Evidence map›Paper›PMID 36845143›Full record

ArticleFrontiers in immunology2023

Mid-titer human convalescent plasma administration results in suboptimal prophylaxis against SARS-CoV-2 infection in rhesus macaques.

Brandon J Beddingfield, Nicholas J Maness, Skye Spencer, Jay Rappaport, Pyone Pyone Aye, Kasi Russell-Lodrigue, Lara A Doyle-Meyers, Robert V Blair, HongMei Gao, David Montefiori and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

11 authors at 2 institutions in 1 country.

Brandon J BeddingfieldDivisions of Microbiology, Tulane National Primate Research Center, Covington, LA, United States.
Nicholas J ManessDivisions of Microbiology, Tulane National Primate Research Center, Covington, LA, United States.
Skye SpencerDivisions of Microbiology, Tulane National Primate Research Center, Covington, LA, United States.
Jay RappaportComparative Pathology, Tulane National Primate Research Center, Covington, LA, United States.
Pyone Pyone AyeVeterinary Medicine, Tulane National Primate Research Center, Covington, LA, United States.
Kasi Russell-LodrigueVeterinary Medicine, Tulane National Primate Research Center, Covington, LA, United States.
Lara A Doyle-MeyersVeterinary Medicine, Tulane National Primate Research Center, Covington, LA, United States.
Robert V BlairComparative Pathology, Tulane National Primate Research Center, Covington, LA, United States.
HongMei GaoDuke Human Vaccine Institute, Duke University Medical Center, Durham, NC, United States.
David MontefioriDuke Human Vaccine Institute, Duke University Medical Center, Durham, NC, United States.
Chad J RoyDivisions of Microbiology, Tulane National Primate Research Center, Covington, LA, United States.
Tulane University · USDuke Medical Center · US

Funding

Tulane NPRC SPF Sheltered Outdoor Enclosure ExpansionP51OD011104 · OD · TULANE UNIVERSITY OF LOUISIANA · PI L Lee HAMM · 2012 to 2026
$142.4M
NIH HHS P51 OD011104
6 · The paper itself

Abstract

Introduction: ARS-CoV-2 is a respiratory pathogen currently causing a worldwide pandemic, with resulting pathology of differing severity in humans, from mild illness to severe disease and death. The rhesus macaque model of COVID-19 was utilized to evaluate the added benefit of prophylactic administration of human post-SARS-CoV-2 infection convalescent plasma (CP) on disease progression and severity. Methods: A pharmacokinetic (PK) study using CP in rhesus monkeys preceded the challenge study and revealed the optimal time of tissue distribution for maximal effect. Thereafter, CP was administered prophylactically three days prior to mucosal SARS-CoV-2 viral challenge. Results: Results show similar viral kinetics in mucosal sites over the course of infection independent of administration of CP or normal plasma, or historic controls with no plasma. No changes were noted upon necropsy via histopathology, although there were differences in levels of vRNA in tissues, with both normal and CP seemingly blunting viral loads. Discussion: Results indicate that prophylactic administration with mid-titer CP is not effective in reducing disease severity of SARS-CoV-2 infection in the rhesus COVID-19 disease model.

Indexed as

COVID-19AnimalsCOVID-19 SerotherapyHumansImmunization, PassiveMacaca mulattaSARS-CoV-2convalescent plasmaCOVID-19prophylaxisrhesus macaqueSARS-CoV-2

Identifiers

PMID36845143
PMCPMC9950397
OpenAlexW4319984369

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.