Evidence map›Paper›PMID 38371947›Full record

ArticleCritical care explorations2022

Temporal Dynamics of Host Immune Response Associated With Disease Severity and Time to Recovery in Patients Hospitalized for COVID-19.

Anthony Sophonsri, Diana Le, Mimi Lou, Pamela Ny, Emi Minejima, Allison B Chambliss, Paul Nieberg, Kimberly Shriner, Annie Wong-Beringer

Open access · goldAbstract read
In one paragraph

Article in Critical care explorations, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. 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.

Anthony SophonsriDepartment of Clinical Pharmacy, University of Southern California, School of Pharmacy, Los Angeles, CA.
Diana LeDepartment of Clinical Pharmacy, University of Southern California, School of Pharmacy, Los Angeles, CA.
Mimi LouDepartment of Clinical Pharmacy, University of Southern California, School of Pharmacy, Los Angeles, CA.
Pamela NyDepartment of Pharmacy, Huntington Hospital, Pasadena, CA.
Emi MinejimaDepartment of Clinical Pharmacy, University of Southern California, School of Pharmacy, Los Angeles, CA.
Allison B ChamblissDepartment of Pathology, University of Southern California, Keck School of Medicine, Los Angeles, CA.
Paul NiebergDepartment of Medicine-Infectious Diseases, Huntington Hospital, Pasadena, CA.
Kimberly ShrinerDepartment of Medicine-Infectious Diseases, Huntington Hospital, Pasadena, CA.
Annie Wong-BeringerDepartment of Clinical Pharmacy, University of Southern California, School of Pharmacy, Los Angeles, CA.
Huntington Hospital · 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

objectivesThe objective of this study was to compare the temporal dynamics of two viral-induced inflammatory proteins interferon gamma inducible protein-10 (IP-10) and tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), as well as C-reactive protein (CRP) among patients hospitalized for COVID-19 and examine their prognostic significance.

designProspective observational cohort study.

settingMulticenter, inpatient. PATIENTS: Adult patients infected with severe acute respiratory syndrome coronavirus 2 between March 2021 and October 2021.

interventionsPatient sera were collected on days 1, 3, 5, and 7 of hospitalization. Levels of IP-10, TRAIL, and CRP were measured using a point-of-need diagnostic immunoassay platform (MeMed BV, MeMed, Haifa, Israel) and compared between patients grouped by disease severity (severe vs nonsevere). MEASUREMENTS AND MAIN

resultsBaseline characteristics were similar regardless of severity except for a higher prevalence of diabetes and heart failure among severe patients. The immune profile at admission was similar between groups; IP-10 and CRP levels generally decreased while TRAIL levels increased over time in all patients. However, the severe group had higher IP-10 (median 713 vs 328 pg/mL;

conclusionsThe observed patterns in host immune response revealed a turning point in COVID-19 disease on hospital day 3 and the potential utility of IP-10 and TRAIL as sensitive markers associated with disease severity and time to recovery.

Indexed as

biomarkerschemokine CXCL10COVID-19inflammationpneumonia

Identifiers

PMID38371947
PMCPMC10871785
OpenAlexW4297810936

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.