Chronic lymphocytic leukaemia (CLL) represents an abnormal clonal expansion of mature antigen-experienced CD5+ B1a cells (Chiorazzi et al, 2005), which present with a highly heterogeneous clinical course depending on associated chromosomal aberrations, somatic mutations within the immunoglobulin variable heavy chain genes (IGHV), and surface CD38 or intracytoplasmic ZAP-70 expression. Given that key signalling components of the B-cell receptor (BCR) are relevant contributors to the variable clinical behaviour of CLL (Stevenson et al, 2011) we explored the influence of functionally relevant germline CD5 variants on CLL prognosis.
English
Leucèmia limfocítica crònica; Receptors cel·lulars; Cèl·lules B; Biologia molecular; Immunologia; Chronic lymphocytic leukemia; Cell receptors; B cells; Molecular biology; Immunology
Blackwell Science
https://doi.org/10.1111/bjh.14037
British Journal of Haematology, 2017, vol. 177,num. 1,p. 147-150
https://doi.org/10.1111/bjh.14037
(c) John Wiley & Sons Ltd, 2016