Related Experiment Video
Updated: Aug 28, 2026

Utilizing the Antigen Capsid-Incorporation Strategy for the Development of Adenovirus Serotype 5-Vectored Vaccine Approaches
Published on: May 6, 2015
Replication-incompetent adenoviruses as vectors for protective immunization against measles virus infection
C Schindler1, A Fooks, J Stephenson
1Institut für Virologie und Immunobiologie, Universität Würzburg, Germany.
Abstract:
Despite the availability of an efficient live-attenuated measles virus vaccine about 1.5 million annual deaths from measles infections and their complications are recorded worldwide. Particularly in developing countries measles remains an unsolved problem and a new vaccine seems necessary. In our animal model of measles virus infection in rats we studied a candidate vaccine based on infectious replication incompetent (E1A-) adenovirus (RAd) where measles virus genes are expressed under the control of the cytomegalovirus immediate early promoter. The aim of the study was to characterize the cell mediated and humoral immunity after immunization with RAd and its protective effect. After challenge with a lethal dose of measles virus no signs of disease or histopathological changes were detected in RAd68-immunized rats. The elimination of measles virus was successful within a few days. The results demonstrate that defective recombinant adenovirus vectors can induce complete protection from experimental measles infection in rats.
Insights
A novel recombinant adenovirus vaccine (RAd) shows promise for measles prevention. In rats, this vaccine candidate effectively protected against lethal measles virus challenge, demonstrating complete immunity and rapid virus elimination.
Area of Science:
- Virology
- Vaccinology
- Immunology
Background:
- Measles causes significant global mortality, especially in developing nations.
- Existing live-attenuated vaccines face challenges, necessitating new approaches.
- A novel vaccine strategy is crucial for controlling measles outbreaks.
Purpose of the Study:
- To evaluate a replication-incompetent adenovirus vector vaccine (RAd) expressing measles virus genes.
- To characterize the cell-mediated and humoral immune responses induced by the RAd vaccine.
- To assess the protective efficacy of the RAd vaccine against experimental measles virus infection.
Main Methods:
- Development of a recombinant adenovirus vector (RAd) expressing measles virus genes under CMV promoter control.
- Immunization of a rat model with the candidate RAd vaccine.
- Challenge with a lethal dose of measles virus to assess protection.
- Monitoring for disease signs, histopathological changes, and virus elimination.
Main Results:
- RAd68-immunized rats showed no signs of measles disease or pathology after lethal virus challenge.
- Complete elimination of measles virus was observed within days post-challenge.
- The defective recombinant adenovirus vector successfully induced complete protection in the animal model.
Conclusions:
- Defective recombinant adenovirus vectors represent a viable platform for developing effective measles vaccines.
- This RAd vaccine candidate demonstrated complete protection against experimental measles infection in rats.
- Further development of this adenovirus-based vaccine strategy holds potential for global measles control.
Related Concept Videos
Vaccines
Poliomyelitis
Respiratory Syncytial Virus Disease

