| Literature DB >> 33234592 |
Hakan Köksal1, Pierre Dillard1, Asta Juzeniene2, Gunnar Kvalheim1, Erlend B Smeland3, June H Myklebust3, Else Marit Inderberg1, Sébastien Wälchli4.
Abstract
CAR T cells targeting the B lymphocyte antigen CD19 have led to remarkable clinical results in B cell leukemia and lymphoma but eliminate all B lineage cells, leading to increased susceptibility to severe infections. As malignant B cells will express either immunoglobulin (Ig) light chain κ or λ, we designed a second-generation CAR targeting Igκ, IGK CAR. This construct demonstrated high target specificity but displayed reduced efficacy in the presence of serum IgG. Since CD19 CAR is insensitive to serum IgG, we designed various combinatorial CAR constructs in order to maintain the CD19 CAR T cell efficacy, but with IGK CAR target selectivity. The Kz-19BB design, combining CD19 CAR containing a 4-1BB costimulatory domain with an IGK CAR containing a CD3zeta stimulatory domain, maintained the target specificity of IgK CAR and was resistant to the presence of soluble IgG. Our results demonstrate that a combinatorial CAR approach can improve target selectivity and efficacy.Entities:
Keywords: B cell malignancies; cell therapy; chimeric antigen receptor (CAR) T cells; immunoglobulin kappa light chain; immunotherapy
Year: 2020 PMID: 33234592 PMCID: PMC7948400 DOI: 10.1074/jbc.RA120.016234
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157