The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jul. 26, 1988

Filed:

Nov. 07, 1984
Applicant:
Inventors:

Akio Mimura, Fuji, JP;

Kaoru Yoshinari, Fuji, JP;

Katsumi Yuasa, Fuji, JP;

Tsuneo Sato, Fuji, JP;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12P / ; C07K / ; A61K / ;
U.S. Cl.
CPC ...
435 68 ; 530351 ;
Abstract

There is provided a proteinaceous biological response modifier having the following properties: (a) molecular weight: 35,000 to 65,000; (b) isoelectric point: 5.0 to 6.1; (c) physiological action on human leukemia cells: to induce human leukemia to differentiate into macrophage-like cells; (d) physiological action on myeloid leukemia cells from mice: to induce myeloid leukemia cells from mice to differentiate into macrophage-like cells; (e) affinity to Concanavalin A Sepharose: not adsorbed; (f) affinity to Blue Sepharose Resin: not adsorbed; (g) pH-stability and thermostability: substantially not inactivated at pH 2 to 10, at 2.degree. C. for 6 hours; not inactivated at 56.degree. C. for 60 minutes; but inactivated by 30% at 70.degree. C. for 60 minutes; (h) sensitivity to enzymes: not inactivated by deoxyribonuclease; not inactivated by glycosidase; and inactivated by protease; (i) flow cytometry analysis: to concentrate cell division cycle of human leukemia cells to G.sub.0 /G.sub.1 phase. There is also provided a process for the production of the proteinaceous biological response modifier comprising culturing human leukemia cells in a differentiation medium in the presence of a substance capable of inducing the human leukemia cells to differentiate into macrophage-like cells; separating the macrophage-like cells from the culture medium; activating the macrophage-like cells in a production medium by a mitogen to enhance the production of the proteinaceous biological response modifier; and isolating the proteinaceous biological response modifier from the production medium. The biological response modifier has anti-tumor activity.


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