Related Experiment Video
Updated: Jul 15, 2026

Induction of Maternal Immune Activation in Mice at Mid-gestation Stage with Viral Mimic Poly(I:C)
Published on: March 25, 2016
Time of perinatal immunization, thimerosal exposure and neurodevelopment at 6 months in breastfed infants
Rejane C Marques1, José G Dórea, Angelo G Manzatto
1Fundação Universidade Federal de Rondônia, Porto Velho, RO, Brasil.
Insights
Early hepatitis-B vaccine (TCV) exposure in Brazilian newborns did not impact neurodevelopment at six months. Breastfeeding appears to protect infants from potential ethylmercury (EtHg) exposure challenges.
Area of Science:
- Pediatrics
- Immunology
- Neuroscience
Background:
- Hepatitis-B vaccine (TCV) administration timing varies for Brazilian newborns based on hospital type.
- Infants born in public hospitals receive TCV within 24 hours, while those in private hospitals receive it 2-4 days later.
- This study investigates the neurodevelopmental (ND) impact of this early TCV exposure difference.
Purpose of the Study:
- To compare neurodevelopment in infants receiving TCV at different postnatal ages.
- To assess the association between TCV ethylmercury (EtHg) dose and neurodevelopmental outcomes.
- To evaluate the protective role of breastfeeding against potential neurodevelopmental delays.
Main Methods:
- Gesell Developmental Schedules used to assess 82 healthy, exclusively breastfed infants at 6 months.
- Evaluated motor skills, language development, comprehension, and social skills.
- Analyzed neurodevelopmental outcomes in relation to TCV immunization timing and ethylmercury exposure.
Main Results:
- No significant neurodevelopmental delays were observed in infants immunized within 24 hours compared to those immunized 2-4 days later.
- Early TCV exposure timing and ethylmercury (EtHg) dose showed no significant association with neurodevelopmental outcomes.
- Gesell Developmental Score did not correlate with ethylmercury levels in parenteral nutrition or hair mercury increase.
Conclusions:
- Early exposure to thimerosal-containing vaccine (TCV) ethylmercury (EtHg) does not predict clinical neurodevelopmental delays at 6 months in breastfed infants.
- Breastfeeding is a significant protective strategy for the central nervous system against early exposure challenges.
- Further research may elucidate the long-term effects and protective mechanisms of breastfeeding.
Aim:
Brazilian newborns immunized with hepatitis-B (thimerosal containing vaccine, TCV) receive the first dose within 24 h if delivered in public hospitals, but at a later time if born in private hospitals. We compared neurodevelopment (ND) in infants born in a state hospital (immunized within 24 h) and in privately run hospitals (immunized 2-4 days postnatally).
Methods:
We used the Gesell Developmental Schedules in 82 healthy exclusively breastfed infants at 6 months to assess motor skills, language development, comprehension capacity and social skills.
Results:
Compared to the group immunized 2-4 days after hospital discharge, the group immunized within 24 h showed no significant difference in ND delays. Despite the variation in gestational age (range 36-42 weeks) and TCV-ethylmercury (EtHg) dose (5.7-11.3 microg Hg/kg b.w.) at birth, time of exposure to TCV showed no significant association with ND. Gesell Developmental Score was not significantly correlated with total parenteral EtHg/unit of body mass neither with the relative increase in hair-Hg (as an additional challenge to prenatal Hg exposure).
Conclusion:
In breastfed infants, differences in early exposure to TCV-EtHg cannot portend clinical neurodevelopment delays at 6 months. We speculate that breastfeeding remains a significant strategy to improve central nervous system protection of infants facing early exposure challenges.
Related Concept Videos
Development of Immunocompetence
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
Vaccinations
Development of the Oral Microbiota
Teratogenicity
Development of Human Microbiota
Immunological Memory
What is Immunological Memory?
Immunological memory is an integral function of the immune system that allows it to recognize and react more rapidly and effectively to pathogens previously encountered. This feature is...

