Evidence map›Paper›PMID 24599269›Full record

ArticlePloS one2014

Sublingual vaccination induces mucosal and systemic adaptive immunity for protection against lung tumor challenge.

Shailbala Singh, Guojun Yang, Kimberly S Schluns, Scott M Anthony, K Jagannadha Sastry

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Shailbala SinghDepartment of Immunology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, United States of America.
Guojun YangDepartment of Immunology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, United States of America.
Kimberly S SchlunsDepartment of Immunology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, United States of America; Immunology Graduate Program, The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas, United States of America.
Scott M AnthonyDepartment of Immunology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, United States of America; Immunology Graduate Program, The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas, United States of America.
K Jagannadha SastryDepartment of Immunology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, United States of America; Immunology Graduate Program, The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas, United States of America.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Training Program in Cancer ImmunobiologyT32CA009598 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ALLISON, JAMES P · 1988 to 2014
$4.9M
Alpha-galactosycleramide as a mucosal adjuvant for HIV antigensR21AI078898 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SASTRY, JAGANNADHA K · 2009 to 2010
$424k
NCI NIH HHS P30 CA016672NCI NIH HHS T32 CA009598NIAID NIH HHS R21 AI078898
6 · The paper itself

Abstract

Sublingual route offers a safer and more practical approach for delivering vaccines relative to other systemic and mucosal immunization strategies. Here we present evidence demonstrating protection against ovalbumin expressing B16 (B16-OVA) metastatic melanoma lung tumor formation by sublingual vaccination with the model tumor antigen OVA plus synthetic glycolipid alpha-galactosylceramide (aGalCer) for harnessing the adjuvant potential of natural killer T (NKT) cells, which effectively bridge innate and adaptive arms of the immune system. The protective efficacy of immunization with OVA plus aGalCer was antigen-specific as immunized mice challenged with parental B16 tumors lacking OVA expression were not protected. Multiple sublingual immunizations in the presence, but not in the absence of aGalCer, resulted in repeated activation of NKT cells in the draining lymph nodes, spleens, and lungs of immunized animals concurrent with progressively increasing OVA-specific CD8+ T cell responses as well as serum IgG and vaginal IgA levels. Furthermore, sublingual administration of the antigen only in the presence of the aGalCer adjuvant effectively boosted the OVA-specific immune responses. These results support potential clinical utility of sublingual route of vaccination with aGalCer-for prevention of pulmonary metastases.

Indexed as

Adaptive ImmunityAdjuvants, ImmunologicAdministration, SublingualAnimalsAntigens, NeoplasmCancer VaccinesCell Line, TumorDendritic CellsFemaleGalactosylceramidesImmunity, HumoralLung NeoplasmsMelanoma, ExperimentalMice, Inbred C57BLMouth MucosaNatural Killer T-CellsAdjuvants, Immunologicalpha-galactosylceramideAntigens, NeoplasmCancer VaccinesGalactosylceramidesOvalbumin

Identifiers

PMID24599269
PMCPMC3943861
OpenAlexW2108824353

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.