Evidence map›Paper›PMID 33506633›Full record

ArticleStem cells translational medicine2021

Resident vs nonresident multipotent mesenchymal stromal cell interactions with B lymphocytes result in disparate outcomes.

Wei Lee, Li-Tzu Wang, Men-Luh Yen, Pei-Ju Hsu, Yu-Wei Lee, Ko-Jiunn Liu, Kuo-I Lin, Yu-Wen Su, Huey-Kang Sytwu, B Linju Yen

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 19 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

10 authors at 3 institutions in 1 country.

Wei LeeGraduate Institute of Life Sciences, National Defense Medical Center (NDMC), Taipei, Taiwan.
Li-Tzu WangDepartment of Obstetrics/Gynecology, National Taiwan University (NTU) Hospital and College of Medicine, NTU, Taipei, Taiwan.
Men-Luh YenDepartment of Obstetrics/Gynecology, National Taiwan University (NTU) Hospital and College of Medicine, NTU, Taipei, Taiwan.
Pei-Ju HsuRegenerative Medicine Research Group, Institute of Cellular and System Medicine, National Health Research Institutes (NHRI), Zhunan, Taiwan.
Yu-Wei LeeRegenerative Medicine Research Group, Institute of Cellular and System Medicine, National Health Research Institutes (NHRI), Zhunan, Taiwan.
Ko-Jiunn LiuNational Institute of Cancer Research, NHRI, Tainan, Taiwan.
Kuo-I LinGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Yu-Wen SuImmunology Research Center, NHRI, Zhunan, Taiwan.
Huey-Kang SytwuNational Institute of Infectious Diseases & Vaccinology, NHRI, Zhunan, Taiwan.
B Linju YenRegenerative Medicine Research Group, Institute of Cellular and System Medicine, National Health Research Institutes (NHRI), Zhunan, Taiwan.ORCID 0000-0002-6905-3018
National Health Research Institutes · TWNational Taiwan University Hospital · TWGenomics Research Center, Academia Sinica · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multipotent human mesenchymal stromal cells (MSCs) from multiple organs including the bone marrow (BM) and placenta harbor clinically relevant immunomodulation best demonstrated toward T lymphocytes. Surprisingly, there is limited knowledge on interactions with B lymphocytes, which originate from the BM where there is a resident MSC. With increasing data demonstrating MSC tissue-specific propensities impacting therapeutic outcome, we therefore investigated the interactions of BM-MSCs-its resident and "niche" MSC-and placental MSCs (P-MSCs), another source of MSCs with well-characterized immunomodulatory properties, on the global functional outcomes of pan-peripheral B cell populations. We found that P-MSCs but not BM-MSCs significantly inhibit proliferation and further differentiation of stimulated human peripheral B populations in vitro. Moreover, although BM-MSCs preserve multiple IL-10-producing regulatory B cell (Breg) subsets, P-MSCs significantly increase all subsets. To corroborate these in vitro findings in vivo, we used a mouse model of B-cell activation and found that adoptive transfer of P-MSCs but not BM-MSCs significantly decreased activated B220

Indexed as

B-LymphocytesMesenchymal Stem CellsPluripotent Stem CellsAnimalsB-Lymphocytes, RegulatoryBone Marrow CellsCell CommunicationCell DifferentiationCell ProliferationFemaleInterleukin-10MicePlacentaPregnancyInterleukin-10bone marrow (BM)human mesenchymal stromal cells (MSCs)interleukin-10 (IL-10)peripheral B lymphocytesplacentaregulatory B cells (Bregs)tissue specificity

Identifiers

PMID33506633
PMCPMC8046079
OpenAlexW3124643774

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.