Haferlach Claudia, Bacher Ulrike
MLL Munich Leukemia Laboratory, Munich, Germany.
Methods Mol Biol. 2011;730:119-30. doi: 10.1007/978-1-61779-074-4_9.
In chronic lymphocytic leukemia of the B-lineage (B-CLL), cytogenetic alterations are highly relevant for prognosis and therapeutic decisions. With conventional techniques, chromosome banding analysis in CLL has been hampered by the low quality of metaphases and low rates of cytogenetic alterations due to a low in vitro proliferation rate of CLL cells. Thus, interphase fluorescence in situ hybridization (FISH) has become the standard technique for cytogenetic analysis in CLL. However, interphase FISH is not able to provide an overview on the whole karyotype. In order to improve chromosome banding analysis in CLL, specific stimulation techniques have been developed. These either use CD40 ligand or oligonucleotides (e.g., CpG) and IL-2 in combination. With the respective techniques, metaphase cultivation is successful in >90% of CLL cases and aberrant karyotypes can be detected in nearly 90% of CLL cases. This has allowed the detection of new clinically relevant subgroups (e.g., complex aberrant karyotype cases) and a more differentiated picture of distinct cytogenetic subtypes, e.g., cases with a 13q deletion. Efforts should continue to define the value of chromosomal banding in CLL focusing as well on the interaction with already established techniques such as interphase FISH or immunophenotyping.
在B淋巴细胞系慢性淋巴细胞白血病(B-CLL)中,细胞遗传学改变与预后及治疗决策高度相关。采用传统技术时,由于CLL细胞体外增殖率低,中期染色体质量差以及细胞遗传学改变发生率低,使得CLL中的染色体显带分析受到阻碍。因此,间期荧光原位杂交(FISH)已成为CLL细胞遗传学分析的标准技术。然而,间期FISH无法提供整个核型的全貌。为了改进CLL中的染色体显带分析,已开发出特定的刺激技术。这些技术要么使用CD40配体,要么将寡核苷酸(如CpG)与白细胞介素-2联合使用。采用相应技术后,在超过90%的CLL病例中成功实现了中期培养,并且在近90%的CLL病例中检测到异常核型。这使得能够检测出新的临床相关亚组(如复杂异常核型病例),并对不同的细胞遗传学亚型(如13q缺失病例)有更清晰的认识。应继续努力确定CLL中染色体显带的价值,同时关注其与已确立的技术(如间期FISH或免疫表型分析)之间的相互作用。