Vaccination Strategies after Elimination of Poliomyelitis
Vaccination Strategies after Elimination of Poliomyelitis
批准号:
7454235
负责人:
Yvonne A. Maldonado
金额:
$50.03万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-07-01 至 2012-06-30
关键词:
AddressAffectAge-MonthsAntibodiesAreaB-LymphocytesBlood CirculationChildChronicConditionCountDataDeveloped CountriesDeveloping CountriesDevelopmentDisease OutbreaksDoseEnrollmentFecesFrequenciesFunctional disorderGenomeGoalsHIVHouseholdHuman poliovirusImmuneIndividualInfantInfectionIntestinesLifeMeasuresMucosal ImmunityNutritional statusOralParalysedPerinatalPoint MutationPoliciesPoliomyelitisPoliovirus VaccinesPoliovirusesPopulationPrevalenceRNAReverse TranscriptionRiskRoleSamplingSeroprevalencesSerotypingSpecimenTestingTimeTreatment ProtocolsVaccinationVaccinesVirulentVirus DiseasesVirus SheddingWorld HealthWorld Health OrganizationZimbabwebasedesigngenome sequencingimmune functionimmunogenicitykillingsmutantneurovirulencetransmission processvaccination strategyvaccine development
中文摘要
描述(申请人提供):1988年世界卫生大会确定的全球根除脊髓灰质炎的目标很可能在未来五年内实现。在过去20年中,脊髓灰质炎病例急剧减少,从1988年的估计350,000例减少到2004年的不到1,300例--减少了99%以上。然而,最近发现了传播中的强毒疫苗衍生脊髓灰质炎病毒(VDPV),它能够导致麻痹性脊髓灰质炎,威胁到根除。此外,众所周知的三种Sabin血清型的点突变与疫苗相关的麻风性脊髓灰质炎(VApp)的发生有关。因此,一旦根除,全球立即停止使用口服脊髓灰质炎疫苗(OPV)是一项高度优先的任务。了解OPV,特别是VDPV和vApp的循环动态,以及人类免疫缺陷病毒(HIV)感染对病毒脱落和灭活脊髓灰质炎疫苗(IPV)免疫原性的影响,对于制定根除后疫苗接种政策至关重要。关于IPV方案免疫原性的信息对于评估IPV是否可用于控制艾滋病毒高流行地区根除后的潜在暴发非常重要。缺乏关键数据,特别是在免疫缺陷患者中,他们可能比免疫功能正常的人更长时间地释放更多的vApp和VDPV,以评估世界卫生组织正在考虑的根除后疫苗接种方案。我们建议及时提供数据,以评估在发展中国家接受口服脊髓灰质炎疫苗接种的健康和免疫缺陷人群的OPV、vApp和VDPV的脱落和传播情况,并评估IPV方案在卫生条件较差的健康和免疫缺陷婴儿中的免疫原性和粘膜免疫,这可能影响IPV的免疫原性。拟议的研究将在居住在艾滋病毒血清阳性率为20%的津巴布韦Chitungwiza感染艾滋病毒和未感染艾滋病毒的婴儿中进行,以解决为世界发展中地区设计脊髓灰质炎疫苗接种战略方面的具体差距。版面描述。麻痹性脊髓灰质炎(脊髓灰质炎)可能很快被根除。然而,由脊髓灰质炎活疫苗引起的脊髓灰质炎可能会发生,并可能威胁到根除脊髓灰质炎的努力。我们提出了一些战略,以确定艾滋病毒感染对发展中国家根除脊髓灰质炎战略的影响,并研究在全球根除脊髓灰质炎中使用灭活脊髓灰质炎疫苗的情况。
英文摘要
DESCRIPTION (provided by applicant): The global eradication of poliomyelitis, a goal set by the World Health Assembly in 1988, may likely be achieved within the next five years. Cases of poliomyelitis have decreased dramatically in the last 20 years, from an estimated 350,000 cases in 1988 to under 1300 in 2004 - a greater than 99% reduction. However, the recent discovery of circulating virulent vaccine derived polioviruses (VDPV), capable of causing paralytic poliomyelitis, threatens eradication. In addition, well-known point mutations of the three Sabin serotypes are associated with development of vaccine-associated paralytic poliomyelitis (VAPP). Thus, global cessation of oral polio vaccine (OPV) use as soon as eradication occurs is a high priority. Understanding the dynamics of circulation of OPV, and especially of VDPV and VAPP, and the impact of human immunodeficiency virus (HIV) infection on viral shedding and on the immunogenicity of inactivated polio vaccine (IPV), is critical for the development of post-eradication vaccination policies. Information about the immunogenicity of IPV regimens is important to assess whether IPV can be used to control potential post-eradication outbreaks in areas of high HIV prevalence. There is a lack of critical data, especially among immunodeficient individuals who may shed more VAPP and VDPV for longer periods than those with normal immune function, to evaluate post-eradication vaccination options being considered by the World Health Organization. We propose to provide data, in a timely fashion, to evaluate the shedding and transmission of OPV, VAPP and VDPV by healthy and immunodeficient populations given OPV in a developing country, and to assess the immunogenicity and mucosal immunity of IPV regimens in healthy and immunodeficient infants living in poor sanitary conditions, which may affect IPV immunogenicity. The proposed studies will be carried among HIV- infected and uninfected infants living in Chitungwiza, Zimbabwe, with an HIV seroprevalence of 20%, to address specific gaps in designing polio vaccination strategies for developing areas of the world. Lay description. Paralytic poliomyelitis (polio) may soon be eradicated. However, polio caused by the live polio vaccine can occur and may threaten efforts to eradicated polio. We propose strategies to identify the effect of HIV infection on polio eradication strategies in a developing country and to study the use of a killed polio vaccine in eradication of poliomyelitis worldwide.
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会议论文
Pediatric Global Health Subspecialty Fellowship
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批准号:10663069
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项目类别:
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资助金额:$39.98万
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财政年份:2022
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负责人:Yvonne A. Maldonado
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依托单位:
Pediatric Global Health Subspecialty Fellowship
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批准号:10411229
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资助金额:$19.3万
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Longevity, Equity, and Aging Research Network (L.E.A.R.N.) Consortium Research Education Core
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批准号:10730181
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Stanford Precision Health for Ethnic and Racial Equity (SPHERE) Transdisciplinary Collaborative Center
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批准号:10272550
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财政年份:2016
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负责人:Yvonne A. Maldonado
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依托单位:
Stanford Precision Health for Ethnic and Racial Equity (SPHERE) Transdisciplinary Collaborative Center
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资助金额:$230.27万
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依托单位:
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资助金额:$6.08万
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依托单位:
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资助金额:$12.55万
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依托单位:
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资助金额:$12.5万
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依托单位:
Training Grant Pediatric Infectious Diseases: Viral Infections in Children
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资助金额:$12.47万
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负责人:Yvonne A. Maldonado
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依托单位:
Training Grant Pediatric Infectious Diseases: Viral Infections in Children
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批准号:8049669
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项目类别:
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资助金额:$12.68万
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财政年份:2009
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负责人:Yvonne A. Maldonado
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依托单位:
Vaccination Strategies after Elimination of Poliomyelitis
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批准号:7230647
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项目类别:
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资助金额:$51.39万
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财政年份:2007
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负责人:Yvonne A. Maldonado
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依托单位:
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资助金额:$50.51万
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Vaccination Strategies after Elimination of Poliomyelitis
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项目类别:
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资助金额:$51.49万
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财政年份:2007
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负责人:Yvonne A. Maldonado
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依托单位:
Vaccination Strategies after Elimination of Poliomyelitis
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财政年份:2001
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负责人:Yvonne A. Maldonado
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依托单位:
ENTEROVIRUS PREVALENCE AND EFFECT ON OPV IMMUNOGENICITY
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批准号:3146488
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项目类别:
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资助金额:$19.61万
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财政年份:1992
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负责人:Yvonne A. Maldonado
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依托单位:
ENTEROVIRUS PREVALENCE AND EFFECT ON OPV IMMUNOGENICITY
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财政年份:1992
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负责人:Yvonne A. Maldonado
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依托单位:
ENTEROVIRUS PREVALENCE AND EFFECT ON OPV IMMUNOGENICITY
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批准号:2066427
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项目类别:
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资助金额:$19.52万
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财政年份:1992
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负责人:Yvonne A. Maldonado
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依托单位:
ENTEROVIRUS PREVALENCE AND EFFECT ON OPV IMMUNOGENICITY
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批准号:3146487
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项目类别:
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资助金额:$15.46万
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财政年份:1992
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负责人:Yvonne A. Maldonado
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依托单位:
海外基金