Journal List > J Korean Med Assoc > v.61(9) > 1101043

Lee: Storage and use of cord blood

Abstract

Cord blood (CB) has been used as an important source for hematopoietic stem cell transplantation and has been stored in public CB banks (CBBs) worldwide since the mid-1990s. Recently, the application of cell-based therapy using CB has expanded its clinical utility for various refractory diseases and immunologic diseases through the manufacture of mesenchymal stem cells or induced pluripotent stem cells and the isolation of mononuclear cells from CB. In this review, I briefly summarize the biologic characteristics and banking process of CB, as well as the current status of public and private CBBs. I also review the current status of stem cell transplantation and cell-based therapy using CBs. Finally, I suggest strategies of banking CBs in anticipation of future medical advances.

Figures and Tables

Figure 1

Cord blood contains hematopoietic stem cells as well as multipotent stem cells such as mesenchymal stem cells which have the ability to regenerate numerous tissue types. RBC, red blood cell; WBC, white blood cell.

jkma-61-557-g001
Figure 2

Cryopreservation process following separation of mononuclear cells from collected cord blood. (A) After removal of the newborn from the operative field, the free end of the cord was wiped with betadine to ensure sterility of the collections. While the placenta was still in utero, the umbilical vein is punctured and the cord blood (CB) is collected by gravity in the collection bag. (B) The CB unit is first centrifuged. (C) The white blood cell-rich supernatant is expressed into the original collection bag and the plasma discarded into the satellite bag after a second centrifugation, leaving a volume of about 25 mL. (D) Cryoprotectant, 10% dimethysuloxide is mixed with separated mononuclear cells from CB. (E) Processed CB units are cryopreserved using an automated microprocessor-controlled rate freezer until −90℃. (F) At the end of the freezing procedure the cells are stored in the liquid phase of a liquid nitrogen freezer.

jkma-61-557-g002
Figure 3

Suggested business model for public and private cord blood banks (CBBs) operating as current good manufacturing practice (cGMP) cell factories. The total nucleated cell counts of cord blood (CB) banking guidelines need to be increased to enhance the utilization rate of stored CBs in public CBBs, and private and public CB samples with low cell doses should be released for use in clinical trials in transplant settings as well as non-transplant settings. cGMP cell factories could manipulate fractionated CBs and generate cellular products that could be released for cell therapies. HSCT, hematopoietic stem cell transplantation; DM, diabetes mellitus; HSC, hematopoietic stem cell; DLI, donor lymphocyte infusion; MSC, mesenchymal stem cell; GVHD, graft versus host disease; HIE, hypoxic ischemic encephalopathy; CMP, cardiomyopathy; BPD, bronchopulmonary dysplasia; Treg, regulatory T; DC, dendrtitic cell; NK natural killer; CAR, chimeric antigen receptors; iPS, induced pluripotent stem cell.

jkma-61-557-g003

References

1. Broxmeyer HE, Douglas GW, Hangoc G, Cooper S, Bard J, English D, Arny M, Thomas L, Boyse EA. Human umbilical cord blood as a potential source of transplantable hemato-poietic stem/progenitor cells. Proc Natl Acad Sci U S A. 1989; 86:3828–3832.
crossref
2. Gluckman E, Broxmeyer HA, Auerbach AD, Friedman HS, Douglas GW, Devergie A, Esperou H, Thierry D, Socie G, Lehn P, Cooper S, English D, Kurtzberg J, Bard J, Boyse EA. 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; 321:1174–1178.
crossref
3. World Marrow Donor Association [Internet]. Leiden: World Marrow Donor Association;cited 2018 Jul 30. Available from: https://collaboration.wmda.info/.
4. Huss R. Isolation of primary and immortalized CD34-hema-topoietic and mesenchymal stem cells from various sources. Stem Cells. 2000; 18:1–9.
crossref
5. Rizk M, Aziz J, Shorr R, Allan DS. Cell-based therapy using umbilical cord blood for novel indications in regenerative therapy and immune modulation: an updated systematic scoping review of the literature. Biol Blood Marrow Transplant. 2017; 23:1607–1613.
crossref
6. Brunstein CG, Miller JS, McKenna DH, Hippen KL, DeFor TE, Sumstad D, Curtsinger J, Verneris MR, MacMillan ML, Levine BL, Riley JL, June CH, Le C, Weisdorf DJ, McGlave PB, Blazar BR, Wagner JE. Umbilical cord blood-derived T regulatory cells to prevent GVHD: kinetics, toxicity profile, and clinical effect. Blood. 2016; 127:1044–1051.
crossref
7. Mehta RS, Shpall EJ, Rezvani K. Cord blood as a source of natural killer cells. Front Med (Lausanne). 2016; 2:93.
crossref
8. Marek-Trzonkowska N, Mysliwiec M, Dobyszuk A, Grabo-wska M, Derkowska I, Juscinska J, Owczuk R, Szadkowska A, Witkowski P, Młynarski W, Jarosz-Chobot P, Bossowski A, Siebert J, Trzonkowski P. Therapy of type 1 diabetes with CD4(+)CD25(high)CD127-regulatory T cells prolongs sur-vival of pancreatic islets: results of one year follow-up. Clin Immunol. 2014; 153:23–30.
crossref
9. Schaub B, Tantisira KG, Gibbons FK, He H, Litonjua AA, Gillman MW, Weiss S, Perkins DL, Gold DR, Finn PW. Fetal cord blood: aspects of heightened immune responses. J Clin Immunol. 2005; 25:329–337.
crossref
10. Broxmeyer HE, Lee MR, Hangoc G, Cooper S, Prasain N, Kim YJ, Mallett C, Ye Z, Witting S, Cornetta K, Cheng L, Yoder MC. Hematopoietic stem/progenitor cells, generation of induced pluripotent stem cells, and isolation of endothelial progenitors from 21- to 23.5-year cryopreserved cord blood. Blood. 2011; 117:4773–4777.
crossref
11. Mitchell R, Wagner JE, Brunstein CG, Cao Q, McKenna DH, Lund TC, Verneris MR. Impact of long-term cryopreservation on single umbilical cord blood transplantation outcomes. Biol Blood Marrow Transplant. 2015; 21:50–54.
crossref
12. Otsubo K, Nosaki K, Imamura CK, Ogata H, Fujita A, Sakata S, Hirai F, Toyokawa G, Iwama E, Harada T, Seto T, Takenoyama M, Ozeki T, Mushiroda T, Inada M, Kishimoto J, Tsuchihashi K, Suina K, Nagano O, Saya H, Nakanishi Y, Okamoto I. Phase I study of salazosulfapyridine in combina-tion with cisplatin and pemetrexed for advanced non-small-cell lung cancer. Cancer Sci. 2017; 108:1843–1849.
crossref
13. Lee YH, Kwon YH, Hwang K, Jun H, Lee MA, Jang HI, Nah JH, Koo HH, Hwang TJ. Analysis of stored and transplanted cord blood units from KoreaCORD: reappraisal of banking guidelines and selection strategy. Transfusion. 2013; 53:123–127.
crossref
14. Lee YH, Cho NC, Je KH, Han H, Han JY, Kim JS, Kim HJ, Cho B, Kim HK. Successful sibling cord blood stem cell trans-plantation for relapsed acute mixed lineage leukemia. Korean J Hematol. 1999; 34:471–476.
15. Yoo KH, Lee SH, Sung KW, Koo HH, Chung NG, Cho B, Kim HK, Kang HJ, Shin HY, Ahn HS, Baek HJ, Han DK, Kook H, Hwang TJ, Kim SY, Lee YH, Hah JO, Im HJ, Seo JJ, Park SK, Jung HJ, Park JE, Lim YJ, Park SS, Lim YT, Yoo ES, Ryu KH, Park HJ, Park BK. Current status of pediatric umbilical cord blood transplantation in Korea: a multicenter retrospective analysis of 236 cases. Am J Hematol. 2011; 86:12–17.
crossref
16. Eapen M, Rubinstein P, Zhang MJ, Stevens C, Kurtzberg J, Scaradavou A, Loberiza FR, Champlin RE, Klein JP, Horowitz MM, Wagner JE. Outcomes of transplantation of unrelated donor umbilical cord blood and bone marrow in children with acute leukaemia: a comparison study. Lancet. 2007; 369:1947–1954.
crossref
17. Wagner JE Jr, Eapen M, Carter S, Wang Y, Schultz KR, Wall DA, Bunin N, Delaney C, Haut P, Margolis D, Peres E, Verneris MR, Walters M, Horowitz MM, Kurtzberg J. Blood and Marrow Transplant Clinical Trials Network. One-unit versus two-unit cord-blood transplantation for hematologic cancers. N Engl J Med. 2014; 371:1685–1694.
crossref
18. Mehta RS, Saliba RM, Cao K, Kaur I, Rezvani K, Chen J, Olson A, Parmar S, Shah N, Marin D, Alousi A, Hosing C, Popat U, Kebriaei P, Champlin R, de Lima M, Skerrett D, Burke E, Shpall EJ, Oran B. Ex vivo mesenchymal precursor cell-expanded cord blood transplantation after reduced-intensity conditioning regimens improves time to neutrophil recovery. Biol Blood Marrow Transplant. 2017; 23:1359–1366.
crossref
19. Kiernan J, Damien P, Monaghan M, Shorr R, McIntyre L, Fergusson D, Tinmouth A, Allan D. Clinical studies of ex vivo expansion to accelerate engraftment after umbilical cord blood transplantation: a systematic review. Transfus Med Rev. 2017; 31:173–182.
crossref
20. Bari S, Seah KK, Poon Z, Cheung AM, Fan X, Ong SY, Li S, Koh LP, Hwang WY. Expansion and homing of umbilical cord blood hematopoietic stem and progenitor cells for clinical transplantation. Biol Blood Marrow Transplant. 2015; 21:1008–1019.
crossref
21. Okada M, Tasaka T, Ikegame K, Aotsuka N, Kobayashi T, Najima Y, Matsuhashi Y, Wada H, Tokunaga H, Masuda S, Utsu Y, Yoshihara S, Kaida K, Daimon T, Ogawa H. A pro-spective multicenter phase II study of intrabone marrow tran-splantation of unwashed cord blood using reduced-intensity conditioning. Eur J Haematol. 2018; 100:335–343.
crossref
22. Park YB, Ha CW, Lee CH, Yoon YC, Park YG. Cartilage rege-neration in osteoarthritic patients by a composite of allogeneic umbilical cord blood-derived mesenchymal stem cells and hyaluronate hydrogel: results from a clinical trial for safety and proof-of-concept with 7 years of extended follow-up. Stem Cells Transl Med. 2017; 6:613–621.
crossref
23. Lee YH, Choi KV, Moon JH, Jun HJ, Kang HR, Oh SI, Kim HS, Um JS, Kim MJ, Choi YY, Lee YJ, Kim HJ, Lee JH, Son SM, Choi SJ, Oh W, Yang YS. Safety and feasibility of countering neurological impairment by intravenous admini-stration of autologous cord blood in cerebral palsy. J Transl Med. 2012; 10:58.
crossref
24. Min K, Song J, Kang JY, Ko J, Ryu JS, Kang MS, Jang SJ, Kim SH, Oh D, Kim MK, Kim SS, Kim M. Umbilical cord blood therapy potentiated with erythropoietin for children with cerebral palsy: a double-blind, randomized, placebo-control-led trial. Stem Cells. 2013; 31:581–591.
crossref
25. Rah WJ, Lee YH, Moon JH, Jun HJ, Kang HR, Koh H, Eom HJ, Lee JY, Lee YJ, Kim JY, Choi YY, Park K, Kim MJ, Kim SH. Neuroregenerative potential of intravenous G-CSF and autologous peripheral blood stem cells in children with cere-bral palsy: a randomized, double-blind, cross-over study. J Transl Med. 2017; 15:16.
crossref
26. Koh H, Hwang K, Lim HY, Kim YJ, Lee YH. Mononuclear cells from the cord blood and granulocytecolony stimulating factor-mobilized peripheral blood: is there a potential for treatment of cerebral palsy? Neural Regen Res. 2015; 10:2018–2024.
crossref
27. Berglund S, Gertow J, Uhlin M, Mattsson J. Expanded umbili-cal cord blood T cells used as donor lymphocyte infusions after umbilical cord blood transplantation. Cytotherapy. 2014; 16:1528–1536.
crossref
TOOLS
ORCID iDs

Young-Ho Lee
https://orcid.org/0000-0003-1498-2773

Similar articles