TY - JOUR
T1 - An innovative method to generate a Good Manufacturing Practice-ready regulatory T-cell product from non-mobilized leukapheresis donors
AU - Zhang, Wei
AU - Smythe, Jon
AU - Frith, Emma
AU - Belfield, Helen
AU - Clarke, Sophie
AU - Watt, Suzanne M.
AU - Danby, Robert
AU - Benjamin, Sylvia
AU - Peniket, Andy
AU - Roberts, David J.
N1 - Publisher Copyright:
© 2015.
PY - 2015
Y1 - 2015
N2 - Background aims: There is real and sustained interest in preparing T-regulatory cells from leukapheresis collections for cellular therapy through the use of simple, effective and reliable methods conforming to Good Manufacturing Practice (GMP). We describe a GMP-ready isolation procedure for CD25+ products with the use of a sterile docking device, pigtail sampling, a laminar flow hood and the CliniMACS system that uses leukapheresis collections made by two apheresis machines. Methods: We used CD8/CD19 depletion followed by CD25-positive selection. The median number of CD4+ cells recovered was 72.5 ± 32.6 × 106, of which 60.5% ± 17.8% were CD25+FOXP3+ cells. Suppression of autologous CD25- cell proliferation by the cryopreserved CD25+ products was 51.3% ± 4.4%, 49.0% ± 3.7% and 39.0% ± 3.6% at CD25+:CD25- ratios of 1:1, 1:2 and 1:4 (n = 6), respectively, comparable to suppression by fresh CD25+ products (53% ± 6.2%, 51% ± 3.3% and 39% ± 7.1%). Results: We found Leukapheresis collections by Cobe Spectra contained more lymphocytes and platelets than collections by Spectra Optia apheresis machine (median, 9.2 × 109 versus 6.7 × 109; P = 0.04) and platelets (median, 610 × 109 versus 170 × 109; P = 0.04). The frequency of CD4+CD25+FOXP3+ was significantly higher in the leukapheresis (4.85%; 95% confidence interval, 1.95% to 5.38%) than in peripheral blood (3.9%; 95% confidence interval, 2.63% to 6.45%) (P = 0.02). The CD8-and CD19-negative depletion step was associated with significant loss of total CD4+ T cells (P = 0.001). Conclusions: Results suggest that functional CD25+ products can be isolated with a GMP-ready method, and good recovery can be obtained with the use of an optimized cryopreservation protocol. These data and methods show the potential, possibilities and future work needed to isolate target cell populations in a reproducible, time-efficient and cost-efficient manner for clinical applications.
AB - Background aims: There is real and sustained interest in preparing T-regulatory cells from leukapheresis collections for cellular therapy through the use of simple, effective and reliable methods conforming to Good Manufacturing Practice (GMP). We describe a GMP-ready isolation procedure for CD25+ products with the use of a sterile docking device, pigtail sampling, a laminar flow hood and the CliniMACS system that uses leukapheresis collections made by two apheresis machines. Methods: We used CD8/CD19 depletion followed by CD25-positive selection. The median number of CD4+ cells recovered was 72.5 ± 32.6 × 106, of which 60.5% ± 17.8% were CD25+FOXP3+ cells. Suppression of autologous CD25- cell proliferation by the cryopreserved CD25+ products was 51.3% ± 4.4%, 49.0% ± 3.7% and 39.0% ± 3.6% at CD25+:CD25- ratios of 1:1, 1:2 and 1:4 (n = 6), respectively, comparable to suppression by fresh CD25+ products (53% ± 6.2%, 51% ± 3.3% and 39% ± 7.1%). Results: We found Leukapheresis collections by Cobe Spectra contained more lymphocytes and platelets than collections by Spectra Optia apheresis machine (median, 9.2 × 109 versus 6.7 × 109; P = 0.04) and platelets (median, 610 × 109 versus 170 × 109; P = 0.04). The frequency of CD4+CD25+FOXP3+ was significantly higher in the leukapheresis (4.85%; 95% confidence interval, 1.95% to 5.38%) than in peripheral blood (3.9%; 95% confidence interval, 2.63% to 6.45%) (P = 0.02). The CD8-and CD19-negative depletion step was associated with significant loss of total CD4+ T cells (P = 0.001). Conclusions: Results suggest that functional CD25+ products can be isolated with a GMP-ready method, and good recovery can be obtained with the use of an optimized cryopreservation protocol. These data and methods show the potential, possibilities and future work needed to isolate target cell populations in a reproducible, time-efficient and cost-efficient manner for clinical applications.
KW - Apheresis machines
KW - CD25 Treg
KW - Cryopreservation
KW - FOXP3
KW - Hematology analyzer
KW - Non-mobilized leukapheresis
UR - http://www.scopus.com/inward/record.url?scp=84945950533&partnerID=8YFLogxK
U2 - 10.1016/j.jcyt.2015.05.015
DO - 10.1016/j.jcyt.2015.05.015
M3 - Article
C2 - 26276008
AN - SCOPUS:84945950533
SN - 1465-3249
VL - 17
SP - 1268
EP - 1279
JO - Cytotherapy
JF - Cytotherapy
IS - 9
ER -