New Nasal Spray Influenza Vaccine for Children (Research Supplement for Post Baccalaureate Diversity Candidate)
儿童新型鼻喷雾流感疫苗(学士学位后多样性候选人的研究补充)
基本信息
- 批准号:10838135
- 负责人:
- 金额:$ 14.58万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-03-10 至 2026-02-28
- 项目状态:未结题
- 来源:
- 关键词:Antiviral AgentsAttenuatedAvian Influenza A VirusCOVID-19ChildCountryDrug resistanceEnvironmentFundingFutureGene ExpressionGene TargetingHealth SciencesHumanInfectionInfluenzaInfluenza TherapeuticInfluenza vaccinationIntegration Host FactorsMedical StudentsMicroRNAsMolecularNosePerformancePostbaccalaureatePreventive vaccinePublic HealthResearchResearch TrainingTexasTherapeuticTwin Multiple BirthUniversitiesVaccinatedVaccinesViralViral GenesVirulentVirusVirus Replicationattenuationefficacy evaluationgraduate studentinfluenza infectioninfluenza virus straininfluenza virus vaccineinfluenzavirusmouse modelnovelnovel therapeuticsnovel vaccinespreventprogramsprophylacticpublic health relevanceseasonal influenzaside effecttherapeutic vaccinetraining opportunitytransmission processundergraduate studentuniversal influenza vaccinevaccine development
项目摘要
New Nasal Spray Influenza Vaccine for Children
(Research Supplement for R15HD109732)
Project Summary/Abstract:
Influenza is still a global public health problem for children despite a vigorous campaign for influenza
vaccination in many countries. Recent emergence of the COVID-19 can also complicate influenza in children
and make it more desirable to vaccinate young children against influenza. Influenza vaccines must be
reformulated annually because of the antigenic shift and drift of circulating influenza viral strains. However,
reformulated seasonal flu vaccines do not always match the circulating strains, and there is the ever-present
threat that avian influenza viruses may adapt for transmission in humans. Additionally, currently available
antiviral drugs against influenza are facing the twin challenges of evolved drug resistance and nonspecific
side effects. Therefore, there is an urgent need for developing novel drugs, vaccines, and combinatory
therapies against influenza virus infection.
In this proposed research, we hypothesize that a universally prophylactic and therapeutic influenza
vaccine for children can be developed through creation of a self-attenuated influenza virus (SAIV) that
expresses artificial microRNAs (amiRNAs) targeting viral and/or host gene expression that are essential for
viral replication. In order to evaluate this hypothesis, we propose the following 3 specific aims for this research:
Specific Aim 1: To evaluate the efficacy of a candidate prophylactic and therapeutic SAIV vaccine
generated by viral gene-targeted attenuation.
Specific Aim 2: To assess the efficacy of a candidate SAIV vaccine generated by host gene-targeted
attenuation.
Specific Aim 3: To produce and evaluate additional dual viral and host factor-targeted prophylactic and
therapeutic SAIV vaccines.
Our proposed SAIV vaccines developed in this research will be extensively investigated in young mouse
model of influenza infection. We anticipate that the proposed research will identify a novel and safe universal
influenza vaccine and molecular therapy that could be further developed as a therapeutic vaccine to prevent
future influenza reinfection in children. Furthermore, this research program will significantly strengthen the
research environment in Texas Tech University Health Sciences Center at El Paso, and provide research
training opportunities for graduate students, medical students, and undergraduate students, throughout the
3-year performance period.
This research supplement fund will support the diversity candidate, Ms. Alejandra Munoz, for 2 year
post-baccalaureate research training through this research program.
新的鼻鼻喷雾流感疫苗
(R15HD109732的研究补充)
项目摘要/摘要:
尽管流感激烈的运动,流感仍然是儿童的全球公共卫生问题
许多国家的疫苗接种。 COVID-19的最新出现也可能使儿童流感复杂化
并使接种幼儿对流感疫苗接种疫苗更为理想。流感疫苗必须是
每年重新构建,因为循环流感病毒菌株的抗原转移和漂移。然而,
重新制定的季节性流感疫苗并不总是与循环菌株相匹配,而且有永远存在的疫苗
禽流感病毒可能适应人类传播的威胁。此外,目前可用
针对流感的抗病毒药面临进化耐药性和非特异性的双重挑战
副作用。因此,迫切需要开发新型药物,疫苗和联合性
针对流感病毒感染的疗法。
在这项拟议的研究中,我们假设一种普遍的预防性和治疗性流感
可以通过创建自我衰减的流感病毒(SAIV)来开发儿童的疫苗
表达靶向病毒和/或宿主基因表达的人造microRNA(AMIRNA),这对于
病毒复制。为了评估这一假设,我们提出了以下3个针对这项研究的特定目标:
特定目的1:评估候选预防和治疗性SAIV疫苗的功效
由病毒基因靶向衰减产生。
特定目的2:评估宿主基因靶向候选的SAIV疫苗的功效
衰减。
特定目的3:生产和评估其他双重病毒和宿主因子的预防性和
治疗性SAIV疫苗。
我们在这项研究中开发的拟议的SAIV疫苗将在年轻小鼠中进行广泛研究
流感感染的模型。我们预计拟议的研究将确定一个新颖且安全的普遍性
流感疫苗和分子疗法可以作为治疗疫苗进一步开发
未来的流感儿童感染。此外,该研究计划将大大加强
德克萨斯理工大学的研究环境El Paso,并提供研究
在整个过程中为研究生,医学生和本科生的培训机会
3年性能期。
该研究补充基金将支持多样性候选人亚历杭德拉·穆诺兹(Alejandra Munoz)女士2年
通过该研究计划进行研究后的研究培训。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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MINGTAO ZENG其他文献
MINGTAO ZENG的其他文献
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{{ truncateString('MINGTAO ZENG', 18)}}的其他基金
Targeted-delivery of small interference RNA against anthrax (1 R21 AI118228-01A1)
针对炭疽病的小干扰 RNA 的靶向递送(1 R21 AI118228-01A1)
- 批准号:
9152506 - 财政年份:2016
- 资助金额:
$ 14.58万 - 项目类别:
Targeted-delivery of small interference RNA against anthrax
针对炭疽病的小干扰 RNA 的靶向递送
- 批准号:
8986413 - 财政年份:2015
- 资助金额:
$ 14.58万 - 项目类别:
Targeted-delivery of small interference RNA against anthrax
针对炭疽病的小干扰 RNA 的靶向递送
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9089923 - 财政年份:2015
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6673546 - 财政年份:2003
- 资助金额:
$ 14.58万 - 项目类别:
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