Evidence map›Paper›PMID 38022535›Full record

ArticleFrontiers in immunology2023

Profound and selective lymphopaenia in primary lymphatic anomaly patients demonstrates the significance of lymphatic-lymphocyte interactions.

Julian Pearce, Linda Hadcocks, Sahar Mansour, Malou van Zanten, Steve Jeffery, Kristiana Gordon, Pia Ostergaard, Peter Mortimer, Derek C Macallan

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 2 institutions in 1 country.

Julian Pearce *Lymphovascular Research Unit, Molecular and Clinical Sciences Research Institute, St George's, University of London, London, United Kingdom.
Linda Hadcocks *Institute for Infection and Immunity, St George's, University of London, London, United Kingdom.
Sahar MansourLymphovascular Research Unit, Molecular and Clinical Sciences Research Institute, St George's, University of London, London, United Kingdom.
Malou van ZantenLymphovascular Research Unit, Molecular and Clinical Sciences Research Institute, St George's, University of London, London, United Kingdom.
Steve JefferyLymphovascular Research Unit, Molecular and Clinical Sciences Research Institute, St George's, University of London, London, United Kingdom.
Kristiana GordonDermatology and Lymphovascular Medicine, St George's University Hospitals NHS Foundation Trust, London, United Kingdom.
Pia OstergaardLymphovascular Research Unit, Molecular and Clinical Sciences Research Institute, St George's, University of London, London, United Kingdom.
Peter MortimerLymphovascular Research Unit, Molecular and Clinical Sciences Research Institute, St George's, University of London, London, United Kingdom.
Derek C MacallanInstitute for Infection and Immunity, St George's, University of London, London, United Kingdom.
St George's, University of London · GBSt George’s University Hospitals NHS Foundation Trust · GB

Funding

British Heart Foundation RG/17/7/33217Medical Research Council MR/P011543/1
6 · The paper itself

Abstract

Introduction: The lymphatic system has a pivotal role in immune homeostasis. To better understand this, we investigated the impact of Primary Lymphatic Anomalies (PLA) on lymphocyte numbers and phenotype. Methods: The study comprised (i) a retrospective cohort: 177 PLA subjects from the National Primary Lymphatic Anomaly Register with clinical and laboratory data, and (ii) a prospective cohort: 28 patients with PLA and 20 healthy controls. Patients were subdivided using established phenotypic diagnostic categories and grouped into simplex (localised tissue involvement only) and systemic (involvement of central lymphatics). Further grouping variables included genital involvement and the likelihood of co-existent intestinal lymphangiectasia. Haematology laboratory parameters were analysed in both cohorts. In the prospective cohort, prospective blood samples were analysed by flow cytometry for markers of proliferation, differentiation, activation, skin-homing, and for regulatory (CD4 Results: In patients with PLA, lymphopaenia was frequent (22% of subjects), affected primarily the CD4 Discussion: Patients with PLA who have dysfunctional lymphatics have a selective reduction in circulating lymphocytes which preferentially depletes naïve CD4

Indexed as

Antigens, Differentiation, T-LymphocyteCD8-Positive T-LymphocytesEdemaHumansPolyestersProspective StudiesRetrospective StudiesAntigens, Differentiation, T-LymphocytePolyesterscellulitislymphangiectasialymphatic diseaseslymphocyte subsetslymphoedemalymphopaenianaïve T cellsWILD syndrome

Identifiers

PMID38022535
PMCPMC10656747
OpenAlexW4388337913

What OpenQuestion holds

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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.