课题基金 / 基金详情

项目摘要

项目成果

Bernard Pragash Arulanandam的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Chlamydia trachomatis is the leading cause of bacterial sexually transmitted disease worldwide. Untreated genital chlamydial infections cause serious sequelae such as pelvic inflammatory disease, ectopic pregnancy, and infertility. A licensed vaccine, which is considered to be the ideal way to limit Chlamydia-induced morbidity, is currently not available. Chlamydial protease- like activity factor (CPAF) is a highly conserved bacterial protein secreted into the host cytosol. Our laboratory has shown the protective efficacy of intranasal vaccination with recombinant(r) CPAF (serovar L2) against genital chlamydial infection and pathology in mice. This protection is mediated by antigen-specific CD4+ T cells and highly dependent on the induction of endogenous IFN-3. Given (1) our extensive immunological characterization of rCPAF vaccination in conferring protective immunity against genital chlamydial infection in the mouse model, and (2) that the pathogenesis and immunity to chlamydial infection in guinea pigs has been shown to be remarkably similar to chlamydial genital infection in humans, we hypothesize that "vaccination with rCPAF will induce protective immunity against inflammatory pathology induced by genital chlamydial infection in guinea pigs". We propose to translate and validate the protective efficacy of rCPAF in an alternative animal model the guinea pig with C. caviae, the causative agent of guinea pig inclusion conjunctivitis (GPIC). The results obtained from these findings will provide important insights into the design of an effective anti-chlamydial vaccine for human use. This study will enable propogation of the guinea pig model of genital chlamydial infection established by Dr. Roger Rank (letter of support), which has been put to limited use in translational vaccine studies. Moreover, the completion of the sequencing of the guinea pig genome will result in the development of immunological reagents for characterization, which will further facilitate the use of this animal model in the scientific community.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1038/icb.2016.122
发表时间: 2017-05
期刊: Immunology and cell biology
影响因子: 4
作者: [Wali S, Gupta R, Yu JJ, Lanka GKK, Chambers JP, Guentzel MN, Zhong G, Murthy AK, Arulanandam BP]
通讯作者: Arulanandam BP
Thioredoxin mediated Acinetobacter baumannii colonization in the GI tract
  • 批准号:
    9092838
  • 项目类别:
  • 资助金额:
    $18.38万
  • 财政年份:
    2016
  • 负责人:
    Bernard Pragash Arulanandam
  • 依托单位:
The Contribution of MicroRNA-182 in Genital Chlamydia trachomatis Infection
  • 批准号:
    9318447
  • 项目类别:
  • 资助金额:
    $7.35万
  • 财政年份:
    2016
  • 负责人:
    Bernard Pragash Arulanandam
  • 依托单位:
Evaluation of CPAF Mediated Anti-Chlamydial Immunity in the Guinea Pig
  • 批准号:
    8030633
  • 项目类别:
  • 资助金额:
    $7.23万
  • 财政年份:
    2011
  • 负责人:
    Bernard Pragash Arulanandam
  • 依托单位:
CPAF induced CD4+ T cell mediated immunity against Chlamydia
  • 批准号:
    8128112
  • 项目类别:
  • 资助金额:
    $13.27万
  • 财政年份:
    2010
  • 负责人:
    Bernard Pragash Arulanandam
  • 依托单位:
海外基金