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Prolonged E55+ retrovirus expression in aged mice is associated with a decline in the anti-virus immune response
M elRefaei1, K J Blank, D M Murasko
1Department of Microbiology and Immunology, MCP Hahnemann University School of Medicine, Philadelphia, Pennsylvania 19129, USA.
Abstract:
E55+ murine leukemia retrovirus (E55+ MuLV) infection of young and aged C57BL/6 (B6) mice was used to investigate the relationship between increased incidences of infection and decreased immune responsiveness of elderly individuals. Young mice decreased E55+ MuLV burden to below detectable levels by 8 weeks postinfection (p.i.). In contrast, virus burden in aged mice did not reach undetectable levels until 20 weeks p.i. A significant T cell proliferative response to E55+ MuLV was detected from 2 to 12 weeks p.i. in young mice, but was never observed in aged mice. Both age groups demonstrated significant E55+ MuLV-specific T-cell-mediated cytotoxic responses at 3 and 4 weeks p.i. and virus neutralizing antibody titers at 2, 4, 8, and 12 weeks p.i. In both cases, responses were consistently higher in young mice (P < 0.04 and P < 0.02, respectively). These results demonstrate that the observed delay in E55+ MuLV clearance by aged mice is associated with an age-related decrease in the immune response to the virus.
Insights
Elderly mice show delayed clearance of E55+ murine leukemia retrovirus (E55+ MuLV) due to a reduced immune response. This study links age-related immune decline to slower viral clearance in aged individuals.
Area of Science:
- Immunology
- Virology
- Gerontology
Background:
- Aging is associated with decreased immune function and increased susceptibility to infections.
- Understanding age-related immune responses to viral pathogens is crucial for public health.
Purpose of the Study:
- To investigate the relationship between aging and the immune response to E55+ murine leukemia retrovirus (E55+ MuLV).
- To compare viral clearance and immune responses in young versus aged mice.
Main Methods:
- Infection of young and aged C57BL/6 (B6) mice with E55+ MuLV.
- Monitoring of viral burden post-infection (p.i.).
- Assessment of T cell proliferation, cytotoxic responses, and neutralizing antibody titers.
Main Results:
- Aged mice exhibited a delayed clearance of E55+ MuLV, taking 20 weeks compared to 8 weeks in young mice.
- Young mice showed significant T cell proliferative responses, which were absent in aged mice.
- Both age groups had cytotoxic T cell responses and neutralizing antibodies, but responses were consistently higher in young mice.
Conclusions:
- Delayed E55+ MuLV clearance in aged mice is linked to an age-related decline in immune responsiveness.
- Immune system aging impacts the ability to control viral infections effectively.
- This study highlights the importance of immune status in viral pathogen resolution across different age groups.
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