Evidence map›Paper›PMID 15057307›Full record

ArticleThe Journal of clinical investigation2004

Remarkably similar antigen receptors among a subset of patients with chronic lymphocytic leukemia.

Fabio Ghiotto, Franco Fais, Angelo Valetto, Emilia Albesiano, Shiori Hashimoto, Mariella Dono, Hideyuki Ikematsu, Steven L Allen, Jonathan Kolitz, Kanti R Rai and 4 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
10.9field-weighted citation impact, top 1% 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

91 citing papers in PubMed, 234 citations in OpenAlex.

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  10. Stereotyped B-Cell Receptor Immunoglobulins in B-Cell Lymphomas.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
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  19. Chronic Lymphocytic Leukemia.Cold Spring Harbor perspectives in medicine · 2021
    Review
  20. Review

31 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 8 institutions in 3 countries.

Fabio GhiottoDepartment of Medicine, North Shore University Hospital and New York University School of Medicine, Manhasset, New York, USA.
Franco Fais
Angelo Valetto
Emilia Albesiano
Shiori Hashimoto
Mariella Dono
Hideyuki Ikematsu
Steven L Allen
Jonathan Kolitz
Kanti R Rai
Marco Nardini
Anna Tramontano
Manlio Ferrarini
Nicholas Chiorazzi
Northwell Health · USAlleanza Contro il Cancro · ITHaradoi Hospital · JPSapienza University of Rome · ITTokyo Women's Medical University · JPUniversity of Genoa · ITUniversity of Pisa · ITYeshiva University · US

Funding

WHITE MATTER STRUCTURAL DEFICITS IN HIGH FUNCTIONING CHILDREN WITH AUTISM SPEM01RR018535 · NCRR · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI SCHWARTZ, GUY · 2003 to 2010
$19.5M
B CELL REPERTOIRES IN CHRONIC LYMPHOCYTIC LEUKEMIAR01CA081554 · NCI · NORTH SHORE UNIVERSITY HOSPITAL · PI CHIORAZZI, NICHOLAS · 2000 to 2012
$2.7M
B CLL SUBGROUPS--MATURATION STAGE AND GENE EXPRESSIONR01CA087956 · NCI · NORTH SHORE UNIVERSITY HOSPITAL · PI CHIORAZZI, NICHOLAS · 2001 to 2004
$1.2M
NCI NIH HHS R01 CA081554NCI NIH HHS R01 CA087956NCI NIH HHS R01 CA81554NCI NIH HHS R01 CA 87956NCRR NIH HHS M01 RR018535
6 · The paper itself

Abstract

Studies of B cell antigen receptors (BCRs) expressed by leukemic lymphocytes from patients with B cell chronic lymphocytic leukemia (B-CLL) suggest that B lymphocytes with some level of BCR structural restriction become transformed. While analyzing rearranged V(H)DJ(H) and V(L)J(L) genes of 25 non-IgM-producing B-CLL cases, we found five IgG(+) cases that display strikingly similar BCRs (use of the same H- and L-chain V gene segments with unique, shared heavy chain third complementarity-determining region [HCDR3] and light chain third complementarity-determining region [LCDR3] motifs). These H- and L-chain characteristics were not identified in other B-CLL cases or in normal B lymphocytes whose sequences are available in the public databases. Three-dimensional modeling studies suggest that these BCRs could bind the same antigenic epitope. The structural features of the B-CLL BCRs resemble those of mAb's reactive with carbohydrate determinants of bacterial capsules or viral coats and with certain autoantigens. These findings suggest that the B lymphocytes that gave rise to these IgG(+) B-CLL cells were selected for this unique BCR structure. This selection could have occurred because the precursors of the B-CLL cells were chosen for their antigen-binding capabilities by antigen(s) of restricted nature and structure, or because the precursors derived from a B cell subpopulation with limited BCR heterogeneity, or both.

Indexed as

B-LymphocytesHumansImmunoglobulin GLeukemia, Lymphocytic, Chronic, B-CellModels, MolecularProtein Structure, TertiaryReceptors, Antigen, B-CellSequence Analysis, ProteinImmunoglobulin GReceptors, Antigen, B-Cell

Identifiers

PMID15057307
PMCPMC379317
OpenAlexW2140384293

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.