研究生: |
唐銘甫 Tang, Neos |
---|---|
論文名稱: |
第二b型忌熱型腸毒素作為黏膜佐劑增強保護性免疫對抗H5N1禽流感病毒 Type IIb Heat Labile Enterotoxin B Subunit as a Mucosal Adjuvant to Enhance Protective Immunity against H5N1 Avian Influenza Viruses |
指導教授: |
吳夙欽
Wu, Suh-Chin 蘇士哲 Sue, Shih-Che |
口試委員: |
呂平江
Lyu, Ping-Chiang 黃明熙 Huang, Ming-Hsi 吳弘毅 Wu, Hung-Yi |
學位類別: |
博士 Doctor |
系所名稱: |
生命科學暨醫學院 - 生物科技研究所 Biotechnology |
論文出版年: | 2024 |
畢業學年度: | 112 |
語文別: | 英文 |
論文頁數: | 54 |
中文關鍵詞: | 大腸桿菌第二b 型忌熱型腸毒素 之B 次單元 、黏膜佐劑 、IL-17A 、H5N1 |
外文關鍵詞: | LTIIb-B5, mucosal adjuvant, IL-17A, H5N1 |
相關次數: | 點閱:3 下載:0 |
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高致病性禽流感病毒目前仍威脅著全球人類與禽類的健康,其中H5N1禽流感病毒從1997年被發現能傳染人類後,至今H5N1的突變株病毒依然可傳播至野外飛禽、家禽、海生哺乳動物(如海獅)、一般陸地哺乳動物(如貂、浣熊、貓),以及人類。目前疫苗接種是預防 H5N1 和其他新型禽流感病毒感染的最主要保護策略,但一般的傳統肌肉注射疫苗無法產生具有對抗原專一性的IgA抗體於黏膜表面,需使用黏膜疫苗才有辦法於黏膜產生對抗原專一性的IgA抗體,然而黏膜免疫系統需仰賴黏膜佐劑突破黏膜免疫系統的耐受性。在本論文中,大腸桿菌第二b 型忌熱型腸毒素 之B 次單元 (LTIIb-B5) 作為黏膜佐劑,與 HA 蛋白一起施打於小鼠的鼻腔免疫。結果顯示:LTIIb-B5 佐劑在血清和支氣管肺泡灌洗液中,引發明顯更高的 IgG、IgA 和中和抗體,從而增強對致命性病毒的保護。 LTIIb-B5 也會在脾臟淋巴細胞和頸部淋巴結中引發更強的 Th17 細胞反應。小鼠被注射抗 IL-17A 單株抗體後,經過致命性病毒的感染測試,小鼠體內的IL-17A 耗竭導致死亡率從 0% 增加至 50%,代表 Th17 的細胞反應對保護性免疫有所關連。這些發現可能為H5N1次單元黏膜疫苗的開發提供有用的資訊。
Infections in humans caused by highly pathogenic avian influenza viruses continue to pose a significant global health threat. Vaccination represents the primary preventive measure against H5N1 and other emerging avian influenza virus infections. However, conventional intramuscular vaccines cannot generate antigen-specific IgA antibodies on mucosal surfaces. Mucosal vaccines are necessary to produce antigen-specific IgA antibodies. Mucosal immunization relies on mucosal adjuvants to overcome the tolerance of the mucosal immune system. This dissertation utilized E. coli type IIb heat labile enterotoxin B subunit (LTIIb-B5) as a mucosal adjuvant in conjunction with HA proteins for intranasal immunizations in a mouse model. The findings demonstrated that the LTIIb-B5 adjuvant induced notably elevated levels of IgG, IgA, and neutralizing antibodies in both sera and bronchoalveolar lavage fluids, thereby enhancing protection against lethal virus challenges. Additionally, LTIIb-B5 elicited a more robust Th17 cellular response in spleen lymphocytes and cervical lymph nodes. Depletion of IL-17A subsequent to vaccinations with anti-IL-17A monoclonal antibodies led to an increase in mortality from 0% to 50%, indicating a potential contribution of the Th17 cellular response to protective immunity. These results offer valuable insights for the development of mucosal H5N1 subunit vaccines.
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