Evidence map›Paper›PMID 35883618›Full record

ReviewCells2022

Exploring the Immunomodulatory Aspect of Mesenchymal Stem Cells for Treatment of Severe Coronavirus Disease 19.

Jitendra Kumar Chaudhary, Deepika Saini, Pankaj Kumar Chaudhary, Anurag Maurya, Ganesh Kumar Verma, Akhilesh Kumar Gupta, Rakesh Roshan, Tarun Kumar Vats, Nidhi Garg, Deepika Yadav and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 23% 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, 10 citations in OpenAlex.

  1. Review
  2. Increasing robustness ofRegenerative therapy · 2025
    Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Protective Effects ofEvidence-based complementary and alternative medicine : eCAM · 2022
    Article
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

13 authors at 5 institutions in 1 country.

Jitendra Kumar ChaudharySchool of Life Sciences, Jawaharlal Nehru University, New Delhi 110067, India.ORCID 0000-0001-8499-9656
Deepika SainiDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Rishikesh 249201, India.ORCID 0000-0003-0564-9098
Pankaj Kumar ChaudharyMolecular Biology & Proteomics Laboratory, Department of Biotechnology, Indian Institute of Technology (IIT), Roorkee 247667, India.ORCID 0000-0002-0570-0140
Anurag MauryaDepartment of Botany, Shivaji College, University of Delhi, New Delhi 110027, India.ORCID 0000-0002-6814-5957
Ganesh Kumar VermaDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Rishikesh 249201, India.ORCID 0000-0002-0887-7785
Akhilesh Kumar GuptaSchool of Medical Science and Technology (SMST), Indian Institute of Technology (IIT), Kharagpur 721302, India.ORCID 0000-0001-5754-2765
Rakesh RoshanDepartment of Zoology, Shivaji College, University of Delhi, New Delhi 110027, India.ORCID 0000-0003-1114-6809
Tarun Kumar VatsDepartment of Zoology, Shivaji College, University of Delhi, New Delhi 110027, India.ORCID 0000-0002-1447-8713
Nidhi GargDepartment of Zoology, Shivaji College, University of Delhi, New Delhi 110027, India.ORCID 0000-0001-6904-4974
Deepika YadavDepartment of Zoology, Shivaji College, University of Delhi, New Delhi 110027, India.ORCID 0000-0002-5496-2251
Nimita KantDepartment of Zoology, Shivaji College, University of Delhi, New Delhi 110027, India.ORCID 0000-0002-9156-4893
Anil Kumar MeenaDepartment of Zoology, Maharshi Dayanand Saraswati University, Ajmer 304001, India.ORCID 0000-0002-8252-462X
Anissa Atif Mirza-ShariffDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Rishikesh 249201, India.ORCID 0000-0002-7531-3445
University of Delhi · INAll India Institute of Medical Sciences Rishikesh · INIndian Institute of Technology Kharagpur · INIndian Institute of Technology Roorkee · INMaharshi Dayanand Saraswati University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is an enveloped, positive sense, single stranded RNA (+ssRNA) virus, belonging to the genus Betacoronavirus and family Coronaviridae. It is primarily transmitted from infected persons to healthy ones through inhalation of virus-laden respiratory droplets. After an average incubation period of 2-14 days, the majority of infected individuals remain asymptomatic and/or mildly symptomatic, whereas the remaining individuals manifest a myriad of clinical symptoms, including fever, sore throat, dry cough, fatigue, chest pain, and breathlessness. SARS-CoV-2 exploits the angiotensin converting enzyme 2 (ACE-2) receptor for cellular invasion, and lungs are amongst the most adversely affected organs in the body. Thereupon, immune responses are elicited, which may devolve into a cytokine storm characterized by enhanced secretion of multitude of inflammatory cytokines/chemokines and growth factors, such as interleukin (IL)-2, IL-6, IL-7, IL-8, IL-9, tumor necrosis factor alpha (TNF-α), granulocyte colony-stimulating factor (GCSF), basic fibroblast growth factor 2 (bFGF2), monocyte chemotactic protein-1 (MCP1), interferon-inducible protein 10 (IP10), macrophage inflammatory protein 1A (MIP1A), platelet-derived growth factor subunit B (PDGFB), and vascular endothelial factor (VEGF)-A. The systemic persistence of inflammatory molecules causes widespread histological injury, leading to functional deterioration of the infected organ(s). Although multiple treatment modalities with varying effectiveness are being employed, nevertheless, there is no curative COVID-19 therapy available to date. In this regard, one plausible supportive therapeutic modality may involve administration of mesenchymal stem cells (MSCs) and/or MSC-derived bioactive factors-based secretome to critically ill COVID-19 patients with the intention of accomplishing better clinical outcome owing to their empirically established beneficial effects. MSCs are well established adult stem cells (ASCs) with respect to their immunomodulatory, anti-inflammatory, anti-oxidative, anti-apoptotic, pro-angiogenic, and pro-regenerative properties. The immunomodulatory capabilities of MSCs are not constitutive but rather are highly dependent on a holistic niche. Following intravenous infusion, MSCs are known to undergo considerable histological trapping in the lungs and, therefore, become well positioned to directly engage with lung infiltrating immune cells, and thereby mitigate excessive inflammation and reverse/regenerate damaged alveolar epithelial cells and associated tissue post SARS-CoV-2 infection. Considering the myriad of abovementioned biologically beneficial properties and emerging translational insights, MSCs may be used as potential supportive therapy to counteract cytokine storms and reduce disease severity, thereby facilitating speedy recovery and health restoration.

Indexed as

COVID-19Mesenchymal Stem CellsAdultCytokine Release SyndromeHumansImmunityImmunomodulationSARS-CoV-2angiotensin converting enzyme 2cytokine stormimmunomodulationmesenchymal stem cellsSevere Acute Respiratory Syndrome Coronavirus-2

Identifiers

PMID35883618
PMCPMC9322532
OpenAlexW4285088942

What OpenQuestion holds

Textmetadata
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.