Journal
ONCOTARGETS AND THERAPY
Volume 12, Issue -, Pages 2187-2191Publisher
DOVE MEDICAL PRESS LTD
DOI: 10.2147/OTT.S189103
Keywords
chimeric antigen receptor; anti-CD19; anti-CD22; humanized; acute lymphoblastic leukemia; relapsed
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Funding
- Project of Invigorating Health Care through Science, Technology and Education, Jiangsu Provincial Key Medical Center [YXZXA2016002]
- Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
- National Natural Science Foundation of Jiangsu Province [BE2018652]
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Background: CD19-modified CAR-T cells greatly influence responses in patients with relapsed/refractory acute lymphoblastic leukemia (ALL). However, recurrence remains a challenge, and reinfusion of CAR-T cells is not always effective. Sequential infusion of humanized CD19-modified and CD22-modified CAR-T cells may overcome this issue and induce remission. Methods: We examined treatment with sequential infusion of humanized CD19-modified and CD22-modified CAR-T cells in a patient with relapsed ALL previously exposed to murine-derived anti-CD19 CAR-T cells. Results: At similar to 6 weeks after treatment, repeated bone marrow smear and flow cytometry analysis revealed no lymphoblasts. Conclusion: Our results suggest that sequential infusion of humanized CD19-modified and CD22-modified CAR-T cells is a valuable option for relapsed patients with prior infusion of murine-derived, CD19-directed CAR-T cells.
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