Evidence map›Paper›PMID 38938578›Full record

ArticleFrontiers in immunology2024

The function of the complement system remains fully intact throughout the course of allogeneic stem cell transplantation.

Beatrice Fageräng, Leon Cyranka, Camilla Schjalm, Karin Ekholt McAdam, Carina Sandem Larsen, Julia Heinzelbecker, Tobias Gedde-Dahl, Reinhard Würzner, Terje Espevik, Geir Erland Tjønnfjord and 4 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Beatrice FagerängDepartment of Immunology, Oslo University Hospital and University of Oslo, Oslo, Norway.
Leon CyrankaDepartment of Clinical Immunology, Laboratory of Molecular Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Camilla SchjalmDepartment of Immunology, Oslo University Hospital and University of Oslo, Oslo, Norway.
Karin Ekholt McAdamDepartment of Immunology, Oslo University Hospital and University of Oslo, Oslo, Norway.
Carina Sandem LarsenDepartment of Hematology, Oslo University Hospital, Oslo, Norway.
Julia HeinzelbeckerDepartment of Immunology, Oslo University Hospital and University of Oslo, Oslo, Norway.
Tobias Gedde-DahlDepartment of Hematology, Oslo University Hospital, Oslo, Norway.
Reinhard WürznerInstitute of Hygiene and Medical Microbiology, Medical University of Innsbruck, Innsbruck, Austria.
Terje EspevikDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Geir Erland TjønnfjordDepartment of Hematology, Oslo University Hospital, Oslo, Norway.
Peter GarredDepartment of Clinical Immunology, Laboratory of Molecular Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Andreas Barratt-DueDivision of Emergencies and Critical Care, Oslo University Hospital, Oslo, Norway.
Tor Henrik Anderson TvedtDepartment of Hematology, Oslo University Hospital, Oslo, Norway.
Tom Eirik MollnesDepartment of Immunology, Oslo University Hospital and University of Oslo, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Hematopoietic stem cell transplantation (HSCT) is associated with immune complications and endothelial dysfunction due to intricate donor-recipient interactions, conditioning regimens, and inflammatory responses. Methods: This study investigated the role of the complement system during HSCT and its interaction with the cytokine network. Seventeen acute myeloid leukemia patients undergoing HSCT were monitored, including blood sampling from the start of the conditioning regimen until four weeks post-transplant. Clinical follow-up was 200 days. Results: Total complement functional activity was measured by WIELISA and the degree of complement activation by ELISA measurement of sC5b-9. Cytokine release was measured using a 27-multiplex immuno-assay. At all time-points during HSCT complement functional activity remained comparable to healthy controls. Complement activation was continuously stable except for two patients demonstrating increased activation, consistent with severe endotheliopathy and infections. Discussion: In conclusion, HSCT patients generally retained a fully functional complement system, whereas activation occurred in patients with severe complications. The complement-cytokine interaction indicates the potential for new complement-targeting therapeutic strategies in HSCT.

Indexed as

Complement ActivationCytokinesHematopoietic Stem Cell TransplantationTransplantation, HomologousAdultAgedComplement System ProteinsFemaleHumansLeukemia, Myeloid, AcuteMaleMiddle AgedTransplantation ConditioningYoung AdultComplement System ProteinsCytokinescomplementcytokinesHSCTimmunosuppressioninnate immunity

Identifiers

PMID38938578
PMCPMC11208304

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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.