Haematologica (May 2011)

Extent of hematopoietic involvement by TET2 mutations in JAK2V617F polycythemia vera

  • Sabina I. Swierczek,
  • Donghoon Yoon,
  • Christine Bellanné-Chantelot,
  • Soo Jin Kim,
  • Cécile Saint-Martin,
  • Francois Delhommeau,
  • Albert Najman,
  • Josef T. Prchal

DOI
https://doi.org/10.3324/haematol.2010.029678
Journal volume & issue
Vol. 96, no. 5

Abstract

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TET2 mutations are found in polycythemia vera and it was initially reported that there is a greater TET2 mutational burden than JAK2V617F in polycythemia vera stem cells and that TET2 mutations precede JAK2V617F. We quantified the proportion of TET2, JAK2V617F mutations and X-chromosome allelic usage in polycythemia vera cells, BFU-Es and in vitro expanded erythroid progenitors and found clonal reticulocytes, granulocytes, platelets and CD34+ cells. We found that TET2 mutations may also follow rather than precede JAK2V617F as recently reported by others. Only a fraction of clonal early hematopoietic precursors and largely polyclonal T cells carry the TET2 mutation. We showed that in vitro the concomitant presence of JAK2V617F and TET2 mutations favors clonal polycythemia vera erythroid progenitors in contrast with non-TET2 mutated progenitors. We conclude that loss-of-function TET2 mutations are not the polycythemia vera initiating events and that the acquisition of TET2 somatic mutations may increase the aggressivity of the polycythemia vera clone.