Evidence map›Paper›PMID 35254660›Full record

ArticleBritish journal of haematology2022

Rituximab-treated patients with lymphoma develop strong CD8 T-cell responses following COVID-19 vaccination.

Jon Riise, Saskia Meyer, Isaac Blaas, Adity Chopra, Trung T Tran, Marina Delic-Sarac, Malu Lian Hestdalen, Ellen Brodin, Even Holth Rustad, Ke-Zheng Dai and 12 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of haematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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  18. B-cell malignancies and COVID-19: a narrative review.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2023
    Review
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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

22 authors at 6 institutions in 1 country.

Jon RiiseDepartment of Oncology, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-0024-0093
Saskia MeyerDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Isaac BlaasDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Adity ChopraDepartment of Immunology, Oslo University Hospital, Oslo, Norway.
Trung T TranDepartment of Immunology, Oslo University Hospital, Oslo, Norway.
Marina Delic-SaracDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Malu Lian HestdalenDepartment of Hematology, Division of Medicine, Akershus University Hospital, Lørenskog, Norway.
Ellen BrodinHematological Research Group, Division of Medicine, Akershus University Hospital, Lørenskog, Norway.
Even Holth RustadDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Ke-Zheng DaiDepartment of Immunology, Oslo University Hospital, Oslo, Norway.
John Torgils VaageInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Lise Sofie Haug Nissen-MeyerDepartment of Immunology, Oslo University Hospital, Oslo, Norway.
Fredrik SundDepartment of Oncology, University Hospital of North Norway, Tromsø, Norway.
Karin F WaderDepartment of Oncology, St Olav University Hospital, Trondheim, Norway.
Anne T BjornevikDepartment of Oncology, Haukeland University Hospital, Bergen, Norway.
Peter A MeyerDepartment of Oncology and Hematology, Stavanger University Hospital, Stavanger, Norway.
Gro O NygaardDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
Marton KönigDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
Sigbjørn SmelandInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Fridtjof Lund-JohansenDepartment of Immunology, Oslo University Hospital, Oslo, Norway.
Johanna OlweusDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Arne KolstadDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
Oslo University Hospital · NOAkershus University Hospital · NOHaukeland University Hospital · NOStavanger University Hospital · NOSt Olav's University Hospital · NOUniversity Hospital of North Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B-cell depletion induced by anti-cluster of differentiation 20 (CD20) monoclonal antibody (mAb) therapy of patients with lymphoma is expected to impair humoral responses to severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) vaccination, but effects on CD8 T-cell responses are unknown. Here, we investigated humoral and CD8 T-cell responses following two vaccinations in patients with lymphoma undergoing anti-CD20-mAb therapy as single agent or in combination with chemotherapy or other anti-neoplastic agents during the last 9 months prior to inclusion, and in healthy age-matched blood donors. Antibody measurements showed that seven of 110 patients had antibodies to the receptor-binding domain of the SARS-CoV-2 Spike protein 3-6 weeks after the second dose of vaccination. Peripheral blood CD8 T-cell responses against prevalent human leucocyte antigen (HLA) class I SARS-CoV-2 epitopes were determined by peptide-HLA multimer analysis. Strong CD8 T-cell responses were observed in samples from 20/29 patients (69%) and 12/16 (75%) controls, with similar median response magnitudes in the groups and some of the strongest responses observed in patients. We conclude that despite the absence of humoral immune responses in fully SARS-CoV-2-vaccinated, anti-CD20-treated patients with lymphoma, their CD8 T-cell responses reach similar frequencies and magnitudes as for controls. Patients with lymphoma on B-cell depleting therapies are thus likely to benefit from current coronavirus disease 2019 (COVID-19) vaccines, and development of vaccines aimed at eliciting T-cell responses to non-Spike epitopes might provide improved protection.

Indexed as

CD8-Positive T-LymphocytesCOVID-19COVID-19 VaccinesLymphomaRituximabAntibodies, ViralEpitopesHumansSARS-CoV-2Spike Glycoprotein, CoronavirusVaccinationAntibodies, ViralCOVID-19 VaccinesEpitopesRituximabSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2anti-CD20 antibodyCD8 T-cell responsecoronavirus disease 2019 (COVID-19) vaccinationhumoral responselymphomasevere acute respiratory syndrome coronavirus-2 (SARS-CoV-2) epitopes

Identifiers

PMID35254660
PMCPMC9111866
OpenAlexW4221059978

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.