High-throughput analysis of the T cell receptor gene repertoire in low-count monoclonal B cell lymphocytosis reveals a distinct profile from chronic lymphocytic leukemia

Haematologica. 2020 Oct 1;105(10):e515. doi: 10.3324/haematol.2019.221275.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocytes
  • Genes, T-Cell Receptor
  • Humans
  • Leukemia, Lymphocytic, Chronic, B-Cell* / genetics
  • Lymphocyte Count
  • Lymphocytosis* / diagnosis
  • Lymphocytosis* / genetics

Grants and funding

Funding: this project received funding from the Hellenic Foundation for Research and Innovation (HFRI) and the General Secretariat for Research and Technology (GSRT), under grant agreement n. 336 (Project CLLon); the TRANSCAN-2 Joint Transnational Call for Proposals 2014 (JTC 2014), GCH-CLL #143, by the European Commission/DG Research and Innovation; the project “KRIPIS II ODYSSEUS” funded by the Operational Programme "Competitiveness, Entrepreneurship and Innovation" (NSRF 2014-2020) and co-financed by Greece and the European Union (European Regional Development Fund); the Italian Association for Cancer Research (AIRC, Special Program on Metastasis, 5 per mille # 21198 to PG); PRIN 2015ZMRFEA, Italian Ministry of University and Research – MIUR, Roma, Italy ERA-NET TRANSCAN-2 JTC 2016 #179 NOVEL; open access project, ID number LM2011020, funded by the Ministry of Education, Youth and Sports of the Czech Republic under the activity “Projects of major infrastructures for research, development and innovations”.