Evidence map›Paper›PMID 9794383›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)1998

CD40 ligand/trimer DNA enhances both humoral and cellular immune responses and induces protective immunity to infectious and tumor challenge.

S Gurunathan, K R Irvine, C Y Wu, J I Cohen, E Thomas, C Prussin, N P Restifo, R A Seder

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 154 citations in OpenAlex.

  1. Trial
  2. Advances in nucleic acid-based cancer vaccines.Journal of biomedical science · 2025
    Review
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  10. T-cell-independent antitumor effects of CD40 ligation.International reviews of immunology · 2012
    Review
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  20. Toll-like receptors in tumor immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2007
    Review
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

8 authors at 4 institutions in 2 countries.

S GurunathanClinical Immunology Section, Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
K R Irvine
C Y Wu
J I Cohen
E Thomas
C Prussin
N P Restifo
R A Seder
National Institute of Allergy and Infectious Diseases · USIDEX Corporation (United States) · USNational Cancer Institute · USNational Institutes of Health · US

Funding

Building on the success of the adoptive immunotherapy of cancerZ01BC010763 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RESTIFO, NICHOLAS P · 2006 to 2008
$6.4M
Intramural NIH HHS Z01 BC010763Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

CD40/CD40 ligand interactions have a central role in the induction of both humoral and cellular immunity. In this study, we examined whether a plasmid expressing CD40 ligand/trimer (CD40LT) could enhance immune responses in vivo. BALB/c mice were injected with plasmid expressing beta-galactosidase DNA with or without CD40LT DNA or IL-12 DNA, and immune responses were assessed. Mice vaccinated with beta-gal DNA plus CD40LT DNA or IL-12 DNA had a striking increase in Ag-specific production of IFN-gamma, cytolytic T cell activity, and IgG2a Ab. The mechanism by which CD40LT DNA enhanced these responses was further assessed by treating vaccinated mice with anti-IL-12 mAb or CTLA-4 Ig (CTLA4Ig). Production of IFN-gamma and CTL activity was abrogated by these treatments, suggesting that CD40LT DNA was mediating its effects on IFN-gamma and CTL activity through induction of IL-12 and enhancement of B7 expression, respectively. Physiologic relevance for the ability of CD40LT DNA to enhance immune responses by the aforementioned pathways was shown in two in vivo models. First, with regard to CTL activity, mice vaccinated with CD40LT DNA did not develop metastatic tumor following challenge with lethal dose of tumor. Moreover, in a mouse model requiring IL-12-dependent production of IFN-gamma, mice vaccinated with soluble Leishmania Ag and CD40LT DNA were able to control infection with Leishmania major. These data suggest that CD40LT DNA could be a useful vaccine adjuvant for diseases requiring cellular and/or humoral immunity.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, NeoplasmAntibody FormationB7-1 Antigenbeta-GalactosidaseCD28 AntigensCD40 LigandColonic NeoplasmsCytotoxicity, ImmunologicDNA, RecombinantFemaleGenes, ReporterImmunity, CellularImmunoglobulin GInterferon-gammaAdjuvants, ImmunologicAntibodies, NeoplasmB7-1 Antigenbeta-GalactosidaseCD28 AntigensCD40 LigandDNA, RecombinantImmunoglobulin GInterferon-gammaInterleukin-12Membrane GlycoproteinsVaccines, Synthetic

Identifiers

PMID9794383
PMCPMC2239005
OpenAlexW2128983157

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.