Evidence map›Paper›PMID 38328225›Full record

ArticleResearch square2024

Tuberculosis Infectiousness is Associated with Distinct Clinical and Inflammatory Profiles.

David Horne, Videlis Nduba, Lilian Njagi, Wilfred Murithi, Zipporah Mwongera, Gisella Logioia, Glenna Peterson, R Max Segnitz, Kevin Fennelly, Thomas Hawn

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2024. 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, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

David HorneUniversity of Washington.ORCID 0000-0002-4721-9099
Videlis NdubaCentre for Respiratory Diseases Research, Kenya Medical Research Institute.
Lilian NjagiCentre for Respiratory Diseases Research, Kenya Medical Research Institute.ORCID 0000-0002-5067-0788
Wilfred MurithiCentre for Respiratory Diseases Research, Kenya Medical Research Institute.
Zipporah MwongeraCentre for Respiratory Diseases Research, Kenya Medical Research Institute.
Gisella LogioiaUniversity of Washington.
Glenna PetersonUniversity of Washington.
R Max SegnitzUniversity of Washington.ORCID 0000-0001-9806-259X
Kevin FennellyNational Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH).ORCID 0000-0001-9416-0686
Thomas HawnUniversity of Washington.
National Institutes of Health · USKenya Medical Research Institute · KEUniversity of Washington · US

Funding

Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
Aerobiology, immunology, and Mycobacterium tuberculosis transmissionR01AI150815 · NIAID · UNIVERSITY OF WASHINGTON · PI HAWN, THOMAS R, HORNE, DAVID J. · 2020 to 2024
$3.5M
Tuberculosis & HIV Co-Infection Training Program in KenyaD43TW011817 · FIC · UNIVERSITY OF WASHINGTON · PI Thomas R Hawn, VIDELIS NDUBA · 2021 to 2026
$1.6M
Pulmonary Innate Immunity & Resistance to Mycobacterium Tuberculosis InfectionK24AI137310 · NIAID · UNIVERSITY OF WASHINGTON · PI HAWN, THOMAS R · 2018 to 2022
$892k
Mycobacterium tuberculosis aerobiology and novel tools to assess infectiousnessUH2AI152621 · NIAID · UNIVERSITY OF WASHINGTON · PI HORNE, DAVID J. · 2021 to 2022
$365k
FIC NIH HHS D43 TW011817NCATS NIH HHS UL1 TR002319NIAID NIH HHS K24 AI137310NIAID NIH HHS R01 AI150815NIAID NIH HHS UH2 AI152621
6 · The paper itself

Abstract

Interrupting transmission events to prevent new acquisition of infection and disease is a critical part of tuberculosis (TB) control efforts. However, knowledge gaps in understanding the biology and determinants of TB transmission, including poor estimates of individual infectiousness and the lack of accurate and convenient biomarkers, undermine efforts to develop interventions. Cough-generated aerosol cultures have been found to predict TB transmission better than any microbiological or clinical markers in cohorts from Uganda and Brazil. We hypothesized that highly infectious individuals with pulmonary TB (defined as positive for cough aerosol cultures) have elevated inflammatory markers and unique transcriptional profiles compared to less infectious individuals (negative for cough aerosol cultures). We performed a prospective, longitudinal study using a cough aerosol sampling system as in other studies. We enrolled 142 participants with treatment-naïve pulmonary TB in Nairobi, Kenya, and assessed the association of clinical, microbiologic, and immunologic characteristics with Mtb aerosolization and transmission in 143 household members. Contacts of the forty-three aerosol culture-positive participants (30%) were more likely to have a positive IGRA (85% vs 53%, P = 0.005) and a higher median IGRA IFNγ level (P < 0.001, median 4.25 IU/ml (0.90-5.91) vs. 0.71 (0.01-3.56)) compared to aerosol culture-negative individuals. We found that higher bacillary burden, younger age, and larger mean upper arm circumference were associated with positive aerosol cultures. In addition, novel host inflammatory profiles, including elevated serum C-reactive protein and sputum cytokines, were associated with aerosol culture status. Notably, we found pre-treatment whole blood transcriptional profiles associated with aerosol culture status, independent of bacillary load. Together, these findings suggest that TB infectiousness is associated with epidemiologic characteristics and inflammatory signatures and that these features may be used to identify highly infectious persons. These results provide new public health tools and insights into TB pathogenesis.

Identifiers

PMID38328225
PMCPMC10849670
OpenAlexW4390691542

What OpenQuestion holds

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Registered trials

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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.