Evidence map›Paper›PMID 17307938›Full record

ArticleInfection and immunity2007

Primary infection of C57BL/6 mice with Plasmodium yoelii induces a heterogeneous response of NKT cells.

Valérie Soulard, Jacques Roland, Christèle Sellier, Anne Charlotte Gruner, Maria Leite-de-Moraes, Jean-François Franetich, Laurent Rénia, Pierre-André Cazenave, Sylviane Pied

Abstract read
In one paragraph

Article in Infection and immunity, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Frontiers in immunology · 2023
    Review
  4. Review
  5. NK1.1 Expression Defines a Population of CD4Frontiers in immunology · 2018
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Comparative analysis of activation phenotype, proliferation, and IFN-gamma production by spleen NK1.1(+) and NK1.1(-) T cells during Plasmodium chabaudi AS malaria.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2010
    Article
  13. Review
  14. Article
  15. Article
  16. 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

9 authors at 5 institutions in 1 country.

Valérie SoulardUnité d'Immunophysiopathologie Infectieuse, Institut Pasteur, 25-28 rue du Docteur Roux, 75724 Paris Cedex 15, France.
Jacques Roland
Christèle Sellier
Anne Charlotte Gruner
Maria Leite-de-Moraes
Jean-François Franetich
Laurent Rénia
Pierre-André Cazenave
Sylviane Pied
Sorbonne Université · FRCentre National de la Recherche Scientifique · FRInserm · FRHôpital Cochin · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NKT cells are a population of innate-like lymphocytes that display effector functions and immunoregulatory properties. We characterized the NKT cell response induced in C57BL/6 mice during a primary infection with Plasmodium yoelii sporozoites. We observed a heterogeneous NKT cell response that differed between liver and spleen. Hepatic NKT cells found in infected livers consisted mainly of CD1d-dependent CD4+ and double-negative (DN) NKT cells, whereas CD1d-independent NKT cells exhibiting a TCR(high) CD4(high) phenotype were prominent among splenic NKT cells during the infection. Hepatic and splenic NKT cells isolated from infected mice were activated and secreted mainly gamma interferon and tumor necrosis factor alpha in response to stimulation. Finally, P. yoelii-activated hepatic DN NKT cells inhibited the parasite's liver stage in a CD1d-dependent manner in vitro. However, experiments using B6.CD1d-deficient mice showed that CD1d and CD1d-restricted NKT cells are not necessary to control the parasite's development in vivo during neither the preerythrocytic stage nor the erythrocytic stage. Thus, our results show that a primary P. yoelii infection induces a heterogeneous and organ-specific response of NKT cells and that CD1d-dependent NKT cells play a minor role in the control of the development of Plasmodium in vivo in our model.

Indexed as

AnimalsAntigens, CD1CD4 AntigensFemaleKiller Cells, NaturalLiverMalariaMiceMice, Inbred C57BLMice, KnockoutOrgan SpecificityPlasmodium yoeliiSpleenSporozoitesAntigens, CD1CD4 Antigens

Identifiers

PMID17307938
PMCPMC1865793
OpenAlexW2133945584

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.