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Induction of innate immunity by nasal influenza vaccine administered incombination with an adjuvant (cholera toxin)

机译:鼻流感疫苗与佐剂(霍乱毒素)联合给药可诱导先天免疫

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Inactivated influenza vaccine was administered intranasally to BALB/c mice together with an adjuvant (cholera toxin B subunit [CTB] supplemented with a trace amount of the whole toxin, CTB*) and its ability to induce innate immunity and confer protection against influenza was examined. Nasal wash virus titres 3 days after inoculation of homologous Viruses were measured as an index of the ability of the vaccine to confer protection in mice immunized with either CTB*-combined vaccine or CTB* alone 1-21 days previously. The results were as follows. (1) Partial but significant reduction of the nasal-wash Virus titres (prevention) was detected beginning 3 days after the vaccination, that is, 2 days earlier than the appearance of both virus-specific antibody-forming cells (AFCs) in the nasal-associated lymphoid tissue (NALT) and virus-specific IgA antibody responses in the nasal washes of mice immunized with the CTB*-combined vaccine. (2) The protection, detected on day 3 and peaking on day 5 but lost by day 21, was also conferred in mice immunized with CTB* alone. (3) The non-specific prevention was detected at doses of more than 0.3 mu g of CTB*/mouse. (4) The nonspecific protection beginning 3 days after the immunization involved the enhanced expression of cytokine mRNAs (IL-15 and IL-18), considered responsible for natural killer (NK) cell activation, by the non-T cell populations in the NALT. (5) Normal NALT cells, when cultured in vitro with CTB*, secreted IL-IB within a few hours in culture. These results demonstrate that the CTB*-combined vaccine, when given intranasally into mice, can confer nonspecific protection against influenza beginning 3 days after the vaccination and that CTB* also possessed this ability to confer protection non-specifically and temporarily by inducing the secretion of IL-1 beta, one of the most important cytokines that initiates both innate and adaptive immunity, and also NK cell activity.
机译:将灭活的流感疫苗与佐剂(霍乱毒素B亚基[CTB]补充了痕量的全毒素CTB *)一起鼻内注射给BALB / c小鼠,并检查了其诱导先天免疫和赋予抗流感保护能力。接种同源病毒后3天的鼻洗病毒滴度被测量为疫苗在1-21天前用CTB *组合疫苗或单独CTB *免疫的小鼠中提供保护的能力的指标。结果如下。 (1)鼻洗液在疫苗接种后3天开始检测,即检测到部分但显着降低的病毒滴度(预防),即比两个病毒特异性抗体形成细胞(AFC)在鼻中出现的时间早2天CTB *联合疫苗免疫的小鼠的鼻洗液中存在相关的淋巴组织(NALT)和病毒特异性IgA抗体反应。 (2)在单独用CTB *免疫的小鼠中,也提供了在第3天检测到并在第5天达到峰值但在第21天消失的保护作用。 (3)以每只小鼠超过0.3μg CTB *的剂量检测到非特异性预防。 (4)免疫后3天开始的非特异性保护涉及NALT中非T细胞群体增强的细胞因子mRNA(IL-15和IL-18)表达,这被认为是导致自然杀伤(NK)细胞活化的原因。 。 (5)正常NALT细胞在体外与CTB *培养后,会在培养后数小时内分泌IL-IB。这些结果表明,将CTB *组合疫苗鼻内注射给小鼠后,可在接种疫苗后3天开始赋予针对流感的非特异性保护,并且CTB *还具有通过诱导H.O.I分泌而非特异性和暂时性地提供保护的能力。 IL-1 beta是最重要的细胞因子之一,可启动先天和适应性免疫以及NK细胞活性。

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