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Discussion Among non-HLA antigens reported to be involved in Tx damage ( In addition to non-HLA Abs induced by an alloimmune mechanism, Abs directed to self-antigens, such as angiotensin II type 1 receptor (AT1R), perlecan, endothelin type A receptor (ETAR), vimentin, or Rho GDP-dissociation inhibitor 2 (ARHGDIB), have been found to be associated with inferior graft outcome, although their causal role in the pathogenesis of damage is unclear ( de novo GSTT1 Ab pool

While topical treatments and laser therapy are common solutions, glutathione injections offer an effective alternative that targets pigmentation from within

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