Summary: Pregnancy Compensation Hypothesis may explain why women are more prone to developing autoimmune diseases, like multiple sclerosis and lupus, than men.
Source: Arizona State University
Women get autoimmune diseases, such as multiple sclerosis, lupus and rheumatoid arthritis eight times more than men do. On the other hand, women have a smaller risk of getting non-reproductive cancers such as melanoma, colon, kidney and lung cancer.
And while there are some exciting developments in cancer treatments, such as immunotherapies, research is showing that women are responding more favorably than men to this type of intervention.
So why is there such a big difference between women and men when it comes to human diseases?
An interdisciplinary team of scientists at Arizona State University believes it may have the answer.
In a paper published today in the scientific journal “Trends in Genetics,” the team presents a new hypothesis to explain the phenomenon, setting the stage for novel research avenues focused specifically on treating autoimmune diseases and cancer.
“Until now, the differences between women and men in regards to human diseases have not been explained by existing theories,” said Melissa Wilson, assistant professor with ASU’s School of Life Sciences and senior author of the paper.
“We are proposing a new theory called The Pregnancy Compensation Hypothesis.”
“Basically, women’s immune systems evolved to facilitate their survival during the presence of an immunologically invasive placenta and pregnancy, and compensate so they could also survive the assault of parasites and pathogens. But now, in modern, industrialized societies, women are not pregnant all the time so they don’t have a placenta pushing back against the immune system. The changes in their reproductive ecology exacerbate the increased risk of autoimmune disease because immune surveillance is heightened. At the same time, we see a reduction in some diseases, like cancer,” Wilson said.
Heini Natri, the lead author of the study and a postdoctoral scholar with the ASU Center for Evolution and Medicine, said because the immune system varies between the sexes, it should be considered when developing immunotherapies and other treatments.
“We think the Pregnancy Compensation Hypothesis can explain why there’s a big sex difference in these diseases. Going forward, understanding the evolutionary origin of the sex bias in these diseases can help us better understand the mechanisms and particular pieces of the immune system we can target,” said Natri. “Our goal is to actually make treatments better for everyone. We are realizing that cancer is different in men and women. In the study of most cancers and other diseases, and so far in the development of cancer treatments, that has not really been taken into account.”
Effects of industrialization
Another factor that may exacerbate this situation is living a modern-day, urban lifestyle.
In industrialized communities, autoimmune diseases appear to occur at a much higher rate than in non-industrialized populations. The researchers believe the human immune system evolved expecting a given load of parasites. In the modern environment, exposure to those parasites has diminished so the immune system has fewer foreign targets. With this reduced load, the immune system attacks ‘self.’
“There is a mismatch between the ancestral environment humans were adapted to, and the industrialized environment many people currently live in. In terms of an evolutionary timescale, our environment has changed incredibly fast,” said Angela Garcia, also a postdoctoral research fellow with the center.
“We have also shifted from an active lifestyle to a sedentary one. We now have an overabundance of calories available, which potentially allows us to maintain excessive levels of hormones, including the female hormone estradiol. Maintaining such high levels of hormones may increase the chance of triggering autoimmune diseases,” she said.
The researchers suggest that by framing future research within the Pregnancy Compensation Hypothesis, scientists could dive deeper into the characterization of genes, environmental context and the longitudinal history of people.
“We think this is more than a hypothesis. By using modern molecular biologic techniques in genetics and genomics, we can look at the differences between male and female immune systems, and between modern immune profiles and those in pre-industrial populations. By doing so, we may find new ways to prevent cancer and autoimmune diseases,” Ken Buetow, a professor with the school and co-author of the study.
The researchers also suggest there are places where genes are regulated uniquely in males and females, as well as across environmental contexts.
“Going forward, we need to systematically collect environmental variables like pathogenic exposure, levels of stress and reproductive hormones, and parity. We have to understand these areas better,” said Wilson.
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Source: Arizona State University Media Contacts: Sandra Leander – Arizona State University Image Source: The image is credited to Jacob Sahertian/ASU VisLab.
The Pregnancy Pickle: Evolved Immune Compensation Due to Pregnancy Underlies Sex Differences in Human Diseases
There are major sex differences in human disease that cannot be explained by reproductive hormones or environmental exposures alone.
Genes on the sex chromosomes exhibit differences in expression that are independent of reproductive hormones, and could contribute to sex differences in disease.
We propose that the ancestral immune system was strongly shaped by the requirement to compensate for unique immune regulation during pregnancy.
Dimorphism in immune function in response to placentation and pregnancy occurs via direct impact of reproductive hormones on immune function, as well as through heritable variation in sex chromosome dosage.
Although evolution has shaped sex differences in immune function over millions of years, industrialized urban populations experience both exacerbated sex differences in hormonal composition as well as reduced pregnancies compared with nonindustrialized populations.