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> At this point, my blood type changes to the blood type of my donor. And my blood will now have my donor’s DNA, not my own. That's actually really fascinating. This perpetuates for life? This would seem to imply that a person who's received a transplant will, thirty years later, be walking around with two separate sets of DNA, as the other cells in the body presumably would not change. Given that DNA is (indirectly) responsible for the way that cells communicate with one another (among other things), I wonder if this dichotomy creates any complications in other ways. (Not counting potential graft-host disease rejection - I'm talking about further down the line). |
1) Pregnant women -- During pregnancy, and to some extent afterward, the mother's blood contains cells from the fetus she is carrying. Some of these cells migrate to other places of the body. Scientists hypothesize that this is part of why pregnancy may lower cancer risk -- something about how the mother's immune system deals with these foreign cells. This is called fetal microchimerism. http://www.scientificamerican.com/article.cfm?id=fetal-cells...
2) Chimeric people. In rare cases, a human can be born that is made up of two separate DNA profiles. http://en.wikipedia.org/wiki/Chimera_(genetics)