Detection of complement-binding donor-specific anti-HLA antibodies may reveal which of the antibodies present have got the capability to activate the complement cascade, potentially but not inevitably resulting in C4d deposition and complement-mediated damage or antibody-mediated injury in vivo. Such findings do not rule out a possible role for complement-independent mechanisms in allograft damage mediated by complement-binding donor-specific anti-HLA antibodies.12 There are therapeutic implications of identifying critical pathologic pathways in charge of kidney-allograft loss. Since promising therapeutic brokers targeting complement are increasingly used in sufferers undergoing transplantation,38-40 the present study may provide a basis for future scientific trials.Apobec3G is a great candidate to be one of these genes.’ The findings are a striking example of what can be learned from learning rapidly evolving proteins, the research strategy taken by Malik’s lab. Conflicts in nature get this kind of evolutionary switch when two competing biological passions come head to head. Predators and prey often impact the evolution of one another, and the same can happen between proteins and viruses of the cells they infect.
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