A Max-Ad Vaccine for Mucosal Immunity to HIV
一种针对 HIV 粘膜免疫的 Max-Ad 疫苗
基本信息
- 批准号:6511633
- 负责人:
- 金额:$ 20万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-09-30 至 2003-03-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (Provided by Applicant): To date there is no effective HIV vaccine
available. Development of a beneficial HIV vaccine has been challenging due to
the high mutation rate of the virus, in particular the envelope protein. Many
of the 25 or more different HIV vaccines now in clinical trials target the
envelope protein in an effort to raise an antibody response to that protein.
New insight into effective anti-viral vaccines has focused attention on
eliciting cellular immune responses. In addition, mucosal immunity to HIV is
desirable for an effective HIV vaccine, since mucosal tissues are the common
sites of initial infection.
The vaccine being developed by GenStar targets these two issues by the
inclusion of the HIV components known to elicit the best cellular immune
responses and the ability of adenovirus to produce excellent mucosal immunity.
GenStar's proprietary adenoviral vector, Max-Ad, is particularly suited for
this approach, since it is a gutless adenovirus with a very large insert
capacity. This capacity not only allows the inclusion of multiple HIV
components but also the gene for the immunostimulatory cytokine, GM-CSF. In
addition, this virus offers efficient transduction of most cells including
dendritic cells, excellent high titer large-scale production, and the lack of
synthesis of any adenoviral proteins. In the proposed studies we intend to
determine the ability of a Max-Ad/HIV vaccine to elicit cellular immune
responses to HIV through mucosal delivery.
PROPOSED COMMERCIAL APPLICATION:
HIV is a world-wide health problem with over 30 million people infected and 15,000 new cases of HIV infections diagnosed each day. Clearly, a prophylactic vaccine for this infectious disease is urgently needed and would produce significant financial and social returns. The potential for effective immunization via a mucosal route such as intranasal spray is particularly attractive in view of the large population at risk and the ease of administration.
说明(由申请人提供):到目前为止,还没有有效的HIV疫苗
项目成果
期刊论文数量(0)
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会议论文数量(0)
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Sybille L Sauter其他文献
Sybille L Sauter的其他文献
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{{ truncateString('Sybille L Sauter', 18)}}的其他基金
Non-Integrating FIV Vectors for HIV Vaccines
用于 HIV 疫苗的非整合 FIV 载体
- 批准号:
7123310 - 财政年份:2006
- 资助金额:
$ 20万 - 项目类别:
FIV Vectors for the Treatment of Hemophilia A
用于治疗 A 型血友病的 FIV 载体
- 批准号:
6992338 - 财政年份:2005
- 资助金额:
$ 20万 - 项目类别:
Non-Primate FIV Vectors for Treatment of Hemophilia A
用于治疗甲型血友病的非灵长类 FIV 载体
- 批准号:
6444339 - 财政年份:2002
- 资助金额:
$ 20万 - 项目类别:
A Max-Ad Vaccine for Mucosal Immunity to HIV
一种针对 HIV 粘膜免疫的 Max-Ad 疫苗
- 批准号:
6402992 - 财政年份:2001
- 资助金额:
$ 20万 - 项目类别:
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