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Rubella Virus Infection, the Congenital Rubella Syndrome, and the Link to Autism
Anthony R Mawson1, Ashley M Croft2
1Department of Epidemiology and Biostatistics, School of Public Health, College of Health Sciences, Jackson State University, Jackson, MS 39213, USA. amawsn@gmail.com.
Insights
Rubella infection may cause congenital rubella syndrome (CRS) and autism through vitamin A toxicity affecting fetal development. Post-natal liver damage and excess vitamin A may also contribute to regressive autism.
Area of Science:
- Virology
- Developmental Biology
- Toxicology
Background:
- Rubella infection, usually mild, can cause congenital rubella syndrome (CRS) with severe birth defects.
- CRS was linked to autism in the 1960s, but both are now rare due to vaccination.
- Autism rates have increased, with many cases appearing after normal development ('regressive autism').
Purpose of the Study:
- To review evidence suggesting rubella's effects are linked to vitamin A metabolism alterations.
- To propose a model where rubella causes CRS and autism via maternal liver dysfunction and fetal hypervitaminosis A.
- To explore the role of liver-damaging factors and excess vitamin A in regressive autism.
Main Methods:
- Review of existing evidence on rubella, CRS, autism, and vitamin A toxicity.
- Analysis of the proposed mechanism involving hepatic metabolism of vitamin A (retinoids).
- Discussion of potential environmental factors and therapeutic strategies.
Main Results:
- Rubella infection can cause liver dysfunction, leading to excess vitamin A release.
- This endogenous hypervitaminosis A is proposed as the cause of CRS and associated autism.
- Excess vitamin A and liver damage are implicated in regressive autism, presenting CRS-like features.
Conclusions:
- Rubella-induced hypervitaminosis A is a plausible mechanism for CRS and autism.
- This model offers potential strategies for preventing fetal CRS and managing regressive autism.
- Further research is needed to validate the proposed environmental factors and therapeutic interventions.
Abstract:
Rubella is a systemic virus infection that is usually mild. It can, however, cause severe birth defects known as the congenital rubella syndrome (CRS) when infection occurs early in pregnancy. As many as 8%-13% of children with CRS developed autism during the rubella epidemic of the 1960s compared to the background rate of about 1 new case per 5000 children. Rubella infection and CRS are now rare in the U.S. and in Europe due to widespread vaccination. However, autism rates have risen dramatically in recent decades to about 3% of children today, with many cases appearing after a period of normal development ('regressive autism'). Evidence is reviewed here suggesting that the signs and symptoms of rubella may be due to alterations in the hepatic metabolism of vitamin A (retinoids), precipitated by the acute phase of the infection. The infection causes mild liver dysfunction and the spillage of stored vitamin A compounds into the circulation, resulting in an endogenous form of hypervitaminosis A. Given that vitamin A is a known teratogen, it is suggested that rubella infection occurring in the early weeks of pregnancy causes CRS through maternal liver dysfunction and exposure of the developing fetus to excessive vitamin A. On this view, the multiple manifestations of CRS and associated autism represent endogenous forms of hypervitaminosis A. It is further proposed that regressive autism results primarily from post-natal influences of a liver-damaging nature and exposure to excess vitamin A, inducing CRS-like features as a function of vitamin A toxicity, but without the associated dysmorphogenesis. A number of environmental factors are discussed that may plausibly be candidates for this role, and suggestions are offered for testing the model. The model also suggests a number of measures that may be effective both in reducing the risk of fetal CRS in women who acquire rubella in their first trimester and in reversing or minimizing regressive autism among children in whom the diagnosis is suspected or confirmed.
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