Evidence map›Paper›PMID 23386724›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Langerin negative dendritic cells promote potent CD8+ T-cell priming by skin delivery of live adenovirus vaccine microneedle arrays.

Veronique Bachy, Catherine Hervouet, Pablo D Becker, Laurent Chorro, Leo M Carlin, Shanthi Herath, Timos Papagatsias, Jean-Baptiste Barbaroux, Sea-Jin Oh, Adel Benlahrech and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 citations in OpenAlex.

  1. Pooled it
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  15. Transdermal vaccination via 3D-printed microneedles induces potent humoral and cellular immunity.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Development of vaccine formulations: past, present, and future.Drug delivery and translational research · 2021
    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

16 authors at 4 institutions in 2 countries.

Veronique BachyPeter Gorer Department of Immunobiology, King's College School of Medicine, London SE1 9RT, United Kingdom.
Catherine Hervouet
Pablo D Becker
Laurent Chorro
Leo M Carlin
Shanthi Herath
Timos Papagatsias
Jean-Baptiste Barbaroux
Sea-Jin Oh
Adel Benlahrech
Takis Athanasopoulos
George Dickson
Steven Patterson
Sung-Yun Kwon
Frederic Geissmann
Linda S Klavinskis
W. L. Gore & Associates (Germany) · DEImperial College London · GBRoyal Holloway University of London · GBKing's College School · GB

Funding

Medical Research Council G0200284Medical Research Council G0900867
6 · The paper itself

Abstract

Stabilization of virus protein structure and nucleic acid integrity is challenging yet essential to preserve the transcriptional competence of live recombinant viral vaccine vectors in the absence of a cold chain. When coupled with needle-free skin delivery, such a platform would address an unmet need in global vaccine coverage against HIV and other global pathogens. Herein, we show that a simple dissolvable microneedle array (MA) delivery system preserves the immunogenicity of vaccines encoded by live recombinant human adenovirus type 5 (rAdHu5). Specifically, dried rAdHu5 MA immunization induced CD8(+) T-cell expansion and multifunctional cytokine responses equipotent with conventional injectable routes of immunization. Intravital imaging demonstrated MA cargo distributed both in the epidermis and dermis, with acquisition by CD11c(+) dendritic cells (DCs) in the dermis. The MA immunizing properties were attributable to CD11c(+) MHCII(hi) CD8α(neg) epithelial cell adhesion molecule (EpCAM(neg)) CD11b(+) langerin (Lang; CD207)(neg) DCs, but neither Langerhans cells nor Lang(+) DCs were required for CD8(+) T-cell priming. This study demonstrates an important technical advance for viral vaccine vectors progressing to the clinic and provides insights into the mechanism of CD8(+) T-cell priming by live rAdHu5 MAs.

Indexed as

NeedlesSkinAdenoviridaeAntigens, CDCD8-Positive T-LymphocytesFlow CytometryGenetic VectorsLectins, C-TypeMannose-Binding LectinsMicroscopy, ConfocalViral VaccinesAntigens, CDCD207 protein, humanLectins, C-TypeMannose-Binding LectinsViral Vaccines

Identifiers

PMID23386724
PMCPMC3581957
OpenAlexW1971277965

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.