Evidence map›Paper›PMID 35509311›Full record

ArticleFrontiers in microbiology2022

Antibody and T Cell Immune Responses to SARS-CoV-2 Peptides in COVID-19 Convalescent Patients.

Ekaterina Garanina, Shaimaa Hamza, Robert J Stott-Marshall, Ekaterina Martynova, Maria Markelova, Yuriy Davidyuk, Venera Shakirova, Neha Kaushal, Manoj Baranwal, Ilsiyar M Khaertynova and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

2 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Neutralizing Antibodies in COVID-19 Serum from Tatarstan, Russia.International journal of molecular sciences · 2023
    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

13 authors at 4 institutions in 3 countries.

Ekaterina GaraninaIntitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Shaimaa HamzaIntitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Robert J Stott-MarshallFaculty of Medicine and Health Sciences, School of Veterinary Medicine and Science, University of Nottingham, Loughborough, United Kingdom.
Ekaterina MartynovaIntitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Maria MarkelovaIntitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Yuriy DavidyukIntitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Venera ShakirovaDepartment of Infectious Diseases, Kazan State Medical University, Kazan, Russia.
Neha KaushalDepartment of Biotechnology, Thapar Institute of Engineering and Technology, Patiala, India.
Manoj BaranwalDepartment of Biotechnology, Thapar Institute of Engineering and Technology, Patiala, India.
Ilsiyar M KhaertynovaDepartment of Infectious Diseases, Kazan State Medical University, Kazan, Russia.
Albert RizvanovIntitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Toshana L FosterFaculty of Medicine and Health Sciences, School of Veterinary Medicine and Science, University of Nottingham, Loughborough, United Kingdom.
Svetlana KhaiboullinaIntitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Kazan Federal University · RUKazan State Medical University · RUThapar Institute of Engineering & Technology · INUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying immunogenic targets of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is critical to advance diagnostic and disease control strategies. We analyzed humoral (ELISA) and T-cell (ELISpot) immune responses to spike (S) and nucleocapsid (N) SARS-CoV-2 proteins as well as to human endemic coronavirus (eCoV) peptides in serum from convalescent coronavirus disease 2019 (COVID-19) patients from Tatarstan, Russia. We identified multiple SARS-CoV-2 peptides that were reactive with serum antibodies and T cells from convalescent COVID-19. In addition, age and gender associated differences in the reactivity to S and N protein peptides were identified. Moreover, several SARS-CoV-2 peptides tested negatively correlated with disease severity and lung damage. Cross-reactivity to eCoV peptides was analyzed and found to be lower in COVID-19 compared to controls. In this study, we demonstrate the changing pattern of immunogenic peptide reactivity in COVID-19 serum based on age, gender and previous exposure to eCoVs. These data highlight how humoral immune responses and cytotoxic T cell responses to some of these peptides could contribute to SARS-CoV-2 pathogenesis.

Indexed as

antibody humoral immune responseCOVID-19peptidesSARS-CoV-2spike protein

Identifiers

PMID35509311
PMCPMC9058163
OpenAlexW4223997139

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.