ArticleClinics (Sao Paulo, Brazil)2026
Immune parameters in hospitalized COVID-19 patients during SARS-CoV2 delta and omicron waves.
Article in Clinics (Sao Paulo, Brazil), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
14 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Understanding immune mechanisms associated with COVID-19 severity remains important for interpreting clinical outcomes. We investigated virological and immunological profiles in 39-patients hospitalized with COVID-19 at InCor Hospital during the Delta and Omicron waves and included 28-non-hospitalized individuals with moderate COVID-19 as a comparator group for cytokine analyses. SARS-CoV-2 infection was confirmed by RT-PCR from nasopharyngeal swabs, and viral variants were identified by next-generation sequencing. RNAemia was assessed by RT-PCR and analyzed as a binary variable. Serum cytokines were quantified by cytometric bead array, while humoral responses were evaluated by anti-Spike RBD IgG levels using CLIA and a Wuhan-Hu-1-based pseudovirus neutralization assay. RNAemia was more frequent in ICU-admitted patients than in non-ICU patients, supporting an association with disease severity. Cytokine profiling showed increased IL-6, IL-8, TNF, IL-17 A and IL-10 levels in hospitalized patients compared with moderate COVID-19 individuals, but did not distinguish recovered from deceased patients. Neutralizing antibody titers measured against a Wuhan-Hu-1 spike pseudovirus were significantly higher in recovered individuals than decease patients, underscoring the relevance of antibody functionality. These data emphasize the relevance of viral dissemination and functional humoral immunity as potential biomarkers for COVID-19 progression and outcome, with RNAemia and neutralizing antibody levels showing a stronger exploratory association in this cohort.
Indexed as
Identifiers
42880124What OpenQuestion holds
Registered trials
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.