The introduction of polyclonal B cell mitogens led to the discovery of the first cytogenetic abnormality, trisomy 12, in CLL in 1980 [1]. With the use of more effective mitogens, initially tetradecanoyl phorbol acetate (TPA) [2], then CD40 ligand [3], and most recently CpG oligonucleotides combined with Interleukin 2 [4, 5], metaphases can be obtained in the majority of cases of CLL and clonal abnormalities are identifiable in approximately 80 % [6].
CITATION STYLE
Oscier, D., Gardiner, A., & Strefford, J. C. (2013). Molecular biology and cytogenetics of chronic lymphocytic leukemia. In Neoplastic Diseases of the Blood (pp. 91–101). Springer New York. https://doi.org/10.1007/978-1-4614-3764-2_8
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