Evidence map›Paper›PMID 36499448›Full record

ReviewInternational journal of molecular sciences2022

Antigen-Specific T Cells and SARS-CoV-2 Infection: Current Approaches and Future Possibilities.

Zuzana Nova, Tomas Zemanek, Norbert Botek

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. 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
0.1field-weighted citation impact, top 54% 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

3 authors at 2 institutions in 2 countries.

Zuzana NovaLambda Life a.s., Levocska 3617/3, 851 01 Bratislava, Slovakia.ORCID 0000-0002-0804-4185
Tomas ZemanekLambda Life a.s., Levocska 3617/3, 851 01 Bratislava, Slovakia.ORCID 0000-0001-9081-307X
Norbert BotekLambda Life a.s., Levocska 3617/3, 851 01 Bratislava, Slovakia.
University Hospital Olomouc · CZUniversity of Trnava · SK

Funding

The Ministry of Education, Science, Research and Sport of the Slovak Republic ITMS2014+: 313011ATT8
6 · The paper itself

Abstract

COVID-19, a significant global health threat, appears to be an immune-related disease. Failure of effective immune responses in initial stages of infection may contribute to development of cytokine storm and systemic inflammation with organ damage, leading to poor clinical outcomes. Disease severity and the emergence of new SARS-CoV-2 variants highlight the need for new preventative and therapeutic strategies to protect the immunocompromised population. Available data indicate that these people may benefit from adoptive transfer of allogeneic SARS-CoV-2-specific T cells isolated from convalescent individuals. This review first provides an insight into the mechanism of cytokine storm development, as it is directly related to the exhaustion of T cell population, essential for viral clearance and long-term antiviral immunity. Next, we describe virus-specific T lymphocytes as a promising and efficient approach for the treatment and prevention of severe COVID-19. Furthermore, other potential cell-based therapies, including natural killer cells, regulatory T cells and mesenchymal stem cells are mentioned. Additionally, we discuss fast and effective ways of producing clinical-grade antigen-specific T cells which can be cryopreserved and serve as an effective "off-the-shelf" approach for rapid treatment of SARS-CoV-2 infection in case of sudden patient deterioration.

Indexed as

COVID-19SARS-CoV-2Cytokine Release SyndromeCytokinesHumansCytokinescellular therapiesCOVID-19immunotherapysevere acute respiratory syndrome coronavirus 2virus-specific T cells

Identifiers

PMID36499448
PMCPMC9737069
OpenAlexW4311093216

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.