Molecular single-cell analysis reveals that CD5-positive peripheral blood B cells in healthy humans are characterized by rearranged Vkappa genes lacking somatic mutation

J Clin Invest. 1997 Oct 1;100(7):1667-76. doi: 10.1172/JCI119691.

Abstract

B cells expressing the CD5 cell surface antigen are involved in certain B cell malignancies and autoimmune diseases. From studies in the mouse, it emerged that CD5+ B cells represent a separate lineage of B lymphocytes that, in contrast to conventional (CD5-) B cells, are not driven into T cell-dependent immune responses in which rearranged variable (V) region genes are diversified by somatic hypermutation. Against this background it came as a surprise that human disease-involved CD5-positive autoreactive B cells as well as B cell chronic lymphocytic leukemias can harbor somatically mutated V region genes. Recent V gene analyses on CD5+ B cells in healthy adults did not give rise to a clear picture about the fraction of somatically mutated among all CD5+ B cells. In this work we used a molecular single-cell analysis to determine reliably the frequency of mutated CD5+ B cells in healthy humans: single, kappa light chain-expressing CD5+ peripheral blood B cells were isolated by flow cytometry, and rearranged Vkappa genes were amplified by PCR. From one donor, CD5+CD19+ B cells were analyzed. Since CD5+ B cells were found among IgM+IgD+ and IgM+IgD- cells (but almost not among class-switched cells) from two other donors, individual cells corresponding to these IgM-expressing subsets were investigated separately. The sequence analysis of rearranged Vkappa genes revealed that most if not all CD5+ B cells in healthy humans carry unmutated V region genes. From one of the donors, a novel polymorphic Jkappa2 gene segment was identified. To explain the discrepancy between the frequent occurrence of disease-associated somatically mutated CD5+ B cells and the low incidence or absence of somatic mutation in normal CD5+ B cells, we speculate that CD5+ B cells usually do not participate in germinal center reactions, but if they occasionally do so, they may be at an increased risk to become involved in autoimmune diseases or B cell malignancies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, CD19
  • B-Lymphocyte Subsets / cytology
  • B-Lymphocyte Subsets / immunology*
  • CD5 Antigens*
  • Flow Cytometry
  • Gene Rearrangement, B-Lymphocyte, Light Chain*
  • Humans
  • Immunoglobulin D / genetics
  • Immunoglobulin M / genetics
  • Immunoglobulin Variable Region / genetics*
  • Leukemia, Lymphocytic, Chronic, B-Cell / etiology
  • Leukemia, Prolymphocytic / etiology
  • Male
  • Mutation
  • Polymerase Chain Reaction
  • Sequence Analysis, DNA

Substances

  • Antigens, CD19
  • CD5 Antigens
  • Immunoglobulin D
  • Immunoglobulin M
  • Immunoglobulin Variable Region

Associated data

  • GENBANK/Z98605
  • GENBANK/Z98606
  • GENBANK/Z98607
  • GENBANK/Z98608
  • GENBANK/Z98609
  • GENBANK/Z98610
  • GENBANK/Z98611
  • GENBANK/Z98612
  • GENBANK/Z98613
  • GENBANK/Z98614
  • GENBANK/Z98615
  • GENBANK/Z98616
  • GENBANK/Z98617
  • GENBANK/Z98618
  • GENBANK/Z98619
  • GENBANK/Z98620
  • GENBANK/Z98621
  • GENBANK/Z98622
  • GENBANK/Z98623
  • GENBANK/Z98624
  • GENBANK/Z98625
  • GENBANK/Z98626
  • GENBANK/Z98627
  • GENBANK/Z98628
  • GENBANK/Z98629
  • GENBANK/Z98630
  • GENBANK/Z98631
  • GENBANK/Z98632
  • GENBANK/Z98633
  • GENBANK/Z98634