Evidence map›Paper›PMID 19946263›Full record

ArticleLeukemia2010

Single-cell analysis reveals oligoclonality among 'low-count' monoclonal B-cell lymphocytosis.

M C Lanasa, S D Allgood, A D Volkheimer, J P Gockerman, J F Whitesides, B K Goodman, J O Moore, J B Weinberg, M C Levesque

Open access · greenAbstract read
In one paragraph

Article in Leukemia, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.0field-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

37 citing papers in PubMed, 69 citations in OpenAlex.

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  11. Pathogenesis of chronic lymphocytic leukemia and the development of novel therapeutic strategies.Journal of clinical and experimental hematopathology : JCEH · 2020
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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

9 authors at 4 institutions in 1 country.

M C LanasaDepartment of Medicine, Duke University Medical Center, 1 Trent Drive, Morris Building Room 25153, Durham, NC 27710, USA. mark.lanasa@duke.edu
S D Allgood
A D Volkheimer
J P Gockerman
J F Whitesides
B K Goodman
J O Moore
J B Weinberg
M C Levesque
Duke Medical Center · USDuke University · USDurham VA Medical Center · USUniversity of Pittsburgh Medical Center · US

Funding

Duke University Center for Translational ResearchP30AI051445 · NIAID · DUKE UNIVERSITY · PI FROTHINGHAM, RICHARD · 2002 to 2006
$8.1M
Prevention of Chronic Lymphocytic Leukemia (CLL)R03CA128030 · NCI · DUKE UNIVERSITY · PI LEVESQUE, MARC C. · 2007 to 2008
$156k
NCI NIH HHS R03 CA128030NIAID NIH HHS AI-51445NIAID NIH HHS P30 AI051445
6 · The paper itself

Abstract

Monoclonal B-cell lymphocytosis (MBL) is a preclinical hematologic syndrome characterized by small accumulations of CD5(+) B lymphocytes. Most MBL share phenotypic characteristics with chronic lymphocytic leukemia (CLL). Although some MBL progress to CLL, most MBL have apparently limited potential for progression to CLL, particularly those MBL with normal absolute B-cell counts ('low-count' MBL). Most CLL are monoclonal and it is not known whether MBL are monoclonal or oligoclonal; this is important because it is unclear whether MBL represent indolent CLL or represent a distinct premalignant precursor before the development of CLL. We used flow cytometry analysis and sorting to determine immunophenotypic characteristics, clonality and molecular features of MBL from familial CLL kindreds. Single-cell analysis indicated four of six low-count MBL consisted of two or more unrelated clones; the other two MBL were monoclonal. 87% of low-count MBL clones had mutated immunoglobulin genes, and no immunoglobulin heavy-chain rearrangements of V(H) family 1 were observed. Some MBL were diversified, clonally related populations with evidence of antigen drive. We conclude that although low-count MBL share many phenotypic characteristics with CLL, many MBL are oligoclonal. This supports a model for step-wise development of MBL into CLL.

Indexed as

AgedAged, 80 and overB-LymphocytesChromosome AberrationsFemaleGenes, ImmunoglobulinHumansImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionImmunophenotypingLeukemia, Lymphocytic, Chronic, B-CellLymphocytosisMaleMiddle AgedImmunoglobulin Heavy ChainsImmunoglobulin Variable Region

Identifiers

PMID19946263
PMCPMC2806490
OpenAlexW2052807764

What OpenQuestion holds

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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.