Evidence map›Paper›PMID 38169327›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2024

Schistosome Infection Impacts Hematopoiesis.

Tobias Wijshake, Joseph Rose, Jipeng Wang, Jacob Zielke, Madeleine Marlar-Pavey, Weina Chen, James J Collins, Michalis Agathocleous

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Loss of vitamin C biosynthesis protects from the pathology of a parasitic infection.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Tobias WijshakeChildren's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0003-1784-2100
Joseph RoseChildren's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, TX.
Jipeng WangDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0003-0107-424X
Jacob ZielkeChildren's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0001-5003-045X
Madeleine Marlar-PaveyChildren's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0001-5819-0407
Weina ChenDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX.
James J CollinsDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX.
Michalis AgathocleousChildren's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, TX.
Children's Medical Center · USThe University of Texas Southwestern Medical Center · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
The Biology of Stem Cells in the Human Parasite Schistosoma MansoniR01AI121037 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI COLLINS, JAMES J · 2016 to 2025
$4.4M
Characterizing sexual development of the human parasite Schistosoma mansoniR01AI150776 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI COLLINS, JAMES J · 2020 to 2024
$2.7M
The role of ascorbate in myelopoiesis and infectionR01DK125713 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI AGATHOCLEOUS, MICHALIS · 2021 to 2025
$1.8M
The role of glycolysis and glucose oxidation in hematopoiesisR01HL161387 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI AGATHOCLEOUS, MICHALIS · 2022 to 2025
$1.6M
NCI NIH HHS P30 CA142543NHLBI NIH HHS R01 HL161387NIAID NIH HHS R01 AI121037NIAID NIH HHS R01 AI150776NIDDK NIH HHS R01 DK125713
6 · The paper itself

Abstract

Helminth infections are common in animals. However, the impact of a helminth infection on the function of hematopoietic stem cells (HSCs) and other hematopoietic cells has not been comprehensively defined. In this article, we describe the hematopoietic response to infection of mice with Schistosoma mansoni, a parasitic flatworm that causes schistosomiasis. We analyzed the frequency or number of hematopoietic cell types in the bone marrow, spleen, liver, thymus, and blood and observed multiple hematopoietic changes caused by infection. Schistosome infection impaired bone marrow HSC function after serial transplantation. Functional HSCs were present in the infected liver. Infection blocked bone marrow erythropoiesis and augmented spleen erythropoiesis, observations consistent with the anemia and splenomegaly prevalent in schistosomiasis patients. This work defines the hematopoietic response to schistosomiasis, a debilitating disease afflicting more than 200 million people, and identifies impairments in HSC function and erythropoiesis.

Indexed as

Bone MarrowSchistosomiasisAnimalsErythropoiesisHematopoiesisHematopoietic Stem CellsHumansMiceSpleen

Identifiers

PMID38169327
PMCPMC10872488
OpenAlexW4390537359

What OpenQuestion holds

Textmetadata
LicenceTDM
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.