Evidence map›Paper›PMID 36592547›Full record

Observational studyJournal of clinical virology : the official publication of the Pan American Society for Clinical Virology2023

Comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study.

Ji-Man Kang, Juhan Lee, Kyu Ha Huh, Dong Jin Joo, Jae Geun Lee, Ha Yan Kim, Myeongjee Lee, Inkyung Jung, Min Young Kim, Sinyoung Kim and 2 more

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Ji-Man KangDepartment of Pediatrics, Severance Children's Hospital, Yonsei University College of Medicine, Seoul, Korea (the Republic of); Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, Korea (the Republic of). Electronic address: umi87c@yuhs.ac.
Juhan LeeDepartment of Surgery, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea (the Republic of); The Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Kyu Ha HuhDepartment of Surgery, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea (the Republic of); The Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Dong Jin JooDepartment of Surgery, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea (the Republic of); The Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Jae Geun LeeDepartment of Surgery, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea (the Republic of); The Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Ha Yan KimBiostatistics Collaboration Unit, Department of Biomedical Systems Informatics, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Myeongjee LeeBiostatistics Collaboration Unit, Department of Biomedical Systems Informatics, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Inkyung JungDivision of Biostatistics, Department of Biomedical Systems Informatics, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Min Young KimDepartment of Pediatrics, Severance Children's Hospital, Yonsei University College of Medicine, Seoul, Korea (the Republic of); Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Sinyoung KimDepartment of Laboratory Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Younhee ParkDepartment of Laboratory Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea (the Republic of). Electronic address: younheep@yuhs.ac.
Myoung Soo KimDepartment of Surgery, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea (the Republic of); The Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea (the Republic of).. Electronic address: ysms91@yuhs.ac.
Yonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSolid organ transplant recipients (SOTRs) are susceptible to severe coronavirus disease 2019 (COVID-19); however, immunogenicity studies of the Omicron variants per vaccination schedules are still lacking. We examined humoral immunogenicity following third-dose mRNA vaccine administration in Korean SOTRs who received primary COVID-19 vaccine series on homologous or heterologous schedules.

methodsWe recruited SOTRs at Severance Hospital from October 27, 2021, to March 31, 2022. Blood samples were collected between 14 days and 5 months after the second and third mRNA vaccine (BNT162b2 or mRNA-1273) doses. SARS-CoV-2 anti-spike IgG titer was analyzed. The neutralization inhibition rate was analyzed using the surrogate neutralization assay for the wild-type, Delta, and Omicron variants.

resultsNo significant differences existed in the SARS-CoV-2 anti-spike IgG positivity rate between the homologous BNT162b2/BNT162b2/BNT162b2 (85%) and other heterologous groups (83% of ChAdOx1/ChAdOx1/BNT162b2, 90% of ChAdOx1/ChAdOx1/mRNA-1273, and 78% of ChAdOx1/BNT162b2/BNT162b2). No significant difference existed in the neutralization inhibition rates between the four groups for wild-type, Delta, and Omicron variants. Median neutralization inhibition rates against the Omicron variant (2-5%) were significantly lower than those against the wild-type (87-97%) and Delta (55-89%) variants (P < 0.001).

conclusionsRegardless of the schedule, the neutralization inhibition rate against the Omicron variant was poor; therefore, additional preventive measures are required in such high-risk populations.

Indexed as

COVID-19Organ Transplantation2019-nCoV Vaccine mRNA-1273Antibodies, NeutralizingAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesHumansImmunoglobulin GmRNA VaccinesSARS-CoV-2Transplant RecipientsVaccination2019-nCoV Vaccine mRNA-1273Antibodies, NeutralizingAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesImmunoglobulin GmRNA VaccinesCOVID-19 vaccineHeterologousKoreaOmicronOrgan transplantationSARS-CoV-2 variants

Identifiers

PMID36592547
PMCPMC9800015
OpenAlexW4313398561

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.