Evidence map›Paper›PMID 37692025›Full record

ArticleCentral-European journal of immunology2023

Phenotypical changes of hematopoietic stem and progenitor cells in COVID-19 patients: Correlation with disease status.

Hosni A M Hussein, Ali A A Thabet, Taha I A Mohamed, Mohamed E Elnosary, Ali Sobhy, Ahmed M El-Adly, Ahmed A Wardany, Elsayed K Bakhiet, Magdy M Afifi, Usama M Abdulraouf and 3 more

Abstract read
In one paragraph

Article in Central-European journal of immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Bioactive Compounds fromCurrent pharmaceutical biotechnology · 2025
    Article
  2. Exploring biosurfactant fromFrontiers in bioengineering and biotechnology · 2024
    Article
  3. Frontiers in bioengineering and biotechnology · 2024
    Article
  4. Article
  5. Persistent CD19Frontiers in cellular and infection microbiology · 2024
    Article
  6. 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.

Hosni A M HusseinDepartment of Botany and Microbiology, Faculty of Science, Al-Azhar University, Assiut, Egypt.
Ali A A ThabetDepartment of Zoology, Faculty of Science, Al-Azhar University, Assiut, Egypt.
Taha I A MohamedDepartment of Botany and Microbiology, Faculty of Science, Al-Azhar University, Assiut, Egypt.
Mohamed E ElnosaryDepartment of Botany and Microbiology, Faculty of Science, Al-Azhar University, Nasr City, Cairo, Egypt.
Ali SobhyDepartment of Clinical Pathology, Faculty of Medicine, Al-Azhar University, Assiut, Egypt.
Ahmed M El-AdlyDepartment of Botany and Microbiology, Faculty of Science, Al-Azhar University, Assiut, Egypt.
Ahmed A WardanyDepartment of Botany and Microbiology, Faculty of Science, Al-Azhar University, Assiut, Egypt.
Elsayed K BakhietDepartment of Botany and Microbiology, Faculty of Science, Al-Azhar University, Assiut, Egypt.
Magdy M AfifiDepartment of Botany and Microbiology, Faculty of Science, Al-Azhar University, Assiut, Egypt.
Usama M AbdulraoufDepartment of Botany and Microbiology, Faculty of Science, Al-Azhar University, Assiut, Egypt.
Samah M FathyDepartment of Zoology, Faculty of Science, Fayoum University, Fayoum, Egypt.
Noha G SayedDepartment of Clinical Pathology, South Egypt Cancer Institute, Assiut University, Assiut, Egypt.
Asmaa M ZahranDepartment of Clinical Pathology, South Egypt Cancer Institute, Assiut University, Assiut, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematopoietic stem cells (HSCs) and hematopoietic progenitor cells (HPCs) play a crucial role in the context of viral infections and their associated diseases. The link between HSCs and HPCs and disease status in COVID-19 patients is largely unknown. This study aimed to monitor the kinetics and contributions of HSCs and HPCs in severe and non-severe COVID-19 patients and to evaluate their diagnostic performance in differentiating between healthy and COVID-19 patients as well as severe and non-severe cases. Peripheral blood (PB) samples were collected from 48 COVID-19 patients, 16 recovered, and 27 healthy controls and subjected to deep flow cytometric analysis to determine HSCs and progenitor cells. Their diagnostic value and correlation with C-reactive protein (CRP), D-dimer, and ferritin levels were determined. The percentages of HSCs and common myeloid progenitors (CMPs) declined significantly, while the percentage of multipotent progenitors (MPPs) increased significantly in COVID-19 patients. There were no significant differences in the percentages of megakaryocyte-erythroid progenitors (MEPs) and granulocyte-macrophage progenitors (GMPs) between all groups. Severe COVID-19 patients had a significantly low percentage of HSCs, CMPs, and GMPs compared to non-severe cases. Contrarily, the levels of CRP, D-dimer, and ferritin increased significantly in severe COVID-19 patients. MPPs and CMPs showed excellent diagnostic performance in distinguishing COVID-19 patients from healthy controls and severe from non-severe COVID-19 patients, respectively. Collectively, our study indicated that hematopoietic stem and progenitor cells are significantly altered by COVID-19 and could be used as therapeutic targets and diagnostic biomarkers for severe COVID-19.

Indexed as

COVID-19hematopoietic progenitor cells (HPCs)hematopoietic stem cells (HSCs)SARS-CoV-2

Identifiers

PMID37692025
PMCPMC10485691

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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.