US2020306319A1PendingUtilityA1
Methods for treating radiation or chemical injury
Est. expiryMar 22, 2031(~4.7 yrs left)· nominal 20-yr term from priority
A61K 35/50A61P 25/06A61P 1/08A61P 39/00A61P 7/04C12N 2531/00C12N 5/0668A61K 2035/124A61P 25/22C12N 5/0663C12N 5/0667A61K 35/35A61P 25/14C12N 5/0605A61P 1/12A61P 25/00A61P 43/00A61P 3/02A61K 35/28A61P 17/14A61P 7/00A61P 7/06G01N 33/50A61P 25/28A61P 25/02C12N 2513/00A61P 1/00
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Claims
Abstract
Methods for treating radiation or chemical injury are described that comprise administering to a subject a therapeutically effective amount of adherent stromal cells. Methods of preparing adherent stromal cells and pharmaceutical compositions comprising the cells are also described.
Claims
exact text as granted — not AI-modified1 .- 126 . (canceled)
127 . A method of mitigating reduction, resulting from exposure to radiation, in a subject's number of endogenous hematopoietic cells, comprising administering to said subject a composition comprising adherent stromal cells (ASC), wherein the ASC are administered before said exposure, and wherein the ASC were cultured under three-dimensional culturing conditions.
128 . The method of claim 127 , wherein said ASC are administered by intramuscular injection.
129 . The method of claim 127 , wherein the origin of the ASC is placenta.
130 . The method of claim 129 , where at least 50% of the ASC are fetal cells.
131 . The method of claim 127 , wherein the origin of the ASC is selected from adipose tissue and bone marrow.
132 . The method of claim 127 , wherein said three-dimensional culturing conditions comprise culturing in a bioreactor.
133 . The method of claim 127 , wherein at least 70% of the ASC are positive for the marker CD200, as detected by flow cytometry compared to an isotype control.
134 . The method of claim 127 , wherein the ASC are administered 1 day before said exposure.
135 . A method of mitigating reduction, resulting from exposure to a chemical, in a subject's number of endogenous hematopoietic cells, comprising administering to said subject a composition comprising adherent stromal cells (ASC), wherein the ASC are administered before said exposure, and wherein the ASC were cultured under three-dimensional culturing conditions.
136 . The method of claim 135 , wherein said ASC are administered by intramuscular injection.
137 . The method of claim 135 , wherein the origin of the ASC is placenta.
138 . The method of claim 137 , where at least 50% of the ASC are fetal cells.
139 . The method of claim 135 , wherein the origin of the ASC is selected from adipose tissue and bone marrow.
140 . The method of claim 135 , wherein said three-dimensional culturing conditions comprise culturing in a bioreactor.
141 . The method of claim 135 , wherein at least 70% of the ASC are positive for the marker CD200, as detected by flow cytometry compared to an isotype control.
142 . The method of claim 135 , wherein the ASC are administered 1 day before said exposure.
143 . The method of claim 135 , wherein said chemical is a chemotherapy agent.
144 . A method of reducing a symptom associated with radiation sickness in a subject, comprising administering to said subject a composition comprising adherent stromal cells (ASC), wherein the ASC are administered before exposure to radiation, and wherein the ASC were cultured under three-dimensional culturing conditions.
145 . The method of claim 144 , wherein said symptom is selected from leukopenia, anemia, thrombocytopenia, nausea, vomiting, and diarrhea.
146 . The method of claim 144 , wherein said ASC are administered by intramuscular injection.Cited by (0)
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