Evidence map›Paper›PMID 30217795›Full record

ArticleBlood advances2018

Blood manufacturing methods affect red blood cell product characteristics and immunomodulatory activity.

Ruqayyah J Almizraq, Philip J Norris, Heather Inglis, Somaang Menocha, Mathijs R Wirtz, Nicole Juffermans, Suchitra Pandey, Philip C Spinella, Jason P Acker, Jennifer A Muszynski

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
10.4field-weighted citation impact, top 2% 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

19 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
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  4. CD71Scandinavian journal of immunology · 2026
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  18. Post-Transfusion Purpura: Current Perspectives.Journal of blood medicine · 2019
    Review
  19. 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

10 authors at 6 institutions in 3 countries.

Ruqayyah J AlmizraqLaboratory Medicine and Pathology, University of Alberta, Edmonton, AB, Canada.ORCID 0000-0001-8494-6538
Philip J NorrisBlood Systems Research Institute, San Francisco, CA.ORCID 0000-0003-0526-2088
Heather InglisBlood Systems Research Institute, San Francisco, CA.
Somaang MenochaDepartment of Pediatrics, Nationwide Children's Hospital, Columbus, OH.
Mathijs R WirtzDepartment of Intensive Care Medicine and.
Nicole JuffermansDepartment of Intensive Care Medicine and.ORCID 0000-0002-3039-6574
Suchitra PandeyLaboratory Medicine and Medicine, University of California, San Francisco, CA.
Philip C SpinellaDivision of Critical Care, Department of Pediatrics, Washington University in St. Louis, St. Louis, MO; and.ORCID 0000-0003-1721-0541
Jason P AckerLaboratory Medicine and Pathology, University of Alberta, Edmonton, AB, Canada.ORCID 0000-0002-1445-827X
Jennifer A MuszynskiDepartment of Pediatrics, Nationwide Children's Hospital, Columbus, OH.ORCID 0000-0002-3329-8048
Amsterdam UMC Location University of Amsterdam · NLNationwide Children's Hospital · USUniversity of Alberta · CAUniversity of California, San Francisco · USBlood Systems Research Institute · USWashington University in St. Louis · US

Funding

Role of microRNA in stored RBC induced innate immune suppressionK08HL123925 · NHLBI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI MUSZYNSKI, JENNIFER · 2015 to 2019
$737k
NHLBI NIH HHS K08 HL123925
6 · The paper itself

Abstract

Transfusion of red cell concentrates (RCCs) is associated with increased risk of adverse outcomes that may be affected by different blood manufacturing methods and the presence of extracellular vesicles (EVs). We investigated the effect of different manufacturing methods on hemolysis, residual cells, cell-derived EVs, and immunomodulatory effects on monocyte activity. Thirty-two RCC units produced using whole blood filtration (WBF), red cell filtration (RCF), apheresis-derived (AD), and whole blood-derived (WBD) methods were examined (n = 8 per method). Residual platelet and white blood cells (WBCs) and the concentration, cell of origin, and characterization of EVs in RCC supernatants were assessed in fresh and stored supernatants. Immunomodulatory activity of RCC supernatants was assessed by quantifying monocyte cytokine production capacity in an in vitro transfusion model. RCF units yielded the lowest number of platelet and WBC-derived EVs, whereas the highest number of platelet EVs was in AD (day 5) and in WBD (day 42). The number of small EVs (<200 nm) was greater than large EVs (≥200 nm) in all tested supernatants, and the highest level of small EVs were in AD units. Immunomodulatory activity was mixed, with evidence of both inflammatory and immunosuppressive effects. Monocytes produced more inflammatory interleukin-8 after exposure to fresh WBF or expired WBD supernatants. Exposure to supernatants from AD and WBD RCC suppressed monocyte lipopolysaccharide-induced cytokine production. Manufacturing methods significantly affect RCC unit EV characteristics and are associated with an immunomodulatory effect of RCC supernatants, which may affect the quality and safety of RCCs.

Indexed as

Cell SeparationImmunomodulationBiomarkersBlood Component RemovalBlood PreservationCoculture TechniquesCytokinesErythrocytesErythrocyte TransfusionExtracellular VesiclesFiltrationFlow CytometryHemolysisHumansLeukocyte CountLeukocytesBiomarkersCytokines

Identifiers

PMID30217795
PMCPMC6156888
OpenAlexW2890359662

What OpenQuestion holds

Textmetadata
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.