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Blood, 15 November 2004, Vol. 104, No. 10, pp. 3312-3317.
Prepublished online as a Blood First Edition Paper on July 29, 2004; DOI 10.1182/blood-2004-03-0950.
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Submitted March 12, 2004
Accepted June 22, 2004
Hairy cell leukemia: at the cross road of somatic mutation and isotype switch
Francesco Forconi*, Surinder S Sahota, Donatella Raspadori, Micaela Ippoliti, Gavin Babbage, Francesco Lauria, and Freda K Stevenson
U.O.C. Ematologia e Trapianti, Dipartimento di Medicina Clinica e Scienze Immunologiche Applicate, University of Siena, Siena, Italy
Molecular Immunology Group, Tenovus Laboratory, Southampton University Hospitals, Southampton, United Kingdom
* Corresponding author; email: forconif{at}unisi.it.
Hairy cell leukemia (HCL) commonly expresses multiple immunoglobulin (Ig) isotypes, a feature rare in other B-cell malignancies or in normal B-cells. In HCL, there is no phenotypic evidence for subpopulations, and single cells from one previous case contained transcripts for several isotypes. This raises the question of the differentiation status of the cell of origin, and of events post-transformation. We have investigated 9 cases, all expressing multiple Ig isotypes. Multiple tumor-derived V(D)J-Cµ, , , transcripts were confirmed in single cells of a further case. All cases were negative for germinal center (GC)-associated markers CD27 and CD38. Seven of 9 had mutated VH-genes, with low levels of intraclonal heterogeneity, but 2/9 were unmutated, indicative of pre-GC origin. Eight of 9 cases expressed activation-induced cytidine deaminase (AID), a molecule essential for somatic mutation and isotype switch. All cases expressed germline IH-CH transcripts which paralleled sIg isotype. Significantly, no circle transcripts indicative of switch deletional recombination were detectable in 9/9 cases. These data indicate heterogeneity in the cell of origin in terms of mutational status, but reveal common features of AID expression and isotype switch events occurring prior to deletional recombination. Both mutational and switching events may be influenced by environmental factors at extrafollicular sites.

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