Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months

SARS-CoV-2 vaccines have shown very high effectiveness in real-world scenarios. However, there is compelling evidence for a fast-paced waning of immunity. The increasing number of new variants that could alter the severity, transmissibility, and potential to evade the immune response raised signific...

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Autores:
Lopera, Tulio J.
Chvatal-Medina, Mateo
Flórez-Álvarez, Lizdany
Zapata-Cardona, Maria I.
Taborda, Natalia A.
Rugeles, Maria T.
Hernández López, Juan Carlos
Tipo de recurso:
Article of investigation
Fecha de publicación:
2022
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
Idioma:
OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/45974
Acceso en línea:
https://hdl.handle.net/20.500.12494/45974
Palabra clave:
SARS-CoV-2
vaccine
neutralizing antibodies
immunity
immunogenicity
variant
Rights
openAccess
License
Atribución
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dc.title.spa.fl_str_mv Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months
title Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months
spellingShingle Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months
SARS-CoV-2
vaccine
neutralizing antibodies
immunity
immunogenicity
variant
title_short Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months
title_full Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months
title_fullStr Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months
title_full_unstemmed Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months
title_sort Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months
dc.creator.fl_str_mv Lopera, Tulio J.
Chvatal-Medina, Mateo
Flórez-Álvarez, Lizdany
Zapata-Cardona, Maria I.
Taborda, Natalia A.
Rugeles, Maria T.
Hernández López, Juan Carlos
dc.contributor.author.none.fl_str_mv Lopera, Tulio J.
Chvatal-Medina, Mateo
Flórez-Álvarez, Lizdany
Zapata-Cardona, Maria I.
Taborda, Natalia A.
Rugeles, Maria T.
Hernández López, Juan Carlos
dc.subject.spa.fl_str_mv SARS-CoV-2
vaccine
neutralizing antibodies
immunity
immunogenicity
variant
topic SARS-CoV-2
vaccine
neutralizing antibodies
immunity
immunogenicity
variant
description SARS-CoV-2 vaccines have shown very high effectiveness in real-world scenarios. However, there is compelling evidence for a fast-paced waning of immunity. The increasing number of new variants that could alter the severity, transmissibility, and potential to evade the immune response raised significant concern. Therefore, elucidating changes in the humoral immune response against viral variants induced by vaccines over time is crucial for improving immunization protocols. We carried out a 6-month longitudinal prospective study in which 60 individuals between 21 and 71 years of age who have received the complete scheme of the BNT162b2 vaccine were followed to determine titers of serum neutralizing activity. The neutralizing capacity was measured at one, three, and six-months post-vaccination by plaque reduction neutralization assay using SARS-CoV-2 B.1 (D614G) and the Gamma, Alpha, Delta, and Mu variants. Data were analyzed using GraphPad 5.0. Neutralizing activity against five different SARS-CoV-2 variants was detected in the serum samples of all vaccinated participants to a different extent after one month, with a progressive decrease according to age and gender. Overall, after one month of vaccination, the neutralizing titer was lower for all evaluated variants when compared to B.1, most remarkable against Delta and Mu, with a reduction of 83.1% and 92.3%, respectively. In addition, the Titer at 3- or 6-months follow-up decreased dramatically for all variants. Our results support the decaying of serum neutralizing activity, both over time and across SARS-CoV-2 variants, being more significant in older men. Since Delta and Mu appear to evade the neutralizing activity, these and further new variants of immune escape mutations should be considered for novel vaccine formulations.
publishDate 2022
dc.date.accessioned.none.fl_str_mv 2022-07-31T17:33:50Z
dc.date.available.none.fl_str_mv 2022-07-31T17:33:50Z
dc.date.issued.none.fl_str_mv 2022-05-02
dc.type.none.fl_str_mv Artículos Científicos
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dc.identifier.bibliographicCitation.spa.fl_str_mv Lopera TJ, Chvatal-Medina M, Flórez-Álvarez L, Zapata-Cardona MI, Taborda NA, Rugeles MT, Hernandez JC. Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months. Front Immunol. 2022 May 2;13:879036. doi: 10.3389/fimmu.2022.879036. PMID: 35585980; PMCID: PMC9108166.
identifier_str_mv 10.3389/fimmu.2022.879036. PMID: 35585980
Lopera TJ, Chvatal-Medina M, Flórez-Álvarez L, Zapata-Cardona MI, Taborda NA, Rugeles MT, Hernandez JC. Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months. Front Immunol. 2022 May 2;13:879036. doi: 10.3389/fimmu.2022.879036. PMID: 35585980; PMCID: PMC9108166.
url https://hdl.handle.net/20.500.12494/45974
dc.relation.ispartofjournal.spa.fl_str_mv Frontiers in Immunology
dc.relation.references.spa.fl_str_mv 1. Johns Hopkins University & Medicine. COVID-19 Map - Johns Hopkins Coronavirus Resource Center. Johns Hopkins Coronavirus Resour Cent, Baltimore, Maryland (2020)
2. Polack FP, Thomas SJ, Kitchin N, Absalon J, Gurtman A, Lockhart S, et al. Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine. N Engl J Med (2020) 383:2603–15. doi: 10.1056/NEJMoa2034577
3. Baden LR, El Sahly HM, Essink B, Kotloff K, Frey S, Novak R, et al. Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine. N Engl J Med (2020) 384:403–16. doi: 10.1056/NEJMoa2035389
4. Tartof SY, Slezak JM, Fischer H, Hong V, Ackerson BK, Ranasinghe ON, et al. Effectiveness of mRNA BNT162b2 COVID-19 Vaccine Up to 6 Months in a Large Integrated Health System in the USA: A Retrospective Cohort Study. Lancet (London England) (2021) 398:1407–16. doi: 10.1016/S0140-6736(21) 02183-8
5. World Health Organization. Tracking SARS-CoV-2 Variants. WHO, Ginebra, Swizertland, (2021). Available at: https://www.who.int/en/activities/trackingSARS-Co
6. Romano M, Ruggiero A, Squeglia F, Maga G, Berisio R. A Structural View of SARS-CoV-2 RNA Replication Machinery: RNA Synthesis, Proofreading and Final Capping. Cells (2020) 9(5):1267. doi: 10.3390/cells9051267
7. Harvey WT, Carabelli AM, Jackson B, Gupta RK, Thomson EC, Harrison EM, et al. SARS-CoV-2 Variants, Spike Mutations and Immune Escape. Nat Rev Microbiol (2021) 19:409–24. doi: 10.1038/s41579-021-00573-0
8. Lopez Bernal J, Andrews N, Gower C, Gallagher E, Simmons R, Thelwall S, et al. Effectiveness of Covid-19 Vaccines Against the B.1.617.2 (Delta) Variant. N Engl J Med (2021) 385:585–94. doi: 10.1056/NEJMoa2108891
9. Folegatti PM, Ewer KJ, Aley PK, Angus B, Becker S, Belij-Rammerstorfer S, et al. Safety and Immunogenicity of the ChAdOx1 Ncov-19 Vaccine Against SARS-CoV-2: A Preliminary Report of a Phase 1/2, Single-Blind, Randomised Controlled Trial. Lancet (2020) 396:467–78. doi: 10.1016/S0140-6736(20) 31604-4
10. Chvatal-Medina M, Mendez-Cortina Y, Patiño PJ, Velilla PA, Rugeles MT. Antibody Responses in COVID-19: A Review. Front Immunol (2021) 12:633184. doi: 10.3389/fimmu.2021.633184
11. Altawalah H. Antibody Responses to Natural SARS-CoV-2 Infection or After COVID-19 Vaccination. Vaccines (2021) 9(8):910. doi: 10.3390/ vaccines9080910
12. Poonia B, Kottilil S. Immune Correlates of COVID-19 Control. Front Immunol (2020) 11:569611. doi: 10.3389/fimmu.2020.569611
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dc.publisher.spa.fl_str_mv Universidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Programa de Medicina, Medellín y Envigado, Colombia, 00000
dc.publisher.program.spa.fl_str_mv Medicina
dc.publisher.place.spa.fl_str_mv Medellín
institution Universidad Cooperativa de Colombia
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spelling Lopera, Tulio J.Chvatal-Medina, MateoFlórez-Álvarez, LizdanyZapata-Cardona, Maria I.Taborda, Natalia A.Rugeles, Maria T.Hernández López, Juan Carlos132022-07-31T17:33:50Z2022-07-31T17:33:50Z2022-05-0210.3389/fimmu.2022.879036. PMID: 35585980https://hdl.handle.net/20.500.12494/45974Lopera TJ, Chvatal-Medina M, Flórez-Álvarez L, Zapata-Cardona MI, Taborda NA, Rugeles MT, Hernandez JC. Humoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six Months. Front Immunol. 2022 May 2;13:879036. doi: 10.3389/fimmu.2022.879036. PMID: 35585980; PMCID: PMC9108166.SARS-CoV-2 vaccines have shown very high effectiveness in real-world scenarios. However, there is compelling evidence for a fast-paced waning of immunity. The increasing number of new variants that could alter the severity, transmissibility, and potential to evade the immune response raised significant concern. Therefore, elucidating changes in the humoral immune response against viral variants induced by vaccines over time is crucial for improving immunization protocols. We carried out a 6-month longitudinal prospective study in which 60 individuals between 21 and 71 years of age who have received the complete scheme of the BNT162b2 vaccine were followed to determine titers of serum neutralizing activity. The neutralizing capacity was measured at one, three, and six-months post-vaccination by plaque reduction neutralization assay using SARS-CoV-2 B.1 (D614G) and the Gamma, Alpha, Delta, and Mu variants. Data were analyzed using GraphPad 5.0. Neutralizing activity against five different SARS-CoV-2 variants was detected in the serum samples of all vaccinated participants to a different extent after one month, with a progressive decrease according to age and gender. Overall, after one month of vaccination, the neutralizing titer was lower for all evaluated variants when compared to B.1, most remarkable against Delta and Mu, with a reduction of 83.1% and 92.3%, respectively. In addition, the Titer at 3- or 6-months follow-up decreased dramatically for all variants. Our results support the decaying of serum neutralizing activity, both over time and across SARS-CoV-2 variants, being more significant in older men. Since Delta and Mu appear to evade the neutralizing activity, these and further new variants of immune escape mutations should be considered for novel vaccine formulations.https://scienti.minciencias.gov.co/cvlac/visualizador/generarCurriculoCv.do?cod_rh=0000283088http://orcid.org/0000-0002-9200-5698https://scienti.colciencias.gov.co/gruplac/jsp/visualiza/visualizagr.jsp?nro=00000000011355juankhernandez@gmail.comUniversidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Programa de Medicina, Medellín y Envigado, Colombia, 00000MedicinaMedellínSARS-CoV-2vaccineneutralizing antibodiesimmunityimmunogenicityvariantHumoral Response to BNT162b2 Vaccine Against SARS-CoV-2 Variants Decays After Six MonthsArtículos Científicoshttp://purl.org/coar/resource_type/c_2df8fbb1http://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articlehttp://purl.org/redcol/resource_type/ARTinfo:eu-repo/semantics/publishedVersionAtribucióninfo:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Frontiers in Immunology1. Johns Hopkins University & Medicine. COVID-19 Map - Johns Hopkins Coronavirus Resource Center. Johns Hopkins Coronavirus Resour Cent, Baltimore, Maryland (2020)2. Polack FP, Thomas SJ, Kitchin N, Absalon J, Gurtman A, Lockhart S, et al. Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine. N Engl J Med (2020) 383:2603–15. doi: 10.1056/NEJMoa20345773. Baden LR, El Sahly HM, Essink B, Kotloff K, Frey S, Novak R, et al. Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine. N Engl J Med (2020) 384:403–16. doi: 10.1056/NEJMoa20353894. Tartof SY, Slezak JM, Fischer H, Hong V, Ackerson BK, Ranasinghe ON, et al. Effectiveness of mRNA BNT162b2 COVID-19 Vaccine Up to 6 Months in a Large Integrated Health System in the USA: A Retrospective Cohort Study. Lancet (London England) (2021) 398:1407–16. doi: 10.1016/S0140-6736(21) 02183-85. World Health Organization. Tracking SARS-CoV-2 Variants. WHO, Ginebra, Swizertland, (2021). Available at: https://www.who.int/en/activities/trackingSARS-Co6. Romano M, Ruggiero A, Squeglia F, Maga G, Berisio R. A Structural View of SARS-CoV-2 RNA Replication Machinery: RNA Synthesis, Proofreading and Final Capping. Cells (2020) 9(5):1267. doi: 10.3390/cells90512677. Harvey WT, Carabelli AM, Jackson B, Gupta RK, Thomson EC, Harrison EM, et al. SARS-CoV-2 Variants, Spike Mutations and Immune Escape. Nat Rev Microbiol (2021) 19:409–24. doi: 10.1038/s41579-021-00573-08. Lopez Bernal J, Andrews N, Gower C, Gallagher E, Simmons R, Thelwall S, et al. Effectiveness of Covid-19 Vaccines Against the B.1.617.2 (Delta) Variant. N Engl J Med (2021) 385:585–94. doi: 10.1056/NEJMoa21088919. Folegatti PM, Ewer KJ, Aley PK, Angus B, Becker S, Belij-Rammerstorfer S, et al. Safety and Immunogenicity of the ChAdOx1 Ncov-19 Vaccine Against SARS-CoV-2: A Preliminary Report of a Phase 1/2, Single-Blind, Randomised Controlled Trial. Lancet (2020) 396:467–78. doi: 10.1016/S0140-6736(20) 31604-410. Chvatal-Medina M, Mendez-Cortina Y, Patiño PJ, Velilla PA, Rugeles MT. Antibody Responses in COVID-19: A Review. Front Immunol (2021) 12:633184. doi: 10.3389/fimmu.2021.63318411. Altawalah H. Antibody Responses to Natural SARS-CoV-2 Infection or After COVID-19 Vaccination. Vaccines (2021) 9(8):910. doi: 10.3390/ vaccines908091012. Poonia B, Kottilil S. Immune Correlates of COVID-19 Control. 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