Evidence map›Paper›PMID 30858151›Full record

ArticleBlood advances2019

Enhancing the antitumor functions of invariant natural killer T cells using a soluble CD1d-CD19 fusion protein.

Rupali Das, Peng Guan, Susan J Wiener, Nishant P Patel, Trevor G Gohl, Elizabeth Evans, Maurice Zauderer, Kim E Nichols

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
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.

Rupali DasDepartment of Physiology, Michigan State University, East Lansing, MI.
Peng GuanDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.
Susan J WienerDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.
Nishant P PatelDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.
Trevor G GohlDepartment of Physiology, Michigan State University, East Lansing, MI.
Elizabeth EvansVaccinex Inc., Rochester, NY; and.
Maurice ZaudererVaccinex Inc., Rochester, NY; and.
Kim E NicholsDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN.ORCID 0000-0002-5581-6555
Children's Hospital of Philadelphia · USMichigan State University · USVaccinex (United States) · USSt. Jude Children's Research Hospital · US

Funding

Roles of CD2 and 2B4 in invariant natural killer T (iNKT) cell functions.K22CA188149 · NCI · MICHIGAN STATE UNIVERSITY · PI DAS, RUPALI · 2015 to 2017
$542k
JAK inhibition as a novel treatment for hemophagocytic lymphohistiocytosisR21AI113490 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI NICHOLS, KIM ERIKA · 2014 to 2015
$490k
NCI NIH HHS K22 CA188149NIAID NIH HHS R21 AI113490
6 · The paper itself

Abstract

Invariant natural killer T (iNKT) cells comprise a unique lineage of CD1d-restricted lipid-reactive T lymphocytes that potently kill tumor cells and exhibit robust immunostimulatory functions. Optimal tumor-directed iNKT cell responses often require expression of the antigen-presenting molecule CD1d on tumors; however, many tumor cells downregulate CD1d and thus evade iNKT cell recognition. We generated a soluble bispecific fusion protein designed to direct iNKT cells to the site of B-cell cancers in a tumor antigen-specific but CD1d-independent manner. This fusion protein is composed of a human CD1d molecule joined to a single chain antibody FV fragment specific for CD19, an antigen widely expressed on B-cell cancers. The CD1d-CD19 fusion protein binds specifically to CD19-expressing, but not CD19-negative cells. Once loaded with the iNKT cell lipid agonist α-galactosyl ceramide (αGC), the CD1d-CD19 fusion induces robust in vitro activation of and cytokine production by human iNKT cells. iNKT cells stimulated by the αGC-loaded CD1d-CD19 fusion also strongly transactivate T-, B-, and NK-cell responses and promote dendritic cell maturation. Importantly, the αGC-loaded fusion induces robust lysis of CD19

Indexed as

AnimalsAntigens, CD19Antigens, CD1dCell Line, TumorCell ProliferationHeterograftsHumansLymphocyte ActivationMiceNatural Killer T-CellsOncogene Proteins, FusionProtein EngineeringSingle-Chain AntibodiesSolubilityTumor BurdenAntigens, CD19Antigens, CD1dCD1D protein, humanOncogene Proteins, FusionSingle-Chain Antibodies

Identifiers

PMID30858151
PMCPMC6418505
OpenAlexW2922013081

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.