US2002037543A1PendingUtilityA1
Purging of cells using viruses
Priority: Jun 26, 2000Filed: Jun 26, 2001Published: Mar 28, 2002
Est. expiryJun 26, 2020(expired)· nominal 20-yr term from priority
Inventors:Harold AtkinsJohn BellConrad J. Heilman, Jr.Brian LichtyRobert M. LorenceMichael RobertsDavid F. Stojdl
A61P 37/06A61P 35/02A61P 35/00A61P 37/02A61P 25/00A61K 35/14C12N 2501/24A61P 29/00A61K 35/28C12N 5/0093A61K 35/766A61K 35/768A61K 35/765
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Claims
Abstract
The subject invention relates to viruses that are able to purge (reduce or eliminate) undesirable cells in a mixture of cells. Undesirable cells can include neoplastic cells, cells mediating graft-versus host diseases, and autoimmune cells. The subject invention also relates to the purging of undesirable cells from bone marrow or peripheral blood cell harvests in the treatment of mammals including cancer patients, transplant recipients, and patients with autoimmune disease.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of reducing or eliminating neoplastic cells in an ex vivo mixture of normal hematopoeitic cells and neoplastic cells by contacting said mixture with a virus.
2 . A method as in claim 1 wherein said virus is an RNA virus.
3 . A method as in claim 1 wherein said neoplastic cells are leukemia cells.
4 . A method as in claim 1 wherein said hematopoietic cells are marrow cells.
5 . A method as in claim 1 wherein said hematopoietic cells are peripheral blood cells.
6 . A method as in claim 2 wherein said RNA virus is a single-strand RNA virus.
7 . A method as in claim 6 wherein said single-strand RNA virus is a non-segmented, negative sense RNA virus.
8 . A method as in claim 7 wherein said non-segmented, negative sense RNA virus is a rhabdovirus.
9 . A method as in claim 8 wherein said rhabdovirus is vesicular stomatitis virus.
10 . A method as in claim 7 wherein said non-segmented, negative sense RNA virus is a paramyxovirus.
11 . A method as in claim 10 wherein said paramyxovirus is Newcastle disease virus.
12 . A method as in claim 6 wherein said single-strand RNA virus is Sindbis virus.
13 . A method as in claim 2 wherein said RNA virus is a double-strand RNA virus.
14 . A method as in claim 13 wherein said double strand RNA virus is a reovirus.
15 . A method as in claim 14 wherein said reovirus is reovirus type 3.
16 . A method as in claim 13 wherein said reovirus is clonal.
17 . A method as in claim 2 wherein said RNA virus is a replication-competent RNA virus.
18 . A method as in claim 2 wherein said RNA virus is a replication-incompetent RNA virus.
19 . A method as in claim 1 wherein said neoplastic cells are lymphoma cells.
20 . A method as in claim 1 further comprising administering a chemotherapeutic agent before, during or after contacting with said virus.
21 . A method as in claim 1 further comprising administering an interferon before, during or after contacting with said virus.
22 . A method of treating cancer in a mammal comprising:
a) removing bone marrow or peripheral blood cells from said mammal, b) contacting said bone marrow or peripheral blood cells ex vivo with an RNA virus, c) performing myeloablative treatment on said mammal, and d) transplanting into said mammal the purged hematopoeitic cells of step b.
23 . A method as in claim 22 wherein said myeloablative treatment is high dose chemotherapy.
24 . A method of treating cancer in a mammal receiving a bone marrow or peripheral blood stem cell transplant comprising contacting the harvested cells of transplant cells ex vivo with a virus, and administering the purged cells to said mammal.Join the waitlist — get patent alerts
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