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- W2938095270 abstract "Antibodies against two G-protein coupled receptors (GPCRs), angiotensin II type 1 receptor (AT1R) and endothelin A receptor (ETAR) are among a growing number of autoantibodies that are found to be associated with allograft dysfunction. AT1R antibodies (AT1Rabs) and ETAR antibodies (ETARabs) have been shown to activate their target receptors and affect signaling pathways. Multiple single center reports have shown an association between presence of these antibodies and acute or chronic rejection and graft loss in kidney, heart, liver, lung and composite tissue transplantations. However, the characteristics of patients that are most likely to develop adverse outcomes, the phenotypes associated with graft damage solely due to these antibodies, and the antibody titer required to cause dysfunction are areas that remain controversial. This review compiles existing knowledge on the effect of antibodies against GPCRs in other diseases in order to bridge the gap in knowledge within transplantation biology. Future areas for research are highlighted and include the need for functional assays and treatment protocols for transplant patients who present with AT1Rabs and ETARabs. Understanding how antibodies that activate GPCRs influence transplantation outcome will have direct clinical implications for preemptive evaluation of transplant candidates as well as the post-transplant care of organ recipients." @default.
- W2938095270 created "2019-04-25" @default.
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- W2938095270 date "2019-08-01" @default.
- W2938095270 modified "2023-10-02" @default.
- W2938095270 title "Antibodies against Angiotensin II Type 1 and Endothelin A Receptors: Relevance and pathogenicity" @default.
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- W2938095270 doi "https://doi.org/10.1016/j.humimm.2019.04.012" @default.
- W2938095270 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8015780" @default.
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- W2938095270 hasPublicationYear "2019" @default.
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