US2011020928A1PendingUtilityA1
Immunovectors which can be used for the intracellular and intranuclear transport
Est. expiryJul 10, 2015(expired)· nominal 20-yr term from priority
A61P 31/18A61P 31/00A61P 35/00C07K 16/18A61K 47/6845A61K 48/00A61P 43/00
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Abstract
A method of transferring a biologically active principle of interest into a cell by coupling an antibody or a fragment of an antibody, which recognizes an epitope contained in a nucleic acid, with the biologically active principle, to form a coupled biologically active principle; and incubating the coupled biologically active principle, which is transferred through the cell membrane and into the cell, with the cell.
Claims
exact text as granted — not AI-modified1 . A method of transferring a biologically active principle of interest into a cell comprising:
a. coupling an antibody or a fragment of an antibody, which recognizes an epitope contained in a nucleic acid, with the biologically active principle, thereby forming a coupled biologically active principle; and b. incubating the coupled biologically active principle with the cell, wherein said coupled principle is transferred through the cell membrane and into the cell.
2 . The method of claim 1 , wherein said biologically active principle is selected from the group consisting of a hapten having biological activity, a hormone, and a medicine.
3 . The method of claim 2 , wherein said biologically active principle is a medicine allowing the immortalization of selected type cells including one of macrophages, dendritic cells, B cells, T cells, and hematopoietic cells.
4 . The method of claim 1 , wherein said biologically active principle is an antiviral agent.
5 . The method of claim 1 , wherein the antibody or fragment of antibody is a monoclonal IgG, a (Fab′) 2 fragment, or a (Fab′) fragment.
6 . The method of claim 1 , wherein the antibody or fragment of antibody is obtained from individuals presenting auto-immune syndromes.
7 . The method of claim 1 , wherein the antibody or fragment of antibody is obtained from individuals presenting disseminated erythematous lupus syndromes.
8 . A hybridoma deposited at the CNCM on Jun. 30, 1996 under the registration number I-1605, I-1606 or I-1607.Cited by (0)
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