Intranasal hepatitis B vaccine composition and method for producing same

Abstract

The present invention provides a hepatitis B vaccine composition for simpler administration via a nasal mucosal spray, which does not require combined use with other administration routes such as subcutaneous administration and does not contain auxiliary components such as adjuvants that may be toxic, a method for producing the same, and methods for treating and preventing hepatitis B. [Solution] A hepatitis B vaccine composition for nasal mucosal spray administration is provided, which comprises a gel base containing a hepatitis B antigen and a carboxyvinyl polymer, and is applicable to the prevention and treatment of hepatitis B.

Description

[Technical field]

[0001] The present invention relates to a hepatitis B vaccine composition for administration by nasal mucosal spray for use in the prevention and treatment of hepatitis B, and a method for producing the same. [Background technology]

[0002] Hepatitis B is a liver disease caused by infection with the hepatitis B virus (HBV), which is transmitted through blood and bodily fluids. Persistent infection of liver cells with HBV can lead to chronic hepatitis, liver cirrhosis, and hepatocellular carcinoma.

[0003] Currently, interferon preparations (IFN) and nucleic acid analogues (NA) are mainly used to treat chronic hepatitis B (CHB). Although IFN has been shown to be effective in some cases in strengthening immunity and effectively sustaining the inhibition of viral proliferation, the HBV elimination rate is generally low and its strong side effects are also a major problem. On the other hand, NA has a high HBV elimination rate of about 95%, but it does not provide a cure and requires lifelong administration, which leaves major problems in terms of compliance and medical economics. It has also been reported that long-term use may lead to the emergence of resistant viruses. Therefore, the development of a new treatment method for CHB was required.

[0004] On the other hand, in Japan, to prevent HBV infection, preventive vaccines are administered to those at high risk of infection (HBV carrier families, medical workers), and some success has been achieved in significantly reducing the number of HBV carriers. On the other hand, immunotherapy using HBV vaccines has been tried as a treatment for CHB, but sufficient therapeutic effects have not yet been achieved.

[0005] HBV has multiple antigens, and the present inventors have attempted immunotherapy focusing on HBs antigen (hepatitis B surface antigen), which induces neutralizing antibodies. In addition, recent advances in research have revealed that acquired immunity against HBc antigen (hepatitis B nucleocapsid antigen) contributes to the inhibition of HBV proliferation and elimination. In this context, the Cuban Institute of Biotechnology and Medical Engineering (CECMED) developed a nasal therapeutic vaccine containing two types of antigens, HBs antigen and HBc antigen, which underwent clinical trials in Bangladesh and was successfully commercialized as HeberNasvac (registered trademark, Non-Patent Document 1). However, as the immune response is insufficient with nasal administration alone, two cycles of vaccination, including subcutaneous administration, are required, and it is not a completely mucosal vaccine for nasal administration.

[0006] As described above, there was a strong desire for a versatile intranasal vaccine formulation for the next generation of HBV vaccines for both therapeutic and preventive purposes; however, this has not yet been fully realized because it has been difficult to obtain a sufficient immune response. [Prior art documents] [Patent documents]

[0007] [Patent Document 1] WO2007 / 123193 [Non-patent literature]

[0008] [Non-Patent Document 1] HeberNasvac Package Insert Summary of the Invention [Problem to be solved by the invention]

[0009] The object of the present invention is to provide a hepatitis B vaccine composition for simpler administration by nasal mucosal spray, which does not require combination with other administration routes such as subcutaneous administration and does not contain auxiliary components such as adjuvants that may be toxic, a method for producing the same, and a method for treating and preventing hepatitis B. [Means for solving the problem]

[0010] In view of the above problems, the present inventors have conducted extensive research and found that a gel base for nasal mucosal spray administration consisting of a carboxyvinyl polymer treated with external shear force to impart spraying properties can be administered via nasal administration of two antigens, HBs antigen and HBc antigen, without the use of an adjuvant, and have thus completed the present invention.

[0011] [1] (i) Hepatitis B surface antigen (HBsAg) and / or hepatitis B nucleocapsid antigen (HBcAg), and (ii) A gel base containing a carboxyvinyl polymer that has been treated with an external shear force to impart sprayability. A hepatitis B vaccine composition for nasal mucosal spray administration comprising:

[0012] [2] The hepatitis B vaccine composition for administration by nasal mucosal spray according to [1], wherein the hepatitis B vaccine (i) is 0.01 to 10 mg / mL per antigen.

[0013] [3] A hepatitis B vaccine composition for nasal mucosal spray administration described in [1] or [2], which contains 0.1 w / v% to 1.0 w / v% carboxyvinyl polymer.

[0014] [4] A Hepatitis B vaccine composition for nasal mucosal spray administration described in any one of [1] to [3], which uses a gel base for spray administration containing a carboxyvinyl polymer that has been treated by applying external shear force to add spray performance such as (1) formulation particle size distribution range, (2) spray density uniformity, and / or (3) spray angle control.

[0015] [5] A hepatitis B vaccine composition for nasal mucosal spray administration described in any of [1] to [4], which is obtained by using a gel base containing 0.5 w / v% to 2.0 w / v% carboxyvinyl polymer, and obtaining a gel base for spray administration containing a carboxyvinyl polymer that has been treated by applying external shear force to add spray performance such as (1) the range of formulation particle size distribution, (2) uniformity of spray density, and / or (3) spray angle control, and then uniformly mixing the gel base with a virus stock solution containing HBs antigen and HBc antigen in a short period of time without applying stress.

[0016] [6] A hepatitis B vaccine composition for nasal mucosal spray administration described in any of [1] to [5], which is produced using a gel base for spray administration that is provided with spray performance such that (1) in the particle size distribution of the formulation, the average particle size of the formulation is in the range of 50 μm to 120 μm, and 50% or more of the particle size distribution is in the range of 10 μm to 100 μm, (2) the spray density becomes an even full cone without bias, and (3) the spray angle is controlled in the range of 30° to 70° by applying an external shear force to a base containing a carboxyvinyl polymer.

[0017] [7] A hepatitis B vaccine composition for nasal mucosal spray administration described in any of [1] to [5], which is produced using a gel base for spray administration that is provided with spray performance such that (1) in the particle size distribution of the formulation, the average particle size of the formulation is in the range of 70 μm to 100 μm and 60% or more of the particle size distribution is in the range of 10 μm to 100 μm, (2) the spray density becomes an even full cone without bias, and (3) the spray angle is controlled in the range of 40° to 60° by applying an external shear force to a base containing a carboxyvinyl polymer.

[0018] [8] A Hepatitis B vaccine composition for nasal mucosal spray administration described in any one of [1] to [7], which uses a gel base for spray administration containing a carboxyvinyl polymer that has been treated by applying external shear force to add (1) a formulation particle size distribution range, (2) spray density uniformity, and (3) spray angle control, so as to enable spray administration using a sprayable device without a pump function.

[0019] [9] A method for preventing and / or treating hepatitis B, comprising administering to a subject in need thereof a hepatitis B vaccine composition for nasal mucosal spray administration described in any one of [1] to [8], using a device capable of spraying a viscous formulation onto the intranasal mucosa from each nostril.

[0020]

[10] Use of the hepatitis B vaccine composition for nasal mucosal spray administration described in any one of [1] to [8] for treating and / or preventing hepatitis B. Effect of the Invention

[0021] According to the present invention, it is possible to provide a hepatitis B vaccine composition for nasal mucosal spray administration that does not require combination with other administration routes such as subcutaneous administration and does not require the use of adjuvants, since a vaccine composition containing HBs antigen and HBc antigen as active ingredients can induce an effective immune response with a small amount of antigen. In addition, as a formulation that is easy to administer and has few side effects, it can be used not only to prevent hepatitis B, but also to treat chronic hepatitis B because it can obtain a sufficient immune response, and its strong activity is expected to lead to a complete cure of CHB through continuous administration. [Brief description of the drawings]

[0022] [Figure 1] The results of the immune response analysis test are shown below, showing the results of neutralizing antibody titers measured one week after the final vaccination. In the graph, "sc" means subcutaneous vaccination, and "in" means intranasal vaccination. The base refers to CVP treated by applying external shear force, (-) means base that does not contain it, and (+) means base that contains it. [Diagram 2] The results of the immune response analysis test are shown below, showing the results of measuring IgA antibodies taken one week after the final vaccination. In the graph, "sc" means subcutaneous vaccination, and "in" means intranasal vaccination. The base refers to CVP treated by applying external shear force, (-) means base that does not contain it, and (+) means base that contains it. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0023] The present invention provides a hepatitis B vaccine composition for nasal mucosal spray administration, which contains a gel base for nasal mucosal spray administration consisting of a carboxyvinyl polymer that has been treated by applying external shear force to impart spraying properties, and a hepatitis B antigen.

[0024] The term "gel base containing a carboxyvinyl polymer treated by applying shear force from the outside to impart spraying performance" used in the present invention means, for example, the "gel base containing a skin / mucosa adhesive" disclosed in WO2007 / 123193, which is a base containing a carboxyvinyl polymer and gellan gum as appropriate, and whose viscosity has been adjusted by applying shear force from the outside. The specific shear force from the outside described in WO2007 / 123193 is not merely stirring or shaking, but is applied by a device that applies shear force known to those skilled in the art, and specifically, a high-speed rotary emulsifier, a colloid mill type emulsifier, a high-pressure emulsifier, a roll mill type emulsifier, an ultrasonic emulsifier, and a membrane type emulsifier can be used. In particular, high-speed rotary emulsifiers of the homomixer type, comb type, and intermittent jet flow generating type are preferred. Such a base is characterized in that it can be adjusted to various viscosities by applying shear force from the outside, and the spray angle and spray density from the spray container can be controlled to suit the purpose.

[0025] The device used for administration by spraying is not limited to any commonly used nasal device, and the composition of the present invention can be used with a sprayable device without a pump function. For example, by using an upward pressure airless spray container as a multi-dose spray container as described in WO2007 / 123193 (see Figures 1 and 2) and WO2007 / 123207 (see Figures 1 to 11), the spray container can be used without remaining in the container at any angle or range of angles, and its usage form is suitable for vaccination of a large number of people in developing countries. In addition, as a disposable type device limited to use for one vaccinator, a nasal spray nozzle disclosed in WO 2015 / 199130 (see Figures 1 to 4) can be used. In the present invention, the hepatitis B virus antigen administered using such a spray administration device is spread over a wide area for a long time on the nasal mucosa, thereby enhancing the immunogenicity of the vaccine.

[0026] Carboxyvinyl polymer, which is the raw material of the base for nasal mucosal spray administration, is a hydrophilic polymer obtained by polymerization of acrylic acid as the main component, and pharmaceutical additives that are commonly used to prepare aqueous gels can be used without any restrictions. The content of the gel base containing a carboxyvinyl polymer that has been treated by applying external shear force to impart spraying performance is 0.1 to 1.0% w / v, calculated as the carboxyvinyl polymer content, and preferably 0.3 to 0.7 w / v%.

[0027] The vaccine of the present invention is characterized in that it contains both or either of the surface type (HBs antigen) and core type (HBc antigen) of hepatitis B virus antigen as antigen. The hepatitis B virus antigen used in the present invention refers to the hepatitis B virus surface antigen and hepatitis B nucleocapsid antigen produced by yeast using recombinant DNA technology. The hepatitis B virus antigen is used in a purified or concentrated virus stock solution for mixing with a gel base for nasal mucosal spray administration. The vaccine of the present invention preferably has a hepatitis B virus antigen concentration of 0.01 to 10 mg / mL, more preferably 0.05 to 5 mg / mL, per vaccine antigen. Hepatitis B virus surface antigen (HBsAg) is a particle (approximately 50-60 nm in diameter) that displays many antigenic proteins on a lipid membrane. The displayed antigenic protein is originally a protein composed of three domains (S, Pre-S1, Pre-S2), and antigens that possess all three domains are classified as L-type antigens (HBsAg L-protein), M-type antigens that lack Pre-S1, and S-type antigens that lack both Pre-S1 and Pre-S2 (HBsAg S-protein). In both cases, antigens are produced using genetically modified yeast.

[0028] Adjuvants are a general term for substances that have regulatory activity such as strengthening or suppressing immune responses. They are immune enhancers added to vaccines to increase the immunogenicity of antigens, and many substances have been investigated so far. On the other hand, while the use of adjuvants improves the immune effect of vaccines, they also have the disadvantage of causing side effects such as inflammation. Naturally, there are several candidates for adjuvants for nasal vaccines, but since there are no adjuvants whose safety has been widely recognized, nasal vaccines containing adjuvants whose efficacy and safety have been established have not yet been approved.

[0029] In the present invention, in the method of mixing the gel base for spray administration with the virus stock solution, "without applying stress" means that heat, pressure, etc. are not applied and high speed stirring is not performed.

[0030] The present inventors have discovered a nasal mucosal spray hepatitis B vaccine composition that, by using a gel base for nasal mucosal spray administration having excellent spraying performance and a high nasal mucosa spreading rate as described above, for the hepatitis B vaccine, makes it possible to obtain an effective vaccine with fewer side effects and with a smaller amount of antigen without the need for concomitant use with other administration routes such as subcutaneous administration and without the use of adjuvants, and that, by combining with a device that enables spraying even with a highly viscous gel base, enables the sprayed formulation to have an average particle size in an appropriate range of 50 μm to 120 μm (preferably, 70 μm to 100 μm), a formulation particle size distribution with 50% or more in the range of 10 μm to 100 μm (preferably, 60% in the range of 10 μm to 100 μm), a spray angle from the device in the range of 30° to 70° (preferably, 40° to 60°) so that the formulation can be administered to a required site in the nasal cavity, and a spray density that is evenly distributed in the full cone into the nasal cavity, and have discovered a method for producing the composition, as well as a preventive method and a therapeutic method using the composition, thereby completing the present invention.

[0031] In the present invention, a "full cone", which represents a uniform spray density without any bias in the spray density, is one of the spray pattern shapes and means a homogeneous circular entire area, while the opposite term is a donut-shaped "hollow cone" which is localized only to the periphery.

[0032] The vaccine of the present invention may further contain a medicamentously acceptable carrier in addition to the hepatitis B virus antigen and the gel base for nasal mucosa spray administration. The carrier may be a carrier that is commonly used in the manufacture of vaccines and intranasal administration preparations, and specifically includes saline, buffered saline, dextrose, water, glycerin, isotonic aqueous buffer, and combinations thereof. In addition, a preservative (e.g., thimerosal), an isotonic agent, a pH adjuster, a surfactant, a stabilizer (e.g., sodium edetate hydrate), an inactivator (e.g., formalin), etc. may be appropriately mixed therein.

[0033] The dosage is determined taking into consideration the age, sex, weight, etc. of the subject, but the antigen can be usually 0.1 to 100 μg, preferably 0.5 to 10 μg, per antigen, administered once or twice or more times. Multiple administrations are preferred, and in this case, administration is preferably performed at intervals of 1 to 4 weeks. EXAMPLES

[0034] The present invention will be described in detail below with reference to examples, but the present invention is not limited to these examples in any way.

[0035] A gel base and a stock solution of hepatitis B virus were prepared by the methods described below, and the two were mixed as follows to prepare a hepatitis B vaccine composition. [Preparation of gel base] Gel base example 1 TIFF0007618632000001.tif54155

[0036] [Virus stock solution containing hepatitis B virus antigen] Virus stock solution example 1 TIFF0007618632000002.tif51153

[0037] Virus stock solution example 2 TIFF0007618632000003.tif51153

[0038] [Mixing gel base and virus stock solution] The above virus stock solution example 1 and virus stock solution example 2 (ratio 1:1) and gel base example 1 were mixed and stirred to obtain a homogeneous intranasal hepatitis B vaccine composition (Example 1 and Example 2). This mixing and stirring can be achieved in a short time by gentle mixing and stirring without applying stress such as heat or pressure to the hepatitis B vaccine antigen. The component amounts and physical property values ​​of the obtained influenza vaccine composition, as well as the added spray performance when sprayed using an appropriate device, are shown below.

[0039] Example 1 TIFF0007618632000004.tif84155

[0040] Example 2 TIFF0007618632000005.tif84155

[0041] A gel base-free nasal hepatitis B vaccine composition was prepared having the following composition: Comparative Example 1 TIFF0007618632000006.tif57153

[0042] Comparative Example 2 TIFF0007618632000007.tif57153

[0043] Immune response analysis test The nasal hepatitis B virus vaccine compositions prepared in Examples 1 and 2, and Comparative Examples 1 and 2 were evaluated for their antibody induction ability as follows, using tree shrews as experimental animals. (Antibody induction in specimens) As specimens, tree shrews (Tupaia belangeri, purchased from Kunming Institute of Zoology, Chinese Academy of Sciences) were randomly divided into 4 groups, 2 groups of 4 or 3 animals each, and antibody induction was performed by nasal administration in the 4 animals group in Example 1 and Example 2, and in the 3 animals group in Comparative Example 1 and Comparative Example 2. For nasal administration, a high-pressure syringe and a liquid spray device were used, and 0.05 mL was sprayed into each nostril (10 μg antigen in total for both nostrils) in each nostril. After the first vaccination, a total of 5 vaccinations were performed at 2-week intervals, and then another vaccination was performed again 4 weeks later. Blood samples were taken at the time of each vaccination and 1 week after the final vaccination, and neutralizing antibody titers were measured and evaluated. Separately, two groups of three treeshrews were prepared, and 0.1 mL (10 μg of each antigen) of Comparative Example 1 and Comparative Example 2 were subcutaneously administered to the back of each tree shrew. The administration was continued in the same manner as in the case of intranasal administration described above, and blood was collected.

[0044] (Measurement of neutralizing antibody titer and serum IgA antibody) The virus solution used to measure the neutralizing antibody titer was prepared by infecting and culturing primary human hepatocytes (PXB cells, Phoenix Bio) with genotype C (C_JPNAT) hepatitis B virus. HepG2-NTCP30 cells were used for the neutralization test, and the neutralizing antibody titer was measured according to the standard method. In addition, serum IgA antibodies against various antigens were detected and measured by ELISA.

[0045] (result) The results of measuring the neutralizing antibody titer and IgA antibody one week after the final vaccination are shown in Table 1 and Figures 1 and 2. Nasal vaccination had a higher antibody induction ability than subcutaneous vaccination, while in nasal vaccination, Examples 1 and 2, which used carboxyvinyl polymer (CVP) treated with external shear force as the base, showed significantly higher antibody induction ability than Comparative Examples 1 and 2, which did not use CVP. [Table 1] TIFF0007618632000008.tif69170

Claims

1. (i) both the hepatitis B surface antigen (HBs antigen) and the hepatitis B nucleocapsid antigen (HBc antigen); and (ii) A gel base containing a carboxyvinyl polymer that has been treated with an external shear force to add sprayability. A hepatitis B vaccine composition for nasal mucosal spray administration for treating hepatitis B, comprising:

2. 2. The hepatitis B vaccine composition for administration via a nasal mucosal spray according to claim 1, wherein the hepatitis B vaccine (i) is present at a concentration of 0.01 to 10 mg / mL per antigen.

3. 3. The hepatitis B vaccine composition for nasal mucosal spray administration according to claim 1 or 2, which contains 0.1 w / v % to 1.0 w / v % of a carboxyvinyl polymer.

4. 4. The hepatitis B vaccine composition for nasal mucosal spray administration according to any one of claims 1 to 3, which uses a gel base for spray administration containing a carboxyvinyl polymer that has been treated by applying shear force from the outside in order to add spray performance such as (1) a range of particle size distribution of the formulation, (2) uniformity of spray density, and / or (3) spray angle control.

5. 5. The hepatitis B vaccine composition for nasal mucosal spray administration according to claim 1, which is obtained by using a gel base containing 0.5 w / v % to 2.0 w / v % carboxyvinyl polymer, treating the gel base for spray administration containing carboxyvinyl polymer by applying external shear force in order to add spray performance such as (1) the range of formulation particle size distribution, (2) uniformity of spray density, and / or (3) spray angle control, and then uniformly mixing the gel base with a virus stock solution containing HBs antigen and HBc antigen in a short period of time without applying stress.

6. 6. A hepatitis B vaccine composition for nasal mucosal spray administration according to any one of claims 1 to 5, which uses a gel base for spray administration containing a carboxyvinyl polymer that has been treated by applying shear force from the outside to add (1) a range of formulation particle size distribution, (2) uniformity of spray density, and (3) spray angle control, so as to enable spray administration using a sprayable device without a pump function.

7. A hepatitis B vaccine composition for nasal mucosal spray administration according to any one of claims 1 to 6, characterized in that it is administered using a device that enables a viscous formulation to be sprayed onto the intranasal mucosa through the nostrils.

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