Cited by 126SARS-CoV-2 and COVID-19 ResearchTransplantation: Methods and OutcomesCOVID-19 Clinical Research Studies

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

BNT162b2 vaccination in heart transplant recipients: Clinical experience and antibody response

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Abstract

Background Data on the safety and efficacy of SARS-CoV-2 vaccines in immunocompromised populations are sparse. Methods We conducted a prospective study of 77 heart transplant (HT) recipients vaccinated with two doses of BNT162b2 vaccine and monitored for adverse events following both doses, the receptor-binding domain (RBD) IgG response, and neutralizing antibodies. Results BNT162b2 vaccination was associated with a low rate of adverse events, characterized mostly by pain at the injection site. By a mean 41 days post second dose there were no clinical episodes of rejection, as suggested by a troponin leak or allograft dysfunction. At a mean 21 days following the second dose, IgG anti-RBD antibodies were detectable in 14 (18%) HT recipients. Immune sera neutralized SARS-CoV-2 pseudo-virus in 8 (57%) of those with IgG anti-RBD antibodies. Immunosuppressive regimen containing mycophenolic acid was associated with lower odds of an antibody response (OR = 0.12, p = 0.042). Conclusions Whether a longer time-frame for observation of an antibody response is required after vaccination in immunosuppressed individuals remains unknown.

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Crossref · 10.1016/j.healun.2021.04.003

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  • Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine

    Polack, F. P., Thomas, S. J., Kitchin, N., Absalon, J., Gurtman, A., Lockhart, S., Perez, J. L., Pérez Marc, G., Moreira, E. D., Zerbini, C., et al. (2020) · New England Journal of Medicine · doi:10.1056/nejmoa2034577 · Cited by 14,592 · cited 1×

    “4% reported at least one systemic reaction.(1) In the nontransplant population, the BNT162b2 vaccine elicits antibody responses against the RBD, and plasma binding and neutralizing activity of the vaccine against SARS-CoV-2 has been demonstrated.”

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Research works printed but not linked: 8

  1. Voysey, 2021, Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against SARS-CoV-2: an interim analysis of four randomised controlled trials in Brazil, South Africa, and the UK, Lancet, 397, 99, 10.1016/S0140-6736(20)32661-1 · DOI · Paper page
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Metadata

Authors
Peled, Y., Ram, E., Lavee, J., Sternik, L., Segev, A., Wieder-Finesod, A., Mandelboim, M., Indenbaum, V., Levy, I., Raanani, E., Lustig, Y., & Rahav, G.
Affiliations
  • Tel Aviv University (IL)
  • Israel Ministry of Health (IL)
Corresponding author
Peled, Yael
Venue
The Journal of Heart and Lung Transplantation
Publisher
Elsevier BV
Published
2021-08
Volume
40
Issue
8
Pages
759-762
ISSN
1053-2498 (ISSN-L)
OpenAlex
W3154374447
Cited by
126
References
1
Citations by year
2025: 5 · 2024: 7 · 2023: 20 · 2022: 54 · 2021: 40
FWCI
9.58
Type
journal article
Language
en
Open access
Locations
  • The Journal of Heart and Lung Transplantation (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Health Sciences › Medicine › Surgery › Transplantation: Methods and Outcomes
  • Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
Keywords
BNT162b2, heart transplant recipients, COVID-19 vaccination, immunosuppression, mycophenolic acid, antibody response, neutralizing antibodies, receptor-binding domain IgG, vaccine safety, adverse events, allograft rejection, immunocompromised patients
MeSH terms
COVID-19, COVID-19 Vaccines, BNT162 Vaccine, Aged, Antibody Formation, Female, Humans, Immunosuppression Therapy, Male, Middle Aged, Postoperative Complications, Prospective Studies, Heart Transplantation

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