USES OF TREHALOSE IN CELL SUSPENSIONS
Disclosed are cellular compositions and methods relating to the use of aqueous trehalose media to suspend cells. A trehalose-containing medium can be used to inhibit cellular clumping, for example upon dilution of more concentrated cellular preparations into the trehalose-containing medium. In certain embodiments cells, after cryopreservation and thawing, are combined with a trehalose-containing medium to prepare a clumping-inhibited cell suspension.
1 . (canceled)
2 . A method for preparing a cellular composition, comprising:
(a) thawing cryopreserved cells to provide a first aqueous liquid medium comprising thawed, viable cells and DNA released from dead cells, wherein said cryopreserved cells are purified uterine derived feline or canine mesenchymal stem cells in a trehalose free cryopreservation medium;
(b) washing the thawed, viable cells and DNA released from dead cells to remove the cryopreservation medium; and
(c) combining the washed thawed, viable cells and DNA released from dead cells with a second aqueous liquid medium containing trehalose to provide a trehalose-containing cell suspension;
(d) wherein said combining is conducted so as to provide a trehalose concentration in the range of about 1.5% to about 7% by weight in the trehalose-containing cell suspension;
(e) wherein said combining is conducted so as to maintain cell viability above ninety percent; and
(f) wherein said trehalose-containing cell suspension is suitable for delivery into the bloodstream of a feline or canine patient.
3 . A method, comprising:
(a) suspending purified uterine derived feline or canine mesenchymal stem cells in a trehalose free cryoprotectant-containing medium to form a cryopreservable cell composition;
(b) subjecting the cryopreservable cell composition to cryopreservation conditions to generate cryopreserved cells;
(c) thawing the cryopreserved cells to provide a first aqueous liquid medium comprising thawed, viable cells and DNA released from dead cells;
(d) washing the thawed, viable cells and DNA released from dead cells to remove the cryoprotectant-containing medium; and
(e) combining the washed thawed, viable cells and DNA released from dead cells with a second aqueous liquid medium containing trehalose to provide a trehalose-containing cell suspension, wherein said combining is conducted so as to provide a trehalose concentration in the range of about 1.5% to about 7% by weight in the trehalose-containing cell suspension.
4 . A method for preparing a diluted cell suspension from a cell concentrate, comprising:
(a) thawing a cryopreserved cell composition having a first viable cell density of at least 3 million cells/mL to provide a first aqueous liquid medium comprising thawed, viable cells and DNA released from dead cells, wherein said first aqueous liquid medium is trehalose free; and
(b) combining the first aqueous medium including thawed, viable cells and DNA released from dead cells with a second aqueous liquid medium containing trehalose to form a trehalose-containing cell suspension having a second viable cell density less than the first cell density, wherein said combining is conducted so as to provide a trehalose concentration in the range of about 1.5% to about 7% by weight in the trehalose-containing cell suspension;
wherein the cryopreserved cell composition comprises purified uterine derived feline or canine mesenchymal stem cells.
5 . The method of claim 2 , wherein the second aqueous liquid medium also contains about 0.9% by weight sodium chloride.
6 . The method of claim 2 , wherein the second aqueous liquid medium has an osmolarity in the range of 200 to 600 mosmol/kg.
7 . The method of claim 2 , wherein said combining comprises:
removing the first aqueous liquid medium from a cryopreservation container; and
combining the second aqueous liquid medium with the first aqueous liquid medium in a second container.
8 . The method of claim 2 , further comprising administering the trehalose-containing cell suspension to a feline or canine patient, wherein the cell suspension is passed through an in-line filter positioned in tubing through which the cell suspension is passed into the blood stream of the patient,
9 . The method of claim 2 , wherein the first aqueous liquid medium is a medium in which the cells had been cryopreserved.
10 . The method of claim 3 , wherein:
the second aqueous liquid medium has a trehalose concentration in the range of 1% to 10% by weight.
11 . The method of claim 2 , wherein the trehalose concentration is 3.3% or about 3.3% by weight.
12 . The method of claim 3 , wherein the trehalose concentration is 3.3% or about 3.3% by weight.
13 . The method of claim 4 , wherein the trehalose concentration is 3.3% or about 3.3% by weight.