Evidence map›Paper›PMID 41376646›Full record

ArticleFrontiers in immunology2025

Immune responses in pulmonary sarcoidosis following COVID-19.

Anna Starshinova, Igor Kudryavtsev, Artem Rubinstein, Tatiana Akisheva, Alexey Golovkin, Zoia Korobova, Anastasia Kulpina, Dmitry Kudlay

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Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors.

Anna Starshinova *Faculty of Mathematics and Computer Science, Saint Petersburg State University, St. Petersburg, Russia.
Igor Kudryavtsev *Faculty of Mathematics and Computer Science, Saint Petersburg State University, St. Petersburg, Russia.
Artem RubinsteinDepartment of Faculty Therapy with a Clinic, Almazov National Medical Research Center, St. Petersburg, Russia.
Tatiana AkishevaDepartment of Immunology, Institution of Experimental Medicine, St. Petersburg, Russia.
Alexey GolovkinDepartment of Faculty Therapy with a Clinic, Almazov National Medical Research Center, St. Petersburg, Russia.
Zoia KorobovaLaboratory of Molecular Immunology, Saint Petersburg Pasteur Institute, St. Petersburg, Russia.
Anastasia KulpinaFaculty of Mathematics and Computer Science, Saint Petersburg State University, St. Petersburg, Russia.
Dmitry KudlayDepartment of Pharmacology, Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/objectives: The complex interplay between sarcoidosis and COVID-19 remains an important area of research, since COVID-19 leads to long-term changes in the immune system. However, COVID-19 is often followed by autoimmune diseases, including newly manifesting sarcoidosis. The goal of this study is to characterize CD4+ T cell subsets, playing a pivotal role in the regulation of innate and adaptive immunity, in the peripheral blood of patients with sarcoidosis after COVID-19. Methods: The peripheral blood samples from patients with sarcoidosis (n = 61) were studied. We divided patients into two distinct groups: sarcoidosis patients with no history of COVID-19 (n= 30) and COVID-19 convalescent patients with sarcoidosis within 12-24 weeks after recovery (n = 31). Healthy controls (n = 40) were similar in terms of age and sex to patients with sarcoidosis. Immunophenotyping of peripheral blood cells was performed using a ten-color flow cytometry. Results: Sarcoidosis patients with COVID-19 history had higher levels of T-helper cells (Th) when compared to COVID-19 naïve patients with sarcoidosis, but lower levels when compared to healthy controls. In COVID-19 convalescent patients with sarcoidosis, we noted higher absolute numbers and percentages of CD45RA-CCR7- and CD45RA+CCR7- cells within Th subset. Among COVID-19 convalescent patients with sarcoidosis we also found higher levels of T helper 1 cells and T helper 2 cells (with CXCR5-CCR6-CXCR3+CCR4- and CXCR5-CCR6-CXCR3-CCR4+ phenotypes, respectively) when compared to other groups. We also noted a statistically significant increase in central memory CXCR5+CCR6-CXCR3- follicular Th cells, as wells as effector memory CXCR5+CCR6-CXCR3- and CXCR5+CCR6+CXCR3- follicular Th cells in both groups of patients with sarcoidosis vs. healthy controls. Conclusions: Our study demonstrated Th cells imbalance in patients with sarcoidosis and COVID-19 history. These findings suggest possible clinical and visual progression of chronic lung sarcoidosis in COVID-19 convalescent patients.

Indexed as

COVID-19Sarcoidosis, PulmonarySARS-CoV-2Adaptive ImmunityAdultAgedFemaleHumansImmunity, InnateImmunophenotypingMaleMiddle Agedautoimmunityfollicular Th cellsgranulomatous diseasespathogenesispost-COVID-19sarcoidosisTh17Th subsets

Identifiers

PMID41376646
PMCPMC12685880

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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.