Evidence map›Paper›PMID 15314077›Full record

ArticleThe Journal of experimental medicine2004

Multiple distinct sets of stereotyped antigen receptors indicate a role for antigen in promoting chronic lymphocytic leukemia.

Bradley T Messmer, Emilia Albesiano, Dimitar G Efremov, Fabio Ghiotto, Steven L Allen, Jonathan Kolitz, Robin Foa, Rajendra N Damle, Franco Fais, Davorka Messmer and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 175 papers.

0numbers the graph read from it
0cells of the map it votes in
175citing papers in PubMed
11.9field-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

175 citing papers in PubMed, 436 citations in OpenAlex.

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  19. Stereotyped B-Cell Receptor Immunoglobulins in B-Cell Lymphomas.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  20. Expression Cloning of Antibodies from Single Human B Cells.Methods in molecular biology (Clifton, N.J.) · 2025
    Article

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

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 5 institutions in 2 countries.

Bradley T MessmerNorth Shore-LIJ Research Institute, 350 Community Dr., Manhasset, NY 11030, USA.
Emilia Albesiano
Dimitar G Efremov
Fabio Ghiotto
Steven L Allen
Jonathan Kolitz
Robin Foa
Rajendra N Damle
Franco Fais
Davorka Messmer
Kanti R Rai
Manlio Ferrarini
Nicholas Chiorazzi
North Shore University Hospital · USAlbert Einstein College of Medicine · USAlleanza Contro il Cancro · ITInternational Centre for Genetic Engineering and Biotechnology · ITSapienza University of Rome · IT

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 CA 81554NCI NIH HHS R01 CA 87956NCRR NIH HHS M01 RR018535
6 · The paper itself

Abstract

Previous studies suggest that the diversity of the expressed variable (V) region repertoire of the immunoglobulin (Ig)H chain of B-CLL cells is restricted. Although limited examples of marked constraint in the primary structure of the H and L chain V regions exist, the possibility that this level of restriction is a general principle in this disease has not been accepted. This report describes five sets of patients, mostly with unmutated or minimally mutated IgV genes, with strikingly similar B cell antigen receptors (BCRs) arising from the use of common H and L chain V region gene segments that share CDR3 structural features such as length, amino acid composition, and unique amino acid residues at recombination junctions. Thus, a much more striking degree of structural restriction of the entire BCR and a much higher frequency of receptor sharing exists among patients than appreciated previously. The data imply that either a significant fraction of B-CLL cells was selected by a limited set of antigenic epitopes at some point in their development and/or that they derive from a distinct B cell subpopulation with limited Ig V region diversity. These shared, stereotyped Ig molecules may be valuable probes for antigen identification and important targets for cross-reactive idiotypic therapy.

Indexed as

Genetic VariationAmino Acid SequenceCluster AnalysisDatabases, GeneticHumansImmunoglobulin Heavy ChainsImmunoglobulin Light ChainsImmunoglobulin Variable RegionLeukemia, Lymphocytic, Chronic, B-CellMolecular Sequence DataMutationReceptors, Antigen, B-CellSequence AlignmentSequence Analysis, DNAImmunoglobulin Heavy ChainsImmunoglobulin Light ChainsImmunoglobulin Variable RegionReceptors, Antigen, B-Cell

Identifiers

PMID15314077
PMCPMC2211936
OpenAlexW2166526425

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.