CN107149675A - A kind of new application of interleukin 12 - Google Patents

A kind of new application of interleukin 12 Download PDF

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Publication number
CN107149675A
CN107149675A CN201610136868.3A CN201610136868A CN107149675A CN 107149675 A CN107149675 A CN 107149675A CN 201610136868 A CN201610136868 A CN 201610136868A CN 107149675 A CN107149675 A CN 107149675A
Authority
CN
China
Prior art keywords
interleukin
sag
new application
hepatitis
inactivity
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201610136868.3A
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Chinese (zh)
Inventor
张宜俊
王翠玲
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangdong Si Feng Biological Science And Technology Co Ltd
Original Assignee
Guangdong Si Feng Biological Science And Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Guangdong Si Feng Biological Science And Technology Co Ltd filed Critical Guangdong Si Feng Biological Science And Technology Co Ltd
Priority to CN201610136868.3A priority Critical patent/CN107149675A/en
Publication of CN107149675A publication Critical patent/CN107149675A/en
Pending legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/19Cytokines; Lymphokines; Interferons
    • A61K38/20Interleukins [IL]
    • A61K38/208IL-12
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/12Viral antigens
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2730/00Reverse transcribing DNA viruses
    • C12N2730/00011Details
    • C12N2730/10011Hepadnaviridae
    • C12N2730/10111Orthohepadnavirus, e.g. hepatitis B virus
    • C12N2730/10134Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein

Abstract

The invention discloses a kind of new application of interleukin 12, it is characterized in that, the purposes that described interleukin 12 treats chronic hepatitis B inactivity Sag carrier's medicines as preparing;It is intended to widen the use scope of cytokine 12, while also providing new medicine for chronic hepatitis B inactivity Sag carrier.

Description

A kind of new application of interleukin 12
Technical field
It is a kind of hepatitis B table specifically the invention discloses a kind of new application of interleukin 12 The new application of face antigen vaccine.
Background technology
There are 2,000,000,000 population infection hepatitis Bs in the whole world, wherein 2.4 hundred million be chronic HBV surface antigen (Sag) carrier.Chronic hepatitis B (CHB) some people is sluggish, but some people Hepatic sclerosis, liver cancer can be caused.
In recent years, using interferon and nucleoside analogue treatment CHB, remarkable progress, Most patients are obtained After treatment, the Cyklokapren of serum paddy third (ALT), HBVDNA, Beagle can recover in peripheral blood It is normal or switch to Sag still lasting masculins in feminine gender, but peripheral blood, it is extremely difficult to serological conversion and (anti-H's is presented It is positive).In these years, domestic and foreign scholars have proposed the concept that chronic hepatitis B feature is cured, That is, treatment chronic hepatitis B except require ALT, HBVDNA, Beagle it is steady in a long-term normal with Outside, still require that peripheral blood Sag is eliminated, and hepatitis B surface antibody, i.e. serum occur by the Sag positives turn It is changed to feminine gender, and anti-H's occurs this is also terminal or target to treatment of chronic.Reach this mesh Mark, is exactly that CHB features are cured.
The content of the invention
In view of the above-mentioned problems, being used as preparation treatment chronic type b it is an object of the invention to provide cytokine -12 The purposes of hepatitis non-active hepatitis B s antigen carries medicine, had both widened the use scope of cytokine -12, New medicine is also provided for chronic hepatitis B non-active hepatitis B s antigen carries simultaneously.
In order to solve the above technical problems, the technical scheme that the present invention is provided is such:
A kind of new application of interleukin 12, described interleukin 12 is used as preparation treatment chronic The purposes of type hepatitis non-active hepatitis B s antigen carries medicine.
It is preferred that, the new application of above-mentioned interleukin 12, described interleukin 12 joint HBsAg Specific antigen epitope peptide treats the use of chronic hepatitis B non-active hepatitis B s antigen carries medicine as preparing On the way.
It is preferred that, the new application of above-mentioned interleukin 12, described HBsAg specific antigen epitopes Peptide is HBsAg specific antigen epitope p peptides.
It is preferred that, the new application of above-mentioned interleukin 12, described hepatitis B inactivity HBsAg Carrier detction index is:HBsAg+, serum titer < 1000IU/ml, HBeAg-, HBV-DNA-.
Compared with existing, technical scheme provided by the present invention uses interleukins - 12 (interleukin-12, IL-12) are used as preparation treatment chronic hepatitis B non-active hepatitis B s antigen carries It is chronic as treatment is prepared that medicine, particularly interleukin 12 combine HBsAg specific antigen epitopes peptide The medicine of hepatitis B non-active hepatitis B s antigen carries, to treat chronic hepatitis B inactivity HBsAg The treatment of carrier provides new medicine;And from the point of view of the result of pharmacodynamic experiment, to treating acute put That penetrates disease has good effect.
Brief description of the drawings
Fig. 1 is that HBsAg specificity P peptides joint rhIL-12 induction human PBMCs s produces IFN-γ amount curve Figure.
Embodiment
With reference to embodiment, the claim to the present invention is described in further detail, but not Any limitation of the invention is constituted, any limited number of time done in the claims in the present invention protection domain Modification, still within the claims of the present invention.
Experimental example 1
The mouse hepatitis B model set up using hydrodynamic(al) force method, HBV virus particles are injected from experiment mice tail vein 42 days afterwards, hepatitis B model is set up, peripheral blood continuous expression HBsAg is positive, and titre is in 50-200IU/ml.
HBsAg specificity P polypeptides (synthetic method) 1~30 μ g/ml;RhIL-12 0.5-4ng/ml, respectively or Joint and the PBMC of Healthy People and Peripheral Blood in Patients with Chronic Hepatitis B are cultivated 72 hours, are collected and are detected supernatant IFN-γ level (ELISA), as a result See Figure 1, points out HBsAg specificity P peptides joint rhIL-12 can be non- A large amount of IFN-γs are significantly often induced, are conducive to promoting HBsAg serological conversions.
Experimental example 2
24, the mouse hepatitis B model set up using hydrodynamic(al) force method, to send out three groups, saline control group, IL-12 Group, P peptides joint rhIL-12 groups, IL-12 and P peptides are to be subcutaneously injected, and once in a week, totally three weeks, are stopped Observation post administration 5 weeks, weekly observation experiment mouse peripheral blood HBsAg levels.
As a result show:HBsAg specificity P peptides joint IL-12, which has, significantly promotes HBsAg serological conversions to act on.
Above-described is only presently preferred embodiments of the present invention, all institutes in the range of the spirit and principles in the present invention Any modifications, equivalent substitutions and improvements made etc., should be included in the scope of the protection.

Claims (4)

1. a kind of new application of interleukin 12, it is characterised in that described interleukin 12 conduct Prepare the purposes for the treatment of chronic hepatitis B inactivity Sag carrier's medicines.
2. the new application of interleukin 12 according to claim 1, it is characterised in that described Interleukin 12 combines Sag specific antigen epitopes peptide as preparation and treats chronic hepatitis B inactivity The purposes of Sag carrier's medicines.
3. the new application of interleukin 12 according to claim 3, it is characterised in that described Sag specific antigen epitopes peptide is Sag specific antigen epitope p peptides.
4. the new application of interleukin 12 according to claim 1 or 2, it is characterised in that institute The hepatitis B inactivity Sag carrier detction indexs stated are:Sag+, serum titer < 1000IU/ml, Beagle-, HBV-DNA-.
CN201610136868.3A 2016-03-10 2016-03-10 A kind of new application of interleukin 12 Pending CN107149675A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610136868.3A CN107149675A (en) 2016-03-10 2016-03-10 A kind of new application of interleukin 12

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610136868.3A CN107149675A (en) 2016-03-10 2016-03-10 A kind of new application of interleukin 12

Publications (1)

Publication Number Publication Date
CN107149675A true CN107149675A (en) 2017-09-12

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610136868.3A Pending CN107149675A (en) 2016-03-10 2016-03-10 A kind of new application of interleukin 12

Country Status (1)

Country Link
CN (1) CN107149675A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1636063A (en) * 2001-11-01 2005-07-06 健方公司 Genetic vaccine against human immunodeficiency virus
CN101361969A (en) * 2008-01-29 2009-02-11 广州市恺泰生物科技有限公司 Therapeutic hepatitis b vaccine and preparation method and use thereof
CN106581672A (en) * 2015-10-15 2017-04-26 广东思峰生物科技有限责任公司 RhIL-12 containing medicine composition for treating non-active hepatitis B

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1636063A (en) * 2001-11-01 2005-07-06 健方公司 Genetic vaccine against human immunodeficiency virus
CN101361969A (en) * 2008-01-29 2009-02-11 广州市恺泰生物科技有限公司 Therapeutic hepatitis b vaccine and preparation method and use thereof
CN106581672A (en) * 2015-10-15 2017-04-26 广东思峰生物科技有限责任公司 RhIL-12 containing medicine composition for treating non-active hepatitis B

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Application publication date: 20170912