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Published on: February 14, 2011
Bacterial infections in cynomolgus monkeys given small molecule immunomodulatory antagonists
1Bristol-Myers Squibb Company, East Syracuse, NY 13057-5050, USA. karen.price@bms.com
Abstract:
Opportunistic infections (OIs) during the course of non-clinical toxicity studies can serve as a clinical indicator of immunosuppression. In monkeys, severity may be magnified since the possibility for fecal-oral and cage-to-cage transmission of bacteria exists, reserve capacity is low, and clinical signs of infection are not easily detected until the infectious process is well underway. This review summarizes a case study presented at the HESI-ILSI ITC-Sponsored workshop on Naturally Occurring Infections in Non-human Primates and Immunotoxicity Implications. It gives an overview on the impact of bacterial infections in monkeys on the development and regulatory assessment of three closely-related representative small molecule immunomodulatory (anti-inflammatory) drug candidates all inhibiting the same drug target. The infections, which sometimes progressed to bacteremia and death, originally manifested in the skin, upper respiratory tract, gastrointestinal tract, and less frequently as soft tissue abscesses. Infections were sporadic and not observed in all studies despite coverage of equivalent or higher systemic exposures or longer durations of treatment. To address concerns regarding inconsistency in the presentation and type of findings and their potential relationship to infection, steps were taken to identify causative agents (via culture, microscopy), implement various intervention and treatment regimens (supportive care, antibiotics, drug holiday), demonstrate reversibility of clinical and immune effects, and study major immune components/mechanisms affected (cytokine/stress protein profiling, immune cell phenotyping, and humoral/innate immune cell function tests). Appropriate diagnosis and characterization of the infection was critical to discrimination of these findings as a secondary pharmacologic effect rather than a direct drug-related target organ effect, and also guided clinical protocol design and regulatory acceptance.
Insights
Opportunistic infections in monkeys can indicate immunosuppression and complicate drug development. Accurate diagnosis is crucial for distinguishing infections from drug effects, ensuring regulatory acceptance.
Area of Science:
- Toxicology
- Immunology
- Non-human Primate Studies
Background:
- Opportunistic infections (OIs) in non-clinical toxicity studies can signal immunosuppression.
- Monkeys are susceptible to OIs due to transmission routes, low reserve capacity, and delayed clinical sign detection.
Purpose of the Study:
- To review the impact of bacterial infections in monkeys on immunomodulatory drug development.
- To discuss strategies for differentiating infection-related findings from direct drug effects.
Main Methods:
- Case study review of bacterial infections in monkeys during immunomodulatory drug development.
- Identification of causative agents, implementation of interventions (supportive care, antibiotics, drug holidays).
- Assessment of clinical and immune effects, including reversibility and immune component analysis.
Main Results:
- Bacterial infections manifested in skin, respiratory, and gastrointestinal tracts, sometimes progressing to bacteremia and death.
- Infections were sporadic and not consistently observed across studies.
- Diagnosis and characterization of infections were critical for regulatory assessment.
Conclusions:
- Distinguishing opportunistic infections from direct drug toxicity is essential in non-human primate studies.
- Effective diagnostic and intervention strategies guide protocol design and regulatory acceptance of immunomodulatory drugs.
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