Evidence map›Paper›PMID 38873612›Full record

ArticleFrontiers in immunology2024

Oropharyngeal microbial ecosystem perturbations influence the risk for acute respiratory infections in common variable immunodeficiency.

Federica Pulvirenti, Maria Giufrè, Tancredi M Pentimalli, Romina Camilli, Cinzia Milito, Annalisa Villa, Eleonora Sculco, Marina Cerquetti, Annalisa Pantosti, Isabella Quinti

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Article in Frontiers in immunology, 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

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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.

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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

10 authors.

Federica PulvirentiReference Center for Primary Immune Deficiencies, Azienda Ospedaliero Universitaria (AOU) Policlinico Umberto I, Rome, Italy.
Maria GiufrèDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Tancredi M PentimalliLaboratory for Systems Biology of Gene Regulatory Elements, Berlin Institute for Medical Systems Biology (BIMSB), Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
Romina CamilliDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Cinzia MilitoDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Annalisa VillaDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Eleonora SculcoDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Marina CerquettiDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Annalisa PantostiDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Isabella QuintiDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The respiratory tract microbiome is essential for human health and well-being and is determined by genetic, lifestyle, and environmental factors. Patients with Common Variable Immunodeficiency (CVID) suffer from respiratory and intestinal tract infections, leading to chronic diseases and increased mortality rates. While CVID patients' gut microbiota have been analyzed, data on the respiratory microbiome ecosystem are limited. Objective: This study aims to analyze the bacterial composition of the oropharynx of adults with CVID and its link with clinical and immunological features and risk for respiratory acute infections. Methods: Oropharyngeal samples from 72 CVID adults and 26 controls were collected in a 12-month prospective study. The samples were analyzed by metagenomic bacterial 16S ribosomal RNA sequencing and processed using the Quantitative Insights Into Microbial Ecology (QIME) pipeline. Differentially abundant species were identified and used to build a dysbiosis index. A machine learning model trained on microbial abundance data was used to test the power of microbiome alterations to distinguish between healthy individuals and CVID patients. Results: Compared to controls, the oropharyngeal microbiome of CVID patients showed lower alpha- and beta-diversity, with a relatively increased abundance of the order Conclusions: CVID patients showed a perturbed oropharynx microbiota enriched with potentially pathogenic bacteria and decreased protective species. Low residual levels of IgA/IgM, chronic lung damage, anti antibiotic prophylaxis contributed to respiratory dysbiosis.

Indexed as

Common Variable ImmunodeficiencyDysbiosisOropharynxRespiratory Tract InfectionsAcute DiseaseAdultAgedBacteriaCase-Control StudiesFemaleHumansMaleMicrobiotaMiddle AgedProspective StudiesRNA, Ribosomal, 16SRNA, Ribosomal, 16Schronic obstructive pulmonary diseasecommon variable immunodeficiencyHaemophilusIgAIgMmicrobiome and dysbiosisoropharyngeal microbiomePneumococcus

Identifiers

PMID38873612
PMCPMC11169596

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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.