Evidence map›Paper›PMID 38750098›Full record

ArticleScientific reports2024

Secretory IgA and course of COVID-19 in patients receiving a bacteria-based immunostimulant agent in addition to background therapy.

Mikhail Kostinov, Oksana Svitich, Alexander Chuchalin, Valery Osiptsov, Ekaterina Khromova, Natalya Abramova, Vitaly Tatevosov, Anna Vlasenko, Vilia Gainitdinova, Dmitrij Pakhomov and 6 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
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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

16 authors.

Mikhail KostinovDepartment of Epidemiology and Modern Vaccination Technologies, Institute of Professional Education, I.M. Sechenov First Moscow State Medical University, Moscow, Russian Federation. monolit.96@mail.ru.ORCID 0000-0002-1382-9403
Oksana SvitichI.I. Mechnikov Research Institute of Vaccines and Sera, Moscow, Russian Federation.ORCID 0000-0003-1757-8389
Alexander ChuchalinDepartment of Hospital Therapy of the Faculty of Pediatrics, Pirogov Russian National Research Medical University (Pirogov Medical University, Moscow, Russian Federation.ORCID 0000-0002-6808-5528
Valery OsiptsovThe Main Military Clinical Hospital of the National Guard Troops of the Russian Federation, Moscow, Russian Federation.ORCID 0000-0003-1027-7620
Ekaterina KhromovaLaboratory of Preventive Vaccination and Immunotherapy of Allergic Diseases, I.I. Mechnikov Research Institute of Vaccines and Sera, Moscow, Russian Federation.ORCID 0000-0002-4003-9976
Natalya AbramovaLaboratory of Molecular Immunology, I.I. Mechnikov Research Institute of Vaccines and Sera, Moscow, Russian Federation.ORCID 0000-0002-7307-0515
Vitaly TatevosovThe Main Military Clinical Hospital of the National Guard Troops of the Russian Federation, Moscow, Russian Federation.ORCID 0000-0002-4136-819X
Anna VlasenkoDepartment of Medical Cybernetics and Informatics Novokuznetsk State Institute for Advanced Medical Education of Physicians, Branch Campus of the Russian Medical Academy of Continuous Professional Education, Novokuznetsk, Russian Federation.ORCID 0000-0001-6454-4216
Vilia GainitdinovaPulmonology Department, N.V. Sklifosovsky Institute of Clinical Medicine, I.M. Sechenov First Moscow State Medical University, Moscow, Russian Federation.ORCID 0000-0002-5999-2150
Dmitrij PakhomovLaboratory of Preventive Vaccination and Immunotherapy of Allergic Diseases, I.I. Mechnikov Research Institute of Vaccines and Sera, Moscow, Russian Federation.ORCID 0000-0002-4073-6085
Kirill MashilovLaboratory of Preventive Vaccination and Immunotherapy of Allergic Diseases, I.I. Mechnikov Research Institute of Vaccines and Sera, Moscow, Russian Federation.
Tatyana OspelnikovaI.I. Mechnikov Research Institute of Vaccines and Sera, Moscow, Russian Federation.ORCID 0000-0002-1580-6096
Natalya MihajlovaI.I. Mechnikov Research Institute of Vaccines and Sera, Moscow, Russian Federation.ORCID 0000-0002-6652-2093
Valentina PolishchukLaboratory of Preventive Vaccination and Immunotherapy of Allergic Diseases, I.I. Mechnikov Research Institute of Vaccines and Sera, Moscow, Russian Federation.ORCID 0000-0003-0533-0909
Ekaterina KurbatovaLaboratory of Therapeutic Vaccines, I.I. Mechnikov Research Institute of Vaccines and Sera, Moscow, Russian Federation.ORCID 0000-0002-0282-4471
Aristitsa KostinovaDepartment of Epidemiology and Modern Vaccination Technologies, Institute of Professional Education, I.M. Sechenov First Moscow State Medical University, Moscow, Russian Federation.ORCID 0000-0002-0584-2376

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucosal immunity plays a major role not only in the prevention but probably also in the outcomes of COVID-19. An enhanced production of secretory immunoglobulin A (sIgA) might contribute to the activation of the immune response mechanisms. To assess the levels of sIgA produced by epithelial cells in the nasal and pharyngeal mucosa and those measured in salivary gland secretions and to study the course of COVID-19 following the combined scheme of intranasal and subcutaneous administration of a bacteria-based immunostimulant agent. This study included 69 patients, aged between 18 and 60, who had moderate COVID-19 infection. They were divided into two groups: Group 1 (control group) included 39 patients who received only background therapy, and Group 2 was made up of 30 patients who received background therapy in combination with the Immunovac VP4 vaccine, a bacteria-based immunostimulant agent, which was given for 11 days starting from the day of admission to hospital. The levels of sIgA were measured by ELISA in epithelial, nasal and pharyngeal swabs, and salivary gland secretions at baseline and on days 14 and 30. The combined scheme of intranasal and subcutaneous administration of the Immunovac VP4 vaccine in the complex therapy of patients with COVID-19 is accompanied by increased synthesis of sIgA in nasal and pharyngeal swabs, more intense decrease in the level of C-reactive protein (CRP) and reduction in the duration of fever and length of hospitalization compared to the control group. Prescribing a immunostimulant agent containing bacterial ligands in complex therapy for COVID-19 patients helps to enhance mucosal immunity and improves the course of the disease.

Indexed as

Adjuvants, ImmunologicCOVID-19Immunoglobulin A, SecretorySARS-CoV-2Administration, IntranasalAdolescentAdultCOVID-19 VaccinesFemaleHumansImmunity, MucosalMaleMiddle AgedYoung AdultAdjuvants, ImmunologicCOVID-19 VaccinesImmunoglobulin A, SecretoryBacterial ligands during COVID-19COVID-19 hospitalizationMicrobial-based immune therapy in COVID-19Mucosal immunitysIgA

Identifiers

PMID38750098
PMCPMC11096160

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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.