Researchers from the USA in
collaboration with some German scientists have developed stem cells that can
evade immune attack of the host. They used CRISPR-Cas9 technology to develop
the cells.
MHC complex defines whether the cells are your own or
foreign. During organ transplantation, MHC of the donor and the recipient
should be matched. If there is a mismatch between the two individuals in their
MHC, the immune cells of the recipient considers the transplanted organ as
foreign and will be destroyed by immune cells. No two individuals have
identical MHC complexes. Normally foreign cells are attacked by immune cells. This
is the main reason for the difficulty in transplantation.
Using CRISPR, the researcher has deleted the genes that code for MHC complex and as a result, there is no more MHC in the cells. Since there is no more MHC, they are not
recognized as foreign and are accepted as their own. One problem is that those
cells that have no MHC are the target of another cell called Natural
killer(NK) cells. NK cells recognized and kill them. However, when CD47 is
expressed on the surface of the cells, it is considered as self and is save
from NK cells. The researchers have developed a stem cell that doesn’t have
MHC but has CD47 on their surface and transplant those cells using humanized
mice model. The studies have found that there is no rejection. This is a huge
step in organ transplantation and we could transplant organs even though the MHC
does not match which is the main difficulty in transplantation.
References:
1. Hypoimmunogenic
derivatives of induced pluripotent stem cells evade immune rejection in fully
immunocompetent allogeneic recipients.
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