Evidence map›Paper›PMID 38335163›Full record

ArticlePloS one2024

Within-host bayesian joint modeling of longitudinal and time-to-event data of Leishmania infection.

Felix M Pabon-Rodriguez, Grant D Brown, Breanna M Scorza, Christine A Petersen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 35% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Tick-borne coinfections modulate CD8Infection and immunity · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Felix M Pabon-RodriguezDepartment of Biostatistics, The University of Iowa College of Public Health, Iowa City, Iowa, United States of America.ORCID 0000-0003-3528-2354
Grant D BrownDepartment of Biostatistics, The University of Iowa College of Public Health, Iowa City, Iowa, United States of America.
Breanna M ScorzaDepartment of Epidemiology, The University of Iowa College of Public Health, Iowa City, Iowa, United States of America.ORCID 0000-0002-3489-0270
Christine A PetersenDepartment of Epidemiology, The University of Iowa College of Public Health, Iowa City, Iowa, United States of America.
University of Iowa · US

Funding

INTERDISCIPLINARY IMMUNOLOGY TRAINING PROGRAMT32AI007260 · NIAID · UNIVERSITY OF IOWA · PI BUTLER, NOAH SULLIVAN, WU, LI · 1986 to 2023
$5.7M
Field trial and modeling of transmission blocking vaccine to prevent Lyme diseaseR01AI139267 · NIAID · UNIVERSITY OF IOWA · PI BROWN, GRANT D, GOMES-SOLECKI, MARIA · 2019 to 2023
$3.6M
Alteration of skin immune environment by sand fly saliva across progressive LeishmaniasisR01AI171971 · NIAID · UNIVERSITY OF IOWA · PI Christine A Petersen · 2022 to 2026
$3.0M
Epidemic modeling framework for complex, multi-species disease processesR01TW010500 · FIC · UNIVERSITY OF IOWA · PI OLESON, JACOB, PETERSEN, CHRISTINE A · 2016 to 2020
$2.4M
FIC NIH HHS R01 TW010500NIAID NIH HHS R01 AI139267NIAID NIH HHS R01 AI171971NIAID NIH HHS T32 AI007260
6 · The paper itself

Abstract

The host immune system plays a significant role in managing and clearing pathogen material during an infection, but this complex process presents numerous challenges from a modeling perspective. There are many mathematical and statistical models for these kinds of processes that take into account a wide range of events that happen within the host. In this work, we present a Bayesian joint model of longitudinal and time-to-event data of Leishmania infection that considers the interplay between key drivers of the disease process: pathogen load, antibody level, and disease. The longitudinal model also considers approximate inflammatory and regulatory immune factors. In addition to measuring antibody levels produced by the immune system, we adapt data from CD4+ and CD8+ T cell proliferation, and expression of interleukin 10, interferon-gamma, and programmed cell death 1 as inflammatory or regulatory factors mediating the disease process. The model is developed using data collected from a cohort of dogs naturally exposed to Leishmania infantum. The cohort was chosen to start with healthy infected animals, and this is the majority of the data. The model also characterizes the relationship features of the longitudinal outcomes and time-to-death due to progressive Leishmania infection. In addition to describing the mechanisms causing disease progression and impacting the risk of death, we also present the model's ability to predict individual trajectories of Canine Leishmaniosis (CanL) progression. The within-host model structure we present here provides a way forward to address vital research questions regarding the understanding of the progression of complex chronic diseases such as Visceral Leishmaniasis, a parasitic disease causing significant morbidity worldwide.

Indexed as

Dog DiseasesLeishmania infantumLeishmaniasisLeishmaniasis, VisceralAnimalsBayes TheoremCD8-Positive T-LymphocytesDogsHumansInterferon-gammaInterferon-gamma

Identifiers

PMID38335163
PMCPMC10857584
OpenAlexW4391678294

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.