Cells carrying nonlymphoma-associated bcl-2/IgH rearrangements (NLABR) are phenotypically related to follicular lymphoma and can establish as long-term persisting clonal populations

Marco Ladetto*, Barbara Mantoan, Federica De Marco, Daniela Drandi, Chiara Aguzzi, Monica Astolfi, Sonia Vallet, Irene Ricca, Maria Dell Aquila, Gloria Pagliano, Luigia Monitillo, Berardino Pollio, Loredana Santo, Carmen Cristiano, Alberto Rocci, Roberto Francese, Chiara Lobetti Bodoni, Alessandra Borchiellini, Piercarla Schinco, Mario BoccadoroCorrado Tarella

*Corresponding author for this work

Research output: Journal article (peer-reviewed)Journal article

12 Citations (Scopus)

Abstract

Objective: Nonlymphoma-associated bcl-2/IgH rearrangements (NLABRs) are frequently amplified by PCR in blood of lymphoma-free subjects (LFS), but the temporal kinetics and phenotypic nature of NLABR-positive cells are unknown. To address these issues we prospectively monitored a panel of NLABR-positive LFS. Methods: LFS have been studied by nested PCR, real-time PCR, and DNA sequencing. Cell selection studies were also performed to define the nature of NLABR-bearing clones. Results: Of 125 donors, 16 (12.8%) were found to be bcl-2/IgH positive and were monitored at least every 6 months for a median time of 22 months (range 6-50). In half of the subjects the same NLABR detected initially was again reamplified at follow-up thrice or more. In 5, the same NLABR was constantly amplified in every follow-up sample. With a median follow-up of 22 months (range 9-50), no stable disappearance of a recurrent clone has been so far recorded. Real-time PCR indicated that persistent NLABR-positive clones are stable over time in the same subject. Cell separation studies indicate that NLABRs belong to CD19+, CD5-, CD23-, CD10+/- cells. Conclusions: Our results indicate that NLABR-positive clones are persistent populations phenotypically related to follicular lymphoma (FL). This suggests the existence of a FL-related clonal expansion of undetermined significance, which might be either a premalignant or a nonmalignant counterpart of FL.

Original languageEnglish
Pages (from-to)1680-1686
Number of pages7
JournalExperimental Hematology
Volume34
Issue number12
DOIs
Publication statusPublished - Dec 2006
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Hematology
  • Genetics
  • Cell Biology
  • Cancer Research

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