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Efficient elimination of primary B-ALL cells in vitro and in vivo using a novel 4-1BB-based CAR targeting a membrane-distal CD22 epitope.

Talía Velasco-HernandezSamanta Romina ZanettiHeleia Roca-HoFrancisco Gutierrez-AgueraPaolo PetazziDiego Sánchez-MartínezOscar MolinaMatteo Libero BaroniJose Luis FusterPaola BalleriniClara BuenoNarcis Fernandez-FuentesPablo EngelPablo Menendez
Published in: Journal for immunotherapy of cancer (2021)
We report a novel, high-affinity hCD22.7 scFv which targets a membrane-distal epitope of CD22. 4-1BB-based hCD22.7-CAR T cells efficiently eliminate clinically relevant B- CD22high and CD22low ALL primary samples in vitro and in vivo. Our study supports the clinical translation of this hCD22.7-CAR as either single or tandem CD22-CD19-CAR for both naive and anti-CD19-resistant patients with B-ALL.
Keyphrases
  • nk cells
  • minimally invasive
  • growth factor
  • signaling pathway
  • cell death
  • cell proliferation
  • oxidative stress
  • cancer therapy
  • recombinant human
  • antiretroviral therapy
  • pi k akt