Evidence map›Paper›PMID 36439376›Full record

ArticleiScience2022

Increased soluble HLA in COVID-19 present a disease-related, diverse immunopeptidome associated with T cell immunity.

Annika Nelde, Jonas Rieth, Malte Roerden, Marissa L Dubbelaar, Naomi Hoenisch Gravel, Jens Bauer, Reinhild Klein, Tobias Hoheisel, Hartmut Mahrhofer, Siri Göpel and 5 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 11 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

15 authors at 3 institutions in 1 country.

Annika NeldeDepartment of Peptide-based Immunotherapy, University and University Hospital Tübingen, 72076 Tübingen, Germany.
Jonas RiethDepartment of Peptide-based Immunotherapy, University and University Hospital Tübingen, 72076 Tübingen, Germany.
Malte RoerdenInstitute for Cell Biology, Department of Immunology, University of Tübingen, 72076 Tübingen, Germany.
Marissa L DubbelaarDepartment of Peptide-based Immunotherapy, University and University Hospital Tübingen, 72076 Tübingen, Germany.
Naomi Hoenisch GravelDepartment of Peptide-based Immunotherapy, University and University Hospital Tübingen, 72076 Tübingen, Germany.
Jens BauerDepartment of Peptide-based Immunotherapy, University and University Hospital Tübingen, 72076 Tübingen, Germany.
Reinhild KleinDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, 72076 Tübingen, Germany.
Tobias HoheiselDepartment of Traumatology and Reconstructive Surgery, BG Trauma Center Tübingen, Eberhard Karls University Tübingen, 72076 Tübingen, Germany.
Hartmut MahrhoferDepartment of Internal Medicine I, University Hospital Tübingen, 72076 Tübingen, Germany.
Siri GöpelDepartment of Internal Medicine I, University Hospital Tübingen, 72076 Tübingen, Germany.
Michael BitzerDepartment of Internal Medicine I, University Hospital Tübingen, 72076 Tübingen, Germany.
Sebastian HörberInstitute for Clinical Chemistry and Pathobiochemistry, Department for Diagnostic Laboratory Medicine, University Hospital Tübingen, 72076 Tübingen, Germany.
Andreas PeterInstitute for Clinical Chemistry and Pathobiochemistry, Department for Diagnostic Laboratory Medicine, University Hospital Tübingen, 72076 Tübingen, Germany.
Jonas S HeitmannCluster of Excellence iFIT (EXC2180) "Image-Guided and Functionally Instructed Tumor Therapies", University of Tübingen, 72076 Tübingen, Germany.
Juliane S WalzDepartment of Peptide-based Immunotherapy, University and University Hospital Tübingen, 72076 Tübingen, Germany.
University of Tübingen · DEUniversity Children's Hospital Tübingen · DEDeutschen Konsortium für Translationale Krebsforschung · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HLA-presented antigenic peptides are central components of T cell-based immunity in infectious disease. Beside HLA molecules on cell surfaces, soluble HLA molecules (sHLA) are released in the blood suggested to impact cellular immune responses. We demonstrated that sHLA levels were significantly increased in COVID-19 patients and convalescent individuals compared to a control cohort and positively correlated with SARS-CoV-2-directed cellular immunity. Of note, patients with severe courses of COVID-19 showed reduced sHLA levels. Mass spectrometry-based characterization of sHLA-bound antigenic peptides, the so-called soluble immunopeptidome, revealed a COVID-19-associated increased diversity of HLA-presented peptides and identified a naturally presented SARS-CoV-2-derived peptide from the viral nucleoprotein in the plasma of COVID-19 patients. Of interest, sHLA serum levels directly correlated with the diversity of the soluble immunopeptidome. Together, these findings suggest an inflammation-driven release of sHLA in COVID-19, directly influencing the diversity of the soluble immunopeptidome with implications for SARS-CoV-2-directed T cell-based immunity and disease outcome.

Indexed as

Immune responseImmune systemImmunology

Identifiers

PMID36439376
PMCPMC9675079
OpenAlexW4309568841

What OpenQuestion holds

Textmetadata
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.