Evidence map›Paper›PMID 32082002›Full record

ArticleMedical archives (Sarajevo, Bosnia and Herzegovina)2019

Expression of NK (CD16+56+) and B cells (CD19) Receptor Molecules as a Reliable Clinical Response Biomarkers of SLE and RA Patients Under the Rituximab Treatment.

Lamija Zecevic, Mevludin Mekic, Djemo Subasic, Majda Hadziabulic, Edmira Isak, Emina Subasic, Kenan Selmanovic

Open access · greenAbstract read
In one paragraph

Article in Medical archives (Sarajevo, Bosnia and Herzegovina), 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
0.3field-weighted citation impact, top 39% 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, 7 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

7 authors at 2 institutions in 1 country.

Lamija ZecevicDepartment of Immunology, Clinical Center University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
Mevludin MekicDepartment for Rheumatology, Clinic for Heart, Blood Vessel and Rheumatism, Clinical Center University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
Djemo SubasicFaculty of Science, University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
Majda HadziabulicPublic Health Center Gornji Vakuf-Uskoplje, Gornji Vakuf-Uskoplje, Bosnia and Herzegovina.
Edmira IsakPublic Health Center Gornji Vakuf-Uskoplje, Gornji Vakuf-Uskoplje, Bosnia and Herzegovina.
Emina SubasicFaculty of Science, University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
Kenan SelmanovicFaculty of Medicine, University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
University of Sarajevo · BAClinical Center University of Sarajevo · BA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionLately, the use of biological therapy in various autoimmune diseases is increasing. The ideal marker for monitoring the effects of modern therapy is still non-existent.

aimTo investigate early response biomarkers of SLE and RA patients under the rituximab treatment are in research phase and each new investigations offer new and original useful data. MATERIAL AND

methodsImmunophenotyping of cells was carried out by a standard method of sample preparation. We investigated by flow cytometric analyses expression of NK and CD19+ cells at ten SLE and five RA patients before and after treatment with rituximab, in laboratory of Department of Clinical immunology in the Clinical Centre University of Sarajevo.

resultsIn both cases, SLE and RA patients, reduced number of CD16+ parameter indicates lower cytotoxic activity of NK cells. Increased number of B cells indicates higher pathological activity leading to severe autoimmune disease allegation.

conclusionDetermining the proportion of NK and B will be useful diagnostic tool in therapeutic strategy, and also in monitoring of effect of biological therapy.

Indexed as

Antigens, CD19Antirheumatic AgentsArthritis, RheumatoidBiomarkersB-LymphocytesCD56 AntigenFlow CytometryGPI-Linked ProteinsHumansImmunophenotypingKiller Cells, NaturalLupus Erythematosus, SystemicReceptors, IgGRituximabTreatment OutcomeAntigens, CD19Antirheumatic AgentsBiomarkersCD19 molecule, humanCD56 AntigenFCGR3B protein, humanGPI-Linked ProteinsNCAM1 protein, humanReceptors, IgGRituximabAutoimmune diseaseB cells and NK cellsBiological drugstherapy

Identifiers

PMID32082002
PMCPMC7007611
OpenAlexW2996863798

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Registered trials

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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.