Biology of Blood and Marrow Transplantation
Volume 16, Issue 8 , Pages 1107-1114, August 2010

Natural Killer Cell-Enriched Donor Lymphocyte Infusions from A 3-6/6 HLA Matched Family Member following Nonmyeloablative Allogeneic Stem Cell Transplantation

  • David A. Rizzieri

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
    • Corresponding Author InformationCorrespondence and reprint requests: David A. Rizzieri, MD, Duke University Medical Center, Marrow and Stem Cell Transplantation Program, Box 3961, Durham NC 27705.
  • ,
  • Robert Storms

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Dong-Feng Chen

      Affiliations

    • Duke University Medical Center Department of Pathology, Durham, North Carolina
  • ,
  • Gwynn Long

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Yiping Yang

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Daniel A. Nikcevich

      Affiliations

    • St. Mary's-Duluth Clinical Cancer Center, Duluth, Minnesota
  • ,
  • Cristina Gasparetto

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Mitchell Horwitz

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • John Chute

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Keith Sullivan

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Therese Hennig

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Debashish Misra

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Christine Apple

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Megan Baker

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Ashley Morris

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Patrick G. Green

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina
  • ,
  • Vic Hasselblad

      Affiliations

    • Duke University Medical Center Department of Bioinfomatics and Biostatistics, Durham, North Carolina
  • ,
  • Nelson J. Chao

      Affiliations

    • Duke University Medical Center Department of Medicine, Division of Cellular Therapy, Durham, North Carloina

Received 12 November 2009; accepted 18 February 2010. published online 25 February 2010.

Infusing natural killer (NK) cells following transplantation may allow less infections and relapse with little risk of acute graft-versus-host disease (aGVHD). We delivered 51 total NK cell-enriched donor lymphocyte infusions (DLIs) to 30 patients following a 3-6/6 HLA matched T cell-depleted nonmyeloablative allogeneic transplant. The primary endpoint of this study was feasibility and safety. Eight weeks following transplantation, donor NK cell-enriched DLIs were processed using a CD56+ selecting column with up to 3 fresh infusions allowed. Toxicity, relapse, and survival were monitored. T cell phenotype, NK cell functional recovery, and KIR typing were assessed for association with outcomes. Fourteen matched and 16 mismatched transplanted patients received a total of 51 NK cell-enriched DLIs. Selection resulted in 96% (standard deviation [SD] 8%) purity and 83% (SD 21%) yield in the matched setting and 97% (SD 3%) purity and 77% (SD 24%) yield in the mismatched setting. The median number of CD3 CD56+ NK cells infused was 10.6 (SD 7.91) × 106 cells/kg and 9.21 (SD 5.6) × 106 cells/kg, respectively. The median number of contaminating CD3+CD56 T cells infused was .53 (1.1) × 106 and .27 (.78) × 106 in the matched and mismatched setting, respectively. Only 1 patient each in the matched (n = 14) or mismatched (n = 16) setting experienced severe aGVHD with little other toxicity attributable to the infusions. Long-term responders with multiple NK cell-enriched infusions and improved T cell phenotypic recovery had improved duration of responses (p = .0045) and overall survival (OS) (P = .0058). A 1-step, high-yield process is feasible, and results in high doses of NK cells infused with little toxicity. NK cell-enriched DLIs result in improved immune recovery and outcomes for some. Future studies must assess whether the improved outcomes are the direct result of the high doses and improved NK cell function or other aspects of immune recovery.

Key Words: NK cells, T cell-depleted transplantation

 

 Financial disclosure: See Acknowledgments on page 1113.

 Current address for Patrick G. Green: Department of Medicine, University of Miami, Miami, FL.

PII: S1083-8791(10)00089-3

doi:10.1016/j.bbmt.2010.02.018

Biology of Blood and Marrow Transplantation
Volume 16, Issue 8 , Pages 1107-1114, August 2010