
Organ transplantation has been a major development in clinical medicine but its success has been marred by the immune system's capacity to respond to "non-self" cells and tissues. A full molecular understanding of this mechanism and the myriad triggers for immune rejection is yet to be elucidated. Consequently, immunosuppressive drugs remain the mainstay of post-transplant management; however, these interventions have side effects such as increased incidence of cancer, post-transplant lymphoproliferative disorders, susceptibility to infection if not managed appropriately and the inconvenience to the patient of lifelong treatment. Novel therapeutic approaches based on molecular understanding of immunological processes are thus needed in this field. The notion that factors influencing successful transplants might be of use as therapeutic approaches is both scientifically and medically appealing. Recent developments in the understanding of successful transplants are expected to provide new opportunities for safer transplantation. This article reviews the present understanding of the molecular basis of rejection and the role of complement in this process as well as the possibility of generating "intelligent" therapy that better target crucial components of hyper-acute rejections.
Graft Rejection, Complement, Antibodies, Epitopes, Xenogeneic, Complement C4b, Animals, Humans, Complement Activation, Allogeneic, Isotypes, Graft Survival, R, Endothelial Cells, Complement System Proteins, Organ Transplantation, Peptide Fragments, Immunoglobulin Isotypes, Treatment Outcome, Acute Disease, Medicine, Hyper acute Rejection, Immunosuppressive Agents
Graft Rejection, Complement, Antibodies, Epitopes, Xenogeneic, Complement C4b, Animals, Humans, Complement Activation, Allogeneic, Isotypes, Graft Survival, R, Endothelial Cells, Complement System Proteins, Organ Transplantation, Peptide Fragments, Immunoglobulin Isotypes, Treatment Outcome, Acute Disease, Medicine, Hyper acute Rejection, Immunosuppressive Agents
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