WO2010098429A1 - 免疫アジュバント組成物、及びその利用 - Google Patents
免疫アジュバント組成物、及びその利用 Download PDFInfo
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- WO2010098429A1 WO2010098429A1 PCT/JP2010/053051 JP2010053051W WO2010098429A1 WO 2010098429 A1 WO2010098429 A1 WO 2010098429A1 JP 2010053051 W JP2010053051 W JP 2010053051W WO 2010098429 A1 WO2010098429 A1 WO 2010098429A1
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Definitions
- the present invention relates to an immune adjuvant composition, a vaccine composition, a non-human animal immunization method, an active immune cell preparation, and a production method thereof.
- Adjuvants are administered in admixture with vaccine antigens to activate innate immunity or to induce antigen-specific immune responses by presenting antigens.
- Various adjuvants are known for animal experiments.
- As an adjuvant made of a general compound not derived from living organisms, for example, sodium hydroxide, aluminum hydroxide, calcium phosphate, alum, carboxyvinyl polymer, etc. are used as adjuvants by utilizing the property of adsorbing antigens such as pathogens. .
- these precipitation adjuvants tend to harden at the site of inoculation.
- liquid paraffin, lanolin, Freund and the like are used as adjuvants by utilizing the property that an oily substance wraps an aqueous antigen solution to form micelles.
- oil-based adjuvants and vaccine antigens becomes an emulsion containing micelles, it is highly viscous, causes pain at the time of inoculation, and the inoculation site tends to harden.
- Patent Document 1 discloses a nucleic acid / polysaccharide complex comprising a CpG oligonucleotide having a natural phosphodiester backbone and a poly (dA) tail, and a ⁇ -1,3-glucan having a molecular weight of 25000 or more. It has been suggested that the body can promote the production of cytokines and antibodies that dominate Th1 cell activity and can be used as an immune adjuvant.
- the main object of the present invention is to provide a novel immune adjuvant composition.
- the present inventor repeated researches to solve the above-described problems, and obtained the following knowledge.
- (i) In homo knockout mice (Zc3h12a ⁇ / ⁇ mice) in which the Zc3h12a gene was disrupted, the number of plasma cells increased and lung infiltration was observed. In addition, the serum immunoglobulin concentration increased and autoantibody production was observed.
- Most Zc3h12a ⁇ / ⁇ mouse splenic T cells also showed effector / memory properties and produced interferon ⁇ in response to T cell receptor stimulation. Thus, destruction of Zc3h12a activated the acquired immune system and increased plasma cells and memory T cells.
- the Zc3h12a gene has a region presumed to be an N-terminal nuclease region and expressed a protein exhibiting ribonuclease activity.
- Zc3h12a ⁇ / ⁇ mice lack the ribonuclease activity of Zc3h12a, which suppresses mRNA degradation of molecules containing specific cytokines. Production is enhanced. (v) Therefore, an inhibitor of the Zc3h12a gene or Zc3h12a protein can be suitably used as an immune adjuvant.
- the present invention has been completed based on the above findings, and provides the following immune adjuvant composition, vaccine composition, activated immune cell preparation and production method thereof.
- Item 1. An immune adjuvant composition comprising as an active ingredient at least one selected from the group consisting of a Zc3h12a gene inhibitor and a Zc3h12a protein inhibitor.
- Item 2. Furthermore, the immune adjuvant composition of claim
- a vaccine composition comprising at least one selected from the group consisting of a Zc3h12a gene inhibitor and a Zc3h12a protein inhibitor, and a vaccine antigen.
- Item 4. Item 4. The vaccine composition according to Item 3, further comprising another immune adjuvant.
- Item 5. Item 5.
- a method for immunizing an animal comprising administering the vaccine composition according to Item 3 or 4 to a non-human animal.
- Item 6. A method for producing active immune cells, comprising a step of bringing immune cells collected from an individual into contact with at least one selected from the group consisting of a Zc3h12a gene inhibitor and a Zc3h12a protein inhibitor to activate the immune cells.
- Item 7. Item 7. An active immune cell produced by the method according to item 6.
- Item 8. At least one compound selected from the group consisting of a Zc3h12a gene inhibitor and a Zc3h12a protein inhibitor for increasing the immunogenicity of a vaccine antigen.
- Item 10 A method for enhancing the immunogenicity of a vaccine antigen, comprising a step of mixing the vaccine antigen with at least one member selected from the group consisting of a Zc3h12a gene inhibitor and a Zc3h12a protein inhibitor.
- Item 11 A composition comprising at least one member selected from the group consisting of a Zc3h12a gene inhibitor and a Zc3h12a protein inhibitor for immunostimulation and a vaccine antigen.
- Item 12 Use of a composition comprising at least one selected from the group consisting of a Zc3h12a gene inhibitor and a Zc3h12a protein inhibitor and a vaccine antigen for the production of a vaccine composition.
- the immune adjuvant composition of the present invention activates acquired immunity in addition to natural immunity by inhibiting the function of the Zc3h12a gene or Zc3h12a protein.
- Conventional adjuvants mainly activate only innate immunity, but the immune adjuvant composition of the present invention activates not only innate immunity but also acquired immunity, and thus becomes a powerful adjuvant.
- it since it is an inhibitor of the Zc3h12a gene or Zc3h12a protein, it can be a nucleic acid such as siRNA or a low molecular weight compound, and a highly safe one can be designed.
- a is a schematic diagram of a mouse Zc3h12a gene (Wild-type allele), a targeting vector (Targeting construct), and a targeted allele.
- b is a figure which shows the result of the Southern blot analysis of the offspring of the heterozygous hybridization.
- (c) shows the results of RT-PCR analysis of wild-type (WT) and Zc3h12a ⁇ / ⁇ macrophage RNA stimulated with LPS.
- a is a figure which shows the result of having investigated the survival rate of the wild type (Zc3h12a ⁇ + / +> ) and Zc3h12a ⁇ -/-> mouse
- b is a histological photograph of sections of spleen (upper), mesenteric lymph node (lower left) and inguinal lymph node (lower right) of wild type and Zc3h12a ⁇ / ⁇ mice.
- c is a histological photograph of lung, spleen and lymph node tissues of wild type and Zc3h12a ⁇ / ⁇ mice.
- FIG. 6 is a histological photograph of liver and pancreas sections of wild type (WT) and Zc3h12a ⁇ / ⁇ mice. It is a figure which shows the measurement result of serum immunoglobulin level (a) in Zc3h12a ⁇ / ⁇ mouse, the production (b) of antinuclear antibody and anti-double-stranded DNA antibody, and the result (c) of histological study. It is a figure which shows the result of having dye
- FIG. 1 It is a figure which shows the result of having dye
- a is a figure which shows the result of having measured the IL-6, IL-12p40, and TNF density
- b is a figure which shows the result of having investigated the expression of IL-6, KC, TNF, I ⁇ B ⁇ , RANTES, IP-10, and ⁇ -actin by Northern blot using LPS-stimulated macrophage-derived RNA.
- FIG. 6 is a heat map representation of the expression of LPS-inducible genes selected based on microarray analysis of wild-type and Zc3h12a ⁇ / ⁇ peritoneal macrophages.
- FIG. 6 is a heat map display and dendrogram obtained as a result of microarray analysis of LPS-inducible genes in wild type and Zc3h12a ⁇ / ⁇ macrophages. It is a figure which shows the result of having measured the transcription factor-DNA binding activity in the nuclear extract of Zc3h12a -/- macrophage stimulated with LPS by electrophoretic mobility shift analysis (EMSA).
- ESA electrophoretic mobility shift analysis
- a is a figure which shows the result of the Northern blot analysis which investigated the destabilization mechanism of mRNA of Zc3h12a.
- b is a figure which shows the time-dependent change of a residual mRNA level.
- HEK293 Tet-off cells were transduced with plasmids, and Northern blot analysis was performed to determine the Zc3h12a response region in the 3′-UTR of IL-6 (a) and time course of residual mRNA levels
- It is a figure (b) which shows the result of having investigated.
- It is a schematic diagram of 3'-UTR of IL-6 and its deletion construct.
- It is a figure which shows the result of having measured the luciferase activity in order to investigate stability of RNA.
- FIG. 2 is a schematic diagram of IL-6 3′-UTR and a construct lacking it. It is a figure which shows the result of having investigated the coupling
- FIG. 2 is a diagram (a) showing the results of measuring the expression of IL-6 by Northern blot analysis and a diagram (b) showing the results of examining the time course of residual mRNA levels.
- the immunoadjuvant composition of the present invention contains as an active ingredient at least one selected from the group consisting of an inhibitor of the Zc3h12a gene and an inhibitor of the Zc3h12a protein.
- Zc3h12a gene Toll-like receptor is a receptor that recognizes microbial components and causes inflammation and immune responses. TLR stimulation activates complex gene expression that controls the magnitude and duration of the immune response. Zc3h12a gene is a modifier of immune response induced by TLR stimulation.
- the nucleotide sequence is registered as accession number NM_025079 in NCBI.
- the inhibitors of Zc3h12a gene may be one which inhibits the expression of Zc3h12a gene, the low molecular compounds, nucleic acids, proteins, glycoproteins and the like.
- low molecular weight compounds are preferable because they are easy to use as pharmaceuticals.
- nucleic acids such as siRNA, shRNA, and stRNA are also preferable because they are easy to design and have low toxicity.
- the design methods of siRNA and shRNA are well known, for example, “Elbashir, SM, Harborth, J., Lendeckel, W., Yalcin, A., Weber, K., and Tuschl, T. (2001).
- RNAs mediate RNA interference in cultured mammalian cells. Nature 411, 494-498. ”And“ Paddison, PJ, Caudy, AA, Sachidanandam, R. & Hannon, GJ Short hairpin activated gene silencing in mammalian cells Methods Mol. Biol. 265, 85-100 (2004) ”. It can also be obtained by requesting ABI or Dharmacon.
- An inhibitor of the Zc3h12a gene can be screened, for example, by the following method.
- a test substance whose expression level is reduced may be screened by luciferase assay or fluorescence detection.
- test cells introduced with a Zc3h12a gene expression plasmid containing regulatory regions and structural genes are brought into contact with the test substance, and the test substances whose Zc3h12a gene expression level decreases due to contact are screened by Western blotting or Northern blotting. You can also
- Inhibitors of Zc3h12a protein The inhibitors of Zc3h12a protein only need to inhibit the activity of this protein, and examples thereof include low molecular weight compounds, nucleic acids, proteins, glycoproteins and the like. In particular, low molecular weight compounds are preferable because they are easy to use as pharmaceuticals.
- the degree of RNA degradation activity may be compared in the presence and absence of a test substance, and a substance that reduces RNA degradation activity may be selected. Specifically, first, first, a human Zc3h12a recombinant protein is synthesized.
- the human Zc3h12a gene (NCBI Accession number NM_025079) is incorporated into a plasmid such as pGEX-6P1, and E. coli BL21-Gold (DE3) pLysS (Stratagene) is transformed to express the protein. After protein expression, the cells were collected and resuspended in PBS. Lyse the cells by sonication, add Triton X-100 to a final concentration of 1% and incubate for 30 minutes at 4 ° C. with gentle shaking. The debris is then removed by centrifugation and the supernatant is incubated with Glutathion Sepharose 4B (GE Healthcare) for 30 minutes at 4 ° C. with gentle shaking.
- Glutathion Sepharose 4B GE Healthcare
- RNA homologous to the sequence of the 3′-UTR conserved domain of IL-6 is synthesized using an in vitro transcription method. Label with [ 32 P] -labeled RNA (5000 cpm) during in vitro transcription.
- RNA and the Zc3h12a protein were mixed with 5 mM Mg (Oac) 2 in the presence of cleavage buffer (25 mM Hepes, 50 mM KOAc, 5 ⁇ M DTT) and Rnasin plus (40U) (Promega). Mix with or without.
- the cleaved RNA is purified by TRIzol (InvitroGen) and analyzed by denaturing PAGE and autoradiography using 6% TBE-Urea gel (InvitroGen).
- the cleaved RNA can be detected as RNA that migrates earlier.
- a test substance may be allowed to act on this system to screen for a substance whose cleavage activity decreases.
- Inhibitors of the Zc3h12a protein can be screened by other methods.
- a Zc3h12a gene expression plasmid and a test substance introduced with a plasmid in which 3′-UTR of a gene such as IL-6 is arranged downstream of a gene expressing luciferase or a fluorescent protein are brought into contact with the test substance by contact.
- a test substance in which the expression level of the Zc3h12a gene decreases may be screened by luciferase assay or fluorescence detection.
- the concentration of the inhibitor in the pharmaceutical immunoadjuvant composition varies depending on the type of the inhibitor, but may be, for example, about 10 ⁇ g / ml to 100 mg / ml.
- the immune adjuvant composition may be in the form of a sterile aqueous or non-aqueous solution, suspension or emulsion. Further, it may contain a pharmaceutically acceptable diluent such as a salt and a buffer, an auxiliary agent, a carrier and the like.
- the immunoadjuvant composition of the present invention may be ingested in a state of being included in human food or drink, animal drinking water or food. That is, the immune adjuvant composition of the present invention includes a food and drink composition.
- the inhibitor concentration in the food and drink may be, for example, about 1 ⁇ g / ml to 100 mg / ml.
- the inhibitor in the immune adjuvant composition of the present invention is a nucleic acid
- the inhibitor may be a liposome preparation.
- Methods for preparing liposome preparations containing nucleic acids are well known. For example, “Whitehead KA, Langer R, Anderson DG. Knocking down barriers: advances in siRNA delivery. Nat Rev Drug Discov. 2009 8 (2): 129- 38. ”.
- the well-known immune adjuvant may be contained in the immune adjuvant composition of this invention.
- Known immunoadjuvants can be used without limitation. Examples of such known immune adjuvants include Freund's complete adjuvant, dead microorganisms such as Mycobacterium tuberculosis, and Amla adjuvant.
- a nucleic acid / polysaccharide complex, hemozoin, ⁇ -hematin, and the like composed of a CpG oligonucleotide having a natural phosphodiester backbone and a poly (dA) tail and a ⁇ -1,3-glucan having a molecular weight of 25000 or more are also included.
- the concentration of the immunoadjuvant used in combination may be, for example, about 1 ⁇ g / ml to 100 mg / ml.
- the immunoadjuvant composition of the present invention includes a plurality of components, they may be mixed or may exist separately.
- the inhibitor described above can be used as a vaccine composition together with a vaccine antigen. By mixing the inhibitor and the vaccine antigen described above, the immunogenicity of the vaccine antigen can be increased.
- the vaccine composition may also contain other immune adjuvants in addition to the inhibitors described above.
- the kind of vaccine is not specifically limited, A well-known vaccine can be used without a restriction
- cedar pollen allergens (Cry j 1, Cry j 2), ragweed allergens (Amba1, Amba2, Amba5, Ambt5, Ambp5), duck allergen (Dacg2) and the like are mentioned as pollen allergens, Casein, lactalbumin, lactoglobulin, ovomucoid, ovalbumin, conalbumin and the like can be mentioned, and house dust allergens include mite allergens (Derf1, Derf2, Zen1, Derp1, Derp2) and the like.
- vaccines for infectious diseases include inactivated complete vaccines, subunit vaccines, toxoids and the like. These vaccines immunize animals against pathogens such as bacteria, viruses, rickettsiae and parasites.
- pathogens such as bacteria, viruses, rickettsiae and parasites.
- vaccines for infectious diseases for example, influenza such as influenza A and B, poliovirus, Japanese encephalitis, Mycobacterium tuberculosis, human papillomavirus, malaria parasite, SARS, avian influenza that can infect humans
- vaccines for infectious diseases such as typhoid fever, paratyphoid fever, plague, whooping cough, typhus rash and the like.
- equine influenza virus equine herpesvirus, equine encephalomyelitis virus, foot-and-mouth disease virus, rabies, feline panleukopenia, cat rhinotracheitis, infectious bovine rhinotracheitis, Type 3 parainfluenza, bovine viral diarrhea, bovine adenovirus, porcine parvovirus, canine adenovirus, canine distemper virus, canine parvovirus, canine parainfluenza, avian influenza, brucellosis, vibriosis, leptospirosis, clostridial infection And vaccines for infectious diseases such as salmonellosis.
- the vaccine may also be a cancer vaccine. Any known cancer vaccine can be used without limitation, and examples include WT1, HER2 / neu in breast cancer, MAGE in malignant melanoma, and CEA in colorectal cancer.
- the vaccine composition may be in the form of a sterile aqueous or non-aqueous solution, suspension or emulsion. Further, it may contain a pharmaceutically acceptable diluent such as a salt and a buffer, an auxiliary agent, a carrier and the like.
- the inhibitor concentration in the vaccine composition may be, for example, about 10 ⁇ g / ml to 100 mg / ml. When other immunoadjuvant is used in combination, the concentration of this immunoadjuvant may be, for example, about 1 ⁇ g / ml to 100 mg / ml.
- the vaccine concentration in the vaccine composition may be, for example, about 1 ⁇ g / ml to 100 mg / ml.
- the vaccine composition of the present invention includes a food and drink composition.
- the inhibitor concentration in the composition may be, for example, about 1 ⁇ g / ml to 100 mg / ml.
- the concentration of this immunoadjuvant may be, for example, about 1 ⁇ g / ml to 100 mg / ml.
- the vaccine concentration may be, for example, about 1 ⁇ g / ml to 100 mg / ml.
- the vaccine composition of the present invention includes a plurality of components, they may be mixed or may exist separately.
- the vaccine composition described above can be administered by mixing the immune adjuvant composition and the vaccine antigen. Moreover, an immune adjuvant composition and a vaccine antigen can also be administered separately. Thereby, an animal can be immunized. In other words, animal immunity (acquired immunity, innate immunity) can be activated. Moreover, when the said inhibitor and another immune adjuvant are contained in an immune adjuvant composition, each adjuvant may be administered separately and may be administered as a mixture.
- the immunoadjuvant composition of the present invention and the vaccine composition of the present invention can be administered therapeutically when they are pharmaceutical compositions, and are administered nontherapeutically when they are food compositions. be able to.
- the immune adjuvant composition and vaccine composition of the present invention can be administered to any animal (human or non-human) having an immune system.
- mammals such as humans, monkeys, cows, horses, pigs, sheep, goats, dogs, cats, guinea pigs, rats and mice; and birds such as chickens, ducks and geese.
- the immunoadjuvant composition and vaccine composition of the present invention include human allergy vaccines and infectious disease vaccines, allergy vaccines and infectious disease vaccines for pet animals such as dogs and cats, and industrial animals such as cattle, pigs and chickens. Useful as an infectious disease vaccine.
- Immune adjuvant compositions and vaccine compositions can be inoculated by routes such as oral, intramuscular, intradermal, subcutaneous, intranasal, intratracheal, and skin.
- the immunoadjuvant composition and vaccine composition of the present invention may be ingested in a state of being included in human food or drink, animal drinking water or food.
- the immune adjuvant composition and vaccine composition of the present invention may be administered once, or may be administered several times at intervals of about 2 days to 8 weeks.
- the dose of vaccine can be varied depending on the type of allergy or infection targeted, the species of animal to be administered, etc., but the dose per dose may be several tens of ng to several mg.
- the dose of the inhibitor may be about 1 ⁇ g / ml to 100 mg / ml.
- the dose of the combined immunoadjuvant may be about 1 ⁇ g / ml to 100 mg / ml.
- the immune adjuvant composition of the present invention can be used to contact and activate immune cells (eg, dendritic cells, lymphocytes) collected from an individual. Thereby, activated immune cells are obtained. By activating activated immune cells to a person, immunity is activated and a vaccine effect can be expected.
- This activated immune cell preparation is usually administered intravenously.
- the collected immune cells may be pre-cultured using a medium such as RPMI under conditions in the presence of cytokines.
- the immune cells and immunoadjuvant composition can then be mixed and incubated at a temperature suitable for the growth of the cells, for example at about 37 ° C. for about 1-24 hours.
- the use ratio of immune cells and immune adjuvant composition may be, for example, about 1: 1 to 1: 10000.
- ELISA kits for measuring mouse IL-4, IL-6, IL-12p40, IL-17, IFN- ⁇ and TNF were purchased from R & D systems.
- a mouse ANA antibody (antinuclear antibody) ELISA kit was purchased from Alpha Diagnostic.
- Monoclonal anti-YY1 antibody (H-10) and HRP-labeled monoclonal anti- ⁇ -tubulin antibody (D-10) were purchased from SantaCruz.
- HRP-conjugated anti-FLAG antibody was purchased from Sigma.
- TLR ligands including MALP-2, Poly I: C, Lipopolysaccharide (LPS) from Salmonella Minnesota Re595 strain, R-848 and CpG oligonucleotide (ODN1668) are found in Kawagoe, T. et al. Sequential control of Toll-like. It was obtained as described in receptor-dependent responses by IRAK1 and IRAK2. Nat Immunol 9, 684-91 (2008). Peritoneal exudate cells were washed with ice-cooled Hank's buffered salt solution (Invitrogen) from the abdominal cavity of mice 3 days after injecting 2 ml of 4.0% thioglycolic acid culture solution (Sigma). Separated by. The HEK293-tet-off cell line was purchased from Clontech. HEK293 cells were purchased from ATCC.
- Zc3h12a cDNA (NCBI Accession No. NM_153159) was inserted into a pFLAG-CMV2 vector (Invitrogen) to prepare a Zc3h12a expression plasmid.
- the pFLAG-CMV2 vector (Invitrogen) was used as an empty plasmid for the control of the Zc3h12a expression plasmid.
- the CCCH domain point mutation (C306R or D141N) and deletion are performed using the Zc3h12a expression plasmid described above, using the QuickChangeII Site-Directed Mutagenesis Kit (Stratagene), and the method described in the instructions attached to this kit. Went according to.
- the respective pGL3 vectors containing the full length (1-403) of IL-6 3′UTR sequence or any part thereof (1-70, 58-173 and 172-403) are Dr. W. Zhao and Dr. Provided by K. Kirkwood (Zhao, W., et al., P38alpha stabilizers interleukin-6 mRNA via multiple AU-rich elements. J Biol Chem 283, 1778-85 (2008)).
- the IL-6 3'UTR cDNA portion (1-92, 1-102, 1-112, 1-132, 1-142, or 122-197) is transferred to the pGL3 vector, Molecular Cloning: A Laboratory Manual , And inserted according to the method described in Cold Spring Harbor Laboratory Press.
- IL-6 CDS and IL-6 CDS + 3 ′ UTR were inserted into pTREtight vector (Clontech) according to the methods described in Molecular Cloning: A Laboratory Manual and Cold Spring Harbor Laboratory Press, respectively, and pTREtight-IL6- CDS and pTREtight-IL6-CDS + 3′UTR were prepared.
- ELISA IL-4, IL-6, IL-12p40, IL-17, IFN- ⁇ and TNF-a in the culture supernatant and mouse ANA-antibody in serum were measured by ELISA according to the manufacturer's protocol.
- ELISA measurement of mouse IgM, IgG1, IgG2a, IgG2b, IgG3 and anti-double-stranded DNA antibodies in serum is performed by Sato, S. et al. Essential function for the kinase TAK1 in innate and adaptive immune responses.
- Flow cytometry Antibodies for flow cytometry measurement were purchased from BD. The spleen cell suspension was prepared by filter and gentle pipetting. Cells were kept in the dark at 4 ° C. for surface staining. The cells were washed with ice-cold FACS buffer (2% FCS, 0.02% NaN 3 in PBS), incubated with each antibody for 15 minutes, and then washed 3 times with FACS buffer. FoxP3 + regulatory T cells were stained using a Mouse Regulatory T Cell Staining Kit (eBioscience) according to the manufacturer's instructions. Intracellular cytokines were stained using BD Cytofix / Cytoparm Plus Fixation / Permeabilization Kit (BD) according to the manufacturer's instructions. Data were measured with a Facs Calibur® or Facs Canto® II flow cytometer (BD) and analyzed using FlowJo (Tree Star software).
- RNA stability was determined using three different methods: (1) Stability of mRNA in macrophages Peritoneal macrophages (1 ⁇ 10 6 ) derived from wild type and Zc3h12a ⁇ / ⁇ mice were each stimulated with LPS (100 ng / ml) for 2 hours. Thereafter, actinomycin D (2 ⁇ g / ml) was added to the medium to stop transcription, and total RNA was prepared for a predetermined period. This RNA was subjected to Northern blot analysis, and IL-6, TNF, KC and ⁇ -actin mRNA levels were measured.
- RNA was subjected to Northern blot analysis, and IL-6 and ⁇ -actin mRNA levels were measured.
- (3) Luciferase assay HEK293 cells were transfected with pGL3-IL-6 3'UTR plasmid or pGL3-empty (empty) plasmid and Zc3h12a expression plasmid or control empty plasmid. After 48 hours of culture, the cells were lysed, and the luciferase activity in the lysate was measured by a Dual-luciferase reporter assay system (Promega). The Renilla-luciferase gene was simultaneously transfected as an internal control.
- RNA cleavage assay The cleavage activity of wild type and mutants of Zc3h12a was measured according to the method described in Miyoshi, K., et al., In vitro RNA cleavage assay for Argonaute-family proteins. Methods Mol Biol 442, 29-43 (2008). . Subsequently, recombinant Zc3h12a protein was incubated with [ 32 P] -labeled RNA transcribed in vitro, and the cleaved RNA was purified and analyzed by denaturing PAGE and autoradiography.
- RNA recombinant protein and in vitro transcribed [ 32 P] -labeled RNA (5000 cpm) were prepared by cleaving buffer (25 mM Hepes, 50 mM KOAc, 5 ⁇ M DTT) and Rnasin plus (40U) (Promega 5 mM Mg (Oac) 2 in the presence of Mixed with or without.
- the cleaved RNA was purified by TRIzol (InvitroGen) and analyzed by denaturing PAGE and autoradiography using 6% TBE-Urea gel (InvitroGen).
- Bone marrow cells were prepared from each of wild-type and Zc3h12a ⁇ / ⁇ mice. The prepared bone marrow cells were intravenously administered to lethally irradiated CD45.1 C57BL / 6 mice (bred at the Institute for Microbial Diseases, Osaka University). Chimeric mice were given 4 weeks of neomycin and ampicillin in their drinking water. Mice were analyzed at least 8 weeks after reconstitution. More than 90% of the spleen cells of the chimeric mice were CD45.2 positive.
- PreScission Protease cleavage buffer 50 mM Tris, 150 mM NaCl, 1 mM EDTA and 1 ⁇ M DTT.
- PreScission Protease (GE Healthcare) (80 U) was added and incubated at 4 ° C. for 4 hours with gentle shaking. The supernatant was collected and stored at ⁇ 80 ° C. as a recombinant protein solution.
- RNA binding assay [ 32 P] -labeled RNA (1 ⁇ 10 6 cpm) and recombinant protein or BSA (Pierce) are mixed in buffer (25 mM Hepes, 50 mM KOAc, 5 ⁇ M DTT) and incubated at room temperature for 20 minutes. did. Heparin was then added to a final concentration of 5 ⁇ g / ml and incubated for an additional 10 minutes. Using FUNA-UV-LINKER FS-800 (Funakoshi Co., Ltd.), the sample was crosslinked by irradiating UV at 254 nm at a distance of 5 cm from the light source for 20 minutes on ice.
- cDNAs were purchased from the manufacturer (Enzo Diagnostics, According to the protocol prepared by Farmingdale, NY), biotin-labeled cRNA was prepared by in vitro transcription reaction performed using T7 RNA polymerase in the presence of biotinylated ribonucleotide.
- cRNA product RNeasy The product was purified using a kit (Qiagen), fragmented, and hybridized with an Affymetrix mouse expression array A430 microarray chip (Affymetrix, Santa Clara, Calif.) according to the manufacturer's protocol.
- Affymetrix mouse expression array A430 microarray chip Affymetrix, Santa Clara, Calif.
- peritoneal macrophages were stimulated with 100 ng / ml LPS.
- RMA Robust multichip average
- the RMA expression value was converted by each probe to fit the mean and standard deviation for 0 and 1, respectively.
- the distance between probes was calculated using Pearson's correlation coefficient as the distance function.
- principal component analysis for RMA values was performed, and Euclidean distances between probes were calculated using the first to fifth principal components. Using these distances, hierarchical clustering was performed by the Ward's method. These calculations and heat map display creation were performed using R and Bioconductor.
- Tissues were fixed with 10% formalin neutral buffer solution, embedded in paraffin, and cut into 5 ⁇ m thick sections. Sections were heated in Target Retrieval Solution (Dako, Glostrup, Denmark) at 98 ° C. for 40 minutes to facilitate antigen detection.
- Target Retrieval Solution Dako, Glostrup, Denmark
- Sections were prepared by using a peroxidase-conjugated goat IgG fraction (MP Biomedicals, LLC, Solon, OH) against mouse IgA ( ⁇ chain) with an antibody diluent (trade name: ChemMate, Dako) 1: diluted to 50, or mouse IgG peroxidase-labeled goat affinity purified F for (whole molecule) (AB ') 2 fragment (peroxidase-conjugated goat affinity purified F (AB') 2 fragment) to (MP Biomedicals, Inc.) antibodies diluted The solution diluted 1:25 with the solution was incubated at room temperature for 30 minutes. Cells immunoreactive with mouse IgA and IgG were visualized using diaminobenzidine (Dako). Sections were lightly counterstained with hematoxylin. The stained sections were observed with an optical microscope.
- Electrostatic surfaces are eF-surf server ( http://ef-site.hgc.jp/eF-surf/ ) and eF-site (Kinoshita, K. & Nakamura, H. eF-site and PDBjViewer: database and It was prepared using viewer for protein functional sites. Bioinformatics 20, 1329-30 (2004)).
- Example 1 Identification of Zc3h12a as an LPS-inducible gene To comprehensively study the expression of genes that induce Toll-like receptors (TLRs), wild-type (WT) mice, LPS-stimulated MyD88 ⁇ / ⁇ mice and TRIF ⁇ / -Using the macrophages from the mice, microarray analysis was performed by the method described above.
- TLRs Toll-like receptors
- WT wild-type mice
- TRIF ⁇ / - LPS-stimulated MyD88 ⁇ / ⁇ mice
- TRIF ⁇ / - TRIF ⁇ /
- RNA derived from macrophages stimulated with LPS 100 ng / ml
- LPS 100 ng / ml
- Northern blot analysis confirmed that Zc3h12a mRNA was rapidly induced in mouse macrophages after LPS stimulation and gradually decreased over time (FIG. 1a).
- Zc3h12a has a CCCH-type zinc finger (Zf) motif and forms a family with homologous proteins Zc3h12b, c and d.
- the HEK293 cells were transfected with Lipofectamine 2000 (Invitrogen) with or without Flag-tagged Zc3h12a.
- Cytoplasm (CP) and nuclear extract (NE) were prepared from HEK293 cells transfected with or without this Flag-tagged Zc3h12a.
- the expression of Zc3h12a was measured by Western blotting using an anti-FLAG antibody.
- Anti- ⁇ tubulin and anti-YY-1 antibody were used as controls for CP and NE, respectively. The result is shown in FIG. The results of this fractionation experiment indicated that the Zc3h12a protein was localized mainly in the cytoplasm rather than in the nucleus (FIG. 1b).
- Example 2 Creation of Zc3h12a ⁇ / ⁇ mice
- Zc3h12a deficient mice Zc3h12a ⁇ / ⁇ mice were created.
- Genomic DNA containing Zc3h12a was separated from genomic DNA derived from GSI-I embryonic stem cells by Elongase (Invitrogen) using PCR.
- the genomic DNA containing the isolated Zc3h12a was characterized by restriction enzyme mapping and sequence analysis.
- the targeting vector was designed by replacing exon 3 with exon 5 containing a CCCH type Zf domain and a neomycin resistance gene.
- a 1.1 kilobase (kb) ClaI-BamI fragment was used as the 3 ′ homology region and a 5.9-kb NotI-SalI fragment was used as the 5 ′ homology region.
- the vector linearized with 30 ⁇ g of NotI in total was introduced into GSI-I embryonic stem cells by electroporation.
- FIG. 2a shows a schematic diagram of the mouse Zc3h12a gene (Wild-type allele), targeting vector (Targeting construct), and target allele.
- H represents HindIII.
- FIG. 2b is a result of Southern blot analysis of heterozygous cross offspring. Genomic DNA was extracted from mouse embryonic fibroblasts (MEF), cut with HindIII, separated by electrophoresis, and hybridized with a radiolabeled probe.
- RNA was subjected to RT-PCR analysis to examine the expression of Zc3h12a mRNA using the two types of primers Fw: ATATGAGTGACCCTTGTGGAACGAAGC (SEQ ID NO: 1) and Rev: TCTGTACACAGCATACATGTGTCCTCC (SEQ ID NO: 2) shown in FIG. ⁇ -actin gene expression was analyzed using the same RNA.
- FIG. 2c shows the results of RT-PCR analysis of RNA of wild type (WT) (Zc3h12a + / + ) and Zc3h12a ⁇ / ⁇ macrophages stimulated with LPS (100 ng / ml) for a predetermined time. RT-PCR analysis showed that Zc3h12a expression was suppressed in Zc3h12a ⁇ / ⁇ macrophages (FIG. 2c).
- FIG. 3b is a photograph of spleen (upper), mesenteric lymph node (lower left) and inguinal lymph node (lower right) of wild type (Zc3h12a + / + ) (upper figure) and Zc3h12a -/- mice (lower figure). is there. Zc3h12a ⁇ / ⁇ mice showed severe splenomegaly and lymphadenopathy (FIG. 3b).
- FIG. 3c is a histological photograph of lung, spleen and lymph node (LN) of wild type (Zc3h12a + / + ) and Zc3h12a ⁇ / ⁇ mice.
- FIG. 4 shows the results of H & E staining of liver and pancreas sections of wild type (WT) and Zc3h12a ⁇ / ⁇ mice. Histological analysis showed the invasion of plasma cells (plasma cells) into the lung and the transepithelium of the bile duct and spleen (FIGS. 3c and 4). Plasma cells also accumulated in Zc3h12a ⁇ / ⁇ lymph nodes (LN) and spleen (FIG. 3c). In LN, granuloma formation was observed, and formation of giant cells fused with macrophages was observed. Despite this, no change in inflammation was seen in the gut or joints of Zc3h12a ⁇ / ⁇ mice (data not shown).
- Table 1 shows the evaluation results of blood cells. Zc3h12a ⁇ / ⁇ mice suffered from severe anemia with an increase in blood cells and platelets (Table 1). The numerical values in Table 1 represent the mean ⁇ standard deviation (SD) of 6 samples.
- FIG. 5a shows serum immunoglobulin levels in Zc3h12a ⁇ / ⁇ mice.
- ANA antinuclear antibodies
- FIG. 5b shows superiority in Zc3h12a ⁇ / ⁇ mice.
- Fig. 5c shows the results (histological photographs) of the immunohistochemical examination of lung sections with anti-IgG and anti-IgA antibodies. Plasma cells that invaded lung and intestinal tissues were readily stained with anti-IgG or anti-IgA antibodies (FIG. 5c).
- FIG. 6 shows the results of examining cell abnormalities and enhanced cytokine production in Zc3h12a ⁇ / ⁇ mice.
- Figures 6a-c show the results of splenocyte analysis by flow cytometry.
- FIG. 6a shows IgM and IgD expression in splenic CD19 + B cells
- FIG. 6b shows the percentage of plasma cells in the spleen
- FIG. 6c shows CD62L and CD44 expression in splenic T cells, respectively.
- similar results were obtained in three different experiments.
- FIG. 7a is a diagram showing the results of staining spleen cells of wild-type and Zc3h12a ⁇ / ⁇ mice with antibodies and analyzing them by flow cytometry.
- FIG. 7b shows the results of staining spleen cells with anti-Foxp3 antibody and CD4 antibody and analyzing them by flow cytometry.
- FIG. 8 shows the results of examining the production of interferon ⁇ , IL-17, and IL-4 in response to CD3 / CD28 stimulation in splenic T cells. Error bars indicate two sets of standard deviations (SD). Similar results were obtained in three different experiments.
- FIG. 9a shows the results of spleen cells stained with anti-CD4 antibody, permeabilized, stained for interferon ⁇ and IL-17, and analyzed by flow cytometry.
- Spleen cells were stimulated by incubating with 50 ng / ml phorbol myristate acetate (PMA) (Sigma), 5 mM calcium ionophore A23187 (Sigma) and Golgistop (BD) for 4 hours at 37 ° C. in complete medium. And used for the above analysis.
- the numbers in the figure indicate the percentage of cells in the quadrant.
- FIG. 10a and b are diagrams showing the results of staining spleen cells of wild-type and Zc3h12a ⁇ / ⁇ mice with antibodies and analyzing them by flow cytometry.
- FIG. 11 shows the results of examining the involvement of hematopoietic cells in the accumulation of plasma cells and effector / immune memory T cells in Zc3h12a ⁇ / ⁇ mice.
- spleen cells of wild type and Zc3h12a ⁇ / ⁇ bone marrow chimeras were stained with antibodies and analyzed by flow cytometry.
- IgM - was shown to be, which is most Zc3h12a - - IgD / - mice B cells undergo class switching in splenic (FIG. 6a). Furthermore, CD138 + CD19 dull plasma cells are abundant in the spleen of Zc3h12a ⁇ / ⁇ mice (FIG. 6b). In addition, CD69 expression is up-regulated in splenic CD3 + T cells and peripherally accumulated CD44 high CD62L ⁇ T cells (FIGS. 6c and 7a).
- Example 4 Next, the production of cytokines from macrophages was examined. Wild type (Zc3h12a + / + ) and Zc3h12a ⁇ / ⁇ mouse peritoneal macrophages were analyzed using MLP-2 (1, 10 ng / ml), Poly I: C (100 ⁇ g / ml), LPS (10, 100 ng / ml), Stimulation was carried out for 24 hours with either R-848 (10 nM) or CpG-DNA (0.1, 1 ⁇ M). IL-6, IL-12p40 and TNF concentrations in the supernatant of the medium were measured by ELISA. The result is shown in FIG. In FIG.
- FIG. 12a “med” is a macrophage (control) that was not stimulated with the substance. Error bars indicate two sets of standard deviations (SD). Similar results were obtained in three different experiments.
- FIG. 13 is a heat map representation of the expression of LPS-inducible genes selected based on microarray analysis of wild type (Zc3h12a + / + ) and Zc3h12a ⁇ / ⁇ peritoneal macrophages.
- microarray analysis of LPS-inducible genes in wild type and Zc3h12a ⁇ / ⁇ macrophages was performed. As described above, wild type and Zc3h12a ⁇ / ⁇ macrophages were stimulated with 100 ng / ml LPS for 0, 1, 2 and 4 hours and total RNA was subjected to microarray analysis using an Affymetrix mouse Genome 430 2.0 microarray chip. Data were processed as described above, and 1045 genes upregulated more than 5-fold more than LPS-inducible genes in wild-type or Zc3h12a ⁇ / ⁇ macrophages either 1, 2 or 4 hours after stimulation.
- TLR2 TLR2
- TLR3 TLR3
- LPS TLR4
- TLR7 TLR7
- CpG-DNA TLR9
- microarray analysis was performed. Microarray analysis of LPS-inducible genes in macrophages showed that most LPS-inducible genes were equally expressed in wild type cells and Zc3h12a ⁇ / ⁇ cells (FIG. 14). Despite this, a specific set of genes was highly expressed in Zc3h12a ⁇ / ⁇ macrophages. These include IL-6, Ifng, Calcr, Sprr2d, etc. (FIG. 13).
- Example 5 Several proteins with CCCH-type Zf motifs have been reported to be involved in mRNA metabolism such as mRNA splicing, polyadenylation, and regulation of mRNA decay. Thus, we hypothesized that Zc3h12a may play a role in mRNA instability, and examined this possibility using IL-6.
- FIG. 16 shows the results showing that Zc3h12a destabilizes mRNA from a set of genes through its 3′-UTR.
- FIG. 16a is a diagram showing the results obtained by extracting total RNA (10 ⁇ g) and subjecting it to RNA blot analysis for examining the expression of IL-6, TNF, KC, and ⁇ -actin probe. Similar results were obtained in three different experiments.
- FIG. 16b shows the time course of residual mRNA. In FIG. 16b, autoradiographs were quantified and the ratio of IL-6, Tnf and Cxcl1 to Actb was used to determine residual mRNA levels.
- Example 6 Determination of Zc3h12a responsive region in 3'-UTR of IL-6
- TAKARA Tet-On Gene Expression System
- FIG. 17 shows that EK293 Tet-off cells were simultaneously transduced with pTREtight-IL6-CDS or pTREtight-IL6-CDS + 3′UTR and a Zc3h12a expression plasmid or a control empty plasmid, and RNA extracted from the cells was extracted.
- FIG. 17a cells were split 3 hours after transfection and incubated overnight. Next, Dox (1 ⁇ g / ml) treatment was performed to prepare total RNA, and IL-6 and ⁇ -actin levels were determined by Northern blot analysis.
- FIG. 17b autoradiographs were quantified and the ratio of IL-6 to Actb was used to determine residual mRNA levels.
- FIG. 19 is a diagram showing the results of measuring luciferase activity. Error bars indicate two sets of standard deviations (SD). Similar results were obtained in three different experiments.
- a pGL3 plasmid containing various sequences of IL-6 (FIG. 19a) 3′-UTR and b-Globin 3′-UTR (FIG. 19b) and a Zc3h12 expression plasmid or control
- the empty plasmid was used to transfect HEK293 cells, and 48 hours later, the luciferase activity of the lysate of the cells was measured.
- FIG. 19a pGL3 plasmid containing various sequences of IL-6 (FIG. 19a) 3′-UTR and b-Globin 3′-UTR (FIG. 19b) and a Zc3h12 expression plasmid or control
- the empty plasmid was used to transfect HEK293 cells, and 48 hours later, the lucifera
- HEK293 cells were transfected with pGL3 containing 3′-UTR against IL-6, IL-12p40, CTR or interferon ⁇ and Zc3h12a expression plasmid or control empty plasmid, After a time, the luciferase activity of the cell lysate was measured.
- FIG. 18 is a schematic diagram of IL-6 3′-UTR and its defective construct.
- Mouse IL-6 mRNA contains five adenine-uridine-rich elements (ARE) in its 3'-UTR ( Figure 18) (Zhao, W. et al., P38alpha stabilizes interleukin-6 mRNA via multiple AU-rich elements. J Biol Chem 283, 1778-85 (2008)).
- ARE adenine-uridine-rich elements
- IL-6 3'-UTR (56-173) contains two AREs and CE (Fig. 19a).
- IL-6 3'-UTR (122-197) was not destabilized by Zc3h12a, suggesting that ARE is not critical for Zc3h12a-mediated IL-6 mRNA destabilization.
- IL-6IL3'-UTR (1-142) containing no ARE was destabilized by the expression of Zc3h12a (Fig. 19a).
- a luciferase reporter construct with a shortened IL-6 3'-UTR, it was found that IL-6 (1-102) but not IL-6 (1-92) is destabilized by Zc3h12a (FIG. 20).
- FIG. 20 FIG.
- FIG. 20 shows a schematic diagram of IL-6 3′-UTR and a construct lacking it.
- the 3'-UTR luciferase activity of pGL3- ⁇ -globin was not affected by the expression of Zc3h12a, but when IL-6 3'-UTR (77-108) was added to b-globin 3'-UTR, Responded ( Figure 19b).
- IL-6 3'-UTR 77-108
- FIG. 19c shows that CE of IL-6 3'-UTR is important for mRNA destabilization mediated by Zc3h12a.
- Expression of Zc3h12a reduced the luciferase activity of the reporter with IL-12p40 and calcitonin receptor (CTR) 3'-UTR but not 3'-UTR of interferon gamma (Fig. 19c).
- CTR calcitonin receptor
- FIG. 21 shows the results of examining the binding of IL-6 to 3′UTR (1-403) mRNA by UV crosslinking assay.
- FIG. 22a shows that HEK293 Tet-off cells were co-transformed with pTREtight-IL6-CDS + 3′UTR and expression plasmids encoding various amounts of Flag-Zc3h12a or variants thereof (C306R and ⁇ CCCH). After the transfection, the cells were treated with Dox for a predetermined time, and the results of IL-6 expression determined by Northern blot analysis are shown.
- FIG. 22a shows that HEK293 Tet-off cells were co-transformed with pTREtight-IL6-CDS + 3′UTR and expression plasmids encoding various amounts of Flag-Zc3h12a or variants thereof (C306R and ⁇ CCCH).
- FIG. 22b shows the results of measuring the expression level of Zc3h12 mutant protein by immunoblotting.
- the arrow in FIG. 22b indicates the expressed Zc3h12a protein.
- FIG. 23a shows that HEK293 Tet-off cells were co-transfected with pTREtight-IL6-CDS + 3′UTR and an expression plasmid encoding Flag-Zc3h12a or variants thereof (C306R and ⁇ CCCH), then The results are shown in which cells were treated with Dox for a predetermined time and the expression of IL-6 was measured by Northern blot analysis. Autoradiographs were quantified and the ratio of IL-6 to Actb was used to determine residual mRNA levels (FIG. 23b).
- FIG. 23 c shows the results of measuring the expression level of Zc3h12a mutant protein by immunoblotting.
- FIG. 24 shows the sequence alignment of the N-terminal and CCCH domains in mouse and human Zc3h12a.
- the colored portions are in a common arrangement.
- Black circles ( ⁇ ) indicate asparagine residues conserved in other PIN domain structures, and asterisks indicate CCCH Zinc finger.
- Sequence alignment suggested that the conserved N-terminal domain (139-297) in Zc3h12a (just before the Zf domain (300-324)) shares a distant relationship to the PIN domain-like SCOP superfamily (FIG. 24).
- FIG. 25 is a structural model of the N-terminal domain of Zc3h12a prepared by structural modeling.
- FIG.26 and FIG.27a is data which show the result of having measured the endoribonuclease activity of Zc3h12a.
- the synthesized RNA was incubated with a predetermined amount of protein (varied amount).
- the left lane is an RNA size marker.
- FIG. 26a shows the results of examining the expression levels of synthesized Zc3h12a and Zc3h12a (D141N), and
- FIG. 26b shows the IL-6 3′UTR mRNA (1-1-in the presence or absence of 5 mM Mg 2+.
- FIG. 27a shows the results of an in vitro cleavage assay of 5 ′ end labeled or 3 ′ end labeled IL-6 3′UTR mRNA (1-403) with varying amounts of recombinant Zc3h12a protein.
- FIG. 27b shows the results of a kinetic analysis of the ribonuclease activity of Zc3h12a.
- 5′-end labeled or 3′-end labeled IL-6 3′UTR mRNA (1-403) was incubated with recombinant Zc3h12a protein for a predetermined time.
- FIG. 28a shows the results of measuring IL-6 expression by Northern blot analysis.
- HEK293 Tet-off cells were co-transfected with pTREtight-IL6 full and Zc3h12a (D141N). The cells were then treated with Dox for a predetermined time, and IL-6 expression was measured by Northern blot analysis.
- FIG. 28b shows the time course of residual mRNA levels.
- the Zc3h12a D141N mutant did not degrade RNA, suggesting that the conserved pocket actually functions as a ribonuclease active site (FIGS. 26a and c).
- the Zc3h12a D141N mutant could not destabilize RNA containing 3′-UTR of IL-6, suggesting that ribonuclease activity is essential for the function of Zc3h12a (FIGS. 23a and 28).
- Zc3h12a did not affect the expression of TNF mRNA in macrophages, suggesting that TTP and Zc3h12a regulate the decay of different cytokine mRNAs.
- Zc3h12a targeted RNA sequences other than ARE.
- the ARE of IL-6 appears to be regulated by an unknown Zc3h12a independent mechanism.
- Zc3h12a has been reported to be a monocyte chemoattractant protein 1 (MCP-1) inducible protein (Zhou, L. et al. Monocyte chemoattractant protein-1 induces a novel transcription factor that causes cardiac myocyte apoptosis and ventricular dysfunction. Circ Res 98, 1177-85 (2006)), Zc3h12a protein overexpression was shown to suppress cytokine production in macrophages through inhibition of NF- ⁇ B activation (Liang, J. et al.
- MCP-1 monocyte chemoattractant protein 1
- the Zc3h12a protein has an intrinsic ribonuclease activity that is responsible for IL-6 mRNA decay. This mechanism is unique compared to other ARE-mediated mRNA decay pathway controls. For example, TTP has been shown to remove poly A tails and replenish deadenylases to facilitate subsequent exonuclease degradation of target mRNA (Anderson, P. Post-transcriptionalscriptioncontrol of cytokine production. Nat Immunol 9, 353-9 (2008)). Thus, it is interesting that Zc3h12a has a nuclease activity that does not exhibit sequence specificity at least in vitro. Target specificity may be determined by the binding partner of Zc3h12a. Or, under certain conditions, Zc3h12a may have a sequence suitable for degradation.
- the mechanism by which Zc3h12a induces mRNA decay is an interesting topic.
- the ribonuclease domain is conserved in four members of the Zc3h12 family, and homologs of this protein family were found in microorganisms such as Drosophila melanogaster (Gene ID: CG10889), Caenorhabditis elegans (Gene ID: C30F12.1) .
- Drosophila melanogaster Gene ID: CG10889
- Caenorhabditis elegans Gene ID: C30F12.1
- Roquin Another RING-type ubiquitin ligase protein containing a CCCH zinc-finger motif called Roquin is essential for suppression of autoimmunity by regulating the expression of ICOS costimulatory molecules (Vinuesa, C. G. et al. A RING -type ubiquitin ligase family member required to repress follicular helper T cells and autoimmunity. Nature 435, 452-8 (2005)). Roquin and some microRNAs seem to share the 3'-UTR RNA segment of ICOS to suppress degradation (Yu, D. et al. Roquin represses autoimmunity by limiting inducible T-cell co-stimulator messenger RNA.
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Abstract
Description
動物実験用には種々のアジュバントが知られている。生物に由来しない一般化合物からなるアジュバントとしては、例えば、水酸化ナトリウム、水酸化アルミニウム、リン酸カルシウム、ミョウバン、カルボキシビニルポリマーなどが、病原体などの抗原を吸着する性質を利用してアジュバントとして用いられている。しかし、これらの沈降性アジュバントは、接種部位が硬結し易い。また、流動パラフィン、ラノリン、フロイントなどが、油性物質が抗原水溶液を包んでミセルを形成する性質を利用してアジュバントとして用いられている。しかし、これらの油性アジュバントとワクチン抗原との混合物はミセルを含む乳濁液になるため、粘性が高く、接種時に疼痛を引き起こし、また、接種部位が硬結し易い。
一般に効果の強いアジュバントは毒性も強いため、安全でかつ効果的なアジュバントの開発が求められている。
天然物由来のアジュバントとして、特許文献1には、天然型のホスホジエステルバックボーン及びポリ(dA)テールを有するCpGオリゴヌクレオチドと、分子量25000以上のβ-1,3-グルカンとからなる核酸/多糖複合体が、Th1細胞活性を優位にするサイトカインや抗体の産生を促進し、免疫アジュバントとして利用できることが示唆されている。
(i) Zc3h12a遺伝子を破壊したホモノックアウトマウス(Zc3h12a-/-マウス)では、形質細胞数が増加しているとともに、肺への浸潤が認められた。また、血清中の免疫グロブリン濃度が増大し、自己抗体の生産が見られた。
(ii) また、殆どのZc3h12a-/-マウスの脾臓のT細胞は、エフェクター/メモリー特性を示し、T細胞レセプター刺激に対する応答においてインターフェロンγを生産した。このように、Zc3h12aを破壊することにより、獲得免疫系が活性化し、形質細胞、メモリーT細胞が増加した。
(iii) Zc3h12a-/- マウスから単離したマクロファージは、TLR(Toll-like receptor)リガンドに対する応答においてIL-6、IL-12p40の産生が大きく亢進していた。一方、TLRリガンドに対する応答においてTNFの生産は亢進していなかった。このように、Zc3h12aを破壊することにより、特定のサイトカインの産生が亢進した。
(iv) Zc3h12a蛋白質はZinc finger領域を有し、RNAと結合した。
(iv) Zc3h12a遺伝子は、N-末端ヌクレアーゼ領域と推定される領域を有しており、リボヌクレアーゼ活性を示す蛋白を発現した。特定のmRNAは分解することにより恒常性を維持しているところ、Zc3h12a-/-マウスでは、Zc3h12aのリボヌクレアーゼ活性が欠如することにより、特定のサイトカインを含む分子のmRNAの分解が抑制されて、その産生を亢進している。
(v) 従って、Zc3h12a遺伝子又はZc3h12a蛋白質のインヒビターは、免疫アジュバントとして好適に使用できる。
項1. Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種を有効成分として含む免疫アジュバント組成物。
項2. さらに、その他の免疫アジュバントを含む項1に記載の免疫アジュバント組成物。
項3. Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種と、ワクチン抗原とを含むワクチン組成物。
項4. さらに、その他の免疫アジュバントを含む項3に記載のワクチン組成物。
項5. 項3又は4に記載のワクチン組成物を非ヒト動物に投与する、動物の免疫方法。
項6. 個体から採取された免疫細胞と、Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種とを接触させて、免疫細胞を賦活化させる工程を含む、活性免疫細胞の製造方法。
項7. 項6に記載の方法で製造された活性免疫細胞。
項8. ワクチン抗原の免疫原性を高めるための、Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種の化合物。
項9. Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種の化合物の、免疫アジュバントの製造のための使用。
項10. Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種とワクチン抗原とを混合する工程を含む、ワクチン抗原の免疫原性を高める方法。
項11. 免疫賦活のための、Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種と、ワクチン抗原とを含む組成物。
項12. Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種と、ワクチン抗原とを含む組成物の、ワクチン組成物の製造のための使用。
また、Zc3h12a遺伝子、又はZc3h12a蛋白質のインヒビターであるため、siRNAのような核酸や低分子化合物とすることができ、安全性の高いものを設計できる。
(I)免疫アジュバント組成物
本発明の免疫アジュバント組成物は、Zc3h12a遺伝子のインヒビター、及びZc3h12a蛋白質のインヒビターからなる群より選ばれる少なくとも1種を有効成分として含むものである。
Toll-like receptor (TLR)は、微生物の成分を認識し、炎症及び免疫反応を引き起こすレセプターである。TLR刺激は、免疫反応の大きさと持続を制御する複合的な遺伝子発現を活性化する。Zc3h12a遺伝子は、TLR刺激により誘導される免疫反応のmodifierである。その塩基配列は、NCBIにおいて、アクセッション番号NM_025079として登録されている。
このインヒビターは、Zc3h12a遺伝子の発現を阻害するものであればよく、低分子化合物、核酸、タンパク質、糖タンパク質などが挙げられる。特に、医薬品として使用し易い点で、低分子化合物が好ましい。また、設計が容易であり、毒性が少ない点で、siRNA、shRNA、stRNAのような核酸も好ましい。
siRNA、shRNAの設計方法は良く知られており、それぞれ、例えば、”Elbashir, S. M., Harborth, J., Lendeckel, W., Yalcin, A., Weber, K., and Tuschl, T. (2001). Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature 411, 494-498.”、及び”Paddison, P. J., Caudy, A. A., Sachidanandam, R. & Hannon, G. J. Short hairpin activated gene silencing in mammalian cells. Methods Mol. Biol. 265, 85-100 (2004)”に記載されている。また、ABI社、Dharmacon社などに依頼すれば入手できる。
Zc3h12a遺伝子のインヒビターは、例えば、以下の方法でスクリーニングできる。Zc3h12a遺伝子発現プラスミド及びIL-6などの遺伝子の3’-UTRをluciferaseや蛍光蛋白質などを発現する遺伝子の下流に配したプラスミドを導入した試験細胞と被検物質とを接触させ、接触によりZc3h12a遺伝子の発現量が低下する被検物質を、ルシフェラーゼアッセイや蛍光検出によりスクリーニングすればよい。
また、制御領域及び構造遺伝子を含むZc3h12a遺伝子の発現プラスミドを導入した試験細胞と被検物質とを接触させ、接触によりZc3h12a遺伝子の発現量が低下する被検物質を、ウェスタンブロッティングやノーザンブロッティングによりスクリーニングすることもできる。
Zc3h12aタンパク質のインヒビターは、このタンパク質の活性を阻害するものであればよく、低分子化合物、核酸、タンパク質、糖タンパク質などが挙げられる。特に、医薬品として使用し易い点で、低分子化合物が好ましい。
Zc3h12aタンパク質のインヒビターのスクリーニングは、例えば、被検物質の存在下、及び非存在下で、RNA分解活性の程度を比較し、RNA分解活性を低下させる物質を選択すればよい。
具体的には、まず、ヒトZc3h12a組み換え蛋白質を合成する。ヒトZc3h12a遺伝子(NCBI Accession number NM_025079)をpGEX-6P1などのプラスミドに組み込み、大腸菌(E. coli)BL21-Gold(DE3)pLysS (Stratagene社) を形質転換し、タンパク質を発現させる。タンパク質発現後、細胞を回収し、PBSに再懸濁した。超音波によって細胞を溶解させ、Triton X-100を最終濃度1%となるように加え、30分間、4℃で穏やかに振とうしながらインキュベートする。次いで、遠心分離によって残骸を除去し、上澄みをGlutathion Sepharose 4B (GE Healthcare社)とともに30分間4℃で、穏やかに振とうしながらインキュベートする。樹脂を回収し、PBSで5回洗浄した後、PreScission Protease cleavage buffer (50 mM Tris, 150 mM NaCl, 1 mM EDTA and 1μM DTT)に再懸濁する。PreScission Protease (GE Healthcare社) (80U)を加えて、穏やかに振とうしながら4時間4℃でインキュベートする。上澄みを回収し、Zc3h12aタンパク質溶液として、-80℃で保存する。
次に、IL-6の3’-UTR conserved domainの配列と相同なRNAをin vitro転写法を用いて合成する。in vitro転写の際に[32P]標識RNA(5000 cpm)でラベルする。
このラベルしたRNAとZc3h12aタンパク質を、切断バッファー (25 mM Hepes, 50 mM KOAc, 5μM DTT)と、Rnasin plus (40U)(Promega社)の存在下、5 mM Mg(Oac)2 有り又はなしで、混合する。切断されたRNAをTRIzol (InvitroGen社)によって精製し、6% TBE-Urea gel (InvitroGen社)を用いるdenaturing PAGE及びオートラジオグラフィーによって分析する。切断されたRNAはより早く泳動されるRNAとして検出できる。このシステムに被検物質を作用させ、切断活性が低下する物質をスクリーニングすればよい。切断活性を検出する方法はこれに限らない。
Zc3h12aタンパク質のインヒビターは、その他の方法でもスクリーニングできる。例えば、Zc3h12a遺伝子発現プラスミド及びIL-6などの遺伝子の3’-UTRをluciferaseや蛍光蛋白質などを発現する遺伝子の下流に配したプラスミドを導入した試験細胞と被検物質とを接触させ、接触によりZc3h12a遺伝子の発現量が低下する被検物質を、ルシフェラーゼアッセイや蛍光検出によりスクリーニングすればよい。
免疫アジュバント組成物中の上記インヒビター濃度は、インヒビターの種類によって異なるが、例えば約10 μg/ml ~100 mg/mlとすればよい。
免疫アジュバント組成物は、無菌の水性又は非水性の溶液、懸濁液、又はエマルションの形態であってもよい。さらに、塩、緩衝剤等の医薬的に許容できる希釈剤、助剤、担体等を含んでいてもよい。
また、本発明の免疫アジュバント組成物は、ヒトの飲食品、動物の飲料水や餌に含ませた状態で摂取するものであってもよい。即ち、本発明の免疫アジュバント組成物には、飲食品組成物も包含される。飲食品中の上記インヒビター濃度は、例えば約1μg/ml ~100 mg/mlとすればよい。
本発明の免疫アジュバント組成物中の上記インヒビターが核酸である場合、このインヒビターはリポソーム製剤であってもよい。核酸を含むリポソーム製剤の調製方法は、良く知られており、例えば、”Whitehead KA, Langer R, Anderson DG.Knocking down barriers: advances in siRNA delivery. Nat Rev Drug Discov. 2009 8(2):129-38.”に記載されている。
本発明の免疫アジュバント組成物に複数の成分が含まれる場合、それらは、混合されていてもよく、別々に存在させてもよい。
上記説明したインヒビターは、ワクチン抗原とともにワクチン組成物とすることができる。上記説明したインヒビターとワクチン抗原とを混合することにより、ワクチン抗原の免疫原性を高めることができる。また、このワクチン組成物は、上記説明したインヒビターに加えて、その他の免疫アジュバントも含んでいてよい。
ワクチンの種類は特に限定されず、公知のワクチンを制限無く使用できる。このような公知のワクチンとして、例えば、食物アレルゲン、ハウスダストアレルゲン、スギ花粉のような花粉アレルゲン、動物の体毛のようなアレルゲンなどのアレルギーワクチンが挙げられる。具体的には、花粉アレルゲンとして、スギ花粉アレルゲン(Cry j 1、Cry j 2)、ブタクサアレルゲン(Amba1、Amba2、Amba5、Ambt5、Ambp5)、カモガヤアレルゲン(Dacg2)等が挙げられ、食物アレルゲンとして、カゼイン、ラクトアルブミン、ラクトグロブリン、オボムコイド、オボアルブミン、コンアルブミン等が挙げられ、ハウスダストアレルゲンとして、ダニ類アレルゲン(Derf1、Derf2、Zen1、Derp1、Derp2)等が挙げられる。
感染症用ワクチンとしては、ヒトを対象とする場合、例えば、A型、B型インフルエンザ等のインフルエンザ、ポリオウイルス、日本脳炎、結核菌、ヒトパピローマウイルス、マラリア原虫、SARS、ヒトに感染し得るトリインフルエンザ、腸チフス、パラチフス、ペスト、百日咳、発疹チフス等の感染症用ワクチンが挙げられる。また、非ヒト動物を対象とする場合、例えば、ウマインフルエンザウイルス、ウマヘルペスウイルス、ウマ脳髄膜炎ウイルス、口蹄疫ウイルス、狂犬病、ネコ汎白血球減少症、ネコ鼻気管炎、感染性ウシ鼻気管炎、3型パラインフルエンザ、ウシのウイルス性下痢、ウシアデノウイルス、ブタパルボウイルス、イヌアデノウイルス、イヌジステンパーウイルス、イヌパルボウイルス、イヌパラインフルエンザ、トリインフルエンザ、ブルセラ症、ビブリオ症、レプトスピラ症、クロストリジウム感染症、サルモネラ症等の感染症用ワクチンが挙げられる。
また、ワクチンは癌ワクチンであってもよい。癌ワクチンは公知のものを制限なく使用でき、例えば、WT1、乳癌などにおけるHER2/neu、悪性黒色腫におけるMAGE、大腸癌におけるCEAなどが挙げられる。
ワクチン組成物中の上記インヒビター濃度は、例えば約10μg/ml~100 mg/mlとすればよい。また、その他の免疫アジュバントを併用する場合、この免疫アジュバントの濃度は、例えば約1μg/ml~100 mg/mlとすればよい。また、ワクチン組成物中のワクチン濃度は、例えば約1μg/ml~100 mg/mlとすればよい。
本発明のワクチン組成物には、飲食品組成物も包含される。飲食品組成物である場合、組成物中のインヒビター濃度は、例えば約1μg/ml~100 mg/mlとすればよい。また、その他の免疫アジュバントを併用する場合、この免疫アジュバントの濃度は、例えば約1μg/ml ~100 mg/mlとすればよい。また、ワクチン濃度は、例えば約1μg/ml ~100 mg/mlとすればよい。
本発明のワクチン組成物に複数の成分が含まれる場合、それらは、混合されていてもよく、別々に存在させてもよい。
上記説明したワクチン組成物は、免疫アジュバント組成物とワクチン抗原とを混合して投与することができる。また、免疫アジュバント組成物とワクチン抗原とを別々に投与することもできる。これにより、動物を免疫することができる。換言すれば、動物の免疫(獲得免疫、自然免疫)を賦活化することができる。また、免疫アジュバント組成物中に、上記インヒビターとその他の免疫アジュバントとが含まれる場合、各アジュバントは別々に投与されてもよく、混合物として投与されてもよい。また、本発明の免疫アジュバント組成物、及び本発明のワクチン組成物は、医薬組成物である場合は、治療的に投与することができ、食品組成物である場合は、非治療的に投与することができる。
本発明の免疫アジュバント組成物、及びワクチン組成物は、免疫系を有するあらゆる動物(ヒト、非ヒト)を投与対象とすることができる。例えば、ヒト、サル、ウシ、ウマ、ブタ、ヒツジ、ヤギ、イヌ、ネコ、モルモット、ラット、マウス等の哺乳動物;ニワトリ、アヒル、ガチョウ等の鳥類が挙げられる。
特に本発明の免疫アジュバント組成物、及びワクチン組成物は、ヒトのアレルギーワクチン及び感染症ワクチン、イヌ、ネコ等のペット動物のアレルギーワクチン及び感染症ワクチン、並びにウシ、ブタ、ニワトリ等の産業動物の感染症ワクチンとして有用である。
本発明の免疫アジュバント組成物及びワクチン組成物は、単回投与されてもよいし、約2日間~8週間の間隔で数回にわたって投与されてもよい。
ワクチン投与量は、対象とするアレルギーや感染症の種類、投与する動物種等により変えることができるが、1回投与量を数十ng~数mgとすればよい。
インヒビターの投与量は、1回投与量を約1μg/ml~100 mg/mlとすればよい。また、その他の免疫アジュバントを併用する場合、併用される免疫アジュバントの1回投与量は、約1μg/ml~100 mg/mlとすればよい。
本発明の免疫アジュバント組成物は、個体から採取された免疫細胞(例えば、樹状細胞、リンパ球)と接触させ、これを賦活化するのに用いることができる。これにより、活性化された免疫細胞が得られる。活性化された免疫細胞を、人に投与することにより、免疫を賦活化し、ワクチン効果を期待できる。この活性化免疫細胞製剤は、通常、静脈内投与すればよい。
採取された免疫細胞は、例えば、RPMIのような培地を用いて、サイトカイン存在下の条件で、予備培養すればよい。次いで、免疫細胞と免疫アジュバント組成物とを混合し、その細胞の生育に適した温度、例えば約37℃で、約1~24時間インキュベートすればよい。
免疫細胞と免疫アジュバント組成物との使用比率は、例えば、約1:1~1:10000とすればよい。
マウスIL-4、IL-6、IL-12p40、IL-17、IFN-γ及びTNF測定のためのELISAキットは、R&D systems社から購入した。マウスANA抗体(抗核抗体)のELISAキットは、Alpha Diagnostic社から購入した。モノクローナル抗YY1抗体(H-10)及びHRP標識モノクローナル抗βチューブリン抗体(HRP-conjugated monoclonal anti-β-tubulin)抗体(D-10)は、SantaCruz社から購入した。HRP標識抗FLAG抗体(HRP-conjugated anti-FLAG antibody)は、Sigma社から購入した。MALP-2を含むTLRリガンド、Poly I:C、Salmonella Minnesota Re595株由来のリポ多糖(LPS)、R-848及びCpGオリゴヌクレオチド(ODN1668)は、Kawagoe, T. et al. Sequential control of Toll-like receptor-dependent responses by IRAK1 and IRAK2. Nat Immunol 9, 684-91 (2008)に記載されたようにして得た。
腹腔滲出細胞(Peritoneal exudate cell)は、2 mlの4.0%チオグリコール酸培養液(Sigma社)を注入してから3日後のマウスの腹腔から、氷冷したHank's buffered salt solution (Invitrogen社)で洗浄することによって分離した。HEK293-tet-off 細胞株は、Clontech社から購入した。HEK293細胞は、ATCCより購入した。
Zc3h12a cDNA(NCBIのAccession No. NM_153159)をpFLAG-CMV2ベクター(Invitrogen社)に挿入して、Zc3h12a発現プラスミドを調製した。pFLAG-CMV2ベクター(Invitrogen社)を、Zc3h12a発現プラスミドのコントロールの空プラスミドとして用いた。CCCHドメインのポイントミューテーション(C306R又はD141N)、及び削除は、上述したZc3h12a発現プラスミドを使用し、QuickChangeII Site-Directed Mutagenesis Kit (Stratagene社)を用いて、このkitに添付の説明書に記載の方法に従って行った。IL-6の3’UTR配列の全長(1-403)又はその部分(1-70、58-173及び172-403のいずれか)を含むそれぞれのpGL3ベクターは、Dr. W. Zhao及びDr. K. Kirkwoodから提供された(Zhao, W., et al., p38alpha stabilizes interleukin-6 mRNA via multiple AU-rich elements. J Biol Chem 283, 1778-85 (2008))。IL-6の3’UTR cDNAの部分(1-92、1-102、1-112、1-132、1-142及び122-197のいずれか)を、pGL3ベクターに、Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Pressに記載の方法に従って挿入した。IL-6の3’UTR (77-108)配列を有する又は有さないβグロビン(1-130)の3’-UTR cDNA、及びIL-12p40 (1-781)、CalcR (1-1601)及びインターフェロンγ(1-631)の3’-UTR cDNAのそれぞれを、Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Pressに記載の方法に従って、pGL3ベクターに挿入した。IL-6のCDS及びIL-6のCDS+3’ UTRを、それぞれMolecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Pressに記載の方法に従って、pTREtightベクター(Clontech社)に挿入し、pTREtight-IL6-CDS及びpTREtight-IL6-CDS+3’UTRを作製した。野生型及び変異型(D141N) Zc3h12a cDNAを(Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Pressに記載の方法に従って、それぞれpGEX-6P1ベクター(GE Healthcare社)に挿入し、pGEX-6P1-Zc3h12a及びZc3h12a D141N変異プラスミドを作製した。IL-6の3’UTR cDNAを、Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Pressに記載の方法に従ってpBluescriptのT7プロモーターの下流に挿入し、pBluescript-IL6 3’UTR (1-430)を作製した。
培地上澄み中のIL-4、IL-6、IL-12p40、IL-17、IFN-γ及びTNF-a、並びに血清中のマウスANA-抗体を、製造者のプロトコールに従ってELISAにより測定した。血清中のマウスのIgM、IgG1、IgG2a、IgG2b、IgG3及び抗二本鎖DNA抗体のELISA測定は、Sato, S. et al. Essential function for the kinase TAK1 in innate and adaptive immune responses. Nat Immunol 6, 1087-95 (2005)、及びFukuyama, et al., The inhibitory Fcgamma receptor modulates autoimmunity by limiting the accumulation of immunoglobulin G+ anti-DNA plasma cells. Nat Immunol 6, 99-106 (2005)に記載の方法に従って行った。
ノーザンブロッティング、免疫ブロッティング及びEMSAは、Sato, S. et al. Essential function for the kinase TAK1 in innate and adaptive immune responses. Nat Immunol 6, 1087-95 (2005)に記載の方法に従って行った。
野生型及びZc3h12a-/-マウスそれぞれから調製した血液の血液学的な分析は、エスアールエル(SRL Inc.)にて行った。
フローサイトメトリー測定のための抗体は、BD社から購入した。脾臓の細胞懸濁液の調製は、フィルターと、穏やかなピペッティングによって行なった。表面染色のために、細胞を暗室に4℃で保持した。細胞を、氷冷したFACS buffer (2%FCS, 0.02% NaN3 in PBS)で洗浄し、各抗体と15分間インキュベートし、次いでFACS bufferで3回洗浄した。FoxP3+調節性T細胞を、Mouse Regulatory T Cell Staining Kit (eBioscience社)を用いて、製造者の作製した使用説明書に従って染色した。細胞内サイトカインは、BD Cytofix/Cytoparm Plus Fixation/Permeabilization Kit (BD社)を用いて、製造者が作製した使用説明書に従って染色した。データは、Facs Calibur(登録商標)又はFacs Canto(登録商標)II flow cytometer(BD社)によって測定し、FlowJo(Tree Star社のソフトウェア)を使用して分析した。
mRNAの安定性は、以下の3種の異なる方法を使用して決定した。
(1)マクロファージにおけるmRNAの安定性
野生型及びZc3h12a-/-マウス由来の腹腔マクロファージ(1×106)を、それぞれLPS (100 ng/ml)で2時間刺激した。その後、アクチノマイシンD(2μg/ml)を培地に加えて転写を停止させ、所定期間において全RNAを調製した。このRNAを、ノーザンブロット分析に供し、IL-6、TNF、KC及びβアクチンmRNA値を測定した。
(2)Tet-off system HEK293tet-off細胞(3×106)に、pTREtight-IL6-CDS(IL-6をコードする配列を有する)又はpTREtight-IL6-CDS+3’UTR(IL-6をコードする配列及び非翻訳領域の3’UTR配列を有する)と、Zc3h12aの野生型若しくは変異型の発現プラスミド又はコントロールの空プラスミドとを用いて形質移入した。3時間後、細胞を3つの60-mm皿に細分し、終夜培養した。pTREtirhtベクターからのmRNAの転写を、Dox (1μg/ml)を添加して停止させ、所定期間において全RNAを調製した。このRNAをノーザンブロット分析に供し、IL-6及びβ-アクチンmRNA値を測定した。
(3)ルシフェラーゼアッセイ
pGL3-IL-6 3’UTRプラスミド又はpGL3-empty(空)プラスミドと、Zc3h12a発現プラスミド又はコントロールの空プラスミドとを用いて、HEK293細胞に形質移入した。培養48時間後、細胞を溶解させ、溶菌液におけるルシフェラーゼ活性を、Dual-luciferase reporter assay system (Promega社)によって測定した。ウミシイタケルシフェラーゼ(renilla-luciferase)遺伝子を、同時に内部コントロールとして形質移入した。
Zc3h12aの野生型及び変異体の切断活性は、Miyoshi, K., et al., In vitro RNA cleavage assay for Argonaute-family proteins. Methods Mol Biol 442, 29-43 (2008)に記載の方法に従って測定した。続いて、組換えZc3h12aタンパク質と、in vitroで転写された[32P]標識RNAとをインキュベートし、切断されたRNAを精製し、denaturing PAGE及びオートラジオグラフィーで分析した。
具体的には、組換えタンパク質及びin vitroで転写された[32P]標識RNA(5000 cpm)を、切断バッファー (25 mM Hepes, 50 mM KOAc, 5μM DTT)と、Rnasin plus (40U)(Promega社)の存在下、5 mM Mg(Oac)2 有り又はなしで、混合した。切断されたRNAをTRIzol (InvitroGen社)によって精製し、6% TBE-Urea gel (InvitroGen社)を用いるdenaturing PAGE及びオートラジオグラフィーによって分析した。
野生型(Wild-type)及びZc3h12a-/-マウスそれぞれから、骨髄細胞を調製した。調製した骨髄細胞を、致命的に照射されたCD45.1 C57BL/6マウス(大阪大学微生物病研究所感染動物実験施設にて繁殖)に静脈投与した。キメラマウスに、飲料水にネオマイシン及びアンピシリンを入れて4週間与えた。再構成後、少なくとも8週間でマウスを分析した。キメラマウスの脾細胞の90%以上が、CD45.2陽性だった。
pGEX-6P1-Zc3h12a又はZc3h12a D141N変異プラスミドで形質転換された大腸菌(E. coli)BL21-Gold(DE3)pLysS (Stratagene社)において、タンパク質を発現させた。タンパク質発現後、細胞を回収し、PBSに再懸濁した。超音波によって細胞を溶解させ、Triton X-100を最終濃度1%となるように加え、30分間、4℃で穏やかに振とうしながらインキュベートした。次いで、遠心分離によって残骸を除去し、上澄みをGlutathion Sepharose 4B (GE Healthcare社)とともに30分間4℃で、穏やかに振とうしながらインキュベートした。樹脂を回収し、PBSで5回洗浄した後、PreScission Protease cleavage buffer (50 mM Tris, 150 mM NaCl, 1 mM EDTA and 1μM DTT)に再懸濁した。PreScission Protease (GE Healthcare社) (80U)を加えて、穏やかに振とうしながら4時間4℃でインキュベートした。上澄みを回収し、組換えタンパク質溶液として、-80℃で保存した。
IL-6の3’UTR配列を有するRNAの合成のためのテンプレートとして、pBluescript-IL6 3’UTR (1-430)プラスミドを使用した。In vitro RNA合成及び[32P]標識化(ラベリング)は、Riboprobe in vitro Transcription system (Promega社)を用いて、製造者の作製した使用説明書に従って行なった。5’-末端の標識化は、標識化していないRNA及びKinase Max 5’-end labeling Kit (ambion社)を用いて、製造者の作製した使用説明書に従って行なった。3’-末端の標識化は、標識化していないRNAと、T4 RNA Ligase (Takara社)及び[32P]pCp (GE Healthcare社)とをインキュベートすることにより行なった。
[32P]標識RNA (1×106 cpm)と、組換えタンパク質又はBSA(Pierce社)とを、バッファー(25 mM Hepes, 50 mM KOAc, 5μM DTT)中で混合し、20分間室温でインキュベートした。次いで、ヘパリンを最終濃度5μg/mlとなるように添加し、さらに10分間インキュベートした。FUNA-UV-LINKER FS-800(フナコシ社)を使用して、氷上で、254 nmのUVを光源から5 cmの距離で20分間照射することによりサンプルを架橋させた。架橋したサンプルを、20分間室温でRNaseT (100 U)で処理し、次いで、RNaseA(1μg)で15分間37℃で処理した。消化後、[32P]標識RNAに結合したタンパク質を、SDS-PAGE及びオートラジオグラフィーによって分析した。
野生型マウス(日本クレアから購入)、MyD88-/-マウス(Adachi O, Kawai T, Takeda K, Matsumoto M, Tsutsui H, Sakagami M, Nakanishi K, Akira S. Targeted disruption of the MyD88 gene results in loss of IL-1- and IL-18-mediated function. Immunity. 1998 Jul;9(1):143-50.に記載の方法で作製)及びTrif-/-マウス(Yamamoto M, Sato S, Hemmi H, Hoshino K, Kaisho T, Sanjo H, Takeuchi O, Sugiyama M, Okabe M, Takeda K, Akira S. Role of adaptor TRIF in the MyD88-independent toll-like receptor signaling pathway. Science. 2003 Aug 1;301(5633):640-3に記載の方法で作製)由来の腹腔マクロファージを、100 ng/mlのLPSで0、1及び4時間刺激した。全RNAを、RNeasy kit (Qiagen社、Hilden, Germany)を用いて抽出し、全RNAの10μgから、T7-(dT) 24プライマーで予備刺激されたSuperScript Choice System (Invitrogen社、Carlsbad, CA)を用いて、二本鎖cDNAを合成した。これらのcDNAを、製造者(Enzo Diagnostics社、 Farmingdale, NY)の作製したプロトコールに従って、ビオチン化リボヌクレオチドの存在下で、T7 RNAポリメラーゼを用いて行なわれるin vitro転写反応によるビオチン標識cRNAの調製に使用した。cRNA産物を、RNeasy kit (Qiagen社)を用いて精製し、断片化し、製造者の作製したプロトコールに従ってAffymetrix mouse expression array A430 microarray chip(Affymetrix社、Santa Clara, CA)とハイブリダイズさせた。Zc3h12a-/-マクロファージにおけるLPS誘導性遺伝子の決定のために、腹腔マクロファージを100 ng/mlのLPSで刺激した。次いで、全RNAをTRIzol (Invitrogen Life Technologies社)で抽出し、RNeasy kitを用いてさらに精製した。精製したRNA100 ngから、Ovation Biotin RNA Amplification and Labeling System (Nugen社)を使用して、製造者が作製したプロトコールに従って、ビオチン標識cDNAを合成した。Affymetrix mouse Genome 430 2.0 microarray chipのハイブリダイゼーション、染色、洗浄及びスキャンは、製造者が作製した使用説明書に従って行なった。Robust multichip average (RMA) expression valuesを、R and Bioconductor affy packageを使用して計算した。階層的なクラスター化のために、刺激後0時間と比較して2又は5倍増加したプローブを選択した。RMA expression valueを、それぞれ0及び1に対する平均及び標準偏差に合うように、各プローブによって変換した。MyD88-/-及びTrif-/-マクロファージにおけるLPS誘導性遺伝子の分析のために、距離関数(distance function)としてPearson’s correlation coefficientを使用して、プローブ間の距離を計算した。Zc3h12a-/-マクロファージにおけるLPS誘導性遺伝子の分析のために、RMA値に対する主成分分析を行い、プローブ間のユークリッド距離(Euclidean distances)を、第一から第5の主成分を用いて計算した。これらの距離を用いて、ウォード法(Ward’s method)によって階層的なクラスター化を行なった。これらの計算及びheat map表示の作成は、R and Bioconductorを用いて行なった。
10%ホルマリン中性バッファー溶液で組織を固定し、パラフィンで包埋し、そして5μmの厚さの切片にした。切片をTarget Retrieval Solution (Dako社、 Glostrup, Denmark)中で、98℃で40分間加熱し、抗原の検出を促進した。切片を、マウスIgA(α鎖)に対するペルオキシダーゼ標識ヤギIgGフラクション(peroxidase-conjugated goat IgG fraction)(MP Biomedicals社、LLC, Solon, OH)を抗体希釈液(商品名:ChemMate、Dako社)で1:50に希釈したもの、又は、マウスIgG(分子全体)に対するペルオキシダーゼ標識ヤギアフィニティー精製F(AB’)2フラグメント(peroxidase-conjugated goat affinity purified F(AB’)2 fragment)(MP Biomedicals社)を抗体希釈液で1:25に希釈したものと、室温で30分間インキュベートした。マウスIgA及びIgGに対して免疫反応した細胞を、ジアミノベンジジン(Dako社)を用いて可視化した。切片を、ヘマトキシリンによって軽く対比染色した。染色した切片を、光学顕微鏡で観察した。
Zc3h12c N-末端ドメインのモデルは、以下のように構築した。
まず、BioInfoBank Meta Server (http://bioinfo.pl)に配列を提出し、トップ10のモデルを、デフォルトのセッティングを使用して構築した。次いで、SeSAW functional annotation server (http://pdbjs6.pdbj.org/SeSAW/)にそれぞれを提出し、最も高いスコアのモデルを選択することにより、ベストモデルを選択した。選択したモデルを、FFAS03 server (http://ffas.ljcrf.edu/ffas-cgi/cgi/ffas.pl)及びModeller(Eswar, N. et al. Comparative protein structure modeling using Modeller. Curr Protoc Bioinformatics Chapter 5, Unit 5 6 (2006))を使用して、構造ゲノミクステンプレート(structural genomics template)2qipから構築した。最も高い3D Jury scoreも有するこのモデルは、フラップエンドヌクレアーゼ(例えば、PDB ID 1ut5)(Feng, M. et al. Roles of divalent metal ions in flap endonuclease-substrate interactions. Nat Struct Mol Biol 11, 450-6 (2004))の活性部位においても保存されている、保存されたアスパラギン酸のクラスター(D141、D226、S242、D244、及びD248)を含んだ。静電的表面は、eF-surf server (http://ef-site.hgc.jp/eF-surf/)及びeF-site(Kinoshita, K. & Nakamura, H. eF-site and PDBjViewer: database and viewer for protein functional sites. Bioinformatics 20, 1329-30 (2004))を使用して調製した。
LPS誘導性遺伝子としてのZc3h12aの同定
Toll-like receptors (TLRs)を誘導する遺伝子の発現を包括的に研究するために、野生型(WT)マウス、LPSで刺激したMyD88-/-マウス及びTRIF-/-マウスからのマクロファージを用いて、上述した方法でマイクロアレイ解析を行った。
Zc3h12a-/-マウスの創製
生体内での免疫応答の制御におけるZc3h12aの機能的役割を研究するために、Zc3h12a欠損 (Zc3h12a-/-)マウスを創製した。
図2cに、LPS (100 ng/ml)で所定時間刺激した野生型(WT)(Zc3h12a+/+)及びZc3h12a-/-マクロファージのRNAのRT-PCR分析の結果を示す。RT-PCR分析は、Zc3h12aの発現がZc3h12a-/-マクロファージにおいて抑制されることを示した(図2c)。
Zc3h12a-/-マウスにおける、胎生期の自己免疫疾患の早期発症
Zc3h12a-/-マウスはメンデルの法則に従い生まれるが、その殆どは、成長が遅滞し、殆どのマウスが生後12週以内に自然に死亡した(図3a)。図3aは、野生型(Zc3h12a+/+)及びZc3h12a-/-マウスの生存率を示す図である(n=10)。図3bは、野生型(Zc3h12a+/+)(上図)及びZc3h12a-/-マウス(下図)の脾臓(上)、腸間膜リンパ節(左下)及び鼠径リンパ節(右下)の写真である。Zc3h12a-/-マウスは、重篤な脾腫とリンパ節腫張を示した(図3b)。図3cは、野生型(Zc3h12a+/+)及びZc3h12a-/-マウスの肺、脾臓及びリンパ節(LN)の組織写真である。図4は、野生型(WT)及びZc3h12a-/-マウスの肝臓及び膵臓切片のH & E染色の結果を示す。組織学的解析は形質細胞(プラズマ細胞)の肺、並びに胆管及び脾臓の経上皮への侵入を示した(図3c及び図4)。形質細胞は、Zc3h12a-/-リンパ節(LN)及び脾臓にも蓄積した(図3c)。LNにおいて、肉芽腫形成が見られ、マクロファージと融合した巨細胞の生成を認めた。これにもかかわらず、炎症の変化はZc3h12a-/- マウスの腸でも関節でも見られなかった(データは示さず)。
Zc3h12a-/-マウスにおける抗核抗体(ANA)及び抗二重鎖DNA抗体の生産を調べた結果を、図5bに示す。統計的優位性は、Student’s t-testによって決定した(*:P< 0.05、**:P< 0.01)抗核抗体及び抗二重鎖DNA抗体の生産が、Zc3h12a-/-マウスで見られた(図5b)。
図5cに、抗IgG及び抗IgA抗体による、肺切片の免疫組織化学的検査の結果(組織写真)を示す。肺及び腸組織に侵入した形質細胞は、抗IgG又は抗IgA抗体で容易に染色された(図5c)。
図8は、脾臓のT細胞における、CD3/CD28刺激への応答におけるインターフェロンγ、IL-17及びIL-4の生産を調べた結果を示す図である。エラーバーは、2組の標準偏差(S.D.)を示す。3つの異なる実験において、同様の結果が得られた。
図9b、及び図10a及びbは、野生型及びZc3h12a-/-マウスの脾細胞を、抗体で染色し、フローサイトメトリーによって分析した結果を示す図である。
図11は、Zc3h12a-/-マウスにおける、形質細胞及びエフェクター/免疫記憶T細胞の蓄積における造血細胞の関与を調べた結果である。図11に示す実験においては、野生型及びZc3h12a-/-骨髄キメラの脾細胞を、抗体で染色し、フローサイトメトリーで分析した。
しかし、T細胞に対するB細胞の比率、及びH CD8+細胞に対するCD4+細胞の比率はZc3h12a-/-マウス脾臓において変わらなかった(図10a及びb)。造血細胞が疾患の進行に十分であるか否かを調べるために、Zc3h12a-/-マウスからの骨髄細胞をレシピエントのC57BL/6マウスに移植した。Zc3h12a-/- BMキメラは、遅れた、しかし重要なリンパ節症の発展と、形質細胞及びCD44highCD62L-T細胞の蓄積を示した。これは、造血細胞が、免疫不全の伸展に寄与することを示している(図11)。
これらの結果は、Zc3h12aが、Igを生産する形質細胞及び肉芽腫の形成によって特徴付けられる重篤な免疫疾患の伸展に必須であることを示している。
次に、マクロファージからのサイトカインの生産について調べた。
野生型(Zc3h12a+/+)及びZc3h12a-/-マウスの腹腔マクロファージをMALP-2 (1、10 ng/ml)、Poly I:C (100μg/ml)、LPS (10、100 ng/ml)、R-848 (10 nM)及びCpG-DNA (0.1、1μM)のいずれかで24時間刺激した。培地の上澄み中のIL-6、IL-12p40及びTNF濃度を、ELISAで測定した。結果を図12aに示す。図12aにおいて、“med”は、上記物質で刺激しなかったマクロファージ(コントロール)である。エラーバーは、2組の標準偏差(S.D.)を示す。3つの異なる実験において、同様の結果が得られた。
また、所定の期間LPS (100 ng/ml)によって刺激されたマクロファージ由来の全RNAを抽出し、IL-6、KC、TNF、IκBα、RANTES、IP-10及びβアクチンの発現を調べるためのノーザンブロットに供した。この結果を図12bに示す。
図13は、野生型(Zc3h12a+/+)及びZc3h12a-/-の腹腔マクロファージのマイクロアレイ分析に基づき選択されたLPS誘導性遺伝子の発現のHeat map表示である。
CCCH-type Zfモチーフを持つ蛋白質のいくつかは、mRNAスプライシング、ポリアデニル化、及びmRNA崩壊の制御のようなmRNAの代謝に関係していることが報告されている。このように、Zc3h12aがmRNAの不安定性において役割をはたしているかもしれないと仮定し、この可能性をIL-6を用いて検討した。
図16に、Zc3h12aが、1セットの遺伝子から、その3’-UTRを通してmRNAを不安定化することを示す結果を示す。図16aは、全RNA(10μg)を抽出し、IL-6、TNF、KC及びβアクチンプローブの発現を調べるためのRNAブロット分析に供した結果を示す図である。3つの異なる実験において、同様の結果が得られた。図16bは、残存mRNAの経時変化を示す。図16bにおいては、オートラジオグラフを定量し、IL-6、Tnf及びCxcl1のActbに対する比を、残存mRNAレベルの決定に使用した。
IL-6の3’-UTRにおけるZc3h12a応答領域の決定
Tet-On Gene Expression System (TAKARA)の説明書に記載の方法に従って、Zc3h12aの発現がIL-6 mRNAを調節するか調べるために、ウイルス転写因子VP-16 (tet-off 293 cells)のトランス活性化ドメインを融合させたテトラサイクリン応答性タンパク質を安定して発現するHEK293細胞を、テトラサイクリン反応性プロモーター(TRE)の調節下、3’ 非翻訳領域(UTR)を有するIL-6をコードする配列(CDS)を内部に有するプラスミド(pTREtight-IL6CDS+3’UTR)を用いて形質移入した。ドキソルビシン (Dox)と処理することによって、IL-6 mRNAの転写を停止させると、mRNAは、インキュベーション時間に依存的に崩壊した(図17a)。Zc3h12aの過剰発現は、IL-6のmRNAの分解を非常に加速した(図17a及びb)。対照的に、Zc3h12aは、3’-UTR配列を内部に有さないmRNA(pTREtight-IL6CDS)の発現には影響を与えなかった(図17a及びb)。
図17aにおいては、細胞は、形質移入から3時間後に分けられ、終夜インキュベートされた。次にDox (1μg/ml)処理を行ない、全RNAを調製し、ノーザンブロット分析によってIL-6及びβアクチンレベルを決定した。図17bにおいては、オートラジオグラフを定量し、IL-6のActbに対する比を、残存mRNAレベルの決定に使用した。
図19a及びbにおいては、IL-6(図19a)の3’-UTR及びb-Globinの3’-UTR(図19b)の種々の配列を内部に有するpGL3プラスミドと、Zc3h12発現プラスミド又はコントロールの空プラスミドとを用いて、HEK293細胞に形質移入し、48時間後に該細胞の溶菌液のルシフェラーゼ活性を測定した。図19cにおいては、HEK293細胞に、IL-6、IL-12p40、CTR又はインターフェロンγに対する3’-UTRを内部に有するpGL3と、Zc3h12a発現プラスミド又はコントロールの空プラスミドとを用いて形質移入し、48時間後に該細胞の溶菌液のルシフェラーゼ活性を測定した。
Zc3h12aが直接RNAと結合するかを、調べた。図21に、UV架橋アッセイによるIL-6の3’UTR (1-403) mRNAに対する結合を調べた結果を示す。ウシ血清アルブミンン(BSA)ではなく、合成されたZc3h12aタンパク質は、in vitroで転写されたIL-6の3’-UTR (1-403)RNAと結合し、Zc3h12aがRNA結合能を有していることが示唆された(図21)。
IL-6 mRNAの不安定化における、CCCH Zfモチーフの役割
Zc3h12aのCCCH配列がIL-6のmRNAの崩壊において重要な役割を果たすことについて実験を行なった。
図22aは、HEK293 Tet-off細胞に、pTREtight-IL6-CDS+3’UTRと、種々の量のFlag-Zc3h12a又はその変異体(C306R及びΔCCCH)をコードする発現プラスミドとを用いて、同時形質移入した後、細胞をDoxで所定時間処理し、IL-6の発現をノーザンブロット分析で決定した結果を示す。図22bは、Zc3h12変異タンパク質の発現量を、免疫ブロッティングによって測定した結果を示す。図22b中の矢印は、発現したZc3h12a蛋白質を示す。
図23aは、HEK293 Tet-off細胞に、pTREtight-IL6-CDS+3’UTRと、Flag-Zc3h12a又はその変異体(C306R及びΔCCCH)をコードする発現プラスミドとを用いて同時形質移入し、次いで、細胞をDoxで所定時間処理し、IL-6の発現をノーザンブロット分析で測定した結果を示す。なお、オートラジオグラフを定量し、IL-6のActbに対する比を、残存mRNAレベルの決定に使用した(図23b)。図23cは、Zc3h12a変異タンパク質の発現レベルを、免疫ブロットによって測定した結果を示す。
図27aは、組換えZc3h12aタンパク質の量を変化させた、5’末端標識又は3’末端標識されたIL-6の3’UTR mRNA (1-403)のin vitroでの切断アッセイの結果を示す。図27bは、Zc3h12aのリボヌクレアーゼ活性の動態分析の結果である。図27に示す実験においては、5’末端標識又は3’末端標識されたIL-6の3’UTR mRNA (1-403)を、組換えZc3h12aタンパク質と所定時間インキュベートした。
これらの実験結果は、Zc3h12aが、結果としてマウスの死亡をもたらす重度の自己免疫応答の発達の阻害に必須であることを明確に証明した。TNFではなく、IL-6及びIL-12p40の生産が、mRNAの崩壊不全によって、Zc3h12a-/-マクロファージにおいて非常に上昇した。CCCH-type zinc fingerタンパク質は、3’-UTRと結合することによって、mRNAの崩壊を調節することが示された。例えば、トリテトラプロリン (TTP) 及びそのホモログであるZfp36l1、Zfp36l2、及びZfp36l3は、TNF、GM-CSF、CXCL1などのmRNAの崩壊に重要である(Anderson, P. Post-transcriptional control of cytokine production. Nat Immunol 9, 353-9 (2008)、及びDatta, S. et al. Tristetraprolin regulates CXCL1 (KC) mRNA stability. J Immunol 180, 2545-52 (2008))。加齢TTP-/-マウスは、TNFの生産によって、自己免疫性関節炎を発症する(Taylor, G. A. et al. A pathogenetic role for TNF alpha in the syndrome of cachexia, arthritis, and autoimmunity resulting from tristetraprolin (TTP) deficiency. Immunity 4, 445-54 (1996))。しかしながら、TTP-/-細胞がTLR刺激の応答においてIL-6量を上昇させることを示した報告はない。興味深いことに、Zc3h12aの損失が、マクロファージにおけるTNF mRNAの発現に影響しないことは、TTP及びZc3h12aが、異なるサイトカインのmRNAの崩壊を調節していることを示唆した。Zc3h12aは、ARE以外のRNA配列を標的とした。そしてIL-6のAREは、未知のZc3h12aに依存しないメカニズムによって調節されているように見える。Zc3h12a-/-マウスにおいて観察された顕著な病理学的発見を考慮すると、IL-6及びIL-12p40以外の遺伝子も、発病に重要にかかわっているように思われた。他の刺激への応答、又は他の型の細胞におけるZc3h12aの標的遺伝子の道程は、Zc3h12a-/-マウスで観察された異常のメカニズムに関する知識を進歩させるであろう。また、Zc3h12aが単球走化性タンパク質1(MCP-1)誘導性タンパク質であることが報告され(Zhou, L. et al. Monocyte chemoattractant protein-1 induces a novel transcription factor that causes cardiac myocyte apoptosis and ventricular dysfunction. Circ Res 98, 1177-85 (2006))、Zc3h12aタンパク質の過剰発現は、NF-κB活性化の阻害を通じてマクロファージにおけるサイトカイン生産を抑制することが示された(Liang, J. et al. A novel CCCH-zinc finger protein family regulates proinflammatory activation of macrophages. J Biol Chem 283, 6337-46 (2008))。しかしながら、本実験はこの報告とは一致せず、Zc3h12aはmRNA崩壊に関与するが、TNFの調節には関与しないことを示した。
Claims (12)
- Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種を有効成分として含む免疫アジュバント組成物。
- さらに、その他の免疫アジュバントを含む請求項1に記載の免疫アジュバント組成物。
- Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種と、ワクチン抗原とを含むワクチン組成物。
- さらに、その他の免疫アジュバントを含む請求項3に記載のワクチン組成物。
- 請求項3に記載のワクチン組成物を動物に投与する、動物の免疫方法。
- 個体から採取された免疫細胞と、Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種とを接触させて、免疫細胞を賦活化させる工程を含む、活性免疫細胞の製造方法。
- 請求項6に記載の方法で製造された活性免疫細胞。
- ワクチン抗原の免疫原性を高めるための、Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種の化合物。
- Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種の化合物の、免疫アジュバントの製造のための使用。
- Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種とワクチン抗原とを混合する工程を含む、ワクチン抗原の免疫原性を高める方法。
- 免疫賦活のための、Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種と、ワクチン抗原とを含む組成物。
- Zc3h12a遺伝子インヒビター、及びZc3h12aタンパク質インヒビターからなる群より選ばれる少なくとも1種と、ワクチン抗原とを含む組成物の、ワクチン組成物の製造のための使用。
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