Evidence map›Paper›PMID 34609964›Full record

ArticleJCI insight2021

Controlled human malaria infection with a clone of Plasmodium vivax with high-quality genome assembly.

Angela M Minassian, Yrene Themistocleous, Sarah E Silk, Jordan R Barrett, Alison Kemp, Doris Quinkert, Carolyn M Nielsen, Nick J Edwards, Thomas A Rawlinson, Fernando Ramos Lopez and 35 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Assembled genome of an EthiopianMicrobiology resource announcements · 2024
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  13. Article
  14. Article
  15. Article
  16. Vaccination withScience translational medicine · 2023
    Article
  17. Article
  18. Molecular therapy. Methods & clinical development · 2022
    Article
  19. Review
  20. Impact of a blood-stage vaccine onmedRxiv : the preprint server for health sciences · 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

45 authors at 7 institutions in 3 countries.

Angela M MinassianThe Jenner Institute and.
Yrene ThemistocleousThe Jenner Institute and.
Sarah E SilkThe Jenner Institute and.
Jordan R BarrettThe Jenner Institute and.
Alison KempWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
Doris QuinkertThe Jenner Institute and.
Carolyn M NielsenThe Jenner Institute and.
Nick J EdwardsThe Jenner Institute and.
Thomas A RawlinsonThe Jenner Institute and.
Fernando Ramos LopezThe Jenner Institute and.
Wanlapa RoobsoongMahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Katherine Jd EllisThe Jenner Institute and.
Jee-Sun ChoThe Jenner Institute and.
Eerik AuninWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
Thomas D OttoWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
Adam J ReidWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
Florian A BachInstitute of Immunology and Infection Research, University of Edinburgh, Edinburgh, United Kingdom.
Geneviève Mc LabbéThe Jenner Institute and.
Ian D PoultonThe Jenner Institute and.
Arianna MariniThe Jenner Institute and.
Marija ZaricThe Jenner Institute and.
Margaux MulatierThe Jenner Institute and.
Raquel Lopez RamonThe Jenner Institute and.
Megan BakerThe Jenner Institute and.
Celia H MittonThe Jenner Institute and.
Jason C SousaWalter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Nattawan RachaphaewMahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Chalermpon KumpitakMahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Nongnuj ManeechaiMahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Chayanut SuansomjitMahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Tianrat PiteekanMahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Mimi M HouThe Jenner Institute and.
Baktash KhozoeeThe Jenner Institute and.
Kirsty McHughThe Jenner Institute and.
David J RobertsNuffield Division of Clinical Laboratory Sciences, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
Alison M LawrieThe Jenner Institute and.
Andrew M BlagboroughDepartment of Pathology, University of Cambridge, Cambridge, United Kingdom.
Fay L NugentThe Jenner Institute and.
Iona J TaylorThe Jenner Institute and.
Kimberly J JohnsonThe Jenner Institute and.
Philip J SpenceInstitute of Immunology and Infection Research, University of Edinburgh, Edinburgh, United Kingdom.
Jetsumon SattabongkotMahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Sumi BiswasThe Jenner Institute and.
Julian C RaynerWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
Simon J DraperThe Jenner Institute and.
Jenner Institute · GBMahidol University · THUniversity of Oxford · GBUniversity of Cambridge · GBWellcome Sanger Institute · GBUniversity of Edinburgh · GBWalter Reed Army Institute of Research · US

Funding

Department of HealthMedical Research Council MC_PC_16056Medical Research Council MR/N00227X/1Wellcome TrustWellcome Trust 106917/Z/15/ZWellcome Trust 107668/Z/15/ZWellcome Trust 108734/Z/15/ZWellcome Trust 203764/Z/16/ZWellcome Trust 206194/Z/17/ZWellcome Trust 209200/Z/17/Z
6 · The paper itself

Abstract

Controlled human malaria infection (CHMI) provides a highly informative means to investigate host-pathogen interactions and enable in vivo proof-of-concept efficacy testing of new drugs and vaccines. However, unlike Plasmodium falciparum, well-characterized P. vivax parasites that are safe and suitable for use in modern CHMI models are limited. Here, 2 healthy malaria-naive United Kingdom adults with universal donor blood group were safely infected with a clone of P. vivax from Thailand by mosquito-bite CHMI. Parasitemia developed in both volunteers, and prior to treatment, each volunteer donated blood to produce a cryopreserved stabilate of infected RBCs. Following stringent safety screening, the parasite stabilate from one of these donors (PvW1) was thawed and used to inoculate 6 healthy malaria-naive United Kingdom adults by blood-stage CHMI, at 3 different dilutions. Parasitemia developed in all volunteers, who were then successfully drug treated. PvW1 parasite DNA was isolated and sequenced to produce a high-quality genome assembly by using a hybrid assembly method. We analyzed leading vaccine candidate antigens and multigene families, including the vivax interspersed repeat (VIR) genes, of which we identified 1145 in the PvW1 genome. Our genomic analysis will guide future assessment of candidate vaccines and drugs, as well as experimental medicine studies.

Indexed as

AnimalsGenomeHealthy VolunteersHumansMalaria, FalciparumMalePlasmodium vivaxInfectious diseaseMalaria

Identifiers

PMID34609964
PMCPMC8675201
OpenAlexW3204561130

What Socratic 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 Socratic graph.