Evidence map›Paper›PMID 30609269›Full record

ArticlePediatric blood & cancer2019

Characterization of natural killer cells expressing markers associated with maturity and cytotoxicity in children and young adults with sickle cell disease.

Allistair A Abraham, Haili Lang, Emily Riehm Meier, Robert S Nickel, Marcus Dean, Nurah Lawal, Barbara Speller-Brown, Yunfei Wang, Leslie Kean, Catherine M Bollard

Open access · greenAbstract read
In one paragraph

Article in Pediatric blood & cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 8 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

10 authors at 3 institutions in 1 country.

Allistair A AbrahamChildren's National Health System, Washington, District of Columbia.ORCID 0000-0003-2019-0887
Haili LangChildren's National Health System, Washington, District of Columbia.
Emily Riehm MeierIndiana Hemophilia and Thrombosis Center, Indianapolis, Indiana.ORCID 0000-0002-7837-9239
Robert S NickelChildren's National Health System, Washington, District of Columbia.ORCID 0000-0003-4277-7523
Marcus DeanChildren's National Health System, Washington, District of Columbia.
Nurah LawalChildren's National Health System, Washington, District of Columbia.
Barbara Speller-BrownChildren's National Health System, Washington, District of Columbia.ORCID 0000-0003-4516-8184
Yunfei WangChildren's National Health System, Washington, District of Columbia.
Leslie KeanSeattle Children's Hospital, Seattle, Washington.
Catherine M BollardChildren's National Health System, Washington, District of Columbia.
Children's National · USIndiana Hemophilia and Thrombosis Center · USSeattle Children's Hospital · US

Funding

Child Health Research Career Development Award (CHRCDA) Program at Children's NationalK12HD001399 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI NATHAN KUPPERMANN · 2001 to 2026
$9.1M
NICHD NIH HHS 5 K12HD001399NICHD NIH HHS K12 HD001399
6 · The paper itself

Abstract

backgroundSickle cell disease (SCD) is increasingly recognized as a red blood cell disorder modulated by abnormally increased inflammation. We have previously shown that in patients with SCD not on a disease-modifying therapy (hydroxyurea or chronic transfusions), natural killer (NK) cell numbers are increased. In the current study, we further investigated the NK cell function to determine if there was evidence of increased activation and cytotoxicity. PROCEDURE: We conducted a cross-sectional study of 44 patients with HbSS/HbSβ

resultsPatients with SCD who were not on disease-modifying therapy had a higher number of NK cells with an immunophenotype associated with increased cytotoxicity (NKG2D

conclusionSCD is associated with increased NK cell function as well as increased NK cell numbers, which appears to be normalized with disease-modifying therapy.

Indexed as

AdolescentAdultAnemia, Sickle CellAntisickling AgentsBiomarkersCase-Control StudiesChildChild, PreschoolCross-Sectional StudiesCytotoxicity, ImmunologicFemaleFollow-Up StudiesHumansHydroxyureaImmunophenotypingInfantAntisickling AgentsBiomarkersHydroxyureahydroxyureaNK cellssickle cell disease

Identifiers

PMID30609269
PMCPMC6707525
OpenAlexW2908170468

What Socratic 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 Socratic graph.