Haploidentical natural killer cells induce remissions in non-Hodgkin lymphoma patients with low levels of immune-suppressor cells

We report a novel phase 2 clinical trial in patients with poor prognosis refractory non-Hodgkin lymphoma (NHL) testing the efficacy of haploidentical donor natural killer (NK) cell therapy (NK dose 0.5–3.27 × 10 7 NK cells/kg) with rituximab and IL-2 (clinicaltrials.gov NCT01181258). Therapy was tol...

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Veröffentlicht in:Cancer Immunology, Immunotherapy Immunotherapy, 2018-03, Vol.67 (3), p.483-494
Hauptverfasser: Bachanova, Veronika, Sarhan, Dhifaf, DeFor, Todd E., Cooley, Sarah, Panoskaltsis-Mortari, Angela, Blazar, Bruce R., Curtsinger, Julie M., Burns, Linda, Weisdorf, Daniel J., Miller, Jeffrey S.
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Sprache:eng
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Zusammenfassung:We report a novel phase 2 clinical trial in patients with poor prognosis refractory non-Hodgkin lymphoma (NHL) testing the efficacy of haploidentical donor natural killer (NK) cell therapy (NK dose 0.5–3.27 × 10 7 NK cells/kg) with rituximab and IL-2 (clinicaltrials.gov NCT01181258). Therapy was tolerated without graft-versus-host disease, cytokine release syndrome, or neurotoxicity. Of 14 evaluable patients, 4 had objective responses (29%; 95% CI 12–55%) at 2 months: 2 had complete response lasting 3 and 9 months. Circulating donor NK cells persisted for at least 7 days after infusion at the level 0.6–16 donor NK cells/µl or 0.35–90% of total CD56 cells. Responding patients had lower levels of circulating host-derived Tregs (17 ± 4 vs. 307 ± 152 cells/µL; p  = 0.008) and myeloid-derived suppressor cells at baseline (6.6 ± 1.4% vs. 13.0 ± 2.7%; p  = 0.06) than non-responding patients. Lower circulating Tregs correlated with low serum levels of IL-10 ( R 2  = 0.64; p  
ISSN:0340-7004
1432-0851
DOI:10.1007/s00262-017-2100-1