Evidence map›Paper›PMID 11877484›Full record

ArticleThe Journal of experimental medicine2002

Natural killer T cell ligand alpha-galactosylceramide enhances protective immunity induced by malaria vaccines.

Gloria Gonzalez-Aseguinolaza, Luc Van Kaer, Cornelia C Bergmann, James M Wilson, John Schmieg, Mitchell Kronenberg, Toshinori Nakayama, Masaru Taniguchi, Yasuhiko Koezuka, Moriya Tsuji

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 142 papers.

0numbers the graph read from it
0cells of the map it votes in
142citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

142 citing papers in PubMed, 314 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Systems analysis of protective immune responses to RTS,S malaria vaccination in humans.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Trial
  4. Article
  5. Article
  6. Article
  7. Developing a potent vaccine againstExpert reviews in molecular medicine · 2024
    Review
  8. Review
  9. Review
  10. Article
  11. How Long Will It Take to Launch an EffectiveInfection and drug resistance · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. Glycolipid-peptide conjugate vaccines elicit CD8Clinical & translational immunology · 2022
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Harnessing NKT cells for vaccination.Oxford open immunology · 2021
    Review

82 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 7 institutions in 2 countries.

Gloria Gonzalez-AseguinolazaDepartment of Medical and Molecular Parasitology, New York University School of Medicine, New York, NY 10010, USA.
Luc Van Kaer
Cornelia C Bergmann
James M Wilson
John Schmieg
Mitchell Kronenberg
Toshinori Nakayama
Masaru Taniguchi
Yasuhiko Koezuka
Moriya Tsuji
New York University · USChiba University · JPKirin (Japan) · JPLa Jolla Institute for Immunology · USUniversity of Pennsylvania · USUniversity of Southern California · USVanderbilt University · US

Funding

EXPRESSION AND FUNCTION OF THE MHC-ENCODED TL MOLECULER01CA052511 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KRONENBERG, MITCHELL · 1991 to 2004
$1.8M
NKT cells: Novel Protective T cells against malariaR21AI047840 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI TSUJI, MORIYA · 2001 to 2001
$431k
PROCESSING AND SELECTION OF HIV CTL EPITOPESR01AI033314 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BERGMANN, CORNELIA C · 1996 to 2000
$337k
ADENOVIRUS--AN EFFICIENT VECTOR OF ANTIMALARIA IMMUNITYR29AI040656 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI TSUJI, MORIYA · 1997 to 2001
$225k
PROCESSING AND SELECTION OF HIV CTL EPITOPESR29AI033314 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BERGMANN, CORNELIA C · 1992 to 1995
–
NCI NIH HHS CA-52511NCI NIH HHS R01 CA052511NIAID NIH HHS AI-01682NIAID NIH HHS AI-33314NIAID NIH HHS AI-40656NIAID NIH HHS AI-47840
6 · The paper itself

Abstract

The important role played by CD8(+) T lymphocytes in the control of parasitic and viral infections, as well as tumor development, has raised the need for the development of adjuvants capable of enhancing cell-mediated immunity. It is well established that protective immunity against liver stages of malaria parasites is primarily mediated by CD8(+) T cells in mice. Activation of natural killer T (NKT) cells by the glycolipid ligand, alpha-galactosylceramide (alpha-GalCer), causes bystander activation of NK, B, CD4(+), and CD8(+) T cells. Our study shows that coadministration of alpha-GalCer with suboptimal doses of irradiated sporozoites or recombinant viruses expressing a malaria antigen greatly enhances the level of protective anti-malaria immunity in mice. We also show that coadministration of alpha-GalCer with various different immunogens strongly enhances antigen-specific CD8(+) T cell responses, and to a lesser degree, Th1-type responses. The adjuvant effects of alpha-GalCer require CD1d molecules, Valpha14 NKT cells, and interferon gamma. As alpha-GalCer stimulates both human and murine NKT cells, these findings should contribute to the design of more effective vaccines against malaria and other intracellular pathogens, as well as tumors.

Indexed as

Adjuvants, ImmunologicAnimalsAntigens, CD1Antigens, CD1dCD8-Positive T-LymphocytesGalactosylceramidesInterferon-gammaKiller Cells, NaturalMalaria VaccinesMiceMice, Inbred BALB CProtozoan ProteinsAdjuvants, ImmunologicAntigens, CD1Antigens, CD1dCD1D protein, humancircumsporozoite protein, ProtozoanGalactosylceramidesInterferon-gammaMalaria VaccinesProtozoan Proteins

Identifiers

PMID11877484
PMCPMC2193764
OpenAlexW2160310527

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.