Non-HLA antibodies may accelerate immune responses after intestinal and multivisceral transplantation

UA Gerlach, N Lachmann, G Ranucci, B Sawitzki… - …, 2017 - journals.lww.com
UA Gerlach, N Lachmann, G Ranucci, B Sawitzki, C Schoenemann, J Pratschke, D Dragun…
Transplantation, 2017journals.lww.com
Background Non-HLA alloantibodies and autoantibodies are involved in allograft rejection
in kidney and heart transplantation. Their role in intestinal transplantation has not yet been
described. We examined the development of antiangiotensin II type I receptor antibodies
(anti-AT 1 R) and antiendothelin type A receptor antibodies associated with the clinical
course and histopathological findings of intestinal transplantation recipients. Methods Thirty-
seven patients underwent intestinal or multivisceral transplantation. Non-HLA antibodies …
Background
Non-HLA alloantibodies and autoantibodies are involved in allograft rejection in kidney and heart transplantation. Their role in intestinal transplantation has not yet been described. We examined the development of antiangiotensin II type I receptor antibodies (anti-AT 1 R) and antiendothelin type A receptor antibodies associated with the clinical course and histopathological findings of intestinal transplantation recipients.
Methods
Thirty-seven patients underwent intestinal or multivisceral transplantation. Non-HLA antibodies (non-HLAabs) were screened in 29 transplant recipients. Antibody-levels greater than 12 U/L were considered positive and were evaluated retrospectively regarding rejection episodes.
Results
Twenty patients developed anti-AT 1 R and/or antiendothelin type A receptor antibodies (non-HLAabs group), 9 did not (control group). The non-HLAabs group had a higher rate of allograft rejection than controls (80% vs 55%), especially a higher rate of antibody-mediated rejections (55% vs 11%, P< 0.01) with detection of donor-specific anti-HLAabs. All rejection episodes in the non-HLAabs group appeared around the time of positive non-HLAabs detection. Five patients had acute cellular rejections at the time of non-HLAabs development, 4 had viral infections.
Conclusions
Our data suggest that antibody-mediated mechanisms targeting antigens beyond HLA may trigger and accelerate immune responses. Given the possibility of pharmacologic targeting of non-HLA receptors, future studies will focus on the explanation of mechanisms how non-HLAabs may enhance rejection and affect long-term allograft survival.
Lippincott Williams & Wilkins