Evidence map›Paper›PMID 36389788›Full record

ArticleFrontiers in immunology2022

Translation suppression underlies the restrained COVID-19 mRNA vaccine response in the high-risk immunocompromised group.

Kangsan Kim, Madhusudhanan Narasimhan, Lenin Mahimainathan, Ray Zhang, Ellen Araj, Elizabeth Kim, William Tharpe, Benjamin M Greenberg, David E Greenberg, Quan-Zhen Li and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 86% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

14 authors at 2 institutions in 2 countries.

Kangsan KimDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
Madhusudhanan NarasimhanDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
Lenin MahimainathanDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
Ray ZhangDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
Ellen ArajDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
Elizabeth KimWilliam P. Clements Jr. University Hospital, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
William TharpeWilliam P. Clements Jr. University Hospital, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
Benjamin M GreenbergDepartment of Neurology and Neurotherapeutics, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
David E GreenbergDepartment of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
Quan-Zhen LiMicroarray Core, Department of Immunology, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
Chi-An ChengSchool of Pharmacy, National Taiwan University, Taipei, Taiwan.
Ravi SarodeDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
Srinivas MalladiDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
Alagarraju MuthukumarDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX, United States.
The University of Texas Southwestern Medical Center · USNational Taiwan University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immunocompromised (IC) patients show diminished immune response to COVID-19 mRNA vaccines (Co-mV). To date, there is no 'empirical' evidence to link the perturbation of translation, a rate-limiting step for mRNA vaccine efficiency (VE), to the dampened response of Co-mV. Materials and methods: Impact of immunosuppressants (ISs), tacrolimus (T), mycophenolate (M), rapamycin/sirolimus (S), and their combinations on Pfizer Co-mV translation were determined by the Spike (Sp) protein expression following Co-mV transfection in HEK293 cells. Results: We observed significantly lower IgG Conclusions: This is the first study to demonstrate that ISs, sirolimus and mycophenolate inhibited Co-mV-induced Sp protein synthesis

Indexed as

COVID-19COVID-19 VaccinesAnimalsHEK293 CellsHumansImmunoglobulin GMicemRNA VaccinesSARS-CoV-2SirolimusTacrolimusCOVID-19 VaccinesImmunoglobulin GmRNA VaccinesSirolimusTacrolimuscovid-19 mRNA vaccinesimmunocompromised patientsmycophenolatesirolimustacrolimustranslation suppression

Identifiers

PMID36389788
PMCPMC9644109
OpenAlexW4307553657

What OpenQuestion holds

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LicenceCC BY
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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.