Evidence map›Paper›PMID 42848769›Full record

ArticlePloS one2026

Functional characterization of neutrophils in patients with multiple myeloma.

Kapina Mwampembwa, Emmanuel Mweni, Humphrey Mwape, Ruth Daka, John Nzobokela, Chrispin Chisanga, Sody Munsaka

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kapina MwampembwaDepartment of Biomedical Sciences, School of Health Sciences, University of Zambia, Lusaka, Zambia.ORCID https://orcid.org/0009-0008-0522-3103
Emmanuel MweniDepartment of Biomedical Sciences, School of Health Sciences, University of Zambia, Lusaka, Zambia.
Humphrey MwapeDepartment of Biomedical Sciences, School of Health Sciences, University of Zambia, Lusaka, Zambia.
Ruth DakaHaematology Section, Pathology Department, the University Teaching Hospital, Lusaka, Zambia.
John NzobokelaPathology Department, Ndola Teaching Hospital, Ndola, Zambia.
Chrispin ChisangaDepartment of Biomedical Sciences, School of Health Sciences, University of Zambia, Lusaka, Zambia.ORCID https://orcid.org/0000-0002-8529-2369
Sody MunsakaDepartment of Biomedical Sciences, School of Health Sciences, University of Zambia, Lusaka, Zambia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma is a hematologic cancer caused by abnormal plasma cell proliferation in the bone marrow and is associated with significant immune dysfunction. Neutrophils, essential components of the innate immune response, may function poorly in patients with multiple myeloma, increasing the risk of infection and affecting disease progression. This study aimed to systematically evaluate the extent of neutrophil dysfunction in patients with newly diagnosed and relapsed multiple myeloma. The study employed a cross-sectional analytical design and recruited 72 participants: 30 multiple myeloma patients and 42 age- and sex-matched healthy controls from the University Teaching Hospital and the Cancer Diseases Hospital of Lusaka, Zambia. 4 mL of venous blood was collected from all participants in ethylenediaminetetraacetic acid vacutainers for laboratory analysis. Neutrophils were isolated from whole blood using Polymorphprep™, and functionality was assessed using in vitro assays, including a phagocytosis assay using fluorescently labeled bacterial particles and a reactive oxygen species assay using the fluorescent probe 2', 7'-Dichlorodihydrofluorescein diacetate, measured by flow cytometry. Statistical analysis was performed using STATA. Neutrophils from multiple myeloma patients demonstrated significantly lower phagocytic capacity (45.0% vs 75.9%, P < 0.001) and reactive oxygen species production (44.7% vs 74.9%, P < 0.001) compared to controls. The logistic regression analysis demonstrated strong associations between multiple myeloma and both reactive oxygen species (OR=5097.6, P < 0.001) and phagocytic dysfunction (OR=7272.7, P < 0.001). By contrast, age, sex, white blood cell count, and absolute neutrophil count were not significantly associated with these outcomes. The study found that patients with multiple myeloma exhibit qualitative impairment of neutrophil function, despite normal quantitative neutrophil counts, underscoring the importance of functional immune monitoring in patient management.

Indexed as

Multiple MyelomaNeutrophilsAdultAgedCase-Control StudiesCross-Sectional StudiesFemaleHumansMaleMiddle AgedPhagocytosisReactive Oxygen SpeciesReactive Oxygen Species

Identifiers

PMID42848769
PMCPMC13649033

What Socratic holds

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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 Socratic graph.