Your Baby's Leftover DNA Is Making You Stronger

Microchimerism, a phenomenon in which women harbor residual fetal cells from their children long after they've given birth, may come with significant health advantages.

Renata Oliveira poses for a picture at the IMIP hospital in Recife, Brazil, January 28, 2016. (Ueslei Marcelino / Reuters)

In pregnancy, women are shape-shifters, their bellies waxing like the moon. After delivery, they hold another kind of magic: microchimerism, a condition in which women harbor cells that originated in their children even decades after birth.

The name, born from Greek myth, refers to the chimera, a fire-breathing lioness with the head of a goat rising up from her body and the tail of a serpent. In ancient mythology, the chimera was an omen of storms and natural disasters. Just what microchimerism foretells still isn’t clear, but a recent study in the International Journal of Epidemiology suggests that these cells may substantially improve the health of the women who house them.

In research published earlier this year, epidemiologists analyzed the data from a previous longitudinal study of 272 elderly Danish women. Out of that group, 70 percent had Y sex chromosomes in their blood, a sign of the presence of male cells.

Although cardiovascular disease was slightly elevated among women with male microchimerism, their overall mortality rate was a whopping 60 percent lower, primarily because of a lower incidence of cancer. Eight-five percent of these women made it to age 80, compared to 67 percent of women without the presence of these cells.

Scientists don’t know for certain what biological mechanisms cause these findings, but past research suggests microchimerism may boost immune surveillance—that is, the body’s ability to recognize and destroy pathogens and cells that might become cancerous—and also play a role in the repair of damaged tissue, helping form new blood vessels to heal wounds. Microchimerism is also associated with a lower risk of Alzheimer’s disease and breast cancer.

These fetal cells migrate all over a mother’s body, becoming part of the heart, the brain, and blood—and fascinating scientist and artists alike. Writer Sarah Gerkensmeyer, mother of two sons, says she likes to think that they never completely left her, and that microchimerism from her younger son Charlie, born in 2011, helped give rise to her short story collection.

“When I was pregnant with him, those weird stories were in me, washing around and fusing together right alongside my developing son,” she wrote last year. “It’s a nice, strange thought, isn’t it? That he gave me those stories to tell.”

Some journalists have asked if the presence of male cells can cause women to think differently, said Mads Kamper-Jørgensen, an associate professor of public health at the University of Copenhagen and the lead author of the International Journal of Epidemiology study.

The answer: No. He also noted that the health benefits of microchimerism are the same whether the cells are male or female. “Sons aren’t any better than daughters.”

The reason why much of the research has focused on microchimerism stemming from males, he explained, is because of the ease in measurement. In blood samples, male Y chromosomes stand out among a woman’s XX. By comparison, finding a daughter’s genetically distinct cells in a mother is expensive and difficult because the chromosomes are all XX. Detecting microchimerism in men is also a challenge, because the female X chromosomes are hard to differentiate from the male XY. (Microchimerism is probably more frequent in women, because pregnancy is a natural avenue for transferring cells, but individuals may also pick up genetically distinct DNA after an organ transplant or transfusions, or in utero if they had a twin.)

A 2004 study found the presence of male genes in 21 percent of women overall—even among those who had only given birth to daughters, had a miscarriage, underwent an abortion, or had never been pregnant. Researchers speculate the unknown DNA could have come from a miscarriage these women never recognized, or from an older brother who transferred cells to their mother, who in turn passed the genes onto subsequent children. Or—here’s where the science starts to feel like sci-fi—women could have picked it up through sexual intercourse, traces of past lovers never lost.

Though the idea is intriguing, it’s also “sort of impossible” to study, Kamper-Jørgensen said, because of the intimate details participants would have to agree to share, and the testing that would have to begin even before women have sexual intercourse and after each new partner.

Kamper-Jørgensen’s current research focuses on preeclampsia, a condition involving elevated blood pressure in pregnancy that causes a higher exchange of cells between fetus and mother, and its association with breast cancer. He’s also investigating the association between microchimersim and allergies in women; those with more children tend to have fewer allergies compared to those who don’t. In another study, he plans to examine microchimerism and its association with rates of brain, cervical, and lung cancer.

“There’s so much [epidemiological] observation out there,” Kamper-Jørgensen said. “Having kids protects you from breast cancer, but we don’t really know why. If you have kids, you live longer, but we don’t really know why. Women live longer than men, but we don’t know why. This phenomenon, this may be it.”