Abstract
Roughly 30% of patients with chronic lymphocytic leukemia (CLL) carry immunoglobulin receptors with highly similar primary sequences. Highly similar, quasi-identical immunoglobulins are termed stereotyped. Patients with CLL can be assigned to different subsets expressing different types of stereotyped immunoglobulin receptors. Reliable identification of stereotypy may assist in the molecular classification of CLL and thus better-guided, compartmentalized research. In several major subsets, stereotypy extends from shared primary sequences to shared clinicobiological features and outcome. Reliable identification of stereotypy in CLL may pave the way for tailored treatment strategies applicable to each major stereotyped subset.
Copyright © 2013 Elsevier Inc. All rights reserved.
Publication types
-
Research Support, Non-U.S. Gov't
-
Review
MeSH terms
-
Animals
-
Antibody Diversity / immunology
-
Humans
-
Immunoglobulin Heavy Chains / genetics
-
Immunoglobulin Heavy Chains / immunology
-
Immunoglobulin Variable Region / genetics
-
Immunoglobulin Variable Region / immunology
-
Immunoglobulins / classification
-
Immunoglobulins / immunology
-
Immunoglobulins / metabolism
-
Leukemia, Lymphocytic, Chronic, B-Cell / classification
-
Leukemia, Lymphocytic, Chronic, B-Cell / genetics
-
Leukemia, Lymphocytic, Chronic, B-Cell / immunology*
-
Receptors, Antigen, B-Cell / genetics
-
Receptors, Antigen, B-Cell / immunology*
-
Receptors, Antigen, B-Cell / metabolism
-
Somatic Hypermutation, Immunoglobulin
Substances
-
Immunoglobulin Heavy Chains
-
Immunoglobulin Variable Region
-
Immunoglobulins
-
Receptors, Antigen, B-Cell