Evidence map›Paper›PMID 27801602›Full record

ArticleExpert review of vaccines2017

A potent adjuvant effect of a CD1d-binding NKT cell ligand in human immune system mice.

Xiangming Li, Jing Huang, Izumi Kaneko, Min Zhang, Shiroh Iwanaga, Masao Yuda, Moriya Tsuji

Open access · greenAbstract read
In one paragraph

Article in Expert review of vaccines, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  9. A humanized mouse model forFrontiers in immunology · 2022
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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

7 authors at 3 institutions in 2 countries.

Xiangming Lia HIV and Malaria Vaccine Program, Aaron Diamond AIDS Research Center , Affiliate of The Rockefeller University , New York , NY , USA.
Jing Huanga HIV and Malaria Vaccine Program, Aaron Diamond AIDS Research Center , Affiliate of The Rockefeller University , New York , NY , USA.
Izumi Kanekob Department of Medical Zoology , Mie University Graduate School of Medicine , Tsu , Mie , Japan.
Min Zhanga HIV and Malaria Vaccine Program, Aaron Diamond AIDS Research Center , Affiliate of The Rockefeller University , New York , NY , USA.
Shiroh Iwanagab Department of Medical Zoology , Mie University Graduate School of Medicine , Tsu , Mie , Japan.
Masao Yudab Department of Medical Zoology , Mie University Graduate School of Medicine , Tsu , Mie , Japan.
Moriya Tsujia HIV and Malaria Vaccine Program, Aaron Diamond AIDS Research Center , Affiliate of The Rockefeller University , New York , NY , USA.
Mie University · JPAaron Diamond AIDS Research Center · USRockefeller University · US

Funding

CD1d/NKT-binding glycolipids in enhancing the immunogenicity of a malaria vaccineR01AI070258 · NIAID · AARON DIAMOND AIDS RESEARCH CENTER · PI TSUJI, MORIYA · 2012 to 2016
$2.2M
NIAID NIH HHS R01 AI070258
6 · The paper itself

Abstract

objectivesA CD1d-binding invariant natural killer T (iNKT)-cell stimulatory glycolipid, namely 7DW8-5, is shown to enhance the efficacy of radiation-attenuated sporozoites (RAS)-based malaria vaccine in mice. In the current study, we aim to determine whether 7DW8-5 can display a potent adjuvant effect in human immune system (HIS) mice.

methodsHIS-A2/hCD1d mice, which possess both functional human iNKT cells and CD8+ T cells, were generated by the transduction of NSG mice with adeno-associated virus serotype 9 expressing genes that encode human CD1d molecules and HLA-A*0201, followed by the engraftment of human hematopoietic stem cells. The magnitudes of human iNKT-cell response against 7DW8-5 and HLA-A*0201-restricted human CD8+ T-cell response against a human malaria antigen in HIS-A2/hCD1d mice were determined by using human CD1d tetramer and human HLA-A*0201 tetramer, respectively.

resultsWe found that 7DW8-5 stimulates human iNKT cells in HIS-A2/hCD1d mice, as well as those derived from HIS-A2/hCD1d mice in vitro. We also found that 7DW8-5 significantly increases the level of a human malarial antigen-specific HLA-A*0201-restricted human CD8+ T-cell response in HIS-A2/hCD1d mice.

conclusionsOur study indicates that 7DW8-5 can display a potent adjuvant effect on RAS vaccine-induced anti-malarial immunity by augmenting malaria-specific human CD8+ T-cell response.

Indexed as

Adjuvants, ImmunologicAnimalsCD8-Positive T-LymphocytesGalactosylceramidesHumansMalaria VaccinesMiceMice, SCIDNatural Killer T-CellsTreatment OutcomeVaccines, Inactivated7DW8-5 glycolipidAdjuvants, ImmunologicGalactosylceramidesMalaria VaccinesVaccines, InactivatedadjuvantCD1dglycolipidhumanized miceMalariaNKT cellsporozoites

Identifiers

PMID27801602
PMCPMC5526659
OpenAlexW2547236059

What OpenQuestion holds

Textmetadata
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.