Evidence map›Paper›PMID 27003592›Full record

ArticleeLife2016

Stem cell progeny contribute to the schistosome host-parasite interface.

James J Collins, George R Wendt, Harini Iyer, Phillip A Newmark

Abstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed.

  1. An injury-responsivebioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Unusual inheritance of a functionalScience advances · 2025
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  10. Combined fluorescentBiology methods & protocols · 2025
    Article
  11. Clinical & translational immunology · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

James J CollinsDepartment of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, United States.
George R WendtDepartment of Pharmacology, UT Southwestern Medical Center, Dallas, United States.
Harini IyerDepartment of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, United States.
Phillip A NewmarkDepartment of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, United States.

Funding

DIVISION OF CELL &MOLECULAR BIOLOGY TRAINING PROGRAMT32GM008203 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 1987 to 2018
$7.0M
Developing comparative and functional genomic approaches to study SchistosomaR21AI099642 · NIAID · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI NEWMARK, PHILLIP A · 2012 to 2013
$424k
Howard Hughes Medical InstituteNIAID NIH HHS HHSN272201000005CNIAID NIH HHS HHSN272201000005INIAID NIH HHS R21 AI099642NIAID NIH HHS R21AI099642NIGMS NIH HHS T32 GM008203PHS HHS HHSN272201000005I
6 · The paper itself

Abstract

Schistosomes infect more than 200 million of the world's poorest people. These parasites live in the vasculature, producing eggs that spur a variety of chronic, potentially life-threatening, pathologies exacerbated by the long lifespan of schistosomes, that can thrive in the host for decades. How schistosomes maintain their longevity in this immunologically hostile environment is unknown. Here, we demonstrate that somatic stem cells in Schistosoma mansoni are biased towards generating a population of cells expressing factors associated exclusively with the schistosome host-parasite interface, a structure called the tegument. We show cells expressing these tegumental factors are short-lived and rapidly turned over. We suggest that stem cell-driven renewal of this tegumental lineage represents an important strategy for parasite survival in the context of the host vasculature.

Indexed as

Host-Parasite InteractionsAdult Stem CellsAnimalsHumansSchistosoma mansoniSchistosomiasis mansonidevelopmental biologyinfectious diseasemicrobiologyparasitic diseasesS. mansonistem cells

Identifiers

PMID27003592
PMCPMC4841766

What OpenQuestion holds

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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.