Evidence map›Paper›PMID 38608679›Full record

ArticleStem cell reports2024

Survivors of polymicrobial sepsis are refractory to G-CSF-induced emergency myelopoiesis and hematopoietic stem and progenitor cell mobilization.

Nirupam Biswas, Amber Bahr, Jennifer Howard, Jesse L Bonin, Rachel Grazda, Katherine C MacNamara

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Neonatal critical illness is associated with pancytopenia development in childhood.medRxiv : the preprint server for health sciences · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
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  8. Observational
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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

6 authors at 1 institution in 1 country.

Nirupam BiswasDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, NY 12208, USA.
Amber BahrDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, NY 12208, USA.
Jennifer HowardDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, NY 12208, USA.
Jesse L BoninDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, NY 12208, USA.
Rachel GrazdaDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, NY 12208, USA.
Katherine C MacNamaraDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, NY 12208, USA. Electronic address: macnamk@amc.edu.
Albany Medical Center Hospital · US

Funding

Hematopoietic Stem Cell Dysfunction and Regeneration in Severe InfectionR35GM131842 · NIGMS · ALBANY MEDICAL COLLEGE · PI MACNAMARA, KATHERINE C. · 2019 to 2023
$2.0M
NIGMS NIH HHS R35 GM131842
6 · The paper itself

Abstract

Sepsis survivors exhibit immune dysfunction, hematological changes, and increased risk of infection. The long-term impacts of sepsis on hematopoiesis were analyzed using a surgical model of murine sepsis, resulting in 50% survival. During acute disease, phenotypic hematopoietic stem and progenitor cells (HSPCs) were reduced in the bone marrow (BM), concomitant with increased myeloid colony-forming units and extramedullary hematopoiesis. Upon recovery, BM HSPCs were increased and exhibited normal function in the context of transplantation. To evaluate hematopoietic responses in sepsis survivors, we treated recovered sham and cecal ligation and puncture mice with a mobilizing regimen of granulocyte colony-stimulating factor (G-CSF) at day 20 post-surgery. Sepsis survivors failed to undergo emergency myelopoiesis and HSPC mobilization in response to G-CSF administration. G-CSF is produced in response to acute infection and injury to expedite the production of innate immune cells; therefore, our findings contribute to a new understanding of how sepsis predisposes to subsequent infection.

Indexed as

Granulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHematopoietic Stem CellsMyelopoiesisSepsisAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLGranulocyte Colony-Stimulating Factorbloodbone marrowextramedullary hematopoiesisG-CSFHSCHSPCmobilizationmyelopoiesissepsis

Identifiers

PMID38608679
PMCPMC11103789
OpenAlexW4394727656

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.