Process for the production of human peptide hormones

Claim 2

In the process for producing human peptide hormone, excluding human erythropoietin, which comprises culturing human cells capable of producing a human peptide hormone on an in vitro nutrient medium under conditions appropriate to accumulate a substantial amount of the human peptide hormone, and recovering the accumulated human peptide hormone from the culture, the improvement, by which the amount of human peptide hormone produced during said in vitro culturing is substantially increased, comprising using as said human cells capable of producing a human peptide hormone, cells obtained by a process comprising: implanting a human×human hybridoma lymphoblastoid cell line capable of producing said human peptide hormone in a non-human warm-blooded animal; feeding the animal to allow said human hybridoma cell line to utilize the nutrient body fluid of the animal for its multiplication; and extracting and disaggregating the resultant tumor, formed in the animal, for use in the in vitro production of said human peptide hormone.

Claim 3

A process as set forth in claim 1, wherein said human peptide hormone is human insulin.

Claim 4

A process as set forth in claim 1, wherein said human peptide hormone is human growth hormone.

Claim 5

A process as set forth in claim 1, wherein said human peptide hormone is human prolactin.

Claim 6

A process as set forth in claim 1, wherein said human peptide hormone is human adrenocorticotropic hormone.

Claim 7

A process as set forth in claim 1, wherein said human peptide hormone is human placental lactogen.

Claim 8

A process as set forth in claim 1, wherein said human peptide hormone is human thyroid-stimulating hormone.

Claim 9

A process as set forth in claim 1, wherein said human peptide hormone is human parathyroid hormone.

Claim 10

A process as set forth in claim 1, wherein said human peptide hormone is human calcitonin.

Claim 11

A process as set forth in claim 1, wherein said non-human warm-blooded animal is a fowl or a mammal.

Claim 12

A process as set forth in claim 1, wherein said non-human warm-blooded animal is a chicken, pigeon, dog, cat, monkey, goat, pig, cow, horse, rabbit, guinea pig, rat, nude rat, hamster, mouse or nude mouse.

Claim 13

A process as set forth in claim 14, wherein said fusing step comprises: suspending said parent human cells together with said human lymphoblastoid line in a salt solution containing an effective amount of a cell fusion inducing agent; allowing the resultant cell suspension to stand for a period sufficient to effect cell fusion; and selecting and cloning a hybridoma line capable of producing human peptide hormone.

Claim 14

A process as set forth in claim 12, wherein said cell fusion inducing agent is Sendai virus or polyethylene glycol.

Claim 15

A process as set forth in claim 1, wherein said human×human hybridoma lymphoblastoid cell line is obtained by fusing parent human cells inherently capable of producing a human peptide hormone with a human lymphoblastoid line.

Claim 16

A process as set forth in claim 14, wherein said parent human cells are normal or tumor human cells.

Claim 17

A process as set forth in claim 14, wherein said human peptide hormone is human insulin and said parent human cells are human insuloma cells.

Claim 18

A process as set forth in claim 14, wherein said human peptide hormine is human insulin and said parent human cells are human pancreas Langerhans island β-cells.

Claim 19

A process as set forth in claim 14, wherein said human peptide hormone is human growth hormone and said parent human cells are human acidophile adenoma cells.

Claim 20

A process as set forth in claim 14, wherein said human peptide hormone is humanprolactin and said parent human cells are human acidophile adenoma cells.

Claim 21

A process as set forth in claim 14, wherein said human peptide hormone is human adrenocorticotropic hormone and said parent human cells are human chromophobe adenoma cells of the pituitary gland.

Claim 22

A process as set forth in claim 2, wherein said human peptide hormone is human placental lactogen and said parent human cells are human chorionic epithelioma cells.

Claim 23

A process as set forth in claim 14, wherein said human peptide hormone is humanplacental lactogen and said parent human cells are human syncytiotrophoblast cells from chorionic villi.

Claim 24

A process as set forth in claim 14, wherein said human peptide hormone is human thyroid-stimulating hormone and said parent human cells are human basophile adenoma cells.

Claim 25

A process as set forth in claim 14, wherein said human peptide hormone is human thyroid-stimulating hormone and said parent human cells are human chromophobe adenoma cells.

Claim 26

A process as set forth in claim 14, wherein said human peptide hormone is human parathyroid hormone and said parent human cells are human parathyroid tumor cells.

Claim 27

A process as set forth in claim 14, wherein said human peptide hormone is human parathyroid hormone and said parent human cells are human kidney carcinoma cells.

Claim 28

A process as set forth in claim 14, wherein said human peptide hormone is human parathyroid hormone and said parent human cells are human ovarian tumor cells.

Claim 29

A process as set forth in claim 14, wherein said human peptide hormone is human calcitonin and said parent human cells are human thyrophyma cells.

Claim 30

A process as set forth in claim 14, wherein said human peptide hormone is human calcitonin and said parent human cells are human carcinoid cells.

Claim 31

A process as set forth in claim 14, wherein said parent human cells are human lung carcinoma cells.

Claim 32

A process in accordance with claim 14, wherein said human lymphoblastoid line is of leukemic origin.

Claim 33

A process as set forth in claim 14, wherein said human lymphoblastoid line is a member selected from the group of cell lines consisting of Namalva, BALL-1, NALL-1, TALL-1 and JBL.

Claim 34

In the process for producing human peptide hormone, excluding human erythropoietin, which comprises culturing human cells capable of producing said peptide hormone on an in vitro nutrient medium under the conditions appropriate to accumulate a substantial amount of the human peptide hormone, and recovering the accumulated human peptide hormone from the culture, the improvement, by which the amount of human peptide hormone produced during said in vitro culturing is substantially increased, comprising using as said human cells capable of producing a human peptide hormone, cells obtained by a process comprising: suspending a human×human hybridoma lymphoblastoid cell line capable of producing said human peptide hormone in a device in which the nutrient body fluid of a non-human warm-blooded animal can be supplied to said human hybridoma cell line; embedding or placing said device in or on a non-human warm-blooded animal in a manner such that the nutrient body fluid of said animal is supplied to the human hybridoma cell line within said device; feeding the animal to allow said human hybridoma cell line to utilize the nutrient body fluid for its multiplication; and harvesting the multiplied human hybridoma cells from the device for use in the in vitro production of said human peptide hormone.

Claim 35

In the process for producing human peptide hormone, excluding human erythropoietin, which comprises culturing human cells capable of producing said peptide hormone on an in vitro nutrient medium under the conditions appropriate to accumulate a substantial amount of the human peptide hormone, and recovering the accumulated human peptide hormone from the culture, the improvement, by which the amount of human peptide hormone produced during said in vitro culturing is substantially increased, comprising using as said human cells capable of producing a human peptide hormone, cells obtained by a process comprising: suspending a human×human hybridoma lymphoblastoid cell line capable of producing said human peptide hormone in a device in which the nutrient body fluid of a non-human warm-blooded animal can be supplied to said human hybridoma cell line; embedding or placing said device in or on a non-human warm-blooded animal in a manner such that the nutrient body fluid of said animal is supplied to the human hybridoma cell line within said device; feeding the animal to allow said human hybridoma cell line to utilize the nutrient body fluid for its multiplication; and harvesting the multiplied human hybridoma cells from the device for use in the in vitro production of said human peptide hormone.

Claim 36

A process as set forth in claim 33, wherein said human peptide hormone is selected from the group consisting of human insulin, human growth hormone, human prolactin, human adrenocorticotropic hormone, human placental lactogen, human thyroid-stimulating hormone, human parathyroid hormone, and human calcitonin.

Claim 37

A process as set forth in claim 33, wherein said device is a diffusion chamber equipped with a membrane filter, ultra-filter or hollow fiber having a nominal pore size in the range of 10 -7 -10 -5 m.

Claim 38

A process as set forth in claim 33, wherein said non-human warm-blooded animal is a fowl or a mammal.

Claim 39

A process as set forth in claim 33, wherein said non-human warm-blooded animal is a chicken, pigeon, dog, cat, monkey, goat, pig, cow, horse, rabbit, guinea pig, rat, nude rat, hamster, mouse or nude mouse.

Claim 40

A process as set forth in claim 33, wherein said fusing step comprises: suspending said parent human cells together with said human lymphoblastoid line in a salt solution containing an effective amount of a cell fusion inducing agent; allowing the resultant cell suspension to stand for a period sufficient to effect cell fusion; and selecting and cloning a hybridoma line capable of producing human peptide hormone.

Claim 41

A process as set forth in claim 38, wherein said cell fusion inducing agent is Sendai virus or polyethylene.

Claim 42

A process as set forth in claim 33, wherein said human×human hybridoma lymphoblastoid cell line is obtained by fusing parent human cells inherently capable of producing a human peptide hormone with a human lymphoblastoid line.

Claim 43

A process as set forth in claim 40, wherein said parent cells are normal or tumor human cells.

Claim 44

A process as set forth in claim 40, wherein said human peptide hormone is human insulin and said parent human cells are human insuloma cells.

Claim 45

A process as set forth in claim 40, wherein said human peptide hormine is human insulin and said parent human cells are human pancreas Langerhans island β-cells.

Claim 46

A process as set forth in claim 40, wherein said human peptide hormone is human growth hormone and said parent human cells are human acidophile adenoma cells.

Claim 47

A process as set forth in claim 40, wherein said human peptide hormone is humanprolactin and said parent human cells are human acidophile adenoma cells.

Claim 48

A process as set forth in claim 40, wherein said human peptide hormone is human adrenocorticotropic hormone and said parent human cells are human chromophobe adenoma cells of the pituitary gland.

Claim 49

A process as set forth in claim 40, wherein said human peptide hormone is human placental lactogen and said parent human cells are human chorionic epithelioma cells.

Claim 50

A process as set forth in claim 40, wherein said human peptide hormone is humanplacental lactogen and said parent human cells are human syncytiotrophoblast cells from chorionic villi.

Claim 51

A process as set forth in claim 40, wherein said human peptide hormone is human thyroid-stimulating hormone and said parent human cells are human basophile adenoma cells.

Claim 52

A process as set forth in claim 40, wherein said human peptide hormone is human thyroid-stimulating hormone and said parent human cells are human chromophobe adenoma cells.

Claim 53

A process as set forth in claim 40, wherein said human peptide hormone is human parathyroid hormone and said parent human cells are human parathyroid tumor cells.

Claim 54

A process as set forth in claim 40, wherein said human peptide hormone is human parathyroid hormone and said parent human cells are human kidney carcinoma cells.

Claim 55

A process as set forth in claim 40, wherein said human peptide hormone is human parathyroid hormone and said parent human cells are human ovarian tumor cells.

Claim 56

A process as set forth in claim 40, wherein said human peptide hormone is human calcitonin and said parent human cells are human thyrophyma cells.

Claim 57

A process as set forth in claim 40, wherein said human peptide hormone is human calcitonin and said parent human cells are human carcinoid cells.

Claim 58

A process as set forth in claim 40, wherein said parent human cells are human lung carcinoma cells.

Claim 59

A process in accordance with claim 40, wherein said human lymphoblastoid line is of leukemic origin.

Claim 60

A process as set forth in claim 40, wherein said human lymphoblastoid line is a member selected from the group of cell lines consisting of Namalva, BALL-1, NALL-1, TALL-1 and JBL.