Evidence map›Paper›PMID 37799713›Full record

ArticleFrontiers in immunology2023

Distinct SARS-CoV-2 specific NLRP3 and IL-1β responses in T cells of aging patients during acute COVID-19 infection.

Shanmuga Sundaram Mahalingam, Sangeetha Jayaraman, Adhvika Arunkumar, Holly M Dudley, Donald D Anthony, Carey L Shive, Jeffrey M Jacobson, Pushpa Pandiyan

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Enrichment ofFrontiers in immunology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Shanmuga Sundaram MahalingamDepartment of Biological Sciences, School of Dental Medicine, Case Western Reserve University, Cleveland, OH, United States.
Sangeetha JayaramanDepartment of Biological Sciences, School of Dental Medicine, Case Western Reserve University, Cleveland, OH, United States.
Adhvika ArunkumarDepartment of Biological Sciences, School of Dental Medicine, Case Western Reserve University, Cleveland, OH, United States.
Holly M DudleyDepartment of Molecular Biology and Microbiology, School of Medicine, Case Western Reserve University, Cleveland, OH, United States.
Donald D AnthonyDepartment of Rheumatology, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, United States.
Carey L ShiveDepartment of Rheumatology, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH, United States.
Jeffrey M JacobsonCenter for AIDS Research, School of Medicine, Case Western Reserve University, Cleveland, OH, United States.
Pushpa PandiyanDepartment of Biological Sciences, School of Dental Medicine, Case Western Reserve University, Cleveland, OH, United States.
Case Western Reserve University · USLouis Stokes Cleveland VA Medical Center · US

Funding

METABOLOME ANALYSES OF SALIVA SAMPLES FROM HIV+ PATIENTS ON cARTR01DE026923 · NIDCR · CASE WESTERN RESERVE UNIVERSITY · PI Pushpa Pandiyan · 2017 to 2026
$4.5M
Microbiology and Immunology Training for HIV and HIV-Related Research in Uganda (MITHU)D43TW010319 · FIC · CASE WESTERN RESERVE UNIVERSITY · PI BOOM, W. HENRY, JOLOBA, MOSES LUTAAKOME · 2016 to 2025
$3.1M
BLRD VA I01 BX005480BLRD VA I01 BX005507FIC NIH HHS D43 TW010319NIDCR NIH HHS R01 DE026923
6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes Coronavirus Disease 2019 (COVID-19) that presents with varied clinical manifestations ranging from asymptomatic or mild infections and pneumonia to severe cases associated with cytokine storm, acute respiratory distress syndrome (ARDS), and even death. The underlying mechanisms contributing to these differences are unclear, although exacerbated inflammatory sequelae resulting from infection have been implicated. While advanced aging is a known risk factor, the precise immune parameters that determine the outcome of SARS-CoV-2 infection in elderly individuals are not understood. Here, we found aging-associated (age ≥61) intrinsic changes in T cell responses when compared to those from individuals aged ≤ 60, even among COVID-positive patients with mild symptoms. Specifically, when stimulated with SARS-CoV-2 peptides

Indexed as

AgingCOVID-19AgedCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesHumansInterleukin-1betaLeukocytes, MononuclearMiddle AgedNLR Family, Pyrin Domain-Containing 3 ProteinProgrammed Cell Death 1 ReceptorSARS-CoV-2IL1B protein, humanInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanProgrammed Cell Death 1 ReceptoragingCD4CD8 IFNγ cells + +COVIDIFN-γIL-1bimmune senescence

Identifiers

PMID37799713
PMCPMC10548880
OpenAlexW4386846500

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.