Evidence map›Paper›PMID 18424737›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

A DNA vaccine prime followed by a liposome-encapsulated protein boost confers enhanced mucosal immune responses and protection.

Kejian Yang, Barbara J Whalen, Rebecca S Tirabassi, Liisa K Selin, Tatyana S Levchenko, Vladimir P Torchilin, Edward H Kislauskis, Dennis L Guberski

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  13. Pathogens (Basel, Switzerland) · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Proteoliposomes in nanobiotechnology.Biophysical reviews · 2012
    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 1 country.

Kejian YangOral Vaccine Institute, 10 New Bond Street, Worcester, MA 01606, USA. Kejian.Yang@gmail.com
Barbara J Whalen
Rebecca S Tirabassi
Liisa K Selin
Tatyana S Levchenko
Vladimir P Torchilin
Edward H Kislauskis
Dennis L Guberski
Biomedical Research Models (United States) · USNortheastern University · USWorcester Polytechnic Institute · USUniversity of Massachusetts Chan Medical School · US

Funding

IMMUNITY IN SYSTEMIC AND MUCOSAL VIRUS INFECTIONSR01AI046578 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SELIN, LIISA KAARINA · 2000 to 2009
$3.1M
NIAID NIH HHS R01 AI046578PHS HHS R31/CCR 922413-01PHS HHS R31/CCR 924378-01PHS HHS R31/CCR 924378-02
6 · The paper itself

Abstract

A variety of DNA vaccine prime and recombinant viral boost immunization strategies have been developed to enhance immune responses in humans, but inherent limitations to these strategies exist. There is still an overwhelming need to develop safe and effective approaches that raise broad humoral and T cell-mediated immune responses systemically and on mucosal surfaces. We have developed a novel mucosal immunization regimen that precludes the use of viral vectors yet induces potent T cell responses. Using hepatitis B surface Ag (HBsAg), we observed that vaccination of BALB/c mice with an i.m. HBsAg-DNA vaccine prime followed by an intranasal boost with HBsAg protein encapsulated in biologically inert liposomes enhanced humoral and T cell immune responses, particularly on mucosal surfaces. Intranasal live virus challenge with a recombinant vaccinia virus expressing HBsAg revealed a correlation between T cell immune responses and protection of immunized mice. A shortened immunization protocol was developed that was successful in both adult and neonatal mice. These results support the conclusion that this new approach is capable of generating a Th-type-1-biased, broad spectrum immune response, specifically at mucosal surfaces. The success of this design may provide a safe and effective vaccination alternative for human use.

Indexed as

Immunization, SecondaryAdministration, IntranasalAnimalsAnimals, NewbornAntibody FormationFemaleHepatitis B Surface AntigensHepatitis B VaccinesHumansImmunity, MucosalLiposomesMiceMice, Inbred BALB CTh1 CellsVaccines, DNAVaccinia virusHepatitis B Surface AntigensHepatitis B VaccinesLiposomesVaccines, DNA

Identifiers

PMID18424737
PMCPMC3633597
OpenAlexW2163510185

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.