Evidence map›Paper›PMID 36151076›Full record

ArticleNature communications2022

Accumulation of mutations in antibody and CD8 T cell epitopes in a B cell depleted lymphoma patient with chronic SARS-CoV-2 infection.

Elham Khatamzas, Markus H Antwerpen, Alexandra Rehn, Alexander Graf, Johannes Christian Hellmuth, Alexandra Hollaus, Anne-Wiebe Mohr, Erik Gaitzsch, Tobias Weiglein, Enrico Georgi and 20 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

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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

30 authors at 7 institutions in 1 country.

Elham Khatamzas *Department of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany. elham.khatamzas@med.uni-heidelberg.de.ORCID 0000-0001-9253-1340
Markus H Antwerpen *Bundeswehr, Institute of Microbiology Munich, Munich, Germany.ORCID 0000-0003-4013-8808
Alexandra RehnBundeswehr, Institute of Microbiology Munich, Munich, Germany.
Alexander GrafLaboratory for Functional Genome Analysis, Gene Center, Ludwig-Maximilians University Munich, Munich, Germany.
Johannes Christian HellmuthDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.ORCID 0000-0001-8409-3037
Alexandra HollausDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
Anne-Wiebe MohrDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.ORCID 0000-0002-5544-4595
Erik GaitzschDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
Tobias WeigleinDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
Enrico GeorgiBundeswehr, Institute of Microbiology Munich, Munich, Germany.
Clemens SchererCOVID-19 Registry of the LMU Munich (CORKUM), University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.ORCID 0000-0003-2816-6793
Stephanie-Susanne StecherDepartment of Medicine II, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.ORCID 0000-0001-6715-1020
Stefanie GruetznerInstitute for Transfusion Medicine and Haemostasis, Medical Faculty, University of Augsburg, Augsburg, Germany.
Helmut BlumLaboratory for Functional Genome Analysis, Gene Center, Ludwig-Maximilians University Munich, Munich, Germany.ORCID 0000-0002-3994-2332
Stefan KrebsLaboratory for Functional Genome Analysis, Gene Center, Ludwig-Maximilians University Munich, Munich, Germany.
Anna ReischerDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
Alexandra LeutbecherDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
Marion SubkleweDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
Andrea DickLaboratory for Immunogenetics, University of Munich, LMU, Munich, Germany.
Sabine ZangeBundeswehr, Institute of Microbiology Munich, Munich, Germany.ORCID 0000-0001-8721-9248
Philipp GirlBundeswehr, Institute of Microbiology Munich, Munich, Germany.ORCID 0000-0003-1370-4114
Katharina MüllerBundeswehr, Institute of Microbiology Munich, Munich, Germany.ORCID 0000-0002-2890-7515
Oliver WeigertDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.ORCID 0000-0002-0987-7373
Karl-Peter HopfnerGene Center and Department of Biochemistry, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID 0000-0002-4528-8357
Hans-Joachim StemmlerDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
Michael von Bergwelt-BaildonDepartment of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
Oliver T KepplerCOVID-19 Registry of the LMU Munich (CORKUM), University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.ORCID 0000-0002-1384-8946
Roman WölfelBundeswehr, Institute of Microbiology Munich, Munich, Germany.ORCID 0000-0002-8756-7821
Maximilian Muenchhoff *COVID-19 Registry of the LMU Munich (CORKUM), University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.ORCID 0000-0001-7016-0470
Andreas Moosmann *Department of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.ORCID 0000-0001-8044-5146
Ludwig-Maximilians-Universität München · DEUniversität der Bundeswehr München · DEGerman Center for Infection Research · DEDeutschen Konsortium für Translationale Krebsforschung · DEImmungenetics (Germany) · DEUniversity Hospital Heidelberg · DEUniversity of Augsburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibodies against the spike protein of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) can drive adaptive evolution in immunocompromised patients with chronic infection. Here we longitudinally analyze SARS-CoV-2 sequences in a B cell-depleted, lymphoma patient with chronic, ultimately fatal infection, and identify three mutations in the spike protein that dampen convalescent plasma-mediated neutralization of SARS-CoV-2. Additionally, four mutations emerge in non-spike regions encoding three CD8 T cell epitopes, including one nucleoprotein epitope affected by two mutations. Recognition of each mutant peptide by CD8 T cells from convalescent donors is reduced compared to its ancestral peptide, with additive effects resulting from double mutations. Querying public SARS-CoV-2 sequences shows that these mutations have independently emerged as homoplasies in circulating lineages. Our data thus suggest that potential impacts of CD8 T cells on SARS-CoV-2 mutations, at least in those with humoral immunodeficiency, warrant further investigation to inform on vaccine design.

Indexed as

COVID-19LymphomaVaccinesCD8-Positive T-LymphocytesCOVID-19 SerotherapyEpitopes, T-LymphocyteHumansImmunization, PassiveMutationNucleoproteinsPeptidesSARS-CoV-2Spike Glycoprotein, CoronavirusEpitopes, T-LymphocyteNucleoproteinsPeptidesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vaccines

Identifiers

PMID36151076
PMCPMC9508331
OpenAlexW4297012035

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.