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Optimization of individualized graft composition: CD3/CD19 depletion combined with CD34 selection for haploidentical transplantation.
Huenecke, Sabine; Bremm, Melanie; Cappel, Claudia; Esser, Ruth; Quaiser, Andrea; Bonig, Halvard; Jarisch, Andrea; Soerensen, Jan; Klingebiel, Thomas; Bader, Peter; Koehl, Ulrike.
Afiliação
  • Huenecke S; Clinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany. sabine.huenecke@kgu.de.
  • Bremm M; Clinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
  • Cappel C; Clinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
  • Esser R; GMP Development Unit, Institute of Cellular Therapeutics, IFB-TX, Hannover Medical School, Hannover, Germany.
  • Quaiser A; Clinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
  • Bonig H; Division for Cell Processing, Institute for Transfusion Medicine and Immunohematology, Goethe-University Frankfurt/Main.
  • Jarisch A; German Red Cross Blood Donor Service, Baden-Württemberg-Hessen, Frankfurt/Main, Germany.
  • Soerensen J; Clinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
  • Klingebiel T; Clinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
  • Bader P; Clinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
  • Koehl U; Clinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Transfusion ; 56(9): 2336-45, 2016 09.
Article em En | MEDLINE | ID: mdl-27346253
ABSTRACT

BACKGROUND:

Excessive T-cell depletion (TCD) is a prerequisite for graft manufacturing in haploidentical stem cell (SC) transplantation by using either CD34 selection or direct TCD such as CD3/CD19 depletion. STUDY DESIGN AND

METHODS:

To optimize graft composition we compared 1) direct or indirect TCD only, 2) a combination of CD3/CD19-depleted with CD34-selected grafts, or 3) TCD twice for depletion improvement based on our 10-year experience with 320 separations in graft manufacturing and quality control.

RESULTS:

SC recovery was significantly higher (85%, n = 187 vs. 73%, n = 115; p < 0.0001), but TCD was inferior (median log depletion, -3.6 vs. -5.2) for CD3/CD19 depletion compared to CD34 selection, respectively. For end products with less than -2.5 log TCD, a second depletion step led to a successful improvement in TCD. Thawing of grafts showed a high viability and recovery of SCs, but low NK-cell yield. To optimize individualized graft engineering, a calculator was developed to estimate the results of the final graft based on the content of CD34+ and CD3+ cells in the leukapheresis product.

CONCLUSION:

Finally, calculated splitting of the starting product followed by CD3/19 depletion together with CD34+ graft manipulation may enable the composition of optimized grafts with high CD34+-cell and minimal T-cell content.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Depleção Linfocítica / Complexo CD3 / Antígenos CD34 / Antígenos CD19 Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Depleção Linfocítica / Complexo CD3 / Antígenos CD34 / Antígenos CD19 Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article