Chimerism
Also called: Tetragametic chimerism · Human chimera
A chimera is one person made of two sets of cells with different DNA. It can happen when two embryos fuse in the first days of pregnancy. Most chimeras never find out. A few discovered it when a DNA test said they were not the mother of their own children.
How common
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How it works
A tetragametic chimera starts as two fertilised eggs, which would normally become fraternal twins. In the first days of pregnancy the two embryos merge into one1. The result is a single person with two cell lines. The two lines can even be different sexes1.
Nothing shows on the outside in most cases. Sometimes there are hints: two eye colours, uneven hair growth, or skin marks that show under UV light1.
A much milder form is common. During pregnancy, cells cross the placenta both ways. Mothers keep small numbers of their children’s cells for decades. This is microchimerism3. A 2012 study found male DNA, probably from sons, in the brains of 37 of the 59 dead women examined6.
How common it is
The 100 figure is a count of found cases, not a rate. Fewer than 100 cases of true human chimerism have been reported since the first one in 19625. Cases are often found only when samples are tested for another reason1. So the count tracks how often people are tested, not how often chimeras are born. The true share of people is unknown. Microchimerism is a separate thing and is common. About 50% to 75% of women carry fetal immune cells after giving birth3. Wide DNA testing of ordinary people is what would change these numbers.
Is it a problem?
Usually not. Most chimeras go through life without knowing they are chimeras1. When the two cell lines are of different sexes, the person can have intersex traits or changed fertility1. The practical issue is that it can confuse blood typing, tissue matching, and DNA parentage tests, as it did for Lydia Fairchild2. No doctor screens for it. It only comes up when a blood, transplant, or genetic test gives a result that does not add up.
History and culture
In 2002, Lydia Fairchild, an American mother, applied for child support enforcement2. DNA tests showed she was not the mother of her two children2. Prosecutors suspected fraud. A test taken at the birth of her third child, with a witness present, also failed to match2. Her lawyer found the case of Karen Keegan, a Boston woman who was also a chimera2. Tests for a kidney transplant had suggested Keegan was not her sons’ mother1. As in Keegan’s case, DNA was taken from Fairchild’s wider family2. Her cervical cells matched her children. Her skin and hair did not2.
One route may start with a twin that is never born. Up to one in every eight multiple pregnancies ends with a twin absorbed early, and its cells can stay in the survivor4. That link is a plausible idea, not a counted number.
Sources and further material
- Wikipedia Chimera (genetics)
- Wikipedia Lydia Fairchild
- Wikipedia Vanishing twin
- NCBI A prenatal case misunderstood as specimen confusion: 46,XY/46,XY chimerism States that fewer than 100 cases of true human chimerism have been reported since 1962.
- doi.org Male Microchimerism in the Human Female Brain Found male DNA in the brains of 37 of the 59 women examined, or 63%.
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