Evidence map›Paper›PMID 36297185›Full record

ArticlePathogens (Basel, Switzerland)2022

Downregulation of sCD40 and sCTLA4 in Recovered COVID-19 Patients with Comorbidities.

Gwendolyne Méndez-Frausto, Susana Godina-González, César E Rivas-Santiago, Edna Nungaray-Anguiano, Gretel Mendoza-Almanza, Bruno Rivas-Santiago, Carlos E Galván-Tejada, Irma E Gonzalez-Curiel

Open access · goldAbstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 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 85% 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

8 authors at 2 institutions in 1 country.

Gwendolyne Méndez-FraustoLaboratorio de Inmunotoxicología y Terapéutica Experimental, Unidad Académica de Ciencias Químicas, Universidad Autónoma de Zacatecas, Zacatecas 98160, Mexico.
Susana Godina-GonzálezLaboratorio de Biomarcadores, Unidad Académica de Ciencias Químicas, Universidad Autónoma de Zacatecas, Zacatecas 98160, Mexico.ORCID 0000-0003-0340-9381
César E Rivas-SantiagoCONACYT-Academic Unit of Chemical Sciences, Autonomous University of Zacatecas, Zacatecas 98160, Mexico.
Edna Nungaray-AnguianoLaboratorio de Inmunotoxicología y Terapéutica Experimental, Unidad Académica de Ciencias Químicas, Universidad Autónoma de Zacatecas, Zacatecas 98160, Mexico.
Gretel Mendoza-AlmanzaCONACYT-Academic Unit of Chemical Sciences, Autonomous University of Zacatecas, Zacatecas 98160, Mexico.
Bruno Rivas-SantiagoUnidad de Investigación Biomédica de Zacatecas, IMSS, Zacatecas 98000, Mexico.ORCID 0000-0002-1521-1519
Carlos E Galván-TejadaUnidad Académica de Ingeniería Eléctrica, Universidad Autónoma de Zacatecas, Zacatecas 98000, Mexico.ORCID 0000-0002-7635-4687
Irma E Gonzalez-CurielLaboratorio de Inmunotoxicología y Terapéutica Experimental, Unidad Académica de Ciencias Químicas, Universidad Autónoma de Zacatecas, Zacatecas 98160, Mexico.ORCID 0000-0002-0044-9196
Universidad Autónoma de Zacatecas "Francisco García Salinas" · MXSecretaría de Ciencia, Humanidades, Tecnología e Innovación · MX

Funding

Consejo Nacional de Ciencia y Tecnología 000000000312908
6 · The paper itself

Abstract

The aim of this study was to analyze molecules associated with regulatory immune response in unvaccinated, recovered COVID-19 patients with and without diabetes mellitus (DM) and hypertension (HTN). We determined anti-SARS-CoV-2 nucleocapsid IgG in plasma by electrochemiluminescence immunoassay. The levels of sCD40, TGF-ß, IL-10, and sCTLA-4 were assessed by ELISA in the serum of the subjects, as well as in healthy donors. We observed that only half of the subjects in the non-comorbid group produced antibodies, whereas all subjects in comorbid groups were IgG-positive for the anti-SARS-CoV-2 nucleocapsid. High levels of sCTL-4 were observed in the non-comorbid group, and the level of IL-10 was observed to increase in seropositive subjects without comorbidities. TGF-ß concentration was similar in all groups studied. Finally, sCD40 decreased in the comorbid group. In conclusion, our results suggest that comorbidities such as DM and HTN alter the production of co-stimulatory inhibitory molecules sCTLA-4 and sCD40 in subjects recovering from mild COVID-19. The alterations observed here were independent of seropositivity, suggesting an effective humoral immune response against COVID-19 separate from the levels of co-stimulatory inhibitory molecules.

Indexed as

COVID-19diabetes mellitushypertensionsCD40sCTLA-4

Identifiers

PMID36297185
PMCPMC9608172
OpenAlexW4303961886

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.