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Published on: October 19, 2014
Surface phenotype and immunoglobulin levels in B-cell chronic lymphocytic leukaemia
A Orfao1, M Gonzalez, J F San Miguel
1Servicio de Hematologia, Hospital Clinico Universitario, Salamanca, Spain.
Insights
Low immunoglobulin (Ig) levels in B-cell chronic lymphocytic leukemia (B-CLL) patients correlate with advanced disease, not specific cell phenotypes. Hypogammaglobulinaemia indicates a higher tumor burden in B-CLL.
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- B-cell chronic lymphocytic leukemia (B-CLL) is a heterogeneous lymphoproliferative disorder.
- Immunoglobulin (Ig) levels and expression are critical in B-CLL pathogenesis and prognosis.
- Understanding the relationship between Ig levels and disease characteristics is vital for patient management.
Purpose of the Study:
- To investigate the association between serum Ig levels and the immunological phenotype of B-CLL.
- To analyze the correlation between Ig levels and clinicohaematological features in B-CLL patients.
- To determine if hypogammaglobulinaemia in B-CLL relates to tumor burden or cellular phenotype.
Main Methods:
- Analysis of serum immunoglobulin levels in 126 B-CLL patients.
- Assessment of B-cell surface phenotype using flow cytometry.
- Correlation of Ig levels with clinical data, including organomegaly, cytopenias, bone marrow patterns, and disease stage.
Main Results:
- 70% of B-CLL patients exhibited decreased Ig levels, predominantly IgM and IgA.
- Hypogammaglobulinaemia was associated with more advanced disease, including organomegaly, anemia/thrombocytopenia, diffuse bone marrow infiltration, and higher lymphocytosis.
- Patients with hypogammaglobulinaemia showed similar surface phenotypes to those with normal Ig levels.
Conclusions:
- Hypogammaglobulinaemia in B-CLL is linked to a higher tumor burden rather than specific B-cell differentiation stages or phenotypes.
- Serum Ig levels serve as a potential indicator of disease severity in B-CLL.
- Further research into the mechanisms underlying hypogammaglobulinaemia in B-CLL is warranted.
Abstract:
The aim of the present study is to analyze the relationship between serum immunoglobulin (Ig) levels and the immunological phenotype and the clinicohaematological features of B-cell chronic lymphocytic leukaemia (B-CLL) in a series of 126 patients. Eighty-eight of the cases (70%) had a decreased concentration of at least one Ig. IgM and IgA were the most frequently decreased (60% and 49% respectively). A serum monoclonal gammapathy was found in 4 patients, Ig M/k in two cases and IgM/l and IgG/k in one case. Patients with hypogammaglobulinaemia had a similar surface phenotype as patients with normal Ig levels (MRFC+, sIg+, CD20+, HLA/DR+, FMC7-, CD5+, CD9+). On the other hand the cases with hypogammaglobulinaemia displayed the features of a more advanced disease, a higher incidence of organomegalies (p less than 0.05), anaemia and/or thrombopenia (p less than 0.05), a diffuse bone marrow pattern (p less than 0.05), advanced clinical stages (p less than 0.05) as well as higher levels of both peripherial blood (p less than 0.02) and bone marrow lymphocytosis (p less than 0.02). These findings suggest that the presence of hypogammaglobulinaemia in B-cell patients is probably more related to a higher tumor burden than to either certain stages of B-cell differentiation or a particular cellular phenotype.
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