Evidence map›Paper›PMID 32833687›Full record

Trial reportThe Journal of clinical investigation2020

SARS-CoV-2-specific T cell responses and correlations with COVID-19 patient predisposition.

Arne Sattler, Stefan Angermair, Helena Stockmann, Katrin Moira Heim, Dmytro Khadzhynov, Sascha Treskatsch, Fabian Halleck, Martin E Kreis, Katja Kotsch

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 147 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
147citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 3% 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

147 citing papers in PubMed, 1 synthesis or guideline pooled it, 219 citations in OpenAlex.

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  6. Upregulation of CCR4 in activated CD8European journal of immunology · 2021
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87 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Arne SattlerDepartment for General, Visceral and Vascular Surgery.
Stefan AngermairDepartment of Anesthesiology and Intensive Care Medicine.
Helena StockmannDepartment of Nephrology and Medical Intensive Care, and.
Katrin Moira HeimDepartment of Infectiology and Pneumonology, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Dmytro KhadzhynovDepartment of Nephrology and Medical Intensive Care, and.
Sascha TreskatschDepartment of Anesthesiology and Intensive Care Medicine.
Fabian HalleckDepartment of Nephrology and Medical Intensive Care, and.
Martin E KreisDepartment for General, Visceral and Vascular Surgery.
Katja KotschDepartment for General, Visceral and Vascular Surgery.
Center for Vascular Biology Research · USHumboldt-Universität zu Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) has emerged as a global pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). So far, viral targets of cellular immunity and factors determining successful mounting of T cell responses are poorly defined. We therefore analyzed cellular responses to membrane, nucleocapsid, and spike proteins in individuals suffering from moderate or severe infection and in individuals who recovered from mild disease. We demonstrate that the CoV-2-specific CD4+ T helper cell response is directed against all 3 proteins with comparable magnitude, ex vivo proliferation, and portions of responding patients. However, individuals who died were more likely to have not mounted a cellular response to the proteins. Higher patient age and comorbidity index correlated with increased frequencies of CoV-2-specific CD4+ T cells, harboring higher portions of IL-2-secreting, but lower portions of IFN-γ-secreting, cells. Diminished frequencies of membrane protein-reactive IFN-γ+ T cells were particularly associated with higher acute physiology and chronic health evaluation II scores in patients admitted to intensive care. CoV-2-specific T cells exhibited elevated PD-1 expression in patients with active disease as compared with those individuals who recovered from previous mild disease. In summary, our data suggest a link between individual patient predisposition with respect to age and comorbidity and impairment of CoV-2-specific Th1-type cellular immunity, thereby supporting a concept of altered T cell function in at-risk patients.

Indexed as

AdultAgedAged, 80 and overAge FactorsCOVID-19Disease SusceptibilityFemaleHumansInterferon-gammaInterleukin-2MaleMiddle AgedProgrammed Cell Death 1 ReceptorSARS-CoV-2Severity of Illness IndexTh1 CellsIFNG protein, humanIL2 protein, humanInterferon-gammaInterleukin-2PDCD1 protein, humanProgrammed Cell Death 1 ReceptorAntigenCOVID-19T cells

Identifiers

PMID32833687
PMCPMC7685725
OpenAlexW3080524815

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.