Evidence map›Paper›PMID 31183814›Full record

ArticleInternational journal of hematology2019

VS38 as a promising CD38 substitute antibody for flow cytometric detection of plasma cells in the daratumumab era.

Shumpei Mizuta, Takahito Kawata, Hiroshi Kawabata, Noriko Yamane, Saya Mononobe, Takao Komai, Yusuke Koba, Naoya Ukyo, Akira Tamekane, Mitsumasa Watanabe

Abstract read
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In one paragraph

Article in International journal of hematology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Article
  5. CD38-specific nanobodies allowFrontiers in immunology · 2022
    Article
  6. Review
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  8. 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

10 authors at 3 institutions in 1 country.

Shumpei MizutaDepartment of Clinical Laboratory, Hyogo Prefectural Amagasaki General Medical Center, 2-17-77 Higashinaniwa-cho Amagasaki, Hyogo, Japan. fgneos0628@yahoo.co.jp.ORCID http://orcid.org/0000-0003-2688-8522
Takahito KawataDepartment of Hematology, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan.
Hiroshi KawabataDepartment of Clinical Laboratory, Hyogo Prefectural Amagasaki General Medical Center, 2-17-77 Higashinaniwa-cho Amagasaki, Hyogo, Japan.
Noriko YamaneDepartment of Clinical Laboratory, Hyogo Prefectural Amagasaki General Medical Center, 2-17-77 Higashinaniwa-cho Amagasaki, Hyogo, Japan.
Saya MononobeDepartment of Clinical Laboratory, Hyogo Prefectural Amagasaki General Medical Center, 2-17-77 Higashinaniwa-cho Amagasaki, Hyogo, Japan.
Takao KomaiDepartment of Clinical Laboratory, Hyogo Prefectural Amagasaki General Medical Center, 2-17-77 Higashinaniwa-cho Amagasaki, Hyogo, Japan.
Yusuke KobaDepartment of Hematology, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan.
Naoya UkyoDepartment of Hematology, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan.
Akira TamekaneDepartment of Hematology, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan.
Mitsumasa WatanabeDepartment of Hematology, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan.
Hyogo Prefectural Amagasaki General Medical Center · JPHyogo University of Health Sciences · JPKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of effective therapies has enabled long-term survival for many patients with multiple myeloma (MM). However, the administration of antibody drugs, such as daratumumab, which bind to plasma cell (PC) surface proteins, may prevent PC detection by flow cytometry. We propose VS38 as an alternative antibody for CD38. VS38 recognizes cytoskeleton-linking membrane protein 63 (CLIMP-63) on the rough endoplasmic reticulum, and this protein may be expressed in secretory cells. We investigated VS38 staining in normal hematopoietic cells from five control samples, as well as PCs from 21 patients with plasma cell disorder (PCD). In normal hematopoietic cells, although VS38-stained monocytes, myeloid cells, and a subpopulation of B cells, PCs were significantly and brightly stained by VS38. There was no significant difference in VS38 staining between normal and abnormal PCs obtained from five patients with monoclonal gammopathy of undetermined significance. Furthermore, PCs in 21 PCD cases were clearly identified by VS38 in all cases, in contrast to CD38, even in daratumumab-administered patients whose CD38 epitopes on PCs were masked. These results suggest that the use of the VS38 antibody in flow cytometry contributes to PC detection, independent of therapeutic treatment.

Indexed as

Antibodies, MonoclonalFlow CytometryADP-ribosyl Cyclase 1Antineoplastic Agents, ImmunologicalHumansMembrane GlycoproteinsMembrane ProteinsMultiple MyelomaNeoplasm ProteinsPlasma CellsADP-ribosyl Cyclase 1Antibodies, MonoclonalAntineoplastic Agents, ImmunologicalCD38 protein, humanCKAP4 protein, humandaratumumabMembrane GlycoproteinsMembrane ProteinsNeoplasm ProteinsCD38DaratumumabFlow cytometryMultiple myelomaVS38

Identifiers

PMID31183814
OpenAlexW2953315474

What OpenQuestion holds

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Read underepoch 390

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.