- Open Access
Effect of anti-CD52 antibody alemtuzumab on ex-vivo culture of umbilical cord blood stem cells
Journal of Hematology & Oncology volume 1, Article number: 19 (2008)
Excessive maturation of hematopoietic cells leads to a reduction of long-term proliferative capability during cord blood (CB) expansion. In this study, we report the effects of anit-CD52 (Alemtuzumab, Campath) on both short- and long-term ex vivo expansion of CB hematopoietic stem cells (HSC) by evaluating the potential role of Alemtuzumab in preserving the repopulating capability in CB HSC and nonlymphoid progenitors.
Ex vivo expansion experiments were carried out using freshly purified CB CD34+ cells in StemSpan™ SFEM medium in the presence of stem cell factor, Flt3-Ligand and thrombopoietin at 50 ng/ml. Alemtuzumab (10 μg/ml) was used to deplete CD52+ cells during the cultures. Flow cytometry was used to monitor CB HSC and their differentiation. Colony forming unit (CFU) assays and long term culture-initiating cell (LTC-IC) assays were performed on cells obtained from day 0 (before culture) and day 14 after cultures. Secondary cultures was performed using CD34+ cells isolated at 35 days from primary cultures and further cultured in StemSpan™ SFEM medium for another 14 days to confirm the long term effect of alemtuzumab in liquid cultures.
Compared to cytokines alone, addition of alemtuzumab resulted in a significant increase in total nucleated cells, absolute CD34+ cells, myeloid and megakaryocytic progenitors, multi-lineage and myeloid CFU and LTC-IC.
The results from current study suggested that the use of alemtuzumab for ex vivo expansion of CBHSC maybe advantageous. Our findings may improve current technologies for CBHSC expansion and increase the availability of CB units for transplantation. However, in vivo studies using animal models are likely needed in further studies to test the hematopoietic effects using such expanded CB products.
Umbilical cord blood transplantation (CBT) is now an established means of hematopoietic stem cell (HSC) transplantation for patients with a variety of malignant and non-malignant disorders [1–3]. As the results of partially matched CBT are similar to those of fully matched unrelated bone marrow transplantation, there has been a significant increase in CBT for patients in need of transplantation with matched unrelated allogeneic HSC. This, coupled with the immediate availability of cord blood units (CBU), has made cord blood an ideal source for pediatric HSC transplantation [4–8].
Due to the low number of HSC in each CBU, double unit CBT has been attempted and the results show that the two CBU have an additive effect, resulting in engraftment times equivalent to a single unit CBU with the cumulative cell dose of both the units [9–12]. However, while this treatment modality has increased cord blood usage in adult patients, many patients remain ineligible, as the total cell dose of two CBU may still be insufficient for many adult patients. In recent years, ex vivo expansion of HSC has been used as another approach for obtaining sufficient CBHSC from a single CBU in order to obtain adequate repopulating HSC from a single CBU. However, despite considerable research, ex vivo expansion of CB HSC has not definitively resulted in improved clinical outcomes in CBT [13–15], and failure or delayed hematopoietic engraftment was encountered in some earlier attempts using ex vivo expanded CB products, despite of satisfactory and impressive results from preclinical ex vivo experiments [16–18]. Stiff and colleagues have successfully transplanted patients with small aliquots of autologous bone marrow (BM, median volume = 36.7 ml with lowest volume = 13 ml) in Aastrom/Replicell stromal-bases close system in serum-containing medium using GM-SCF-IL-3 fusion protein, Flt3-L and erythropoietin as sole-source of HSC in 19 patients with breast cancer. Long-term hematopoietic reconstitution was achieved without an increase in infection or late graft failure for up to 8 years [14, 19]. Rice and colleagues reported that the response to short-term cytokine exposure in different CB hematopoietic cell populations was mainly from the mature cell populations rather than from the stem cell population . Their observation at least partially explained the pitfalls in clinical-scale transplantation using ex vivo CB products. To overcome this problem, new approaches for ex vivo expansion need to be developed, aiming at expansion of the "stem" cell population in cord blood and improving the long-term hematopoietic reconstitution in cord blood transplantation [14, 21].
CD52 is a phosphatidylinositol-linked, 12-amino acid leukocyte differentiation antigen abundantly expressed on the surface of activated lymphocytes, monocytes, macrophages, monocyte-derived dendritic cells and endothelial cells [22–25]. Alemtuzumab, a humanized anti-CD52 monoclonal antibody, was approved by FDA in 2001 for the clinical administration in patients with chronic lymphoblastic leukemia (CLL). Alemtuzumab results in rapid clearance of CD52+ cells by complement-mediated target cell lysis and antibody mediated cellular toxicity [26, 27]. Alemtuzumab is now commonly used for the treatment of lymphoid malignancy, such as chronic lymphoid leukemia (CLL) . Previous publications show that alemtuzumab could also enhance megakaryopoiesis [22, 29]. Based on these earlier observations, we postulated that depletion of CD52+ cells with alemtuzumab in ex vivo expansion experiments of CBU may lead to a higher percentage of CD34+ cells through depletion of more mature CD52+ hematopoietic progenitors. Hence, we embarked on this study to evaluate the potential role of Alemtuzumab in preserving primitive CB HSC during ex vivo cord blood expansion.
Evaluation of the quality of CB CD34+ hematopoietic progenitors and stem cells
The purity of CD34+ cells after immunomagnetic separation was 85.72 ± 5.98% (n = 6). The result was confirmed by Aldeflour staining (Figure 1); 81.05% cells were both CD34+ and Bodipy-aminoacetate (BAAA) brightly stained, 12.65% CD34+cells did not express BAAA activity. In total, there were 86.50% cells brightly expressing BAAA in CD34-enriched cell population. The data are consistent with previous reports [30–32] and provides secondary confirmation of the cell selection efficiency and that primitive and naïve hematopoietic progenitors were present within our initiating cells.
Effect of alemtuzumab on total nucleated cells (TNCs) and CB CD34+ cells
As shown in Figure 2A, TNCs were expanded 20.90 ± 2.89 fold on day 14 with alemtuzumab, which was 1.36-fold more than control (15.33 ± 2.45, p < 0.05). The absolute CD34+ cell count (Figure 2B) was 3.06 × 105 ± 0.58 × 105, in cultures with alemtuzumab, compared to control (1.93 × 105 ± 0.31 × 105. Compared to control cultures, the absolute CD34+ cell numbers were 58.55% higher with alemtuzumab added in the cultures (N = 6, p < 0.05).
Effect of alemtuzumab on lymphoid, megakaryocytic and myeloid cells
As shown on Table 1, the addition of alemtuzumab resulted in a 98.48% reduction in the proportion of absolute CD52+ cells (0.02 × 105 ± 0.02 × 105 versus 1.32 × 105 ± 0.44 × 105 in controls; N = 6 p < 0.05) and 96.36% reduction in the proportion of CD90+ lymphoid progenitors (0.02 × 105 ± 0.01 × 105 versus 0.55 × 105 ± 0.24 × 105 in controls; N = 6 p < 0.05). Mature lymphocyte markers, such as CD3 and CD19 were also tested, but as the current cytokine combination did not favor lymphoid cell proliferation, the percentage was too low (<0.3%) to demonstrate any potential effects on the addition of alemtuzumab. On the other hand, in the presence of alemtuzumab, more expansion of CD13+ myeloid progenitors (44.35%) was observed compared to controls. The expression of glycophorin A appeared to be marginally enhanced by alemtuzumab, but the difference was not statistically significant.
Effect of alemtuzumab on megakaryocytes
As shown in Figure 3A, there was 28.75% greater expansion of CD41+ megakaryocytes in the presence of alemtuzumab on day 7 cultures (1.03 × 105 ± 0.39 × 105 with alemtuzumab vs 0.80 × 105 ± 0.23 × 105 without; N = 6, p < 0.05) and 55.59% greater expansion on day 14 cultures (4.73 × 105 ± 0.71 × 105 with alemtuzumab vs 3.04 × 105 ± 0.52 × 105 without; N = 6, p < 0.05). These observations are consistent with previous reports, which show that Alemtuzumab enhances megakaryopoiesis [22, 29].
Colony Forming Unit (CFU) assay
CFU-GEMM and CFU-GM were significantly improved with 14 days of alemtuzumab expansion culture. As shown in Figure 4A, CFU-GEMM was expanded 2.05 ± 0.42 fold with alemtuzumab compared to 1.48 ± 0.29 fold in control (p < 0.05). CFU-GM was expanded 1.70 ± 0.04 and 1.27 ± 0.07 fold with or without alemtuzumab treatment respectively. Erythroid colonies (BFU-E/CFU-E) were nearly 2-fold decreased compared to initial cells in both conditions (0.4 ± 0.17 vs. 0.54 ± 0.18 fold expansion with or without alemtuzumab, respectively), which partially offset the total CFU (CFU-GM + BFU-E/CFU-E + CFU-GEMM) expansion (1.45 ± 0.23-fold in alemtuzumab treatment groups, p < 0.05 vs. 1.11 ± 0.16 in control, p < 0.05, compared to initiate cells). To further demonstrate the effect of alemtuzumab on expansion, relative CFU expansion fold was calculated (Fig 3B). Expansion cultures carried out in the presence of alemtuzumab resulted in 1.40 ± 0.06, 1.34 ± 0.04 and 1.31 ± 0.04 fold more expansion in CFU-GEMM, CFU-GM and total CFU respectively (p < 0.05).
Long-term culture-initiating cell (LTC-IC) assay
LTC-IC was performed on cells before and after 14 days of culture and, in the absence of alemtuzumab, there was a 53% ~75% decrease in LTC-IC compared to initial CD34+ cells (prior to culture). In the presence of alemtuzumab, LTC-IC was sustained at 1.17 ± 0.20 compared to the initial cells (Figure 4B). Thus, addition of alemtuzumab into the cultures resulted in 1.45- to 2.25- (mean 1.95 ± 0.44) fold greater numbers of LTC-IC compared to controls (p < 0.05).
Secondary cultures of CD34+ cells
Secondary cultures was performed using CD34+ cell isolated from day 35 of ex vivo expansion cultures to confirm the long-term growth of CD34+ cell in liquid cultures. The purity of CD34+ cells was 85.00%, similar to that observed with fresh CB CD34+ cell isolation. The CD34+ cells were further cultured for up to two weeks (49 days) with identical combinations of cytokines with alemtuzumab 10 μg/ml. Secondary cultures without alemtuzumab were used as controls. A significantly higher percentage of CD34+ cells (10.96 ± 5.09% vs. 2.24 ± 0.53%) was observed at day 42 (p < 0.05) and day 49 (2.34 ± 1.14% vs. 0.57 ± 0.39%, p < 0.05, Figure 5), respectively. At day 42, CD52+ cell population was 0.53 ± 0.31% with alemtuzumab vs. 5.59 ± 0.79% without alemtuzumab) and at day 49, CD52+ cells were 0.93 ± 0.55% with alemtuzumab vs. 16.56 ± 2.28% without alemtuzumab. Even at day 42 of culture, absolute CD34+ cells in cultures with alemtuzumab showed a 15% increase while the cultures without alemtuzumab showed a 76% decrease (absolute CD34+ expansion fold: 0.24, Figure 5B). By day 49, both cultures conditions showed a net loss of CD34+ cell numbers (absolute CD34+ numbers as percentage of original: 8% of original in control cultures vs 36% of original with alemtuzumab, Figure 5B).
The results from this study showed that the anti-CD52 antibody Alemtuzumab significantly enhanced ex vivo expansion of CB CD34+ cells and TNC. In addition, compared to both the initiating cells and cytokines-alone control cultures, total CFU, especially CFU-GEMM and CFU-GM were expanded after treatment of alemtuzumab, and LTC-IC numbers preserved, confirming the retention of hematopoietic progenitors. Furthermore, the effects of alemtuzumab were more pronounced when the culture was extended for 49 days (14 days secondary cultures taken from CD34+ cells selected out at day 35 of primary cultures). Although there is a net loss of CD34+ cell at day 49, the alemtuzumab did preserve more CD34+ cells compared to control cultures, which had loss of almost all CD34+ cells by day 49. This is likely because of the fact that differences in preserving progenitor/primitive cell populations become more prominent with longer term cultures, further confirming that alemtuzumab could potentially preserve primitive CD34+ hematopoietic cells.
Although the degree of expansion was modest, our experiments were aimed at comparing expansion with/without alemtuzumab, and were reasonable for this "early phase" cytokine combination, which was targeted at retaining immature stem cell populations rather than an overwhelming increase in absolute cell numbers. Immuno-homeostasis in in vivo transplantation/engraftment are far more complicated that just an ex vivo study and the results of ex vivo expansion caused by addition of alemtuzumab this study was indirect. As there was depletion of CD52 cells associated with the addition of alemtuzumab, future experiments will see if adding back CD52+ cells would abrogate the effect of alemtuzumab. Further optimization with the use of this drug in other cytokine combinations in large-scale expansion cultures is being carried out, including the SCID-repopulating assay.
One important issue in HSC expansion has always been the concern that expanding mature cell populations at the expense of the primitive progenitors could affect durable engraftment capacity . The underlying mechanisms for alemtuzumab enhancement of in vitro cord blood expansion could be secondary to selective depletion of CD52+ populations, such as lymphocytes and monocytes. Moreover, depletion of CD52+ cell populations may result in removal of certain inhibitory cell populations, such as CD26+ lymphocytes and NK cells during ex vivo expansion of CB HSC [20, 34]. The ability to retain the hematopoietic progenitors and stem cells in culture would enhance the likelihood of stable engraftment in recipients of these expanded products. Another potential risk of HSC expansion is the mature lymphocytes arising from these cultures, which could lead to a higher incidence of graft versus host disease (GVHD), thus negating a major benefit of CBT – which is the lowered incidence and severity of GVHD with increased tolerance towards HLA mismatches [3, 35–37]. In our study, mature cells and lymphocytes were actively removed in culture with the maintenance of hematopoietic progenitors and stem cells, and a relative expansion of myeloid and megakaryocytic precursors; thus appearing to circumvent these two theoretical risks of expansion. Moreover, a recent study from Shah et al shows that alemtuzumab is effective in decreasing the incidence of GVHD without increasing the risk of relapse in pediatric patients . Despite an initial proportional decrease in lymphocytes/monocytes, there was no subsequently absolute decrease of CD13+, CD14+ and CD15+ cell numbers, after 14 days of culture. Many clinical cord blood expansion trials now incorporate the expansion of one unit of cord blood following the infusion of another unexpanded unit in a double cord blood transplant setting. The unexpanded unit has, thus served successfully as a backup for potential loss of engraftment potential after cord blood expansion while the expanded unit serves to provide the first wave of myeloid recovery, thus decreasing the long engraftment period of CBT .
In summary, our study shows that the use of alemtuzumab in ex vivo cord blood expansion results in an increase in total cell expansion while preserving hematopoietic CD34+ cell content. Furthermore, the expansion of myeloid and megakaryocytic precursors is also enhanced. This finding may contribute to current technologies in CB expansion and increase the availability of CBT for patients around the world.
CB samples were obtained from the Singapore Cord Blood Bank (SCBB) that failed to meet the banking criteria for storage. This study was approved by the Hospital's Ethics Committee. Further allocation of CBU used for this study was re-confirmed by the SCBB Research Advisory Ethics Committee. A total of nine CBU were used in this study. Three for CFU and LTC-IC study while six for the ex vivo expansion and flow analysis.
CB CD34+ cell isolation
Cord blood CD34+ cells were isolated prior to expansion using a magnetic-cell sorting device (VarioMACS, Miltenyi, Germany). Briefly, mononuclear cells were fractionated by Ficoll-HypaquePlus (Amersham Pharmacia Biotech, Upsala, Sweden) density centrifugation. The CD34+ cell fraction was then isolated using the direct CD34 isolation kit, LS columns and VarioMACS magnetic cell separator (Miltenyi Biotec, Germany) according to the manufacturer's instructions. The purity of the selected population was verified with anti-human CD34+ antibody conjugated with phycoerythrin (PE, Anti-HPCA-1, Becton Dickinson, San Jose, USA) and analysed using the FACSCalibur flow cytometer and CellQuest Pro software (Becton Dickinson). Aldefluor assay was used to evaluate the activity of aldehyde dehydrogenase in the sorted CB CD34+ cells using the reagents from Stem Cell Technology (Stem Cell Technology, Vancouver, Canada) and the FACSCalibur flow cytometric analysis [30, 32, 40].
Ex vivo expansion cultures of cord blood CD34+ cells
105 CD34+ cells isolated from same CBU were cultured in 2 ml StemSpan™ SFEM Medium (10%BSA, 10 μg/ml recombinant human insulin, 200 μg/ml human transferrin, 104M 2-mercaptoethanol and 2 mM L-glutamine in Iscove's MDM, StemCell Technologies, Vancouver, Canada) supplemented with 50 ng/ml of stem cell factor (SCF, from Chemicon, USA), 50 ng/ml of thrombopoietin (TPO, from Chemicon, USA), 50 ng/ml of Flt-3 Ligand (Chemicon, USA), and 25 ng/ml of penicillin (10,000 uits/ml) and streptomycin (40 mg/ml, Gibco, USA). 10 μg/ml of alemtuzumab (Schering AG, Germany) was added with 10% of healthy human serum (collected from a consistent healthy adult donor with Ethics Committee approval) as a source of human complement. All cultures were performed at 37°C with humidified air containing 5% CO2. Culture medium was replenished on day 4, 7, 10, 14 with simultaneous harvest of small aliquots of cells for counts, phenotypic analysis, and culture assays. Trypan blue exclusion was used to determine cell viability. A total of six experiments were performed from six different CBU.
Flow cytometry analysis
The effect of alemtuzumab on CD34+ stem cells populations after ex-vivo expansion of cord blood HSC was analyzed by flow cytometric analysis using a panel of monoclonal antibodies (mAbs), including CD34 and lineage specific mAbs against myeloid, erythroid, megakaryocytic and lymphoid lineages (CD13, CD14, CD90, CD41 and Glycophorin A, from Becton Dickinson, San Jose, USA and CD52, from Serotec, USA). Samples were incubated with mAbs at 4°C for 30 min, washed, fixed, acquired and analyzed using a FACSCalibur flow cytometer. At least 10,000 events were acquired for each analysis.
Colony Forming Unit (CFU) assay
Colony assay was performed triplicate on cells obtained from day 0 (before culture) and day 14 after cultures. Cells were plated on 35 mm petri dishes (Nunc, Denmark) after mixing well with Methocult H4435 medium (1% methylcellulose in Iscove's MDM, 30% fetal bovine serum, 1% bovine serum albumin, 104 M 2-mercaptoethanol, 2 mM L-glutamine, 50 ng/ml SCF, 20 ng/ml, GM-CSF, 20 ng/ml IL-3, 20 ng/ml IL-6, 20 ng/ml G-CSF and 3 U/ml EPO, from Stem Cell Technologies, Vancouver, Canada). After incubation for 14 days at 37°C, granulocyte and macrophage colony forming units (CFU-GM), burst forming unit erythroid/erythroid colony forming units (BFU-E/CFU-E) and granulocyte-erythroid-macrophage-megakaryocyte colony forming units (CFU-GEMM) were enumerated according to manufacturer's guidelines under an inverted microscope (Axiovert 25, Carl Zeiss Pte Ltd, Singapore).
Quantitative bulk culture assay of long-term culture-initiating cell (LTC-IC)
Bulk culture LTC-IC assay was established and maintained in triplicate following manufacturer's instructions (Stem Cell Technologies, Vancouver, Canada). Briefly, stromal layers were initiated with M2-10B4 murine fibroblast cell line (CRL1972) by seeding 1 × 106 cells in a 75 cm2 culture flask in 15 ml RPMI (Gibco, Grand Island, NY, U.S.A) with 10% fetal calf serum (Hyclone, Logan, UT, USA). Half of the medium was changed weekly, and at log-phase growth, cells were trypsinized (Trypsin-EDTA; Invitrogen, U.S.A) and irradiated with an adsorbed dose of 8,000 cGy with a 60Co gamma irradiator (J.L. Shepherd & Associates, Canada). Feeder layers were then cultured in Long-term Culture Medium H5100 (12.5% horse serum, 12.5% FBS, 0.2 mM inositol, 20 mM folic acid, 104M 2-mercaptoethanol, 2 mM L-glutamine in MEM- medium, from Stem Cell Technologies, Vancouver, Canada) supplemented with 106mol/L hydrocortisone 21-hemisuccinate (Stem Cell Technologies, Vancouver, Canada). 24 hours later, freshly isolated day 0 CD34+ cells and day 14 expanded cells were added in triplicates to irradiated M2-10B4 stromal layer. Cultures were maintained at 37°C 5% CO2 and 100% humidity for 5 weeks with 50% volume of medium changed weekly. At the end of the 5th week, all the cells were harvested together (non-adherent cells were pipetted off and adherent cells were trypsinized) and fractions of cells were plated for CFU assay in H4435 medium as described above. After incubation for another 14 days at 37°C, total CFU numbers were counted and normalized against the initial cells. LTC-IC expansion was calculated from the LTC-IC derived total CFU numbers before and after culture under different conditions.
Secondary culture for day 35 CD34+ cells
To study the long term effects of alemtuzumab on hematopoietic progenitors and stem cells, cells were cultured for up to 35 days and CD34+ cells were isolated using MACS from day 35 cultures with alemtuzumab as described above. The purity of CD34+ cells was tested by flow cytometry analysis and selected CD34+ cells were put into secondary culture with the same cytokine combination and 10% human serum, with or without 10 μg/ml alemtuzumab. After a further 7 to 14 days of culture, cells were harvested and analysis of CD34 and CD52 expression profiles was performed.
Data was shown as mean ± SD. Group comparison for the statistical significance was calculated using Wilcoxon matched pairs nonparametric test. A p value of less than 0.05 was considered to be statistically significant.
Gluckman E, Broxmeyer HA, Auerbach AD, Friedman HS, Douglas GW, Devergie A, Esperou H, Thierry D, Socie G, Lehn P: Hematopoietic reconstitution in a patient with Fanconi's anemia by means of umbilical-cord blood from an HLA-identical sibling. N Engl J Med. 1989, 321 (17): 1174-1178.
Rocha V, Sanz G, Gluckman E: Umbilical cord blood transplantation. Curr Opin Hematol. 2004, 11 (6): 375-385. 10.1097/01.moh.0000145933.36985.eb.
Hwang WY, Samuel M, Tan D, Koh LP, Lim W, Linn YC: A meta-analysis of unrelated donor umbilical cord blood transplantation versus unrelated donor bone marrow transplantation in adult and pediatric patients. Biol Blood Marrow Transplant. 2007, 13 (4): 444-453. 10.1016/j.bbmt.2006.11.005.
Ballen KK, Haley NR, Kurtzberg J, Lane TA, Lindgren BR, Miller JP, Newman B, McCullough J: Outcomes of 122 diverse adult and pediatric cord blood transplant recipients from a large cord blood bank. Transfusion. 2006, 46 (12): 2063-2070. 10.1111/j.1537-2995.2006.01032.x.
Grewal SS, Barker JN, Davies SM, Wagner JE: Unrelated donor hematopoietic cell transplantation: marrow or umbilical cord blood?. Blood. 2003, 101 (11): 4233-4244. 10.1182/blood-2002-08-2510.
Huang S, Law P, Young D, Ho AD: Candidate hematopoietic stem cells from fetal tissues, umbilical cord blood vs. adult bone marrow and mobilized peripheral blood. Exp Hematol. 1998, 26 (12): 1162-1171.
Klaus J, Herrmann D, Breitkreutz I, Hegenbart U, Mazitschek U, Egerer G, Cremer FW, Lowenthal RM, Huesing J, Fruehauf S, Moehler T, Ho AD, Goldschmidt H: Effect of CD34 cell dose on hematopoietic reconstitution and outcome in 508 patients with multiple myeloma undergoing autologous peripheral blood stem cell transplantation. Eur J Haematol. 2007, 78 (1): 21-28. 10.1111/j.0902-4441.2006.t01-1-EJH2895.x.
Martin PL, Carter SL, Kernan NA, Sahdev I, Wall D, Pietryga D, Wagner JE, Kurtzberg J: Results of the cord blood transplantation study (COBLT): outcomes of unrelated donor umbilical cord blood transplantation in pediatric patients with lysosomal and peroxisomal storage diseases. Biol Blood Marrow Transplant. 2006, 12 (2): 184-194. 10.1016/j.bbmt.2005.09.016.
Barker JN, Weisdorf DJ, Wagner JE: Creation of a double chimera after the transplantation of umbilical-cord blood from two partially matched unrelated donors. N Engl J Med. 2001, 344 (24): 1870-1871. 10.1056/NEJM200106143442417.
De Lima M, St John LS, Wieder ED, Lee MS, McMannis J, Karandish S, Giralt S, Beran M, Couriel D, Korbling M, Bibawi S, Champlin R, Komanduri KV: Double-chimaerism after transplantation of two human leucocyte antigen mismatched, unrelated cord blood units. Br J Haematol. 2002, 119 (3): 773-776. 10.1046/j.1365-2141.2002.03893.x.
Ruggeri A, Peffault de Latour R, Rocha V, Larghero J, Robin M, Rodrigues CA, Traineau R, Ribaud P, Ferry C, Devergie A, Gluckman E, Socié G: Double cord blood transplantation in patients with high risk bone marrow failure syndromes. Br J Haematol. 2008
Zhang L, Shen B, Hou H, Yan W, Dai Y, Shi Q, Ma X, Ju X, Liu X: [Effects of HLA disparity of two umbilical cord blood units on human engraftment in SCID mice]. Zhonghua Xue Ye Xue Za Zhi. 2002, 23 (12): 624-627.
Haylock DN, Nilsson SK: Expansion of umbilical cord blood for clinical transplantation. Curr Stem Cell Res Ther. 2007, 2 (4): 324-335. 10.2174/157488807782793745.
Hofmeister CC, Zhang J, Knight KL, Le P, Stiff PJ: Ex vivo expansion of umbilical cord blood stem cells for transplantation: growing knowledge from the hematopoietic niche. Bone Marrow Transplant. 2007, 39 (1): 11-23. 10.1038/sj.bmt.1705538.
Robinson S, Niu T, de Lima M, Ng J, Yang H, McMannis J, Karandish S, Sadeghi T, Fu P, del Angel M, O'Connor S, Champlin R, Shpall E: Ex vivo expansion of umbilical cord blood. Cytotherapy. 2005, 7 (3): 243-250. 10.1080/14653240510027172.
Jaroscak J, Goltry K, Smith A, Waters-Pick B, Martin PL, Driscoll TA, Howrey R, Chao N, Douville J, Burhop S, Fu P, Kurtzberg J: Augmentation of umbilical cord blood (UCB) transplantation with ex vivo-expanded UCB cells: results of a phase 1 trial using the AastromReplicell System. Blood. 2003, 101 (12): 5061-5067. 10.1182/blood-2001-12-0290.
Koller MR, Manchel I, Maher RJ, Goltry KL, Armstrong RD, Smith AK: Clinical-scale human umbilical cord blood cell expansion in a novel automated perfusion culture system. Bone Marrow Transplant. 1998, 21 (7): 653-663. 10.1038/sj.bmt.1701157.
Shpall EJ, Quinones R, Giller R, Zeng C, Baron AE, Jones RB, Bearman SI, Nieto Y, Freed B, Madinger N, Hogan CJ, Slat-Vasquez V, Russell P, Blunk B, Schissel D, Hild E, Malcolm J, Ward W, McNiece IK: Transplantation of ex vivo expanded cord blood. Biol Blood Marrow Transplant. 2002, 8 (7): 368-376. 10.1053/bbmt.2002.v8.pm12171483.
Stiff P, Chen B, Franklin W, Oldenberg D, Hsi E, Bayer R, Shpall E, Douville J, Mandalam R, Malhotra D, Muller T, Armstrong RD, Smith A: Autologous transplantation of ex vivo expanded bone marrow cells grown from small aliquots after high-dose chemotherapy for breast cancer. Blood. 2000, 95 (6): 2169-2174.
Christopherson KW, Uralil SE, Porecha NK, Zabriskie RC, Kidd SM, Ramin SM: G-CSF- and GM-CSF-induced upregulation of CD26 peptidase downregulates the functional chemotactic response of CD34+CD38- human cord blood hematopoietic cells. Exp Hematol. 2006, 34 (8): 1060-1068. 10.1016/j.exphem.2006.03.012.
Hutton JF, D'Andrea RJ, Lewis ID: Potential for clinical ex vivo expansion of cord blood haemopoietic stem cells using non-haemopoietic factor supplements. Curr Stem Cell Res Ther. 2007, 2 (3): 229-237. 10.2174/157488807781696221.
Deutsch VR, Nagler A, Slavin S, Condiotti R, Levine RF, Eldor A: Effect of bone marrow T lymphocytes treated with CAMPATH 1 G on megakaryocyte colony formation. Exp Hematol. 1993, 21 (11): 1427-1435.
Hale G: Cd52 (Campath1). J Biol Regul Homeost Agents. 2001, 15 (4): 386-391.
Hale G, Bright S, Chumbley G, Hoang T, Metcalf D, Munro AJ, Waldmann H: Removal of T cells from bone marrow for transplantation: a monoclonal antilymphocyte antibody that fixes human complement. Blood. 1983, 62 (4): 873-882.
Ravandi F, O'Brien S: Alemtuzumab. Expert Rev Anticancer Ther. 2005, 5 (1): 39-51. 10.1586/14737188.8.131.52.
Rowan WC, Hale G, Tite JP, Brett SJ: Cross-linking of the CAMPATH-1 antigen (CD52) triggers activation of normal human T lymphocytes. Int Immunol. 1995, 7 (1): 69-77. 10.1093/intimm/7.1.69.
Xia MQ, Hale G, Waldmann H: Efficient complement-mediated lysis of cells containing the CAMPATH-1 (CDw52) antigen. Mol Immunol. 1993, 30 (12): 1089-1096. 10.1016/0161-5890(93)90155-5.
Flynn JM, Byrd JC: Campath-1H monoclonal antibody therapy. Curr Opin Oncol. 2000, 12 (6): 574-581. 10.1097/00001622-200011000-00010.
Nagler A, Condiotti R, Lubina A, Deutsch VR: Enhancement of megakaryocytopoiesis by Campath-1G-treated natural killer cells. Bone Marrow Transplant. 1997, 20 (7): 525-531. 10.1038/sj.bmt.1700952.
Hess DA, Meyerrose TE, Wirthlin L, Craft TP, Herrbrich PE, Creer MH, Nolta JA: Functional characterization of highly purified human hematopoietic repopulating cells isolated according to aldehyde dehydrogenase activity. Blood. 2004, 104 (6): 1648-1655. 10.1182/blood-2004-02-0448.
Pearce DJ, Taussig D, Simpson C, Allen K, Rohatiner AZ, Lister TA, Bonnet D: Characterization of cells with a high aldehyde dehydrogenase activity from cord blood and acute myeloid leukemia samples. Stem Cells. 2005, 23 (6): 752-760. 10.1634/stemcells.2004-0292.
Storms RW, Trujillo AP, Springer JB, Shah L, Colvin OM, Ludeman SM, Smith C: Isolation of primitive human hematopoietic progenitors on the basis of aldehyde dehydrogenase activity. Proc Natl Acad Sci USA. 1999, 96 (16): 9118-9123. 10.1073/pnas.96.16.9118.
McNiece IK, Almeida-Porada G, Shpall EJ, Zanjani E: Ex vivo expanded cord blood cells provide rapid engraftment in fetal sheep but lack long-term engrafting potential. Exp Hematol. 2002, 30 (6): 612-616. 10.1016/S0301-472X(02)00805-6.
Hamood M, Corazza F, Bujan-Boza W, Sariban E, Fondu P: Natural killer (NK) cells inhibit human umbilical cord blood erythropoiesis. Exp Hematol. 1995, 23 (11): 1187-1191.
Rocha V, Wagner JE, Sobocinski KA, Klein JP, Zhang MJ, Horowitz MM, Gluckman E: Graft-versus-host disease in children who have received a cord-blood or bone marrow transplant from an HLA-identical sibling. Eurocord and International Bone Marrow Transplant Registry Working Committee on Alternative Donor and Stem Cell Sources. N Engl J Med. 2000, 342 (25): 1846-1854. 10.1056/NEJM200006223422501.
Takahashi S, Iseki T, Ooi J, Tomonari A, Takasugi K, Shimohakamada Y, Yamada T, Uchimaru K, Tojo A, Shirafuji N, Kodo H, Tani K, Takahashi T, Yamaguchi T, Asano S: Single-institute comparative analysis of unrelated bone marrow transplantation and cord blood transplantation for adult patients with hematologic malignancies. Blood. 2004, 104 (12): 3813-3820. 10.1182/blood-2004-03-1001.
Takahashi S, Ooi J, Tomonari A, Konuma T, Tsukada N, Oiwa-Monna M, Fukuno K, Uchiyama M, Takasugi K, Iseki T, Tojo A, Yamaguchi T, Asano S: Comparative single-institute analysis of cord blood transplantation from unrelated donors with bone marrow or peripheral blood stem-cell transplants from related donors in adult patients with hematologic malignancies after myeloablative conditioning regimen. Blood. 2007, 109 (3): 1322-1330. 10.1182/blood-2006-04-020172.
Shah AJ, Kapoor N, Crooks GM, Weinberg KI, Azim HA, Killen R, Kuo L, Rushing T, Kohn DB, Parkman R: The effects of Campath 1H upon graft-versus-host disease, infection, relapse, and immune reconstitution in recipients of pediatric unrelated transplants. Biol Blood Marrow Transplant. 2007, 13 (5): 584-593. 10.1016/j.bbmt.2007.01.076.
Tse W, Bunting KD, Laughlin MJ: New insights into cord blood stem cell transplantation. Curr Opin Hematol. 2008, 15 (4): 279-284. 10.1097/MOH.0b013e328304ae2c.
Jones RJ, Barber JP, Vala MS, Collector MI, Kaufmann SH, Ludeman SM, Colvin OM, Hilton J: Assessment of aldehyde dehydrogenase in viable cells. Blood. 1995, 85 (10): 2742-2746.
This work was funded by Department of Clinical Research, SGH (P02) and the Singapore Cancer Syndicate (SCSTS00049). All the authors of this article would like to thank Department of Clinical Research and Singapore Cord Blood Bank for supporting the experiments. We would like to thank Ms Stephanie Fook Chong Man Chung, Senior Biostatistician, Department of Clinical Research, Singapore General Hospital for her statistical advice.
The authors declare that they have no competing interests.
CKL was involved in designed, participated in all assay, analyzed data and drafted the manuscript. LS was involved in designed, flow cytometry and drafted the manuscript. QF was involved in CFU assay, LTC-IC assay and drafted the manuscript. PL was involved in critically evaluating and revising the manuscript. WTC and SNL were involved in sample process, cell cultures, Aldeflour assay and flow cytometry. WYKH was actively involved in concept design, coordination, interpretation of data, drafting and critically revising the manuscript. All authors read and approved the final manuscript.
About this article
Cite this article
Lim, C.K., Sun, L., Feng, Q. et al. Effect of anti-CD52 antibody alemtuzumab on ex-vivo culture of umbilical cord blood stem cells. J Hematol Oncol 1, 19 (2008) doi:10.1186/1756-8722-1-19
- Cord Blood
- Graft Versus Host Disease
- Cord Blood Transplantation
- Stem Cell Technology