Microchimerism is the presence of cells in an individual that have originated from a genetically distinct individual. The most common form of microchimerism is fetomaternal microchimerism, i.e., cells from a fetus pass through the placenta and establish cell lineages within the mother. Microchimerism was also described after the transplantation of human organs in human recipients. Consequently, microchimerism may also be expected in xenotransplantation using pig cells or organs. Indeed, microchimerism was described in patients after xenotransplantations as well as in non-human primates after the transplantation of pig organs. Here, for the first time, a comprehensive review of microchimerism in xenotransplantation is given. Since pig cells contain porcine endogenous retroviruses (PERVs) in their genome, the detection of proviral DNA in transplant recipients may be misinterpreted as an infection of the recipient with PERV. To prevent this, methods discriminating between infection and microchimerism are described. This knowledge will be important for the interpretation of screening results in forthcoming human xenotransplantations.
Keyphrases
- endothelial cells
- induced apoptosis
- cell cycle arrest
- induced pluripotent stem cells
- pluripotent stem cells
- end stage renal disease
- chronic kidney disease
- cell death
- ejection fraction
- endoplasmic reticulum stress
- dna methylation
- bone marrow
- pi k akt
- cell proliferation
- signaling pathway
- single molecule
- cell free
- circulating tumor
- kidney transplantation