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Updated: Jul 28, 2026

Multicolor Flow Cytometry Analyses of Cellular Immune Response in Rhesus Macaques
Published on: April 22, 2010
Responses of infant rhesus monkeys to inoculation with Mason-Pfizer monkey virus materials
Abstract:
Rhesus monkeys neonatally inoculated with Mason-Pfizer monkey virus (M-PMV) and virus-infected cells frequently developed viral and/or bacterial pneumonia and enteritis. Three characteristic hematologic patterns occurred among the inoculated animals and correlated well with the probability of survival. Postmortem examination of the animals revealed lymphadenopathy and thymic atrophy. M-PMV was present in lymph nodes, blood, brain, spleen, thymus, kidneys, and bone marrow. The disease induced in some animals had characteristics suggestive of a slow-virus-induced autoimmune response.
Insights
Neonatal rhesus monkeys infected with Mason-Pfizer monkey virus (M-PMV) developed pneumonia and enteritis. Hematologic patterns and postmortem findings, including lymphadenopathy and thymic atrophy, correlated with survival, suggesting a slow-virus-induced autoimmune response.
Area of Science:
- Veterinary Virology
- Primate Immunology
- Pathology
Background:
- Mason-Pfizer monkey virus (M-PMV) is a known pathogen in non-human primates.
- Neonatal inoculation can lead to distinct disease manifestations.
Purpose of the Study:
- To characterize the clinical, hematologic, and pathologic outcomes of neonatal rhesus monkeys inoculated with M-PMV.
- To investigate the distribution of M-PMV within infected animals.
- To explore potential autoimmune mechanisms in M-PMV-induced disease.
Main Methods:
- Neonatal rhesus monkeys were inoculated with M-PMV and/or infected cells.
- Hematologic parameters were monitored.
- Postmortem examinations were performed, including gross pathology and tissue sample analysis for viral presence.
- Clinical signs and survival rates were recorded.
Main Results:
- Inoculated monkeys frequently developed viral/bacterial pneumonia and enteritis.
- Three distinct hematologic patterns correlated with survival probability.
- Postmortem findings included lymphadenopathy and thymic atrophy.
- M-PMV was detected in multiple organs, including lymph nodes, blood, brain, spleen, thymus, kidneys, and bone marrow.
Conclusions:
- Neonatal M-PMV infection in rhesus monkeys causes significant morbidity, including pneumonia and enteritis.
- Hematologic profiles and postmortem findings are valuable indicators of disease severity and prognosis.
- The widespread viral distribution and observed pathology suggest M-PMV can induce a complex disease, potentially involving autoimmune processes.
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