Abstract: SA-PO1147
Impact of Persistent and Transient Donor-Specific Antibodies Within First Year After Kidney Transplantation
Session Information
- Transplantation: Clinical - Rejection, Recurrent Disease, Incompatibility
November 09, 2019 | Location: Exhibit Hall, Walter E. Washington Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Transplantation
- 1902 Transplantation: Clinical
Authors
- Sharma, Akhil, University of Pittsburgh, Pittsburgh, Pennsylvania, United States
- Jorgensen, Dana R., University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States
- Hariharan, Sundaram, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States
Background
The importance of Donor Specific Antibody (DSA) surveillance within 1st year (yr) post kidney transplant remains unclear. We studied the impact of DSA pattern during the 1st yr post-txp on clinical outcomes.
Methods
931 patients (pts) from 2013-17 were enrolled (HLA Compatible, Flow xmatch negative). Pts were grouped into Transient DSA (T-DSA, n=66; 1 positive test, Class I/II), Persistent DSA (P-DSA, n=115, >1 positive test, Class I/II), and No DSA (N-DSA, n=750) within 1st yr post-txp. DSA testing was done @ 1,3,6,9, & 12 mos. Biopsies (protocol 3&12 mos, & indication) were included. Surrogate marker for this study included incidences of TCMR and ABMR. Outcomes measured were pt survival, graft survival and composite of pt loss, graft loss and eGFR <20ml/min at last follow-up.
Results
During the 1st yr, DSA was detected in 19% of pts (7% T-DSA vs 12% P-DSA). There were no differences in baseline or txp characteristics, other than increased sensitization (cPRA>20%) in P-DSA pts (67% vs 47%, p=0.001). P-DSA pts developed DSA earlier for Class I (75±136 vs 121±132 days, p=0.03) and II (83±141 vs 192±185 days, p<0.001), when compared to T-DSA pts. After 1 yr, DSA detection was far less in N-DSA pts (Class I/II 4/8%) than in T-DSA (Class I/II 53/62%, p<0.001) or P-DSA (Class I/II 64/69%, p<0.001) pts. P-DSA pts experienced more clinical TCMR (14 vs 8%, p=0.04), ABMR (12 vs 0.8%, p<0.001), & less normal biopsies (4 vs 11%, p=0.02) than N-DSA pts, and more ABMR than T-DSA pts (12 vs 0%, p=0.003). There were no differences in sub-clinical TCMR/inflammation, tacrolimus levels, renal function, pt survival, or death censored graft survival among all groups. However, lower composite outcome was noted with T & P-DSA pts (Figure 1).
Conclusion
Persistent and Transient DSA within 1 yr had similar outcomes and lower composite outcome when compared to No DSA pts. Thus, detection of DSA within 1 yr, whether Persistent or Transient, is detrimental to renal allograft.