Evidence map›Paper›PMID 37350148›Full record

ArticleStatistics in medicine2023

Bayesian multivariate longitudinal model for immune responses to Leishmania: A tick-borne co-infection study.

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

Open access · hybridAbstract read
In one paragraph

Article in Statistics in medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Tick-borne coinfections modulate CD8Infection and immunity · 2025
    Article
  2. Article
  3. Article
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

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, USA.ORCID 0000-0003-3528-2354
Grant D BrownDepartment of Biostatistics, The University of Iowa College of Public Health, Iowa City, Iowa, USA.ORCID 0000-0002-7247-7313
Breanna M ScorzaDepartment of Epidemiology, The University of Iowa College of Public Health, Iowa City, Iowa, USA.ORCID 0000-0002-3489-0270
Christine A PetersenDepartment of Epidemiology, The University of Iowa College of Public Health, Iowa City, Iowa, USA.ORCID 0000-0002-7285-4254
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
NIAID NIH HHS R01 AI139267NIAID NIH HHS R01 AI171971NIAID NIH HHS T32 AI007260
6 · The paper itself

Abstract

While many Bayesian state-space models for infectious disease processes focus on population infection dynamics (eg, compartmental models), in this work we examine the evolution of infection processes and the complexities of the immune responses within the host using these techniques. We present a joint Bayesian state-space model to better understand how the immune system contributes to the control of Leishmania infantum infections over the disease course. We use longitudinal molecular diagnostic and clinical data of a cohort of dogs to describe population progression rates and present evidence for important drivers of clinical disease. Among these results, we find evidence for the importance of co-infection in disease progression. We also show that as dogs progress through the infection, parasite load is influenced by their age, ectoparasiticide treatment status, and serology. Furthermore, we present evidence that pathogen load information from an earlier point in time influences its future value and that the size of this effect varies depending on the clinical stage of the dog. In addition to characterizing the processes driving disease progression, we predict individual and aggregate patterns of Canine Leishmaniasis progression. Both our findings and the application to individual-level predictions are of direct clinical relevance, presenting possible opportunities for application in veterinary practice and motivating lines of additional investigation to better understand and predict disease progression. Finally, as an important zoonotic human pathogen, these results may support future efforts to prevent and treat human Leishmaniosis.

Indexed as

CoinfectionDog DiseasesLeishmania infantumLeishmaniasis, VisceralTicksAnimalsBayes TheoremDisease ProgressionDogsHumansImmunityBayesian modelingcanine leishmaniasisco-infectionimmune responseslongitudinal

Identifiers

PMID37350148
PMCPMC11123579
OpenAlexW4381716629

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.