Evidence map›Paper›PMID 31377972›Full record

ArticleJournal of clinical immunology2019

Pattern Recognition Molecules of the Lectin Pathway-Screening of Patients with Suspected Immunodeficiency.

Clara Mistegård Jørgensen, Lisbeth Jensen, Mette Christiansen, Mette Bjerre, Jens Magnus Bernth Jensen, Steffen Thiel

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Article in Journal of clinical immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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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.

Clara Mistegård JørgensenDepartment of Biomedicine, Aarhus University, Wilhelm Meyers Allé 4, 8000, Aarhus, Denmark. clarjo@rm.dk.ORCID http://orcid.org/0000-0002-6359-2192
Lisbeth JensenDepartment of Biomedicine, Aarhus University, Wilhelm Meyers Allé 4, 8000, Aarhus, Denmark.
Mette ChristiansenDepartment of Clinical Medicine - Department of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
Mette BjerreDepartment of Clinical Medicine - Medical Research Laboratory, Aarhus University, Aarhus, Denmark.
Jens Magnus Bernth JensenDepartment of Clinical Medicine - Department of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
Steffen ThielDepartment of Biomedicine, Aarhus University, Wilhelm Meyers Allé 4, 8000, Aarhus, Denmark.
Aarhus University · DKAarhus University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo compare plasma concentrations of all lectin pathway (LP) pattern recognition molecules (PRMs) in patients referred for laboratory evaluation due to recurrent infections with healthy individuals.

methodsPatients were divided into categories according to referral: recurrent airway infections (RAI), recurrent abscesses, common variable immunodeficiency (CVID), lung transplantation candidates (LTX), and 'other causes'. LP PRMs (mannose-binding lectin (MBL), collectin liver 1 (CL-L1), H-ficolin, L-ficolin, M-ficolin) and C-reactive protein (CRP) were determined in 332 patients and 150 healthy blood donors using time-resolved immunofluorometric assays.

resultsNone of the LP PRMs was found in lower concentration in the patient categories; however, several PRMs were detected in higher concentrations. M-ficolin was found in higher concentrations in all patient categories. Patients suffering from RAI had higher concentrations of CL-L1 and H-ficolin. Patients suffering from abscesses exhibited higher concentrations of MBL and CL-L1, whereas LTX had higher concentrations of MBL. Patients with other causes of referral had higher concentrations of MBL and CL-L1. Prevalence of combined deficiencies of PRMs in patient categories and controls did not differ. CRP was used as a marker of ongoing inflammation and was significantly higher among all patient categories. Furthermore, CRP was found to correlate with both M-ficolin and L-ficolin.

conclusionThe results suggest that neither single nor combined deficiencies of LP PRMs are more frequent among patients referred for an immunological evaluation than in healthy individuals. Future studies are needed and should focus on deficiencies of LP PRMs combined with deficiencies in other parts of the immune system.

Indexed as

BiomarkersC-Reactive ProteinDenmarkDisease SusceptibilityEnzyme-Linked Immunosorbent AssayFemaleHumansImmunologic Deficiency SyndromesLectinsMaleMass ScreeningSignal TransductionBiomarkersC-Reactive ProteinLectinsComplementImmunodeficiencyImmunological evaluationLectin pathwayScreening

Identifiers

PMID31377972
OpenAlexW2965350200

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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.