Pentaisomaltose, an Alternative to DMSO. Engraftment of Cryopreserved Human CD34+ Cells in Immunodeficient NSG Mice

Research output: Contribution to journalLetterResearchpeer-review

Standard

Pentaisomaltose, an Alternative to DMSO. Engraftment of Cryopreserved Human CD34+ Cells in Immunodeficient NSG Mice. / Svalgaard, Jesper Dyrendom; Talkhoncheh, Mehrnaz Safaee; Haastrup, Eva Kannik; Munthe-Fog, Lea; Clausen, Christian; Hansen, Morten Bagge; Andersen, Pernille; Gørløv, Jette Sønderskov; Larsson, Jonas; Fischer-Nielsen, Anne.

In: Cell Transplantation, Vol. 27, No. 9, 09.2018, p. 1407-1412.

Research output: Contribution to journalLetterResearchpeer-review

Harvard

Svalgaard, JD, Talkhoncheh, MS, Haastrup, EK, Munthe-Fog, L, Clausen, C, Hansen, MB, Andersen, P, Gørløv, JS, Larsson, J & Fischer-Nielsen, A 2018, 'Pentaisomaltose, an Alternative to DMSO. Engraftment of Cryopreserved Human CD34+ Cells in Immunodeficient NSG Mice', Cell Transplantation, vol. 27, no. 9, pp. 1407-1412. https://doi.org/10.1177/0963689718786226

APA

Svalgaard, J. D., Talkhoncheh, M. S., Haastrup, E. K., Munthe-Fog, L., Clausen, C., Hansen, M. B., Andersen, P., Gørløv, J. S., Larsson, J., & Fischer-Nielsen, A. (2018). Pentaisomaltose, an Alternative to DMSO. Engraftment of Cryopreserved Human CD34+ Cells in Immunodeficient NSG Mice. Cell Transplantation, 27(9), 1407-1412. https://doi.org/10.1177/0963689718786226

Vancouver

Svalgaard JD, Talkhoncheh MS, Haastrup EK, Munthe-Fog L, Clausen C, Hansen MB et al. Pentaisomaltose, an Alternative to DMSO. Engraftment of Cryopreserved Human CD34+ Cells in Immunodeficient NSG Mice. Cell Transplantation. 2018 Sep;27(9):1407-1412. https://doi.org/10.1177/0963689718786226

Author

Svalgaard, Jesper Dyrendom ; Talkhoncheh, Mehrnaz Safaee ; Haastrup, Eva Kannik ; Munthe-Fog, Lea ; Clausen, Christian ; Hansen, Morten Bagge ; Andersen, Pernille ; Gørløv, Jette Sønderskov ; Larsson, Jonas ; Fischer-Nielsen, Anne. / Pentaisomaltose, an Alternative to DMSO. Engraftment of Cryopreserved Human CD34+ Cells in Immunodeficient NSG Mice. In: Cell Transplantation. 2018 ; Vol. 27, No. 9. pp. 1407-1412.

Bibtex

@article{512808f6ab6f4f9fa417f25482d427ee,
title = "Pentaisomaltose, an Alternative to DMSO. Engraftment of Cryopreserved Human CD34+ Cells in Immunodeficient NSG Mice",
abstract = "Hematopoietic stem cell transplantation often involves the cryopreservation of stem cell products. Currently, the standard cryoprotective agent (CPA) is dimethyl sulfoxide (DMSO), which is known to cause concentration-related toxicity and side effects when administered to patients. Based on promising in vitro data from our previous study using pentaisomaltose (a 1 kDa subfraction of Dextran 1) as an alternative to DMSO for cryopreservation of hematopoietic progenitor cells (HPCs) from apheresis products, we proceeded to a preclinical model and compared the two CPAs with respect to engraftment of human hematopoietic stem and progenitor cells (HSPCs) in the immunodeficient NSG mouse model. Human HPCs from apheresis products were cryopreserved with either pentaisomaltose or DMSO, and the following outcomes were measured: (1) the post-thaw recovery of cryopreserved cells and clonogenic potential of CD34+ cells and (2) hematopoietic engraftment in NSG mice. We found that recovery and colony-forming cells data were comparable between pentaisomaltose and DMSO. The engraftment data revealed comparable human CD45+ levels in peripheral blood at 8 weeks and bone marrow at 16 weeks post transplantation. Additionally, the frequencies of CD34+CD38low/negative and myeloid/lymphoid cells in the bone marrow were comparable. We here demonstrated that long-term engrafting HSPCs were well preserved in pentaisomaltose and comparable to cells cryopreserved with DMSO. Although a clinical trial is necessary to translate these results into human use, the present data represent an important step toward the replacement of DMSO with a non-toxic alternative.",
author = "Svalgaard, {Jesper Dyrendom} and Talkhoncheh, {Mehrnaz Safaee} and Haastrup, {Eva Kannik} and Lea Munthe-Fog and Christian Clausen and Hansen, {Morten Bagge} and Pernille Andersen and G{\o}rl{\o}v, {Jette S{\o}nderskov} and Jonas Larsson and Anne Fischer-Nielsen",
year = "2018",
month = sep,
doi = "10.1177/0963689718786226",
language = "English",
volume = "27",
pages = "1407--1412",
journal = "Cell Transplantation",
issn = "0963-6897",
publisher = "Cognizant Communication Corporation",
number = "9",

}

RIS

TY - JOUR

T1 - Pentaisomaltose, an Alternative to DMSO. Engraftment of Cryopreserved Human CD34+ Cells in Immunodeficient NSG Mice

AU - Svalgaard, Jesper Dyrendom

AU - Talkhoncheh, Mehrnaz Safaee

AU - Haastrup, Eva Kannik

AU - Munthe-Fog, Lea

AU - Clausen, Christian

AU - Hansen, Morten Bagge

AU - Andersen, Pernille

AU - Gørløv, Jette Sønderskov

AU - Larsson, Jonas

AU - Fischer-Nielsen, Anne

PY - 2018/9

Y1 - 2018/9

N2 - Hematopoietic stem cell transplantation often involves the cryopreservation of stem cell products. Currently, the standard cryoprotective agent (CPA) is dimethyl sulfoxide (DMSO), which is known to cause concentration-related toxicity and side effects when administered to patients. Based on promising in vitro data from our previous study using pentaisomaltose (a 1 kDa subfraction of Dextran 1) as an alternative to DMSO for cryopreservation of hematopoietic progenitor cells (HPCs) from apheresis products, we proceeded to a preclinical model and compared the two CPAs with respect to engraftment of human hematopoietic stem and progenitor cells (HSPCs) in the immunodeficient NSG mouse model. Human HPCs from apheresis products were cryopreserved with either pentaisomaltose or DMSO, and the following outcomes were measured: (1) the post-thaw recovery of cryopreserved cells and clonogenic potential of CD34+ cells and (2) hematopoietic engraftment in NSG mice. We found that recovery and colony-forming cells data were comparable between pentaisomaltose and DMSO. The engraftment data revealed comparable human CD45+ levels in peripheral blood at 8 weeks and bone marrow at 16 weeks post transplantation. Additionally, the frequencies of CD34+CD38low/negative and myeloid/lymphoid cells in the bone marrow were comparable. We here demonstrated that long-term engrafting HSPCs were well preserved in pentaisomaltose and comparable to cells cryopreserved with DMSO. Although a clinical trial is necessary to translate these results into human use, the present data represent an important step toward the replacement of DMSO with a non-toxic alternative.

AB - Hematopoietic stem cell transplantation often involves the cryopreservation of stem cell products. Currently, the standard cryoprotective agent (CPA) is dimethyl sulfoxide (DMSO), which is known to cause concentration-related toxicity and side effects when administered to patients. Based on promising in vitro data from our previous study using pentaisomaltose (a 1 kDa subfraction of Dextran 1) as an alternative to DMSO for cryopreservation of hematopoietic progenitor cells (HPCs) from apheresis products, we proceeded to a preclinical model and compared the two CPAs with respect to engraftment of human hematopoietic stem and progenitor cells (HSPCs) in the immunodeficient NSG mouse model. Human HPCs from apheresis products were cryopreserved with either pentaisomaltose or DMSO, and the following outcomes were measured: (1) the post-thaw recovery of cryopreserved cells and clonogenic potential of CD34+ cells and (2) hematopoietic engraftment in NSG mice. We found that recovery and colony-forming cells data were comparable between pentaisomaltose and DMSO. The engraftment data revealed comparable human CD45+ levels in peripheral blood at 8 weeks and bone marrow at 16 weeks post transplantation. Additionally, the frequencies of CD34+CD38low/negative and myeloid/lymphoid cells in the bone marrow were comparable. We here demonstrated that long-term engrafting HSPCs were well preserved in pentaisomaltose and comparable to cells cryopreserved with DMSO. Although a clinical trial is necessary to translate these results into human use, the present data represent an important step toward the replacement of DMSO with a non-toxic alternative.

U2 - 10.1177/0963689718786226

DO - 10.1177/0963689718786226

M3 - Letter

C2 - 30056762

VL - 27

SP - 1407

EP - 1412

JO - Cell Transplantation

JF - Cell Transplantation

SN - 0963-6897

IS - 9

ER -

ID: 220858348