Evidence map›Paper›PMID 34085278›Full record

Trial reportBritish journal of haematology2021

Single dose of BNT162b2 mRNA vaccine against severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) induces neutralising antibody and polyfunctional T-cell responses in patients with chronic myeloid leukaemia.

Patrick Harrington, Katie J Doores, Deepti Radia, Amy O'Reilly, Ho Pui Jeff Lam, Jeffrey Seow, Carl Graham, Thomas Lechmere, Donal McLornan, Richard Dillon and 11 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in British journal of haematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 7 pooled it
4.0field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 7 syntheses or guidelines pooled it, 62 citations in OpenAlex.

  1. Pooled it
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  3. Pooled it
  4. Guideline
  5. Pooled it
  6. Pooled it
  7. Pooled it
  8. Review
  9. Article
  10. The characterization of CD8Emerging microbes & infections · 2024
    Review
  11. Review
  12. mRNA vaccines and their delivery strategies: A journey from infectious diseases to cancer.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. mRNA Vaccines against SARS-CoV-2: Advantages and Caveats.International journal of molecular sciences · 2023
    Review
  18. Review
  19. Impact of the COVID-19 pandemic on the diagnosis and treatment of onco-hematologic patients: a discussion paper.Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2023
    Review
  20. 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

21 authors at 2 institutions in 1 country.

Patrick HarringtonDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0001-5704-466X
Katie J DooresDepartment of Infectious Diseases, School of Immunology and Microbial Sciences, King's College London, London, UK.
Deepti RadiaDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0002-3578-0102
Amy O'ReillyDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Ho Pui Jeff LamDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Jeffrey SeowDepartment of Infectious Diseases, School of Immunology and Microbial Sciences, King's College London, London, UK.
Carl GrahamDepartment of Infectious Diseases, School of Immunology and Microbial Sciences, King's College London, London, UK.
Thomas LechmereDepartment of Infectious Diseases, School of Immunology and Microbial Sciences, King's College London, London, UK.
Donal McLornanDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0003-1224-091X
Richard DillonDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Yogita ShanmugharajDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Andreas EspehanaDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Claire WoodleyDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Jamie SaundersDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Natalia Curto-GarciaDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0003-1437-4583
Jennifer O'SullivanDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0003-0502-7133
Kavita RajDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Shahram KordastiDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Michael H MalimDepartment of Infectious Diseases, School of Immunology and Microbial Sciences, King's College London, London, UK.
Claire HarrisonDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Hugues de LavalladeDepartment of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0002-4988-2564
King's College London · GBGuy's and St Thomas' NHS Foundation Trust · GB

Funding

Blood Cancer UK
6 · The paper itself

Abstract

Patients receiving targeted cancer treatments such as tyrosine kinase inhibitors (TKIs) have been classified in the clinically extremely vulnerable group to develop severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), including patients with chronic myeloid leukaemia (CML) taking TKIs. In addition, concerns that immunocompromised individuals with solid and haematological malignancies may not mount an adequate immune response to a single dose of SARS-CoV-2 BNT162b2 (Pfizer-BioNTech) vaccine have been raised. In the present study, we evaluated humoral and cellular immune responses after a first injection of BNT162b2 vaccine in 16 patients with CML. Seroconversion and cellular immune response before and after vaccination were assessed. By day 21 after vaccination, anti-Spike immunoglobulin G was detected in 14/16 (87·5%) of the patients with CML and all developed a neutralising antibody response [serum dilution that inhibits 50% infection (ID

Indexed as

COVID-19AdultAgedAntibodies, NeutralizingAntibodies, ViralBNT162 VaccineCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCOVID-19 VaccinesFemaleHematologic NeoplasmsHumansImmunity, CellularImmunoglobulin GLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleAntibodies, NeutralizingAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesImmunoglobulin GProtein Kinase InhibitorsSpike Glycoprotein, CoronavirusBNT162b2 vaccinechronic myeloid leukaemiaSARS-CoV2 vaccinetyrosine kinase inhibitor

Identifiers

PMID34085278
PMCPMC8239833
OpenAlexW3164216481

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.