Evidence map›Paper›PMID 37195999›Full record

ArticlePLoS pathogens2023

Distinct immune responses associated with vaccination status and protection outcomes after malaria challenge.

Damian A Oyong, Fergal J Duffy, Maxwell L Neal, Ying Du, Jason Carnes, Katharine V Schwedhelm, Nina Hertoghs, Seong-Hwan Jun, Helen Miller, John D Aitchison and 5 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01994525 (Phase 1 Trial With Challenge to Assess the Safety and Biomarkers of Protection in Malaria-naïve Adults of Immunization Via Mosquito Bite With Radiation-Attenuated Plasmodium Falciparum Sporozoites), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.2field-weighted citation impact, top 8% 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.

NCT01994525 phase1completednot on this map

Phase 1 Trial With Challenge to Assess the Safety and Biomarkers of Protection in Malaria-naïve Adults of Immunization Via Mosquito Bite With Radiation-Attenuated Plasmodium Falciparum Sporozoites (IMRAS)

TypeinterventionalSponsorU.S. Army Medical Research and Development CommandRan2014 to 2017Enrolled54ConditionsMalariaArmsPfRAS, Placebo, Challenge
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Article
  6. CD8Frontiers in immunology · 2024
    Review
  7. Human transcriptional signature of protection afterHuman vaccines & immunotherapeutics · 2023
    Article
  8. 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

15 authors at 2 institutions in 1 country.

Damian A OyongCenter for Global Infectious Disease Research (CGIDR), Seattle Children's Research Institute, Seattle, Washington, United States of America.
Fergal J DuffyCenter for Global Infectious Disease Research (CGIDR), Seattle Children's Research Institute, Seattle, Washington, United States of America.
Maxwell L NealCenter for Global Infectious Disease Research (CGIDR), Seattle Children's Research Institute, Seattle, Washington, United States of America.
Ying DuCenter for Global Infectious Disease Research (CGIDR), Seattle Children's Research Institute, Seattle, Washington, United States of America.
Jason CarnesCenter for Global Infectious Disease Research (CGIDR), Seattle Children's Research Institute, Seattle, Washington, United States of America.
Katharine V SchwedhelmVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Nina HertoghsCenter for Global Infectious Disease Research (CGIDR), Seattle Children's Research Institute, Seattle, Washington, United States of America.
Seong-Hwan JunVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Helen MillerVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
John D AitchisonCenter for Global Infectious Disease Research (CGIDR), Seattle Children's Research Institute, Seattle, Washington, United States of America.
Stephen C De RosaVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Evan W NewellVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
M Juliana McElrathVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Suzanne M McDermottCenter for Global Infectious Disease Research (CGIDR), Seattle Children's Research Institute, Seattle, Washington, United States of America.
Kenneth D StuartCenter for Global Infectious Disease Research (CGIDR), Seattle Children's Research Institute, Seattle, Washington, United States of America.ORCID 0000-0002-4064-9758
Infectious Disease Research Institute · USFred Hutch Cancer Center · US

Funding

Systems Biology CoreU19AI128914 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI Margaret Juliana McElrath, KENNETH D STUART · 2017 to 2026
$29.5M
TR&D Project 4. The Imaging Stage: Multiscale Spatiotemporal Modeling of Macromolecular Systems in Cellular NeighborhoodsP41GM109824 · NIGMS · ROCKEFELLER UNIVERSITY · PI ROUT, MICHAEL P · 2014 to 2023
$18.8M
NIAID NIH HHS U19 AI128914NIGMS NIH HHS P41 GM109824
6 · The paper itself

Abstract

Understanding immune mechanisms that mediate malaria protection is critical for improving vaccine development. Vaccination with radiation-attenuated Plasmodium falciparum sporozoites (PfRAS) induces high level of sterilizing immunity against malaria and serves as a valuable tool for the study of protective mechanisms. To identify vaccine-induced and protection-associated responses during malarial infection, we performed transcriptome profiling of whole blood and in-depth cellular profiling of PBMCs from volunteers who received either PfRAS or noninfectious mosquito bites, followed by controlled human malaria infection (CHMI) challenge. In-depth single-cell profiling of cell subsets that respond to CHMI in mock-vaccinated individuals showed a predominantly inflammatory transcriptome response. Whole blood transcriptome analysis revealed that gene sets associated with type I and II interferon and NK cell responses were increased in prior to CHMI while T and B cell signatures were decreased as early as one day following CHMI in protected vaccinees. In contrast, non-protected vaccinees and mock-vaccinated individuals exhibited shared transcriptome changes after CHMI characterized by decreased innate cell signatures and inflammatory responses. Additionally, immunophenotyping data showed different induction profiles of vδ2+ γδ T cells, CD56+ CD8+ T effector memory (Tem) cells, and non-classical monocytes between protected vaccinees and individuals developing blood-stage parasitemia, following treatment and resolution of infection. Our data provide key insights in understanding immune mechanistic pathways of PfRAS-induced protection and infective CHMI. We demonstrate that vaccine-induced immune response is heterogenous between protected and non-protected vaccinees and that inducted-malaria protection by PfRAS is associated with early and rapid changes in interferon, NK cell and adaptive immune responses. Trial Registration: ClinicalTrials.gov NCT01994525.

Indexed as

MalariaMalaria, FalciparumMalaria VaccinesAnimalsHumansImmunityInterferonsPlasmodium falciparumSporozoitesVaccinationInterferonsMalaria Vaccines

Identifiers

PMID37195999
PMCPMC10228810
OpenAlexW4376958598

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.