For many promising target cells (e.g.: haematopoeitic progenitors), the susceptibility to standard adeno-associated viral (AAV) vectors is low. Advancements in vector development now allows the generation of target cell-selected AAV capsid mutants.
To determine its suitability, the method was applied on a chronic myelogenous leukaemia (CML) cell line (K562) to obtain a CML-targeted vector and the resulting vectors tested on leukaemia, non-leukaemia, primary human CML and CD34 + peripheral blood progenitor cells (PBPC); standard AAV2 and a random capsid mutant vector served as controls.
Transduction of CML (BV173, EM3, K562 and Lama84) and AML (HL60 and KG1a) cell lines with the capsid mutants resulted in an up to 36-fold increase in CML transduction efficiency (K562: 2-fold, 60% ± 2% green fluorescent protein (GFP) + cells; BV173: 9-fold, 37% ± 2% GFP + cells; Lama84: 36-fold, 29% ± 2% GFP + cells) compared to controls. For AML (KG1a, HL60) and one CML cell line (EM3), no significant transduction (<1% GFP + cells) was observed for any vector. Although the capsid mutant clone was established on a cell line, proof-of-principle experiments using primary human cells were performed. For CML (3.2-fold, mutant: 1.75% ± 0.45% GFP + cells, p = 0.03) and PBPC (3.5-fold, mutant: 4.21% ± 3.40% GFP + cells) a moderate increase in gene transfer of the capsid mutant compared to control vectors was observed.