Evidence map›Paper›PMID 41365001›Full record

ArticleAmerican journal of otolaryngology

Preservation of adaptive immunity is associated with survival in invasive fungal sinusitis.

Iris Lee, Sonam Verma, John S Schneider, Nyssa F Farrell, Peggy L Kendall, Lauren T Roland

Abstract readComparative Study
In one paragraph

Article in American journal of otolaryngology. 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
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.

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

6 authors.

Iris LeeDivision of Rheumatology, Department of Medicine, Washington University in St Louis, United States of America.
Sonam VermaDivision of Allergy and Immunology, Department of Medicine, Washington University in St Louis, United States of America.
John S SchneiderDepartment of Otolaryngology - Head and Neck Surgery, Washington University in St Louis, United States of America.
Nyssa F FarrellDepartment of Otolaryngology - Head and Neck Surgery, Washington University in St Louis, United States of America.
Peggy L KendallDivision of Allergy and Immunology, Department of Medicine, Washington University in St Louis, United States of America.
Lauren T RolandDepartment of Otolaryngology - Head and Neck Surgery, Washington University in St Louis, United States of America. Electronic address: rolandl@wustl.edu.

Funding

Washington University Institute of Clinical and Translational Sciences (KL2) KL2TR002346 · NCATS · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 2017 to 2026
$14.0M
NCATS NIH HHS KL2 TR002346
6 · The paper itself

Abstract

backgroundInvasive Fungal Sinusitis (IFS) is a deadly and morbid disease of the paranasal sinuses. Immunocompromised patients are at risk of developing IFS, and survival at 6 months is approximately 50%. Previously studied treatments such as granulocyte stimulating factor have not improved survival. Thus, the immune cells responsible for survival in this vulnerable population are not well defined.

objectiveThe goal of this study was to immunophenotype cells associated with IFS survival.

methodsBlood samples from consenting patients were collected at the time of surgery for IFS between April 2022 and December 2023. Peripheral blood mononuclear cells (PBMCs) were evaluated for major lymphoid and myeloid subsets using mass Cytometry by Time of Flight (CyTOF) between IFS survivors and non-survivors, defined by vital status 6 months after the time of diagnosis. Data were analyzed using the dimensionality reduction algorithm optimized t-distributed stochastic neighbor embedding (opt-SNE).

resultsSeven patients had PBMCs viable for analysis (3 survivors and 4 non-survivors). Total white blood cell counts were lower in non-survivors. Total T cell and B cell counts were decreased in non-survivors as compared to survivors, but there were no differences in other immune cell populations, such as NK cells or monocytes. Percentage differences were identified as deficiencies in CD4 T cells, particularly memory cells, in the IFS non-survivors.

conclusionFuture work includes the investigation of CD4 T cells as a biomarker for IFS survival and the study of T cell manipulation or stimulation in IFS patients.

Indexed as

Adaptive ImmunityInvasive Fungal InfectionsLeukocytes, MononuclearSinusitisAdultAgedBiomarkersCD4-Positive T-LymphocytesFemaleHumansImmunocompromised HostImmunophenotypingLeukocyte CountMaleMiddle AgedSurvival RateBiomarkersAdaptive immunityAspergillusInvasive fungal sinusitisMucorSinonasalSinusitis

Identifiers

PMID41365001
PMCPMC13098752

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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.