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Placenta plays potent role in autism risk

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Paul H. Patterson, Elaine Y. Hsiao
2 October 2012

Hot spot: The placenta amplifies maternal signals and molecules, which in certain circumstances can up autism risk.

As the central organ regulating maternal-fetal interactions and embryonic development, the placenta is perfectly positioned to mediate environmental and genetic risk factors during prenatal development1, 2. It may also relay risk factors for autism to the fetus.

There is increasing evidence implicating the placenta in autism risk. For example, abnormal inclusions of trophoblasts, the cells that comprise the placenta, are found more frequently in placentas from mothers of children who develop autism than in controls3. Also, placental inflammation is associated with impairments in communication and social interaction in the child, as measured by low ratings on the Modified Checklist for Autism in Toddlers4.

Rather than passively conveying nutrients to the fetus, the placenta senses the mother’s hormonal and nutritional state. It then adjusts its hormonal and nutritional output to the fetus accordingly.

The placenta is also an active filter — for example, it regulates the transfer of steroid hormones and antibodies. It can also amplify signals coming from the mother, including those involved in nutrition and endocrine function. Under certain circumstances, such as stress and inflammation, however, this amplification can harm the fetus.

It is not clear whether problems with the placenta are directly responsible for a subset of autism spectrum disorders in people. However, at least in sheep, inducing inflammation in the utero-placental compartment is sufficient to cause neurological deficits reminiscent of autism6.

Infection risk:

What causes placental inflammation?                                                                         

A number of clinically relevant insults during pregnancy are known. Researchers are studying one of these, maternal infection, in rodent and non-human primate models by mimicking a viral or bacterial infection.

Maternal immune activation induces cytokines, molecular signals of the immune system, in the placenta. The cytokines can, in turn, activate immune cells within the placenta7, 8, 9, 10, 11, 12, causing them to send signals to trophoblast cells that eventually lead to an altered placental hormonal balance11.

Stimulating a pregnant woman’s immune system through viral or bacterial infection is also associated with a higher risk of autism in the child. A study of more than 10,000 individuals with autism in Denmark demonstrated an association between maternal infection and autism in the child15. A study published earlier this year of more than 4,000 people with autism in Sweden showed similar results16.

Changes in fetal levels of serotonin are likely to affect brain development. Serotonin regulates early events in development — for example, by directing axons to their correct place in the brain and the generation of new neurons. Maternal infection in animal models also alters tryptophan/kynurenine levels in the fetal brain and causes impairments in serotonin signaling in the offspring19.

Cell source:

The placenta also serves as a primary source for hematopoietic stem cells (HSCs) during pregnancy. These cells give rise to all blood and lymphatic immune cells, and at least some are known to originate in the placenta and are believed to seed the fetal liver at a later stage of pregnancy.

Their development and maturation is guided by environmental cues, such as cytokines. So, inflammatory insults that alter cytokine balances in the placenta could skew the development of HSCs, leading to immune dysfunction later in life.

In support of this theory, both fetal and adult bone marrow HSCs are abnormal in mice born to mothers who had an infection during pregnancy. Also, PDGF-B, a growth factor that regulates placental HSC differentiation, is modulated by cytokines such as interleukin-6, interleukin-1 beta and TNF-alpha20. Changes in placental levels of these cytokines may affect HSC development.

These results suggest a potential mechanism for how early-life challenges can lead to persistent immune abnormalities, which studies increasingly suggest is a feature of autism21.

Changes in the placental environment may be the link between autism risk factors such as maternal infection and preterm birth, and autism symptoms such as immune dysfunction and elevated serotonin in the blood. These effects — in addition to the detrimental consequences of placental pathology such as lack of oxygen or malnutrition — can lead to long-term impairments in neurodevelopment.

Paul Patterson is the Anne P. and Benjamin F. Biaggini Professor of Biological Sciences at the California Institute of Technology, in Pasadena. Elaine Hsiao is a graduate student in his laboratory. 


1: Rosenberg R.E. et al. Arch. Pediatr. Adolesc. Med. 163, 907–14 (2009) PubMed

2: Hallmayer J. et al. Arch. Gen. Psychiatry 68, 1095–1102 (2011) PubMed

3: Anderson G.M. et al. Biol. Psychiatry 61, 487-91 (2007) PubMed

4: Limperopoulos C. et al. Pediatrics 121, 758-765 (2008) PubMed

5: Moore G.S. et al. Am. J. Obstet. Gynecol. 206, 314.e1-9 (2012) PubMed

6: Hutton L.C. et al. Dev. Neurosci. 29, 341-354 (2007) PubMed

7: Boksa P. Brain Behav. Immun. 24, 881-897 (2010) PubMed

8: Carpentier P.A. et al. Am. J. Pathol. 178, 2802-2810 (2011) PubMed

9: Fatemi S.H. et al. Neuropharmacology 62, 1290-1298 (2012) PubMed

10: Girard S. et al. Am. J. Obstet. Gynecol. 206, 358e1-9 (2012) PubMed

11: Hsiao E.Y. and P.H. Patterson Dev. Neurobiol. 72, 1317-1326 (2012) PubMed

12: Mandal M. et al. Brain Behav. Immun. 25, 863-871 (2011) PubMed

13: Abdallah M.W. et al. Brain Behav. Immun. 26, 170–176 (2012) PubMed

14: Goines P.E. et al. Mol. Autism 2, 13 (2011) Pubmed

15: Atladottir H.O. et al. J. Autism Dev. Disord. 40, 1423-1430 (2010) PubMed

16: Lee B.K. et al. International Meeting for Autism Research, Toronto, 2012 Abstract

17: Manuelpillai U. et al.  Am. J. Obstet. Gynecol. 192, 280-8 (2005) PubMed

18: Bonnin A. et al. Nature 472, 347-350 (2011) PubMed

19: Kannan S, et al. International Meeting for Autism Research, San Diego, 2011 Abstract

20: Chhabra A, et al. Dev. Cell 22, 651-659 (2012) PubMed

21: Onore C. et al. Brain Behav. Immun. 26, 383-392 (2012) PubMed


Name: Paul Whiteley
2 October 2012 - 2:28PM

An extension of the Barker hypothesis perhaps?


BBC Horizon: The nine months that made you: http://www.bbc.co.uk/programmes/b013ywz4

Name: Paul Patterson
3 October 2012 - 8:08PM

David Barker is right on - my book has a section on him.

Name: usethebrainsgodgiveyou1
2 October 2012 - 4:18PM

My son's birthmother was pregnant and possibly suffering from untreated hypothyroidism. Worldwide, lack of iodine is the most easily preventable cause of birth defects. I wonder if the 2 are related.

Name: Natasa
5 October 2012 - 11:48AM

The following paper is very interesting and possibly of high relevance , showing differential transmission of maternal CMV infection and differential postnatal outcomes in triples.

Only one of the three infants was later diagnosed with autism.

“The third-born triplet suffered from symptomatic CMV infection with a high viral load (6.0 × 10⁶ copy/mL). The triamniotic-trichorionic placentas were not fused to each other. The histopathologic analysis showed that CMV-positive cells were frequently found in the decidua, villi, and amnion of the third-born triplet's placenta but were limited and scattered in the decidua or villi but not amnion of the other 2 placentas. The third-born triplet underwent ganciclovir therapy. None of the infants had physical or auditory problems at 4 years of age, whereas the third-born triplet had been diagnosed with an autistic disorder.”
Differential transmission and postnatal outcomes in triplets with intrauterine cytomegalovirus infection. Kitajima J et al. Pediatr Dev Pathol. 2012 Mar-Apr;15(2):151-5.

Name: subtrician
18 October 2012 - 11:42PM

could Chemtrails cause autism

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