Evidence map›Paper›PMID 19464560›Full record

ArticleVaccine2009

Alpha-C-galactosylceramide as an adjuvant for a live attenuated influenza virus vaccine.

Sarah A Kopecky-Bromberg, Kathryn A Fraser, Natalie Pica, Elena Carnero, Thomas M Moran, Richard W Franck, Moriya Tsuji, Peter Palese

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
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  7. Article
  8. Ceramide and Related Molecules in Viral Infections.International journal of molecular sciences · 2021
    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

8 authors at 3 institutions in 1 country.

Sarah A Kopecky-BrombergDepartment of Microbiology, Mount Sinai School of Medicine, New York, NY 10029-6574, United States.
Kathryn A Fraser
Natalie Pica
Elena Carnero
Thomas M Moran
Richard W Franck
Moriya Tsuji
Peter Palese
Icahn School of Medicine at Mount Sinai · USAaron Diamond AIDS Research Center · USCity University of New York · US

Funding

Viral Pathogenesis and TherapeuticsU54AI057158 · NIAID · WADSWORTH CENTER · PI LEVY, DAVID E · 2003 to 2014
$100.8M
TRAINING PROGRAM: MECHANISMS OF VIRUS-HOST INTERACTIONST32AI007647 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI Domenico Tortorella · 2000 to 2026
$11.5M
Live attenuated vaccines for epidemic and pandemic fluU01AI070469 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GARCIA-SASTRE, ADOLFO · 2006 to 2010
$9.7M
TH1 AND TH2 RESPONSES IN VIRAL IMMUNITYR01AI041111 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI MORAN, THOMAS M · 1998 to 2010
$3.2M
NIAID NIH HHS 1 U01 AI070469NIAID NIH HHS R01 AI041111NIAID NIH HHS R01 AI 41111NIAID NIH HHS T32 AI007647NIAID NIH HHS U01 AI070469NIAID NIH HHS U54 AI057158NIAID NIH HHS U54AI057158PHS HHS T32 A1007645
6 · The paper itself

Abstract

There is a substantial need to develop better influenza virus vaccines that can protect populations that are not adequately protected by the currently licensed vaccines. While live attenuated influenza virus vaccines induce superior immune responses compared to inactivated vaccines, the manufacturing process of both types of influenza virus vaccines is time consuming and may not be adequate during a pandemic. Adjuvants would be particularly useful if they could enhance the immune response to live attenuated influenza virus vaccines so that the amount of vaccine needed for a protective dose could be reduced. The glycolipid, alpha-galactosylceramide (alpha-GalCer), has recently been shown to have adjuvant activity for both inactivated and replicating recombinant vaccines. The goal of these experiments was to determine whether a derivative of alpha-GalCer, alpha-C-galactosylceramide (alpha-C-GalCer) can enhance the immune response elicited by a live attenuated influenza virus vaccine containing an NS1 protein truncation and reduce the amount of vaccine required to provide protection after challenge. Our results indicated that the adjuvant reduced both morbidity and mortality in BALB/c mice after challenge with wild type influenza virus. The adjuvant also increased the amount of influenza virus specific total IgG, IgG1, and IgG2a antibodies as well as IFN-gamma secreting CD8(+) T cells. By using knockout mice that are not able to generate NKT cells, we were able to demonstrate that the mechanism of adjuvant activity is dependent on NKT cells. Thus, our data indicate that stimulators of NKT cells represent a new avenue of adjuvants to pursue for live attenuated virus vaccines.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, ViralCD8-Positive T-LymphocytesChick EmbryoFemaleGalactosylceramidesInfluenza VaccinesInterferon-gammaKiller Cells, NaturalMaleMiceMice, Inbred BALB COrthomyxoviridae InfectionsSeverity of Illness IndexSurvival AnalysisAdjuvants, Immunologicalpha-galactosylceramideAntibodies, ViralGalactosylceramidesInfluenza VaccinesInterferon-gammaVaccines, Attenuated

Identifiers

PMID19464560
PMCPMC2818010
OpenAlexW2087404142

What OpenQuestion holds

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LicenceTDM
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.