Evidence map›Paper›PMID 33298881›Full record

ArticleCell death discovery2020

Mesenchymal stem cells protect against malaria pathogenesis by reprogramming erythropoiesis in the bone marrow.

Reva S Thakur, Vikky Awasthi, Anirban Sanyal, Samit Chatterjee, Swati Rani, Rubika Chauhan, Meenu Kalkal, Mrinalini Tiwari, Veena Pande, Jyoti Das

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 13 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.

Reva S ThakurParasite-Host Biology, National Institute of Malaria Research, Dwarka, New Delhi, 110077, India.
Vikky AwasthiParasite-Host Biology, National Institute of Malaria Research, Dwarka, New Delhi, 110077, India.
Anirban SanyalParasite-Host Biology, National Institute of Malaria Research, Dwarka, New Delhi, 110077, India.
Samit ChatterjeeDepartment of Zoology, University of Rajasthan, Jaipur, 302004, India.
Swati RaniParasite-Host Biology, National Institute of Malaria Research, Dwarka, New Delhi, 110077, India.
Rubika ChauhanParasite-Host Biology, National Institute of Malaria Research, Dwarka, New Delhi, 110077, India.
Meenu KalkalParasite-Host Biology, National Institute of Malaria Research, Dwarka, New Delhi, 110077, India.
Mrinalini TiwariDepartment of Genetics and Epigenetics, Institute of Nuclear Medicine & Allied Science, Timarpur, New Delhi, 110054, India.
Veena PandeDepartment of Biotechnology, Kamaun University, Nanital, 263001, India.
Jyoti DasParasite-Host Biology, National Institute of Malaria Research, Dwarka, New Delhi, 110077, India. drjyoti203@gmail.com.
National Institute of Malaria Research · INInstitute of Nuclear Medicine & Allied Sciences · INUniversity of Rajasthan · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malaria remains a major public health problem worldwide. The immune mechanisms that mediate protection against malaria are still unclear. Previously, we reported that mesenchymal stem cells (MSCs) play a critical role in host protection against malaria by altering the dynamic balance of T regulatory cells and effector T cells producing inflammatory cytokines. Here, we report that MSCs reprogram haematopoiesis in primary (bone marrow) and secondary (spleen) lymphoid organs to provide host protection against malaria. Adoptive transfer of MSCs from malaria-infected mice to naïve recipient mice that were subsequently infected with malaria parasites dramatically accelerated the formation of colony-forming units-erythroid cells in the bone marrow. Adoptively transferred MSCs also induced expression of the key erythroid cell differentiation factor GATA-1 in the spleen of recipient animals. Interestingly, we further observed a subtle increase in the CD34

Identifiers

PMID33298881
PMCPMC7667156
OpenAlexW3103982476

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.