Beth C. Sanders, John W. Alexander-Miller, Martha A. Immun Ageing Research BACKGROUND: Immune responses to COVID-19 mRNA vaccines have not been well characterized in frail older adults. We postulated that frailty is associated with impaired antibody and cellular mRNA vaccine responses. METHODS: We followed older adults in a retirement facility with longitudinal clinical and serological samples from the first Moderna mRNA-1273 vaccine dose starting in February 2021 through their 3rd (booster) vaccine dose. Outcomes were antibody titers, antibody avidity, and AIM+ T cell function and phenotype. Statistical analysis used linear regression with clustered error for antibody titers over multiple timepoints with clinical predictors including, age, sex, prior infection status, and clinical frailty scale (CFS) score. T cell function analysis used linear regression models with clinical predictors and cellular memory phenotype variables. RESULTS: Participants (n = 15) had median age of 90 years and mild, moderate, or severe frailty scores (n = 3, 7, or 5 respectively). Over the study time course, anti-spike antibody titers were 10-fold higher in individuals with lower frailty status (p = 0.001 and p = 0.005, unadjusted and adjusted for prior COVID-19 infection). Following the booster, titers to spike protein improved regardless of COVID-19 infection or degree of frailty (p = 0.82 and p = 0.29, respectively). Antibody avidity significantly declined over 6 months in all participants following 2 vaccine doses (p < 0.001), which was further impaired with higher frailty (p = 0.001). Notably, avidity increased to peak levels after the booster (p < 0.001). Overall antibody response was inversely correlated with a phenotype of immune-senescent T cells, CD8 + CD28- TEMRA cells (p = 0.036, adjusted for COVID-19 infection). Furthermore, there was increased detection of CD8 + CD28- TEMRA cells in individuals with greater frailty (p = 0.056, adjusted for COVID-19). CONCLUSIONS: We evaluated the immune responses to the Moderna COVID-19 mRNA vaccine in frail older adults in a retirement community. A higher degree of frailty was associated with diminished antibody quantity and quality. However, a booster vaccine dose at 6 months overcame these effects. Frailty was associated with an increased immune-senescence phenotype that may contribute to the observed changes in the vaccine response. While the strength of our conclusions was limited by a small cohort, these results are important for guiding further investigation of vaccine responses in frail older adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12979-023-00327-x. BioMed Central 2023-01-17 /pmc/articles/PMC9843107/ /pubmed/36650551 http://dx.doi.org/10.1186/s12979-023-00327-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Semelka, Charles T.
DeWitt, Michael E.
Blevins, Maria W.
Holbrook, Beth C.
Sanders, John W.
Alexander-Miller, Martha A.
Frailty impacts immune responses to Moderna COVID-19 mRNA vaccine in older adults
title Frailty impacts immune responses to Moderna COVID-19 mRNA vaccine in older adults
title_full Frailty impacts immune responses to Moderna COVID-19 mRNA vaccine in older adults
title_fullStr Frailty impacts immune responses to Moderna COVID-19 mRNA vaccine in older adults
title_full_unstemmed Frailty impacts immune responses to Moderna COVID-19 mRNA vaccine in older adults
title_short Frailty impacts immune responses to Moderna COVID-19 mRNA vaccine in older adults
title_sort frailty impacts immune responses to moderna covid-19 mrna vaccine in older adults
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843107/
https://www.ncbi.nlm.nih.gov/pubmed/36650551
http://dx.doi.org/10.1186/s12979-023-00327-x
work_keys_str_mv AT semelkacharlest frailtyimpactsimmuneresponsestomodernacovid19mrnavaccineinolderadults
AT dewittmichaele frailtyimpactsimmuneresponsestomodernacovid19mrnavaccineinolderadults
AT blevinsmariaw frailtyimpactsimmuneresponsestomodernacovid19mrnavaccineinolderadults
AT holbrookbethc frailtyimpactsimmuneresponsestomodernacovid19mrnavaccineinolderadults
AT sandersjohnw frailtyimpactsimmuneresponsestomodernacovid19mrnavaccineinolderadults
AT alexandermillermarthaa frailtyimpactsimmuneresponsestomodernacovid19mrnavaccineinolderadults