Evidence map›Paper›PMID 30761123›Full record

ArticleFrontiers in immunology2019

CD56

Lazar Vujanovic, Christopher Chuckran, Yan Lin, Fei Ding, Cindy A Sander, Patricia M Santos, Joel Lohr, Afshin Mashadi-Hossein, Sarah Warren, Andy White and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% 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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 75 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Enhanced CD56 Expression and Increased Number of CD56American journal of reproductive immunology (New York, N.Y. : 1989) · 2026
    Article
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  8. Review
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  13. Review
  14. Differential impact of TIM-3 ligands on NK cell function.Journal for immunotherapy of cancer · 2025
    Article
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  16. Article
  17. Article
  18. Article
  19. Article
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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

13 authors at 3 institutions in 1 country.

Lazar VujanovicUniversity of Pittsburgh Hillman Cancer Center, Pittsburgh, PA, United States.
Christopher ChuckranDepartment of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.
Yan LinUniversity of Pittsburgh Hillman Cancer Center, Pittsburgh, PA, United States.
Fei DingUniversity of Pittsburgh Hillman Cancer Center, Pittsburgh, PA, United States.
Cindy A SanderUniversity of Pittsburgh Hillman Cancer Center, Pittsburgh, PA, United States.
Patricia M SantosUniversity of Pittsburgh Hillman Cancer Center, Pittsburgh, PA, United States.
Joel LohrDepartment of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.
Afshin Mashadi-HosseinNanoString Technologies, Seattle, WA, United States.
Sarah WarrenNanoString Technologies, Seattle, WA, United States.
Andy WhiteNanoString Technologies, Seattle, WA, United States.
Alan HuangNanoString Technologies, Seattle, WA, United States.
John M KirkwoodUniversity of Pittsburgh Hillman Cancer Center, Pittsburgh, PA, United States.
Lisa H ButterfieldUniversity of Pittsburgh Hillman Cancer Center, Pittsburgh, PA, United States.
University of Pittsburgh · USNanostring Technologies (United States) · USUPMC Hillman Cancer Center · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
Therapuetic Immune Targeting of EphA2 Expressed by Melanoma & Its Tumor-AssociateP50CA121973 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KIRKWOOD, JOHN MUNN · 2008 to 2018
$22.9M
Training Program in Skin Biology and CancerT32CA175294 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KIRKWOOD, JOHN MUNN · 2014 to 2018
$973k
NCI NIH HHS P30 CA047904NCI NIH HHS P50 CA121973NCI NIH HHS T32 CA175294
6 · The paper itself

Abstract

Natural killer (NK) cells are innate cytotoxic and immunoregulatory lymphocytes that have a central role in anti-tumor immunity and play a critical role in mediating cellular immunity in advanced cancer immunotherapies, such as dendritic cell (DC) vaccines. Our group recently tested a novel recombinant adenovirus-transduced autologous DC-based vaccine that simultaneously induces T cell responses against three melanoma-associated antigens for advanced melanoma patients. Here, we examine the impact of this vaccine as well as the subsequent systemic delivery of high-dose interferon-α2b (HDI) on the circulatory NK cell profile in melanoma patients. At baseline, patient NK cells, particularly those isolated from high-risk patients with no measurable disease, showed altered distribution of CD56

Indexed as

Antigen PresentationAntigen-Presenting CellsBiomarkersCancer VaccinesCD56 AntigenClinical Trials, Phase I as TopicCombined Modality TherapyCytotoxicity, ImmunologicHumansImmunophenotypingImmunotherapyInterferon-alphaKiller Cells, NaturalLymphocyte ActivationMelanomaNeoplasm StagingBiomarkersCancer VaccinesCD56 AntigenInterferon-alphaReceptors, IgGCD56dim CD16−dendritic cellsinterferon-αmelanomanatural killer cell subsetsrecombinant adenoviral vector

Identifiers

PMID30761123
PMCPMC6361792
OpenAlexW2915039064

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.