Evidence map›Paper›PMID 31477704›Full record

ArticleNature communications2019

Innate immunity limits protective adaptive immune responses against pre-erythrocytic malaria parasites.

Nana K Minkah, Brandon K Wilder, Amina A Sheikh, Thomas Martinson, Lisa Wegmair, Ashley M Vaughan, Stefan H I Kappe

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed, 52 citations in OpenAlex.

  1. Trial
  2. Trial
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  4. Androgens inhibit protective CD8Nature communications · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. CD8Frontiers in immunology · 2024
    Review
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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

7 authors at 2 institutions in 1 country.

Nana K MinkahCenter for Global Infectious Disease Research, Seattle Children's Research Institute, 307 Westlake Ave N, Seattle, WA, USA.
Brandon K WilderCenter for Global Infectious Disease Research, Seattle Children's Research Institute, 307 Westlake Ave N, Seattle, WA, USA.
Amina A SheikhCenter for Global Infectious Disease Research, Seattle Children's Research Institute, 307 Westlake Ave N, Seattle, WA, USA.
Thomas MartinsonCenter for Global Infectious Disease Research, Seattle Children's Research Institute, 307 Westlake Ave N, Seattle, WA, USA.
Lisa WegmairCenter for Global Infectious Disease Research, Seattle Children's Research Institute, 307 Westlake Ave N, Seattle, WA, USA.
Ashley M VaughanCenter for Global Infectious Disease Research, Seattle Children's Research Institute, 307 Westlake Ave N, Seattle, WA, USA.
Stefan H I KappeCenter for Global Infectious Disease Research, Seattle Children's Research Institute, 307 Westlake Ave N, Seattle, WA, USA. stefan.kappe@seattlechildrens.org.
Oregon Health & Science University · USUniversity of Washington · US

Funding

Innate immune responses to malaria liver stage infectionR01AI114699 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI KAPPE, STEFAN HI · 2015 to 2019
$2.5M
NIAID NIH HHS R01 AI114699
6 · The paper itself

Abstract

Immunization with attenuated whole Plasmodium sporozoites constitutes a promising vaccination strategy. Compared to replication-deficient parasites, immunization with replication-competent parasites confers better protection and also induces a type I IFN (IFN-1) response, but whether this IFN-1 response has beneficial or adverse effects on vaccine-induced adaptive immunity is not known. Here, we show that IFN-1 signaling-deficient mice immunized with replication-competent sporozoites exhibit superior protection against infection. This correlates with superior CD8 T cell memory including reduced expression of the exhaustion markers PD-1 and LAG-3 on these cells and increased numbers of memory CD8 T cells in the liver. Moreover, the adoptive transfer of memory CD8 T cells from the livers of previously immunized IFN-1 signaling-deficient mice confers greater protection against liver stage parasites. However, the detrimental role of IFN-1 signaling is not CD8 T cell intrinsic. Together, our data demonstrate that liver stage-engendered IFN-1 signaling impairs hepatic CD8 T cell memory via a CD8 T cell-extrinsic mechanism.

Indexed as

Adaptive ImmunityAnimalsCD8-Positive T-LymphocytesErythrocytesFemaleImmunity, InnateImmunizationInterferon Type ILiverMalariaMalaria VaccinesMice, Inbred C57BLMice, KnockoutPlasmodium yoeliiSporozoitesVaccines, AttenuatedInterferon Type IMalaria VaccinesVaccines, Attenuated

Identifiers

PMID31477704
PMCPMC6718385
OpenAlexW2971688962

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.