Summary: A new PNAS study reveals why men are less likely to develop multiple sclerosis than women. According to researchers, a ‘guardian molecule’ that is triggered by testosterone appears to have a protective effect in men. When female mice were treated with the molecule, their symptoms of the disease were eliminated.
Source: Northwestern University.
Men are much less likely to get multiple sclerosis (MS) than women and one reason is that they are protected by high levels of testosterone.
Scientists have now discovered how it works. Using a mouse model of MS, they have identified a guardian molecule — triggered by testosterone — that appears to protect males from disease. When female mice with disease are treated with this protective molecule, their symptoms were eliminated, reports a new study from Northwestern Medicine.
“This suggests a mechanism for the reduced incidence of multiple sclerosis and other autoimmune diseases in males compared to females,” said lead study author Melissa Brown, professor of microbiology/immunology at Northwestern University Feinberg School of Medicine. “These findings could lead to an entirely new kind of therapy for MS, which we greatly need.”
The paper will be published in the Proceedings of the National Academy of Sciences on Jan. 29.
Women have three-to-four times the incidence of MS compared to men and the lower incidence in males is related, in part, to higher levels of testosterone. But until now, scientists haven’t understood how the hormone provides protection. The new study discovered how testosterone does it, and how females can glean the benefits.
“This is why it’s vital to study sex differences in research,” Brown said.
The discovery stemmed from an earlier lucky mistake in the lab in which male mice were used instead of female mice, because a graduate student hadn’t yet learned to identify the nearly imperceptible genitals of male mouse pups.
In MS, immune cells attack the myelin sheath, a membrane that wraps around the nerve axons within the brain and spinal cord. The sheath acts as insulation and assists in sending nerve signals from the brain and spinal cord to the rest of the body. The damage to the myelin sheath interrupts normal nerve signal conduction and can result in a variety of symptoms including sensory disturbances, loss of motor function and cognitive deficits.
Northwestern scientists showed that testosterone caused mast cells, a type of immune cell, to produce the guardian molecule, cytokine IL-33, in male mice. The guardian molecule triggers a cascade of chemicals that prevents the development of another type of immune cell, so-called Th17 cells, that can directly attack the myelin.
In this model of disease, similar to MS in humans, females develop more of a disease-causing Th17 immune response than males. These Th17 cells, attack and destroy the myelin. But that damaging response was reversed in females by treatment with IL-33.
“Because testosterone levels are seven-to-eight times lower in adult women compared to men, we speculate there are insufficient levels in females to activate this protective pathway,” Brown said. “But we showed we can activate the pathway with the guardian molecule, IL-33.”
In addition to a higher incidence of MS in women, there are also sex-determined differences in the average age of onset and subtype of the disease. Women generally develop MS at a younger age and usually have a relapsing-remitting course of disease. Men develop the disease later in life and it usually continues to worsen without periods of improvement. The development of the disease in men also correlates with age-related reduction of testosterone levels.
While there have been some new breakthroughs in developing effective drug therapies for MS patients, most of these work by suppressing the immune system, making patients more susceptible to certain infections and/or causing a general malaise.
Limited clinical trials in male MS patients have shown that testosterone treatment over 12 months can partially reverse evidence of myelin- and nerve-degeneration and alleviate symptoms. However, short-term testosterone administration is not a viable therapy for either men or women because of the multitude of undesirable side effects.
“Our findings have identified new and more specific cellular and molecular targets for immune intervention that we hope will lead to better therapies that leave most of the immune system intact,” Brown said. “This testosterone-driven protective pathway should also be studied in other female-biased autoimmune diseases.”
About this neuroscience research article
Funding: This work was supported by grants R21 NS081598 and F31 NS084691 from the National Institutes of Neurological Disorders and Stroke of the National Institutes of Health and the National Multiple Sclerosis Society.
[cbtabs][cbtab title=”MLA”]Northwestern University “Men Hold Secret to Protect Women From Multiple Sclerosis.” NeuroscienceNews. NeuroscienceNews, 29 January 2018. <https://neurosciencenews.com/testosterone-multiple-sclerosis-8401/>.[/cbtab][cbtab title=”APA”]Northwestern University (2018, January 29). Men Hold Secret to Protect Women From Multiple Sclerosis. NeuroscienceNews. Retrieved January 29, 2018 from https://neurosciencenews.com/testosterone-multiple-sclerosis-8401/[/cbtab][cbtab title=”Chicago”]Northwestern University “Men Hold Secret to Protect Women From Multiple Sclerosis.” https://neurosciencenews.com/testosterone-multiple-sclerosis-8401/ (accessed January 29, 2018).[/cbtab][/cbtabs]
The cellular and molecular basis of sex-dimorphic autoimmune diseases, such as the CNS demyelinating disease multiple sclerosis (MS), remains unclear. Our studies in the SJL mouse model of MS, experimental autoimmune encephalomyelitis (EAE), reveal that sex-determined differences in Il33 expression by innate immune cells in response to myelin peptide immunization regulate EAE susceptibility. IL-33 is selectively induced in PLP139–151-immunized males and activates type 2 innate lymphoid cells (ILC2s), cells that promote and sustain a nonpathogenic Th2 myelin-specific response. Without this attenuating IL-33 response, females generate an encephalitogenic Th17-dominant response, which can be reversed by IL-33 treatment. Mast cells are one source of IL-33 and we provide evidence that testosterone directly induces Il33 gene expression and also exerts effects on the potential for Il33 gene expression during mast cell development. Thus, in contrast to their pathogenic role in allergy, we propose a sex-specific role for both mast cells and ILC2s as attenuators of the pathogenic Th response in CNS inflammatory disease.