Evidence map›Paper›PMID 37649544›Full record

ArticlePractical laboratory medicine2023

Immune biomarkers associated with COVID-19 disease severity in an urban, hospitalized population.

Allison B Chambliss, Mayada Aljehani, Brian Tran, Xingyao Chen, Elizabeth Elton, Carolina Garri, Nolan Ung, Naim Matasci, Mitchell E Gross

Open access · goldAbstract read
In one paragraph

Article in Practical laboratory medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

9 authors at 2 institutions in 1 country.

Allison B ChamblissDepartment of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Mayada AljehaniLawrence J. Ellison Institute for Transformative Medicine, Los Angeles, CA, USA.
Brian TranLawrence J. Ellison Institute for Transformative Medicine, Los Angeles, CA, USA.
Xingyao ChenLawrence J. Ellison Institute for Transformative Medicine, Los Angeles, CA, USA.
Elizabeth EltonLawrence J. Ellison Institute for Transformative Medicine, Los Angeles, CA, USA.
Carolina GarriLawrence J. Ellison Institute for Transformative Medicine, Los Angeles, CA, USA.
Nolan UngLawrence J. Ellison Institute for Transformative Medicine, Los Angeles, CA, USA.
Naim MatasciLawrence J. Ellison Institute for Transformative Medicine, Los Angeles, CA, USA.
Mitchell E GrossLawrence J. Ellison Institute for Transformative Medicine, Los Angeles, CA, USA.
Larry Ellison Foundation · USUniversity of Southern California · US

Funding

Southern California Clinical and Translational Science InstituteUL1TR001855 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Thomas A Buchanan, Michele D. Kipke · 2016 to 2026
$81.3M
Southern California Clinical and Translational Science InstituteUL1TR000130 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BUCHANAN, THOMAS A · 2012 to 2015
$36.0M
NCATS NIH HHS UL1 TR000130NCATS NIH HHS UL1 TR001855
6 · The paper itself

Abstract

Objectives: We sought to identify immune biomarkers associated with severe Coronavirus disease 2019 (COVID-19) in patients admitted to a large urban hospital during the early phase of the SARS-CoV-2 pandemic. Design: The study population consisted of SARS-CoV-2 positive subjects admitted for COVID-19 (n = 58) or controls (n = 14) at the Los Angeles County University of Southern California Medical Center between April 2020 through December 2020. Immunologic markers including chemokine/cytokines (IL-6, IL-8, IL-10, IP-10, MCP-1, TNF-α) and serologic markers against SARS-CoV-2 antigens (including spike subunits S1 and S2, receptor binding domain, and nucleocapsid) were assessed in serum collected on the day of admission using bead-based multiplex immunoassay panels. Results: We observed that body mass index (BMI) and SARS-CoV-2 antibodies were significantly elevated in patients with the highest COVID-19 disease severity. IP-10 was significantly elevated in COVID-19 patients and was associated with increased SARS-CoV-2 antibodies. Interactions among all available variables on COVID-19 disease severity were explored using a linear support vector machine model which supported the importance of BMI and SARS-CoV-2 antibodies. Conclusions: Our results confirm the known adverse association of BMI on COVID-19 severity and suggest that IP-10 and SARS-CoV-2 antibodies could be useful to identify patients most likely to experience the most severe forms of the disease.

Indexed as

AntibodiesChemokinesCOVID-19CytokinesImmunologySARS-CoV-2

Identifiers

PMID37649544
PMCPMC10462676
OpenAlexW4382983340

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.