Variability in PolyIC induced immune response: Implications for preclinical maternal immune activation models

Milo Careaga1, Sandra L Taylor2, Carolyn Chang3

  • 1Department of Psychiatry and Behavioral Sciences, University of California, Davis, USA; The MIND Institute, University of California, Davis, USA.

Journal of Neuroimmunology
|September 11, 2018
PubMed

Insights

Maternal immune activation (MIA) using Polyinosinic-polycytidylic acid (PolyIC) in rats shows high molecular weight PolyIC causes significant cytokine responses, unlike low molecular weight PolyIC, impacting neurodevelopmental disorder research.

Area of Science:

  • Neuroscience
  • Immunology
  • Developmental Biology

Background:

  • Maternal infection during pregnancy is linked to increased risk of neurodevelopmental disorders in offspring.
  • Maternal immune activation (MIA) models, particularly using Polyinosinic-polycytidylic acid (PolyIC), are crucial for studying these risks.
  • The impact of PolyIC's molecular weight on its immune-activating properties requires further investigation.

Purpose of the Study:

  • To investigate the influence of Polyinosinic-polycytidylic acid (PolyIC) molecular weight on maternal immune activation (MIA) in a preclinical rat model.
  • To determine if different molecular weights of PolyIC elicit varying cytokine responses and behavioral changes.

Main Methods:

  • Nulliparous rats were injected with either high molecular weight (HMW) or low molecular weight (LMW) PolyIC.
  • Cytokine levels and sickness behavior were assessed post-injection.

Main Results:

  • High molecular weight PolyIC induced a pronounced cytokine response and significant sickness behavior.
  • Low molecular weight PolyIC did not elicit the same level of cytokine response or observable sickness behavior.

Conclusions:

  • PolyIC molecular weight is a critical factor influencing the immune response in MIA models.
  • Experimental design considerations, specifically PolyIC molecular weight, are essential for reproducible and reliable MIA research.
  • Future studies should account for PolyIC molecular weight when investigating maternal infection effects on offspring neurodevelopment.

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