» Articles » PMID: 11863422

Retroviral Transduction and Engraftment Ability of Primate Hematopoietic Progenitor and Stem Cells Transduced Under Serum-free Versus Serum-containing Conditions

Overview
Journal Mol Ther
Publisher Cell Press
Date 2002 Feb 28
PMID 11863422
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

The ability to efficiently transduce hematopoietic stem and progenitor cells under serum-free conditions would be desirable for safety and standardization of clinical gene therapy protocols. Using rhesus macaques, we studied the transduction efficiency and engraftment ability of CD34-enriched SCF/G-CSF mobilized progenitor cells (PBSC) transduced with standard amphotropic marking vectors under serum-free and serum-containing conditions. Supernatants were collected from producer cells 16 hours after serum-free medium or medium containing 10% fetal calf serum was added. Vector titers were approximately two- to threefold higher when producer cells were cultured in serum-containing medium. However, retroviral transduction of rhesus CFU-GM was improved using serum-free vector-containing medium. For analysis of engraftment with transduced cells, three macaques had CD34+ peripheral blood stem cells split into two fractions for transduction. One fraction was transduced using serum-free vector-containing medium, and the other fraction was transduced using standard serum-containing medium. The two fractions were re-infused simultaneously following total body irradiation. In all three animals, there was equivalent marking from both vectors for 7-9 months post-transplantation. These data are encouraging regarding the removal of serum-containing medium from clinical hematopoietic cell transduction protocols, given the lack of a detrimental effect on transduction and engraftment with transduced cells.

Citing Articles

Effective and stable gene transduction in rhesus macaque iPSCs capable of T-lineage differentiation utilizing the piggyBac system.

Tanaka M, Iwamoto Y, Wang B, Imai E, Yoshida M, Iriguchi S Regen Ther. 2024; 27:104-111.

PMID: 38545443 PMC: 10966093. DOI: 10.1016/j.reth.2024.03.002.


Hematopoietic Stem Cell Gene-Addition/Editing Therapy in Sickle Cell Disease.

Germino-Watnick P, Hinds M, Le A, Chu R, Liu X, Uchida N Cells. 2022; 11(11).

PMID: 35681538 PMC: 9180595. DOI: 10.3390/cells11111843.


Serum-free Erythroid Differentiation for Efficient Genetic Modification and High-Level Adult Hemoglobin Production.

Uchida N, Demirci S, Haro-Mora J, Fujita A, Raines L, Hsieh M Mol Ther Methods Clin Dev. 2018; 9:247-256.

PMID: 29766032 PMC: 5948232. DOI: 10.1016/j.omtm.2018.03.007.


Optimal conditions for lentiviral transduction of engrafting human CD34+ cells.

Uchida N, Hsieh M, Hayakawa J, Madison C, Washington K, Tisdale J Gene Ther. 2011; 18(11):1078-86.

PMID: 21544097 PMC: 6525965. DOI: 10.1038/gt.2011.63.


Myeloablative irradiation in non-human primates.

Watts K, Beard B, Wood B, Kiem H J Med Primatol. 2009; 38(6):425-32.

PMID: 19638102 PMC: 2796123. DOI: 10.1111/j.1600-0684.2009.00368.x.