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Use of In vivo Imaging to Monitor the Progression of Experimental Mouse Cytomegalovirus Infection in Neonates
Published on: July 6, 2013
Vaccines for cytomegalovirus
1David.Bernstein@cchmc.org
Abstract:
Cytomegalovirus (CMV) is a leading cause of congenital infection worldwide and therefore is recognized as an important target for vaccine development. Data from natural infections and work done with animal models, including models of congenital infection, provide the rationale for their development. CMV vaccine evaluations were begun in the mid-1970's with an attenuated live virus vaccine, Towne, but this vaccine has not consistently provided protection. Most recently, data from a trial with a subunit glycoprotein B (gB) vaccine administered with the adjuvant MF59 became available. This trial, conducted in post-partum women, demonstrated that the vaccine decreased CMV infections, increasing optimism that a protective CMV vaccine could be developed. Other approaches for CMV that have entered clinical trials include replicons, DNA vaccines, prime boost strategies, and chimeric live viruses. The replicon vaccine included gB and the T cell targets phosphoprotein (pp)65 and Immediate Early (IE)1 while the DNA vaccine was given with a new adjuvant and included gB and pp65. The optimal composition for a CMV vaccine remains to be defined but trials continue with the gB vaccine and others.
Insights
Developing a Cytomegalovirus (CMV) vaccine is crucial for preventing congenital infections. Recent trials show promise with subunit glycoprotein B vaccines, though optimal composition is still under investigation.
Area of Science:
- Virology
- Immunology
- Vaccinology
Background:
- Cytomegalovirus (CMV) is a primary cause of congenital infections globally.
- Developing an effective CMV vaccine is a significant public health priority.
- Previous vaccine candidates, like the live attenuated Towne vaccine, have shown limited efficacy.
Purpose of the Study:
- To review the progress and challenges in developing a vaccine against Cytomegalovirus.
- To evaluate different vaccine strategies and their potential for preventing CMV infection and transmission.
Main Methods:
- Review of historical and recent clinical trial data for CMV vaccines.
- Analysis of various vaccine platforms including live attenuated, subunit, replicon, and DNA vaccines.
- Examination of vaccine components such as glycoprotein B (gB), phosphoprotein (pp)65, and Immediate Early (IE)1 antigens.
Main Results:
- A subunit glycoprotein B (gB) vaccine with MF59 adjuvant demonstrated a reduction in CMV infections in a trial with postpartum women.
- Early CMV vaccine trials using the Towne vaccine showed inconsistent protection.
- Multiple vaccine approaches, including replicons and DNA vaccines, are in clinical trials.
Conclusions:
- Recent advances, particularly with gB-based vaccines, offer optimism for developing a protective CMV vaccine.
- The optimal formulation and composition for a CMV vaccine are still being determined.
- Ongoing clinical trials continue to explore various CMV vaccine candidates.
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