Low performance of sinovac vaccine particularly with belatacept therapy in a study with different types of COVID-19 vaccines in transplanted patients

The huge impact of SARS-CoV-2 infections on organ transplant recipients makes it necessary to optimize vaccine efficacy in this population. To effectively implement multiple strategies, it is crucial to understand the performance of each type of available vaccine. In our study, the antibody titer wa...

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Autores:
Arias-Murillo, Jazmín Roció
Salinas-Nova, María Angélica
Caicedo, Tatiana
Galindo-Borda, Marisol
Meneses-Gil, Ximena
Montero, Camilo
Girón, Fernando
Pedraza, Nestor
Aroca, Gustavo
Ospina-Martínez, Martha Lucía
Mercado-Reyes, Marcela
Tipo de recurso:
Fecha de publicación:
2023
Institución:
Universidad Simón Bolívar
Repositorio:
Repositorio Digital USB
Idioma:
eng
OAI Identifier:
oai:bonga.unisimon.edu.co:20.500.12442/12114
Acceso en línea:
https://hdl.handle.net/20.500.12442/12114
https://doi.org/10.1016/j.transproceed.2023.02.034
https://www.sciencedirect.com/science/article/pii/S0041134523000696
Palabra clave:
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openAccess
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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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dc.title.eng.fl_str_mv Low performance of sinovac vaccine particularly with belatacept therapy in a study with different types of COVID-19 vaccines in transplanted patients
title Low performance of sinovac vaccine particularly with belatacept therapy in a study with different types of COVID-19 vaccines in transplanted patients
spellingShingle Low performance of sinovac vaccine particularly with belatacept therapy in a study with different types of COVID-19 vaccines in transplanted patients
title_short Low performance of sinovac vaccine particularly with belatacept therapy in a study with different types of COVID-19 vaccines in transplanted patients
title_full Low performance of sinovac vaccine particularly with belatacept therapy in a study with different types of COVID-19 vaccines in transplanted patients
title_fullStr Low performance of sinovac vaccine particularly with belatacept therapy in a study with different types of COVID-19 vaccines in transplanted patients
title_full_unstemmed Low performance of sinovac vaccine particularly with belatacept therapy in a study with different types of COVID-19 vaccines in transplanted patients
title_sort Low performance of sinovac vaccine particularly with belatacept therapy in a study with different types of COVID-19 vaccines in transplanted patients
dc.creator.fl_str_mv Arias-Murillo, Jazmín Roció
Salinas-Nova, María Angélica
Caicedo, Tatiana
Galindo-Borda, Marisol
Meneses-Gil, Ximena
Montero, Camilo
Girón, Fernando
Pedraza, Nestor
Aroca, Gustavo
Ospina-Martínez, Martha Lucía
Mercado-Reyes, Marcela
dc.contributor.author.none.fl_str_mv Arias-Murillo, Jazmín Roció
Salinas-Nova, María Angélica
Caicedo, Tatiana
Galindo-Borda, Marisol
Meneses-Gil, Ximena
Montero, Camilo
Girón, Fernando
Pedraza, Nestor
Aroca, Gustavo
Ospina-Martínez, Martha Lucía
Mercado-Reyes, Marcela
description The huge impact of SARS-CoV-2 infections on organ transplant recipients makes it necessary to optimize vaccine efficacy in this population. To effectively implement multiple strategies, it is crucial to understand the performance of each type of available vaccine. In our study, the antibody titer was measured, and the presence of antibodies against SARS-CoV-2 was evaluated after 90 days of immunization; furthermore, the differences between hybrid immunity, immunity by vaccination, and immunosuppressant type were identified. As a result, of the patients included in this study (n = 160), 53% showed antibodies against SARS-CoV-2 90 days after the first dose in patients who had completed the vaccination schedule. Antibody titers were higher in patients with hybrid immunity, and the proportion of nonresponsive patients was higher among those who received the immunosuppressant belatacept in their post-transplant regimen (P = .01). Only 15% of patients treated with this medicine seroconverted and patients vaccinated with Corona- Vac and treated with belatacept showed no response. In conclusion, a reduced response to vaccines against SARS-CoV-2 was identified in the transplant population, and this response varied with the type of vaccine administered and the immunosuppressive treatment.
publishDate 2023
dc.date.accessioned.none.fl_str_mv 2023-03-29T21:15:51Z
dc.date.available.none.fl_str_mv 2023-03-29T21:15:51Z
dc.date.issued.none.fl_str_mv 2023
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
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dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/article
dc.type.spa.spa.fl_str_mv Artículo científico
dc.identifier.citation.eng.fl_str_mv This research was funded by the National Institute of Health, project code CEMIN-19-2021, an investment project strengthening the coordination of blood banks and donation and transplant networks, national code BPIN-2018011000083, and resources of the hospitals with transplant programs participating.
dc.identifier.issn.none.fl_str_mv 18732623
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12442/12114
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.transproceed.2023.02.034
dc.identifier.url.none.fl_str_mv https://www.sciencedirect.com/science/article/pii/S0041134523000696
identifier_str_mv This research was funded by the National Institute of Health, project code CEMIN-19-2021, an investment project strengthening the coordination of blood banks and donation and transplant networks, national code BPIN-2018011000083, and resources of the hospitals with transplant programs participating.
18732623
url https://hdl.handle.net/20.500.12442/12114
https://doi.org/10.1016/j.transproceed.2023.02.034
https://www.sciencedirect.com/science/article/pii/S0041134523000696
dc.language.iso.eng.fl_str_mv eng
language eng
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eu_rights_str_mv openAccess
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dc.publisher.spa.fl_str_mv Elsevier
dc.source.none.fl_str_mv Vol. XX No. XX Año 2023
institution Universidad Simón Bolívar
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spelling Arias-Murillo, Jazmín Roció92dc0e81-028b-498a-84e8-f647ff0eaabcSalinas-Nova, María Angélicaa53281b2-9ab6-4172-b9f6-93e17b5b72ceCaicedo, Tatiana743025da-908f-4376-b208-6e78b3d582a3Galindo-Borda, Marisol4d516cca-b759-474d-887f-1ac48f878c5eMeneses-Gil, Ximena44e3006a-5948-44ab-a3f3-9ab74a33ef44Montero, Camilo065b8673-a76b-4053-a2c0-8cebf5e98c94Girón, Fernandoad1e6e84-6203-4069-a907-7fd2a0c0f294Pedraza, Nestor7a1d7ad2-c87e-40c2-ac44-eec38624e493Aroca, Gustavoe6bdfa35-1a1c-42aa-aee3-89159433d484Ospina-Martínez, Martha Lucía6bf92bb7-1918-4a05-a8b1-4aeed1e28b37Mercado-Reyes, Marcela4051c239-53db-43d2-8387-89d8d2d814e22023-03-29T21:15:51Z2023-03-29T21:15:51Z2023This research was funded by the National Institute of Health, project code CEMIN-19-2021, an investment project strengthening the coordination of blood banks and donation and transplant networks, national code BPIN-2018011000083, and resources of the hospitals with transplant programs participating.18732623https://hdl.handle.net/20.500.12442/12114https://doi.org/10.1016/j.transproceed.2023.02.034https://www.sciencedirect.com/science/article/pii/S0041134523000696The huge impact of SARS-CoV-2 infections on organ transplant recipients makes it necessary to optimize vaccine efficacy in this population. To effectively implement multiple strategies, it is crucial to understand the performance of each type of available vaccine. In our study, the antibody titer was measured, and the presence of antibodies against SARS-CoV-2 was evaluated after 90 days of immunization; furthermore, the differences between hybrid immunity, immunity by vaccination, and immunosuppressant type were identified. As a result, of the patients included in this study (n = 160), 53% showed antibodies against SARS-CoV-2 90 days after the first dose in patients who had completed the vaccination schedule. Antibody titers were higher in patients with hybrid immunity, and the proportion of nonresponsive patients was higher among those who received the immunosuppressant belatacept in their post-transplant regimen (P = .01). Only 15% of patients treated with this medicine seroconverted and patients vaccinated with Corona- Vac and treated with belatacept showed no response. In conclusion, a reduced response to vaccines against SARS-CoV-2 was identified in the transplant population, and this response varied with the type of vaccine administered and the immunosuppressive treatment.pdfengElsevierAttribution-NonCommercial-NoDerivatives 4.0 Internacionalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Vol. XX No. XX Año 2023Low performance of sinovac vaccine particularly with belatacept therapy in a study with different types of COVID-19 vaccines in transplanted patientsinfo:eu-repo/semantics/articleArtículo científicohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_2df8fbb1Pereira MR, Mohan S, Cohen DJ, et al. COVID-19 in solid organ transplant recipients: initial report from the US epicenter. Am J Transplant 2020;20:1800–8.TagedEndAkalin E, Azzi Y, Bartash R, et al. Covid-19 and kidney transplantation. N Engl J Med 2020;382:2475–7.TagedEndArias-Murillo YR, Benavides-V CA, Salinas-N MA, Osorio- Arango K, Plazas-Sierra C, Cortés JA. SARS-CoV2/COVID-19 infection in transplant recipients and patients on the transplant waiting list in Colombia. Transplant Proc 2021;53:1237–44.TagedEndMagicova M, Zahradka I, Fialova M, et al. Determinants of immune response to anti-SARS-CoV-2 mRNA vaccines in kidney transplant recipients: a prospective cohort study. Transplantation 2022;106:842–52.Sanders JF, Bemelman FJ, Messchendorp AL, et al. The RECOVAC immune-response study: the immunogenicity, tolerability, and safety of COVID-19 vaccination in patients with chronic kidney disease, on dialysis, or living with a kidney transplant. Transplantation 2022;106:821–34.Benotmane I, Gautier-Vargas G, Cognard N, et al. Weak anti- SARS-CoV-2 antibody response after the first injection of an mRNA COVID-19 vaccine in kidney transplant recipients. Kidney Int 2021;99:1487–9.TagedEndBoyarsky BJ, Werbel WA, Avery RK, et al. Antibody response to 2-dose SARS-CoV-2 mRNA vaccine series in solid organ transplant recipients. JAMA 2021;325:2204–6.TagedEndRozen-Zvi B, Yahav D, Agur T, et al. Antibody response to SARS-CoV-2 mRNA vaccine among kidney transplant recipients: a prospective cohort study. Clin Microbiol Infect 2021;27(1173):e1–.e4.TagedEndBenotmane I, Gautier-Vargas G, Cognard N, et al. Low immunization rates among kidney transplant recipients who received 2 doses of the mRNA-1273 SARS-CoV-2 vaccine. Kidney Int 2021;99:1498– 500.TagedEndHaskin O, Ashkenazi-Hoffnung L, Ziv N, et al. Serological response to the BNT162b2 COVID-19 mRNA vaccine in adolescent and young adult kidney transplant recipients. Transplantation 2021;105:e226–33.TagedEndCucchiari D, Egri N, Bodro M, et al. Cellular and humoral response after MRNA-1273 SARS-CoV-2 vaccine in kidney transplant recipients. Am J Transplant 2021;21:2727–39.TagedEndBalcells ME, Le Corre N, Dur an J, et al. Reduced immune response to inactivated SARS-CoV-2 vaccine in a cohort of immunocompromised patients in Chile. Clin Infect Dis 2022;75:e594–602.TagedEndMiele M, Bus a R, Russelli G, et al. Impaired anti-SARS-CoV-2 humoral and cellular immune response induced by Pfizer-BioNTech BNT162b2 mRNA vaccine in solid organ transplanted patients. Am J Transplant 2021;21:2919–21.TagedEndMarinaki S, Adamopoulos S, Degiannis D, et al. Immunogenicity of SARS-CoV-2 BNT162b2 vaccine in solid organ transplant recipients. Am J Transplant 2021;21:2913–5.Grupper A, Rabinowich L, Schwartz D, et al. Reduced humoral response to mRNA SARS-CoV-2 BNT162b2 vaccine in kidney transplant recipients without prior exposure to the virus. Am J Transplant 2021;21:2719–26.Hall VG, Ferreira VH, Ierullo M, et al. Humoral and cellular immune response and safety of two-dose SARS-CoV-2 mRNA-1273 vaccine in solid organ transplant recipients. Am J Transplant 2021;21:3980–9.TagedEndR€ossler A, Riepler L, Bante D, von Laer D, Kimpel J. SARSCoV- 2 omicron variant neutralization in serum from vaccinated and convalescent persons. N Engl J Med 2022;386:698–700.TagedEndEren Sadio glu R, Demir E, Evren E, et al. Antibody response to two doses of inactivated SARS-CoV-2 vaccine (CoronaVac) in kidney transplant recipients. Transpl Infect Dis 2021;23:e13740.TagedEndDheir H, Tocoglu A, Toptan H, et al. Short and mid-term SARS-CoV-2 antibody response afterinactivated COVID-19 vaccine in hemodialysis and kidneytransplant patients. J Med Virol 2022;94: 3176–83.TagedEndMariana S, Florencia R, Jose S, et al. Short and mid-term SARS-CoV-2 antibody response afterinactivated COVID-19 vaccine in hemodialysis and kidneytransplant patients. Clin Kidney J 2022;15: 527–33.Bruminhent J, Setthaudom C, Chaumdee P, et al. SARS-CoV- 2-specific humoral and cell-mediated immune responses after immunization with inactivated COVID-19 vaccine in kidney transplant recipients (CVIM 1 study). Am J Transplant 2022;22:813–22.Seija M, Rammauro F, Santiago J, et al. Short and mid-term SARS-CoV-2 antibody response afterinactivated COVID-19 vaccine in hemodialysis and kidney transplant patients. Clin Kidney J 2022;15: 527–33.TagedEndCorreia AL, Leal R, Pimenta AC, et al. The type of SARSCoV- 2 vaccine influences serological response in kidney transplant recipients. Clin Transplant 2022;36:e14585.TagedEndPrendecki M, Thomson T, Candice L, et al. Willicombe M in collaboration with the OSC. Comparison of humoral and cellular responses in kidney transplant recipients receiving BNT162b2 and ChAdOx1 SARS-CoV-2 vaccines. medRxiv, in press.Gangappa S, Wrammert J, Wang D, et al. Kinetics of antibody response to influenza vaccination in renal transplant recipients. Transpl Immunol 2019;53:51–60.TagedEndOu MT, Boyarsky BJ, Chiang TPY, et al. Immunogenicity and reactogenicity after SARS-CoV-2 mRNA vaccination in kidney transplant recipients taking Belatacept. Transplantation 2021;105:2119–23.Chavarot N, Ouedrani A, Marion O, et al. Poor anti-SARSCoV- 2 humoral and T-cell responses after 2 injections of mRNA vaccine in kidney transplant recipients treated with Belatacept. Transplantation 2021;105:e94–5.TagedEndAbravanel F, Marion O, Del Bello A, et al. Humoral and cellular immune responses of solid organ transplant patients on Belatacept to three doses of mRNA-based anti-SARS-CoV-2 vaccine. Vaccines (Basel) 2022;10:354.TagedEndNoble J, LangelloA, Bouchut W, Lupo J, Lombardo D, Rostaing L. Immune response post−SARS-CoV-2 mRNA vaccination in kidney transplant recipients receiving Belatacept. Transplantation 2021;105:e259–60.Hammerman A, Sergienko R, Friger M, et al. Effectiveness of the BNT162b2 vaccine after recovery from Covid-19. 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