Evidence map›Paper›PMID 41249610›Full record

ReviewJournal of clinical immunology2025

Evaluating Pediatric Reference Ranges for Extended Immunophenotyping from a Finnish Cohort against Published References.

Elli Äärimaa, Anssi Kesäläinen, Samuel Askeli, Anne Toivonen, Okko Savonius, Oscar Brück, Pauliina Lusila, Kim Vettenranta, Santtu Heinonen, Timo Jahnukainen and 4 more

Abstract readReview
In one paragraph

Review in Journal of clinical immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Elli Äärimaa *Translational Immunology Research Program, University of Helsinki, Helsinki, 00014, Finland. elli.aarimaa@helsinki.fi.
Anssi Kesäläinen *Translational Immunology Research Program, University of Helsinki, Helsinki, 00014, Finland. anssi.kesalainen@helsinki.fi.
Samuel AskeliTranslational Immunology Research Program, University of Helsinki, Helsinki, 00014, Finland. samuel.askeli@helsinki.fi.
Anne ToivonenClinical Microbiology, HUS Diagnostic Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Okko SavoniusDepartment of Pediatric Nephrology and Transplantation, New Children's Hospital, Pediatric Research Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Oscar BrückHematoscope Lab, Comprehensive Cancer Center, Department of Clinical Chemistry, HUS Diagnostic Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Pauliina LusilaNew Children's Hospital, Pediatric Research Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Kim VettenrantaNew Children's Hospital, Pediatric Research Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Santtu HeinonenNew Children's Hospital, Pediatric Research Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Timo JahnukainenDepartment of Pediatric Nephrology and Transplantation, New Children's Hospital, Pediatric Research Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Minna KoskenvuoDivision of Pediatric Hematology, Oncology and Stem Cell Transplantation, New Children's Hospital, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Sanna SiitonenClinical Chemistry, HUS Diagnostic Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Sari LehtimäkiClinical Chemistry, HUS Diagnostic Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Eliisa KekäläinenTranslational Immunology Research Program, University of Helsinki, Helsinki, 00014, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flow cytometric immunophenotyping of lymphocytes and dendritic cells, and functional lymphocyte mitogen response tests are used in the diagnostics of inborn errors of immunity (IEI), especially in pediatrics. These routinely used tests lack sufficient age-matched reference values in children. We established reference values for lymphocyte and dendritic cell subsets for four age groups from 68 healthy children under 12 years of age. These values were then compared to prior publicly available articles and 46 clinical samples from children with confirmed IEI diagnosis. Mitogen response results were also compared between 27 children and 177 adults. In the literature review, we found considerable variability in lymphocyte subset definitions and statistical approaches. Most IEI patients had increased transitional and naïve B, and decreased memory B cells. CHH patients had increased γδ T and DNTs. Lymphocyte stimulation via FASCIA method provides weaker stimulation results in children than in adults, which seems to result from a larger proportional count of naïve lymphocytes in children. The established reference values can be used in diagnostics of pediatric immunological conditions in laboratories that use similar analytic methods. Lower lymphocyte mitogen response results in children need to be taken into consideration when interpreting the results of lymphocyte functional tests.

Indexed as

Dendritic CellsImmunophenotypingLymphocyte SubsetsAdultChildChild, PreschoolCohort StudiesFemaleFinlandFlow CytometryHumansInfantInfant, NewbornMaleReference ValuesFlow cytometryImmunodeficiencyImmunophenotypingLymphocyte subsetsPediatricsReference values

Identifiers

PMID41249610
PMCPMC12628421

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.