DESENSITIZATION THERAPY IN HYPERIMMUNIZED LIVING DONOR KIDNEY TRANSPLANT RECIPIENTS AND ITS IMPACT ON GRAFT FUNCTION AND ACUTE REJECTION RATE IN THE FIRST YEAR POST-TRANSPLANT

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DESENSITIZATION THERAPY IN HYPERIMMUNIZED LIVING DONOR KIDNEY TRANSPLANT RECIPIENTS AND ITS IMPACT ON GRAFT FUNCTION AND ACUTE REJECTION RATE IN THE FIRST YEAR POST-TRANSPLANT
Hugo Leonardo
Reynoso de la Torre
Jorge Andrade Sierra gugo_leonardo@hotmail.com Instituto Mexicano del Seguro Social Department of Nephrology and Organ Transplant Unit, Specialties Hospital, National Western Medical Centre Guadalajara
Mauricio Carvallo Venegas gugo_leonardo@hotmail.com Instituto Mexicano del Seguro Social Department of Nephrology and Organ Transplant Unit, Specialties Hospital, National Western Medical Centre Guadalajara, Jalisco
Diana Laura Muñoz Montes de Oca gugo_leonardo@hotmail.com Instituto Mexicano del Seguro Social Department of Nephrology and Organ Transplant Unit, Specialties Hospital, National Western Medical Centre Guadalajara, Jalisco
 
 
 
 
 
 
 
 
 
 
 
 

Desensitization treatment may increase the possibility of successful kidney transplantation from living and deceased donors in hyperimmunized patients. Decreasing/eliminating levels of donor-specific antibodies, decreasing the incidence of hyperacute rejection, and allowing successful transplantation, with adequate long-term transplant survival.

The aim of this study is to determine graft function and rejection rate in patients who received pre-transplant desensitization therapy with plasmapheresis (PF), immunoglobulins (IG) and rituximab (RTX). As a secondary objective, determine the incidence of infectious events during the post-transplant period. 

Descriptive analysis and retrospective cohort from January-2018 to December-2022. Including 38 patients, ≥18 years with a positive DSA flow crossmatch test and a negative complement-dependent cytotoxic (CDC) crossmatch test, who underwent pre-transplant desensitization therapy with PF, IG, and RTX. All patients had a maintenance immunosuppression regimen based on mycophenolic acid (MMF), prednisone and tacrolimus. Sociodemographic data, kidney function was assessed using the CKD-EPI 2021 formula, infectious and acute rejection events were recorded and analyzed.

The function of the graft at 12 months was 80 ± 28.5 (SD) ml/min/1.73m2 by CKD-EPI 2021. Acute rejection rate was 18.4% (7). 100% of the documented cases of acute rejection were antibody-mediated. The MFI class I of the patients who developed rejection was 7001 ± 1269 (p= 0.17), and MFI class II 7083 ± 3264 (p=0.58) (Figure 1). Two patients developed hyperacute rejection, both positive in DSA flow crossmatch class II, with a MFI DSA class I 6782 ± 1639 and class II of 8958 ± 5828. The first patient with positive antigen B and DR, and the second patient with positive antigen for C and DR. 36.5% patients had urinary tract infection, with a cumulative number of urinary tract infection events of 27. Four patients developed respiratory tract infections (10.5%), death was reported in 2 of them due to the infection.

Patients with acute rejection

7

Dialysis Time,  (years)

4 (IQR, 1-5)

HLA antigens matching  (n)

Class I

Class II

 

3 (IQR, 1-3)

4 (IQR, 2-5)

Positive DSA flow crossmatch test (%)

Class I

Class II

Both classes

 

2 (28.6%)

5 (71.4%)

0 (0%)

DSA, MFI (SD)

Class I

Class II

 

6725 ± 4763

9764 ± 4473

Type of DSA

A

B

C

DQ

DR

DP

 

1 (14.3%)

 2 (28.6%)

1 (14.3%)

1 (14.3%)

2 (28.6%)

2 (5.3%)

Type of Donor (%)

Related

Not related

 

2 (28.6%)

5 (71.4%)

Transplant n (%)

First

Second

 

0 (0%)

7 (100%)

Hyperacute rejection (%)

2 (28.5%)

Rejection submission time (%)

<6 months

>6 months

 

5 (71.4%)

2 (28.5%)

Graft loss (%)

2 (28.5%)

Number of patients N

38

Age (years)

31 (IQR, 28-35) 

Conclusions

Despite 7 episodes of acute rejection, graft function at 12 months was successful, with a mean eGFR of 80 ml/min. The binary logistic regression model concluded that the variable most associated with acute rejection was the number of shared class I antigens (p=0.005) (Figure 2). With these results we conclude that hyperimmunized patients can have an opportunity and access a high-risk transplant with successful results.


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