Evidence map›Paper›PMID 39013877›Full record

ArticleNature communications2024

Controlled human hookworm infection remodels plasmacytoid dendritic cells and regulatory T cells towards profiles seen in natural infections in endemic areas.

Mikhael D Manurung, Friederike Sonnet, Marie-Astrid Hoogerwerf, Jacqueline J Janse, Yvonne Kruize, Laura de Bes-Roeleveld, Marion König, Alex Loukas, Benjamin G Dewals, Taniawati Supali and 4 more

Abstract read
In one paragraph

Article in Nature communications, 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

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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
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

14 authors.

Mikhael D Manurung *Leiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0003-2728-1829
Friederike Sonnet *Leiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands.
Marie-Astrid HoogerwerfLeiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-3088-3380
Jacqueline J JanseLeiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands.
Yvonne KruizeLeiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands.
Laura de Bes-RoeleveldLeiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands.
Marion KönigLeiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-9892-218X
Alex LoukasCentre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Australia.
Benjamin G DewalsLaboratory of Immunology-Vaccinology, FARAH, University of Liège, Liège, Belgium.ORCID 0000-0003-1497-0799
Taniawati SupaliDepartment of Parasitology, Faculty of Medicine, University of Indonesia, Jakarta, Indonesia.
Simon P JochemsLeiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-4835-1032
Meta RoestenbergLeiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-5052-2830
Mariateresa CoppolaLeiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-1387-7229
Maria YazdanbakhshLeiden University Center for Infectious Diseases (LU-CID), Leiden University Medical Center, Leiden, The Netherlands. m.yazdanbakhsh@lumc.nl.ORCID 0000-0002-7666-1441

Funding

Stichting Dioraphte (Dioraphte Foundation) 18040403
6 · The paper itself

Abstract

Hookworm infection remains a significant public health concern, particularly in low- and middle-income countries, where mass drug administration has not stopped reinfection. Developing a vaccine is crucial to complement current control measures, which necessitates a thorough understanding of host immune responses. By leveraging controlled human infection models and high-dimensional immunophenotyping, here we investigated the immune remodeling following infection with 50 Necator americanus L3 hookworm larvae in four naïve volunteers over two years of follow-up and compared the profiles with naturally infected populations in endemic areas. Increased plasmacytoid dendritic cell frequency and diminished responsiveness to Toll-like receptor 7/8 ligand were observed in both controlled and natural infection settings. Despite the increased CD45RA

Indexed as

Dendritic CellsNecator americanusT-Lymphocytes, RegulatoryAdultAnimalsEndemic DiseasesFemaleHookworm InfectionsHumansImmunophenotypingMaleNecatoriasisYoung Adult

Identifiers

PMID39013877
PMCPMC11252261

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.