CN1438030A - Method for preparing tumor specific transfer factors - Google Patents
Method for preparing tumor specific transfer factors Download PDFInfo
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- CN1438030A CN1438030A CN03114543A CN03114543A CN1438030A CN 1438030 A CN1438030 A CN 1438030A CN 03114543 A CN03114543 A CN 03114543A CN 03114543 A CN03114543 A CN 03114543A CN 1438030 A CN1438030 A CN 1438030A
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Abstract
The preparation method of tumor transspecific factor is characterized by that it includes the processes of preparing antigen, immunizing animal and preparing tumor transspecific factor. Said method uses animal organ immunized by tumor antigen as raw material, its main components are small molecule polypeptide, amino acid and nucleotide, etc. and it contains no globulin, and does not result in anaphylactic reaction, and has the functions of transferring cell information, mediating cell immune reaction and specifically inhibiting and killing correspondent tumor cell.
Description
One, technical field
The present invention relates to biotechnology, particularly relate to a kind of preparation method of tumor specific transfer factor.
Two, background technology
Till the present, medical circle generally adopts operating method to treat most malignant tumor.Yet because the aggressive of tumorigenic invisible and development, the metastasis or the subclinical metastasis of oncocyte appearred in tumor patients more than half in fact at the beginning of making a definite diagnosis, and the patient has finally still been seized life by cancer.How to control postoperative recurrence, eliminate subclinical metastasis, overcome the invalid effect of radiotherapy, alleviate the chemotherapy harmful effect that inhibition brings to body's immunity, become century property one big problem the diffusibility focus.After conventional operation, radiotherapy, chemotherapy, the Biotherapeutics of tumor has become the new model of oncotherapy, the main body of tumor biotherapy is an immunotherapy of tumors, its mechanism of action: the one, the stagnation or the apoptosis of inducing tumor cell self growth, the 2nd, activate the generation that has the T cell of antineoplastic specificity and cytotoxic activity in the body, reach the purpose of specific killing tumor.Yet tumor is not only systemic disease, also is systemic disease, and tumor treatment also must be carried out whole body therapeutic except that topical therapeutics such as operation and radiotherapy.From present International Development situation, the treatment of tumor active specific immunotherapy has shown more good potential applicability in clinical practice.Treat tumor with tumor specific transfer factor and just be based on the above-mentioned mechanism of action, the generation of the T cell of tumor specific transfer factor energy active cell cytotoxic activity and the secretion of cytokine, rebuild, repair and transfer body's immunity, initiatively specifically excitating organism to the humoral immunization and the cell immunocompetent of tumor cell, specificity suppresses, kills and wounds corresponding tumor cell, excision primary tumor patient is had the effect that control is shifted, eliminated the residual cancer cell, reach the purpose of treatment malignant tumor.To lymphocytic specificity activation with to the specificity inhibition of tumor cell and the common existence of lethal effect is the treatment foundation and the characteristics of tumor specific transfer factor, makes tumor specific transfer factor become a kind of safe and effective active specific immunotherapy and treats ideal medicine.
Three, summary of the invention
The object of the present invention is to provide a kind of preparation method of tumor specific transfer factor, utilize tumor specific transfer factor, adopt biotechnology to make efficient, special antitumor drug the specificity inhibition of tumor cell and the characteristics of lethal effect.
For achieving the above object, the present invention adopt the preparation method of technical scheme form by following step:
A. prepare antigen: prepare the cancerous tissue of required raw material for the cancer patient, preparation process is: after the homogenate, with 5000～10000 rev/mins speed after centrifugal 20～60 minutes, abandon precipitation, centrifugal 20～60 minutes again with 8000～12000 rev/mins speed, receive the supernatant degerming at last, qualitative, quantitative, packing is preserved;
B. animal immune: immunologic process is: take multiple spot subcutaneous injections such as groin, nape, abdominal cavity, and totally 8～12 points, immunity is 1 time weekly, and immunity is 4 times altogether, and first immunisation and immunity for the second time adopt antigen to add adjuvant; Antigen is only used in third and fourth time immunity.
C. prepare tumor specific transfer factor: will rub through animal spleen, the lymph node of cancer cell antigen immunity, after the homogenate, freeze thawing: solidification point is-20～-70 ℃, melt temperature is 20～30 ℃, freeze thawing 2～5 times, last low temperature dialysis, quantitative and qualitative, aseptic subpackaged.Four, the specific embodiment
Concrete implementation step of the present invention is:
1. preparation antigen:
Get the fresh cancer specimen that operation is downcut, homogenate with 1～3 times of volume, homogenate disperses, the homogenate condition is: 0.9%NaCL, 20mmol/L phosphate buffer (PBS)-1mmol/L disodiumedetate (EDTA-2Na) (PH7.4), or 20mmol/L Tris hydrochloric acid (TrisHCl) buffer (PH7.4); Centrifugal: as 5000～10000 rev/mins, 20～60 minutes, to abandon precipitation; Centrifugal again: receive supernatant, centrifugal: 8000～12000 rev/mins, 20～60 minutes, receive the supernatant degerming, qualitative, quantitative, packing is preserved.
2. immune animal:
Select healthy goat up to specification, every heavily about 20Kg takes multiple spot subcutaneous injections such as groin, nape, abdominal cavity, and totally 8～12 points immune 1 time weekly, are total to immunity 4 times.0～30 milligram/time of first immunisation antigen 1 adds the complete freund adjuvant of equivalent; The 2nd immunity: 0～30 milligram/time of antigen 1 adds the incomplete freund adjuvant of equivalent; 3rd, 4 immunity: single with 50～100 milligrams/time of antigens.Check the sensitization state of goat with the skin test method.
3. preparation tumor specific transfer factor:
To handle clean through Lien Naemorhedi, the lymph node of tumor antigen immunity, rub homogenate, freeze thawing under-20～-70 ℃ of low temperature and under 20～30 ℃ of temperature, multigelation like this 2～5 times, to normal saline dialysis (5000～14000D bag filter), under 2～10 ℃ of conditions of temperature, receive extracellular fluid dialysis, aseptic sucking filtration, qualitative, quantitative, and do biological activity assay, packing.
Characteristics of the present invention: 1. preparation process adopts secondary centrifuging, can improve antigenic purity; 2. Pei Zhi homogenate is beneficial to antigenic release dissolving and protects antigenic integrity; 3. Mian Yi number of times and consumption not only can guarantee the quality of tumor specific transfer factor but also can improve its output; 4. dialysis condition can improve the purity of tumor specific transfer factor.
Advantage of the present invention: tumor specific transfer factor itself is not had an immunogenicity, can prolonged and repeatedly inject, safe in utilization, effect is obvious, be a safe and effective practical new new technique of prevention at present and treatment malignant tumor, have market application foreground and certain social value widely.And better curative effect is all arranged for digestive system tumor, pulmonary carcinoma, renal carcinoma, breast carcinoma, malignant melanoma, the easy recurrent tumor of intracranial etc.
Embodiments of the invention:
1. preparation antigen: collect the fresh cancer specimen that operation is downcut, reject cancer normal structure on every side, with PH7.4,20mmol/L phosphate buffer (PBS)-1mmol/L disodiumedetate (EDTA-2Na) buffer solution for cleaning, immersion, homogenate disperse, under 4 ℃, 7000 rev/mins conditions centrifugal 30 minutes; Receive supernatant, under 4 ℃, 12000 rev/mins conditions centrifugal 50 minutes once more, receive the supernatant degerming, stay small part to survey protein content, packing ,-20 ℃ are frozen standby.
2. immune animal: select to meet " management of laboratory animal rules " goat, 20 kilograms every, adopt multiple spot subcutaneous injections such as groin, nape, abdominal cavity, totally 8～12 points, 0.5 milliliter every, immunity is 1 time weekly, and immunity is four times altogether.First immunisation is got 20 milligrams of/time cancer antigens and is added the complete freund adjuvant of equivalent; Immunity is for the second time got 20 milligrams of/time cancer antigens and is added the incomplete freund adjuvant of equivalent; Back secondary immunity is with 80 milligrams of/time cancer antigens.Check the sensitization state of goat with the skin test method.
3. preparation tumor specific transfer factor: the Lien Naemorhedi of the immunity of learning from else's experience, lymph node, wipe out peplos, fat, fibrous tissue, with shredding behind the sterile saline cyclic washing, homogenate,-70 ℃ to 30 ℃ multigelations 5 times, the microscopy smudge cells reaches more than 90%, the centrifugal precipitation of abandoning is got supernatant, received 4 ℃ of normal saline dialysiss of supernatant dress bag filter 30～40 hours, below the bag filter molecular weight 5000D, receive the extracellular fluid dialysis filtration sterilization, with the 8.0abs of the highest absworption peak place (251nm) is 1 tumor specific transfer factor unit (units per ml), presses the packing of biological product packing rules, and 2 milliliters every contain 2 units.
The calibrating of tumor specific transfer factor finished product:
Outward appearance: no foreign body does not have colourless or faint yellow transparent, the clarifying liquid of precipitation
Sterility test: " Chinese pharmacopoeia appendix XIH checked that it is fixed to meet by two ones of versions in 2000.
PH value: PH6.0～7.2, " Chinese pharmacopoeia appendix VIH inspection should be up to specification according to two ones of versions in 2000.
Content of peptides: Folin-phenol method, 1.0～1.5 mg/ml
Ribose content: 3.5-vesorcinol colorimetry 0.6～0.7 mg/ml
E
252± 2nm: characteristic absorption peak is arranged
E
250nm、1cm：15～18
E
260/280nm：E
260/280＝2.0～2.3
Protein: get 2 milliliters of this product and add 2 milliliters of joltings of 20% sulfosalicylic acid, must not produce muddiness
Thermal source: " Chinese pharmacopoeia appendix XIE inspection should be up to specification by two ones of versions in 2000
Hypersensitive test: 5 of healthy guinea pigs getting body weight 250～350 gram, lumbar injection this product is 0.5 milliliter next day of inferior continuously, after placing for 2 weeks, again from 1.0 milliliters of vena femoralis injection this product, inject in back 15 minutes, observe animal must not have continuously time dry cough, continuous 3 fore paws grab nose, obviously perpendicular hair, extremity feel like jelly, couch, phenomenons such as dyspnea, spasm, collapse and death.
Undue toxicity: get 5 of the healthy mices of body weight 17～20 gram,, death must not be arranged in 72 hours respectively by 0.5 milliliter of tail vein injection this product; During if any death, should get 10 retrials of mice of body weight 18～19 grams in addition, all mice must not have death in 72 hours.
Acute toxicity test: 40 of mices are divided into two groups at random.One group of intramuscular injection is subjected to reagent (dividing the secondary administration) for 20 milliliters/kilogram, and another group disposable vein injection is subjected to reagent for 30 milliliters/kilogram, is subjected to the reagent amount to be equivalent to clinical adult respectively and intends with dosage 250 times and 375 times, observes continuously 7 days.The result shows: 40 mices all survive, and also do not observe tangible toxic reaction after the administration.The mice well-grown, diet is as usual, weight increase, the behavioral activity no abnormality seen, hair color is smooth.Off-test is taken off neck with mice and is put to death postmortem, and main organs such as the perusal heart, liver, spleen, lung, kidney are not seen obvious pathological change.
Determination of activity and result:
E-rosette experiment: get 4 of identical small test tubes, 2 add Hanks liquid respectively and oppose for 0.2 milliliter and look after, and 2 add test liquid respectively and make to measure pipe for 0.2 milliliter in addition.Every pipe adds 0.1 milliliter of lymphocyte suspension, and mixing is put 37 ℃ of water bath with thermostatic control activation 60 minutes.Take out, centrifugal (200g, 10 minutes), abandoning supernatant adds 0.1 milliliter of 0.5% sheep red blood cell (SRBC) suspension, shakes up.Put 37 ℃ of incubations 10 minutes, centrifugal (100g, 5 minutes), abandoning supernatant horizontally rotates mixing gently with cell, adds 0.1 milliliter of fixative, gently mixing.Put 4 ℃ of refrigerators 15 minutes.Take out, every pipe is got 1 and placed respectively on the microscope slide, and is topped in treating that dye liquor drips dyeing with the coverslip of the even dyeing liquor of cloth in advance.Count with the high power lens microscopy.All lymphocytic cell surfaces adhere to 4 above sheep red blood cell (SRBC) persons, promptly are calculated as the percentage rate of rosette cell, obtain the meansigma methods of each group.The result: the active rosette percentage rate of the active rosette percentage control tube of sample cell improves more than 10%.
MTT-LAI experiment: experiment grouping: matched group for singly add culture fluid, singly add common transfer factor, singly add tumor antigen and common transfer factor+tumor antigen; Experimental group is tumor specific transfer factor+corresponding tumor antigen.Experimental procedure: mouse spleen lymphocyte is diluted to 1 * 10 with the RPMI-1640 liquid that contains 10% calf serum
6Individual/milliliter, every hole adds Cell sap 100 microlitres in 96 porocyte culture plates.Add culture fluid or each sample by the experiment grouping again to every hole.Application of sample finishes, and in 37 ℃ of cultivations 2.5 hours, the upset orifice plate discarded supernatant in the hole with orifice plate.In each hole, add 180 microlitres then and do not contain the RPMI-1640 liquid of calf serum and the MTT solution of 20 microlitres (5 mg/ml), hatched again 4 hours for 37 ℃.Centrifugal (1000g, 15 minutes) microwell plate is abandoned supernatant, and every hole adds the blue chemical compound (Formazan) of 200 microlitre dimethyl sulfoxide to form in the dissolved cell, and room temperature was placed 15 minutes.In ELISA-reader DYNATECH MR4000 570nm colorimetric.Establish three parts in multiple hole for every group.The adhesion inhibition index is calculated as follows:
The result: the leukocyte adhesion depression effect of tumor specific transfer factor+corresponding tumor antigen group (LAI index %) is far above other each matched group (P＜0.01), the result differs highly significant, and the LAI effect that the prompting tumor specific transfer factor shifts is at corresponding tumor antigen.Illustrate: tumor specific transfer factor+corresponding tumor antigen, as gastric cancer specific transfer factor+gastric cancer antigen, pulmonary carcinoma specific transfer factor+LuCA, breast carcinoma specific transfer factor+breast cancer antigen or the like.
Claims (4)
1, the preparation method of tumor specific transfer factor is characterized in that, is made up of following step:
A. prepare antigen: prepare the cancerous tissue of required raw material for the cancer patient, preparation process is: after the homogenate, with 5000～10000 rev/mins speed after centrifugal 20～60 minutes, abandon precipitation, centrifugal 20～60 minutes again with 8000～12000 rev/mins speed, receive the supernatant degerming at last, qualitative, quantitative, packing is preserved;
B. animal immune: immunologic process is: take multiple spot subcutaneous injections such as groin, nape, abdominal cavity, and totally 8～12 points, immunity is 1 time weekly, and immunity is 4 times altogether, and first immunisation and immunity for the second time adopt antigen to add adjuvant; Antigen is only used in third and fourth time immunity.
C. prepare tumor specific transfer factor: will rub through animal spleen, the lymph node of cancer cell antigen immunity, after the homogenate, freeze thawing: solidification point is-20～-70 ℃, melt temperature is 20～30 ℃, freeze thawing 2～5 times, last low temperature dialysis, quantitative and qualitative, aseptic subpackaged.
2, the preparation method of tumor specific transfer factor according to claim 1, it is characterized in that: the homogenate condition is: 0.9%NaCL, 20mmol/L phosphate buffer (PBS)-1mmol/L disodiumedetate (EDTA-2Na) (PH7.4), or 20mmol/L Tris hydrochloric acid (TrisHCl) buffer (PH7.4).
3, the preparation method of tumor specific transfer factor according to claim 1, it is characterized in that: immune condition is: first immunisation: antigen adds the complete freund adjuvant of equivalent; Immunity for the second time: antigen adds the incomplete freund adjuvant of equivalent, and the antigen consumption is 10～30 milligrams/time; Last twice immunity: only using antigen, antigen consumption is 50～100 milligrams/time.
4, the preparation method of tumor specific transfer factor according to claim 1 is characterized in that: the dialysis condition is: with 5000～14000 dalton's bag filters, carry out under 2～10 ℃ of conditions of temperature.
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101967194A (en) * | 2010-09-14 | 2011-02-09 | 中国人民解放军第四军医大学 | Recombinant human cell restin MHD fusion protein and preparation method thereof |
| CN101314032B (en) * | 2007-05-30 | 2011-04-06 | 遵义医学院 | Preparation technique for specified transfer factor oral preparation for typhoid fever, paratyphoid fever |
| CN110616247A (en) * | 2019-08-16 | 2019-12-27 | 大连百利天华制药有限公司 | Spleen aminopeptide oral freeze-dried powder activity rapid determination method |
-
2003
- 2003-03-17 CN CNB031145434A patent/CN1179749C/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101314032B (en) * | 2007-05-30 | 2011-04-06 | 遵义医学院 | Preparation technique for specified transfer factor oral preparation for typhoid fever, paratyphoid fever |
| CN101967194A (en) * | 2010-09-14 | 2011-02-09 | 中国人民解放军第四军医大学 | Recombinant human cell restin MHD fusion protein and preparation method thereof |
| CN110616247A (en) * | 2019-08-16 | 2019-12-27 | 大连百利天华制药有限公司 | Spleen aminopeptide oral freeze-dried powder activity rapid determination method |
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| CN1179749C (en) | 2004-12-15 |
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Granted publication date: 20041215 Termination date: 20130317 |