Evidence map›Paper›PMID 28466551›Full record

ArticleVox sanguinis2017

Functionality testing of stem cell grafts to predict infectious complications after allogeneic hematopoietic stem cell transplantation.

J Nilsson, I Granrot, J Mattsson, B Omazic, M Uhlin, S Thunberg

Open access · greenAbstract read
In one paragraph

Article in Vox sanguinis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

6 authors at 2 institutions in 1 country.

J NilssonClinical Immunology and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden.
I GranrotClinical Immunology and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden.
J MattssonCentre for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Stockholm, Sweden.
B OmazicClinical Immunology and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden.
M UhlinClinical Immunology and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-2177-6727
S ThunbergDepartment of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital · SEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesAllogeneic hematopoietic stem cell transplantation (HSCT) is a routine clinical procedure performed to treat patients with haematological malignancies, primary immune deficiencies or metabolic disorders. Infections during lymphopenia after allogeneic HSCT are associated with high mortality and morbidity. Typical infectious agents are Epstein-Barr virus, cytomegalovirus, herpes simplex virus, varicella-zoster virus and fungi. The study aim was to evaluate whether measurement of the responses of antigen-specific T-cells, recognizing infectious pathogens would correlate to protective functions in the stem cell recipient post-transplant. MATERIALS AND

methodsTwenty-one grafts were analysed by flow cytometry and cells were stimulated in vitro with relevant infectious antigens, followed by evaluation of T-cell proliferation and cytokine production. Results were compared to the recipients' clinical records 1-year post-transplantation.

resultsWe show that an extensive repertoire of transferred antigen-specific T-cells from allogeneic donor grafts against infectious agents, involved in post-transplant infections, are linked to an absence of infectious complications for the recipient up-to 1-year post-transplant. The protective effect was associated with antigen-specific T-cell proliferation and IL-1β secretion.

conclusionOur results suggest that assaying T-cell function before HSCT could determine individual risks for infectious complications and thus aid in clinical decision-making regarding prophylactic and pre-emptive anti-infective therapy.

Indexed as

AdenoviridaeAdolescentAdultAgedCandidaChildChild, PreschoolCytomegalovirusFemaleFlow CytometryHematologic NeoplasmsHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHerpesvirus 3, HumanHerpesvirus 4, HumanHumansallogeneic hematopoietic stem cell transplantationFASCIAinfectious complicationsstem cell productstransferred immunity

Identifiers

PMID28466551
PMCPMC7169299
OpenAlexW2611563518

What OpenQuestion holds

Textmetadata
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.