| Literature DB >> 35421218 |
Clara Bueno1,2,3, Susana Barrera2,4, Alex Bataller1,5, Valentín Ortiz-Maldonado5, Natalina Elliot6, Sorcha O'Byrne6, Guanlin Wang7,8, Montse Rovira8, Francisco Gutierrez-Agüera1, Juan L Trincado1,3, María González-González2,4, Mireia Morgades9, Marc Sorigué9,10, Paloma Bárcena2,4, Samanta Romina Zanetti1, Montse Torrebadell11,12,13, Nerea Vega-Garcia11,12, Susana Rives13,14, Mar Mallo10, Francesc Sole10, Adam J Mead6,13, Irene Roberts6,7,15, Supat Thongjuea6,7,14, Bethan Psaila6,15, Manel Juan3,16,17, Julio Delgado2,3,5,16, Alvaro Urbano-Ispizúa1,3,5,16, Josep María Ribera3,9,10, Alberto Orfao2,4, Anindita Roy6,7,15, Pablo Menendez1,2,3,18,19.
Abstract
CD19-directed immunotherapies have revolutionized the treatment of advanced B-cell acute lymphoblastic leukemia (B-ALL). Despite initial impressive rates of complete remission (CR) many patients ultimately relapse. Patients with B-ALL successfully treated with CD19-directed T cells eventually relapse, which, coupled with the early onset of CD22 expression during B-cell development, suggests that preexisting CD34+CD22+CD19- (pre)-leukemic cells represent an "early progenitor origin-related" mechanism underlying phenotypic escape to CD19-directed immunotherapies. We demonstrate that CD22 expression precedes CD19 expression during B-cell development. CD34+CD19-CD22+ cells are found in diagnostic and relapsed bone marrow samples of ∼70% of patients with B-ALL, and their frequency increases twofold in patients with B-ALL in CR after CD19 CAR T-cell therapy. The median of CD34+CD19-CD22+ cells before treatment was threefold higher in patients in whom B-ALL relapsed after CD19-directed immunotherapy (median follow-up, 24 months). Fluorescence in situ hybridization analysis in flow-sorted cell populations and xenograft modeling revealed that CD34+CD19-CD22+ cells harbor the genetic abnormalities present at diagnosis and initiate leukemogenesis in vivo. Our data suggest that preleukemic CD34+CD19-CD22+ progenitors underlie phenotypic escape after CD19-directed immunotherapies and reinforce ongoing clinical studies aimed at CD19/CD22 dual targeting as a strategy for reducing CD19- relapses. The implementation of CD34/CD19/CD22 immunophenotyping in clinical laboratories for initial diagnosis and subsequent monitoring of patients with B-ALL during CD19-targeted therapy is encouraged.Entities:
Mesh:
Substances:
Year: 2022 PMID: 35421218 DOI: 10.1182/blood.2021014840
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 25.476