Bacterial infections in cynomolgus monkeys given small molecule immunomodulatory antagonists

Karen D Price1

  • 1Bristol-Myers Squibb Company, East Syracuse, NY 13057-5050, USA. karen.price@bms.com

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.