Onjisaponins, from the root of Polygala tenuifolia Willdenow, as effective adjuvants for nasal influenza and diphtheria–pertussis–tetanus vaccines
Active substances from hot water extracts from 267 different Chinese and Japanese medicinal herbs were screened for mucosal adjuvant activity with influenza HA vaccine in mice. The extract from the root of Polygala tenuifolia was found to contain potent mucosal adjuvant activity. The active substanc...
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Published in | Vaccine Vol. 19; no. 32; pp. 4824 - 4834 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Oxford
Elsevier Ltd
14.09.2001
Elsevier |
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Abstract | Active substances from hot water extracts from 267 different Chinese and Japanese medicinal herbs were screened for mucosal adjuvant activity with influenza HA vaccine in mice. The extract from the root of
Polygala tenuifolia was found to contain potent mucosal adjuvant activity. The active substances were purified and identified as onjisaponins A, E, F, and G. When each onjisaponin (10 μg) was intranasally (i.n.) inoculated with influenza vaccine (10 μg) in mice, serum hemagglutination-inhibiting (HI) antibody titers increased 3–14 times over control mice administered vaccine alone after 4 weeks. When each onjisaponin (10 μg) was i.n. inoculated with the vaccine (10 μg) followed by i.n. vaccination of the vaccine alone after 3 weeks, serum HI antibody titers increased 27–50 fold over those mice given i.n. vaccinations without onjisaponins. These same conditions also significantly increased nasal anti-influenza virus IgA antibody titers. Two inoculations with onjisaponin F (1 μg) and influenza HA vaccine (1 μg) at 3 weeks intervals, significantly increased serum HI antibody and nasal anti-influenza virus IgA and IgG antibody titers after only 1 week over mice given HA vaccine alone after the secondary vaccination. Intranasal vaccination with onjisaponin F inhibited proliferation of mouse adapted influenza virus A/PR/8/34 in bronchoalveolar lavages of infected mice. Separate intranasal vaccinations with onjisaponins A, E, F, and G (10 μg) each and diphtheria–pertussis–tetanus (DPT) vaccine (10 μg) of mice followed by i.n. vaccination with DPT vaccine alone after 4 weeks showed significant increases in serum IgG and nasal IgA antibody titers after 2 weeks following secondary vaccination over mice vaccinated with DPT vaccine alone. All onjisaponins showed little hemolytic activity at concentrations up to 100 μg/ml. The results of this study suggest that onjisaponins may provide safe and potent adjuvants for intranasal inoculation of influenza HA and DPT vaccines. |
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AbstractList | Active substances from hot water extracts from 267 different Chinese and Japanese medicinal herbs were screened for mucosal adjuvant activity with influenza HA vaccine in mice. The extract from the root of
Polygala tenuifolia was found to contain potent mucosal adjuvant activity. The active substances were purified and identified as onjisaponins A, E, F, and G. When each onjisaponin (10 μg) was intranasally (i.n.) inoculated with influenza vaccine (10 μg) in mice, serum hemagglutination-inhibiting (HI) antibody titers increased 3–14 times over control mice administered vaccine alone after 4 weeks. When each onjisaponin (10 μg) was i.n. inoculated with the vaccine (10 μg) followed by i.n. vaccination of the vaccine alone after 3 weeks, serum HI antibody titers increased 27–50 fold over those mice given i.n. vaccinations without onjisaponins. These same conditions also significantly increased nasal anti-influenza virus IgA antibody titers. Two inoculations with onjisaponin F (1 μg) and influenza HA vaccine (1 μg) at 3 weeks intervals, significantly increased serum HI antibody and nasal anti-influenza virus IgA and IgG antibody titers after only 1 week over mice given HA vaccine alone after the secondary vaccination. Intranasal vaccination with onjisaponin F inhibited proliferation of mouse adapted influenza virus A/PR/8/34 in bronchoalveolar lavages of infected mice. Separate intranasal vaccinations with onjisaponins A, E, F, and G (10 μg) each and diphtheria–pertussis–tetanus (DPT) vaccine (10 μg) of mice followed by i.n. vaccination with DPT vaccine alone after 4 weeks showed significant increases in serum IgG and nasal IgA antibody titers after 2 weeks following secondary vaccination over mice vaccinated with DPT vaccine alone. All onjisaponins showed little hemolytic activity at concentrations up to 100 μg/ml. The results of this study suggest that onjisaponins may provide safe and potent adjuvants for intranasal inoculation of influenza HA and DPT vaccines. Active substances from hot water extracts from 267 different Chinese and Japanese medicinal herbs were screened for mucosal adjuvant activity with influenza HA vaccine in mice. The extract from the root of Polygala tenuifolia was found to contain potent mucosal adjuvant activity. The active substances were purified and identified as onjisaponins A, E, F, and G. When each onjisaponin (10 microg) was intranasally (i.n.) inoculated with influenza vaccine (10 microg) in mice, serum hemagglutination-inhibiting (HI) antibody titers increased 3-14 times over control mice administered vaccine alone after 4 weeks. When each onjisaponin (10 microg) was i.n. inoculated with the vaccine (10 microg) followed by i.n. vaccination of the vaccine alone after 3 weeks, serum HI antibody titers increased 27-50 fold over those mice given i.n. vaccinations without onjisaponins. These same conditions also significantly increased nasal anti-influenza virus IgA antibody titers. Two inoculations with onjisaponin F (1 microg) and influenza HA vaccine (1 microg) at 3 weeks intervals, significantly increased serum HI antibody and nasal anti-influenza virus IgA and IgG antibody titers after only 1 week over mice given HA vaccine alone after the secondary vaccination. Intranasal vaccination with onjisaponin F inhibited proliferation of mouse adapted influenza virus A/PR/8/34 in bronchoalveolar lavages of infected mice. Separate intranasal vaccinations with onjisaponins A, E, F, and G (10 microg) each and diphtheria-pertussis-tetanus (DPT) vaccine (10 microg) of mice followed by i.n. vaccination with DPT vaccine alone after 4 weeks showed significant increases in serum IgG and nasal IgA antibody titers after 2 weeks following secondary vaccination over mice vaccinated with DPT vaccine alone. All onjisaponins showed little hemolytic activity at concentrations up to 100 microg/ml. The results of this study suggest that onjisaponins may provide safe and potent adjuvants for intranasal inoculation of influenza HA and DPT vaccines. Active substances from hot water extracts from 267 different Chinese and Japanese medicinal herbs were screened for mucosal adjuvant activity with influenza HA vaccine in mice. The extract from the root of Polygala tenuifolia was found to contain potent mucosal adjuvant activity. The active substances were purified and identified as onjisaponins A, E, F, and G. When each onjisaponin (10 mu g) was intranasally (i.n.) inoculated with influenza vaccine (10 mu g) in mice, serum hemagglutination-inhibiting (HI) antibody titers increased 3-14 times over control mice administered vaccine alone after 4 weeks. When each onjisaponin (10 mu g) was i.n. inoculated with the vaccine (10 mu g) followed by i.n. vaccination of the vaccine alone after 3 weeks, serum HI antibody titers increased 27-50 fold over those mice given i.n. vaccinations without onjisaponins. These same conditions also significantly increased nasal anti-influenza virus IgA antibody titers. Two inoculations with onjisaponin F (1 mu g) and influenza HA vaccine (1 mu g) at 3 weeks intervals, significantly increased serum HI antibody and nasal anti-influenza virus IgA and IgG antibody titers after only 1 week over mice given HA vaccine alone after the secondary vaccination. Intranasal vaccination with onjisaponin F inhibited proliferation of mouse adapted influenza virus A/PR/8/34 in bronchoalveolar lavages of infected mice. Separate intranasal vaccinations with onjisaponins A, E, F, and G (10 mu g) each and diphtheria-pertussis-tetanus (DPT) vaccine (10 mu g) of mice followed by i.n. vaccination with DPT vaccine alone after 4 weeks showed significant increases in serum IgG and nasal IgA antibody titers after 2 weeks following secondary vaccination over mice vaccinated with DPT vaccine alone. All onjisaponins showed little hemolytic activity at concentrations up to 100 mu g/ml. The results of this study suggest that onjisaponins may provide safe and potent adjuvants for intranasal inoculation of influenza HA and DPT vaccines. |
Author | Kato, Toshio Aizawa, Chikara Nagamine, Takashi Nagai, Takayuki Yamada, Haruki Suzuki, Yujiro Yabe, Takeshi Kiyohara, Hiroaki Susa, Eizaburo Hagiwara, Yukari Tamura, Shin-ichi |
Author_xml | – sequence: 1 givenname: Takayuki surname: Nagai fullname: Nagai, Takayuki organization: Oriental Medicine Research Center, The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8642, Japan – sequence: 2 givenname: Yujiro surname: Suzuki fullname: Suzuki, Yujiro organization: Research Center for Biologicals, The Kitasato Institute, 6-111 Arai, Kitamoto-shi, Saitama 364-0026, Japan – sequence: 3 givenname: Hiroaki surname: Kiyohara fullname: Kiyohara, Hiroaki organization: Oriental Medicine Research Center, The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8642, Japan – sequence: 4 givenname: Eizaburo surname: Susa fullname: Susa, Eizaburo organization: Research Center for Biologicals, The Kitasato Institute, 6-111 Arai, Kitamoto-shi, Saitama 364-0026, Japan – sequence: 5 givenname: Toshio surname: Kato fullname: Kato, Toshio organization: Research Center for Biologicals, The Kitasato Institute, 6-111 Arai, Kitamoto-shi, Saitama 364-0026, Japan – sequence: 6 givenname: Takashi surname: Nagamine fullname: Nagamine, Takashi organization: Research Center for Biologicals, The Kitasato Institute, 6-111 Arai, Kitamoto-shi, Saitama 364-0026, Japan – sequence: 7 givenname: Yukari surname: Hagiwara fullname: Hagiwara, Yukari organization: Research Center for Biologicals, The Kitasato Institute, 6-111 Arai, Kitamoto-shi, Saitama 364-0026, Japan – sequence: 8 givenname: Shin-ichi surname: Tamura fullname: Tamura, Shin-ichi organization: Department of Pathology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan – sequence: 9 givenname: Takeshi surname: Yabe fullname: Yabe, Takeshi organization: Oriental Medicine Research Center, The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8642, Japan – sequence: 10 givenname: Chikara surname: Aizawa fullname: Aizawa, Chikara organization: Research Center for Biologicals, The Kitasato Institute, 6-111 Arai, Kitamoto-shi, Saitama 364-0026, Japan – sequence: 11 givenname: Haruki surname: Yamada fullname: Yamada, Haruki email: yamadaha@kitasato-u.ac.jp |
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Keywords | Adjuvant Mucosal immunity Onjisaponin Influenza vaccine DPT vaccine Infection Root Respiratory disease Viral disease Influenza Bacteriosis Vaccine Tetanus Diphtheria Whooping cough |
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Snippet | Active substances from hot water extracts from 267 different Chinese and Japanese medicinal herbs were screened for mucosal adjuvant activity with influenza HA... |
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SubjectTerms | Adjuvant Adjuvants, Immunologic - administration & dosage Adjuvants, Immunologic - isolation & purification Administration, Intranasal Animals Antibodies, Bacterial - biosynthesis Antibodies, Bacterial - immunology Antibodies, Viral - biosynthesis Antibodies, Viral - immunology Biological and medical sciences Bordetella pertussis - immunology Chick Embryo Chromatography, High Pressure Liquid Corynebacterium diphtheriae - immunology Diphtheria-Tetanus-Pertussis Vaccine - chemistry Diphtheria-Tetanus-Pertussis Vaccine - immunology DPT vaccine Epidemiology. Vaccinations Ferrets Fundamental and applied biological sciences. Psychology General aspects Hemagglutinin Glycoproteins, Influenza Virus - immunology Hemolytic Plaque Technique Infectious diseases Influenza A virus - immunology Influenza vaccine Influenza Vaccines - chemistry Influenza Vaccines - immunology Medical sciences Mice Microbiology Molecular Structure Mucosal immunity Nasal Mucosa - immunology Onjisaponin onjisaponins Plant Extracts - chemistry Plant Roots - chemistry Polygala tenuifolia Polygalaceae - chemistry Saponins - administration & dosage Saponins - chemistry Saponins - immunology Saponins - isolation & purification Sheep Solvents Species Specificity Triterpenes - administration & dosage Triterpenes - chemistry Triterpenes - immunology Triterpenes - isolation & purification Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies Virology Water |
Title | Onjisaponins, from the root of Polygala tenuifolia Willdenow, as effective adjuvants for nasal influenza and diphtheria–pertussis–tetanus vaccines |
URI | https://dx.doi.org/10.1016/S0264-410X(01)00215-8 https://www.ncbi.nlm.nih.gov/pubmed/11535335 https://search.proquest.com/docview/18114415 https://search.proquest.com/docview/71147638 |
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