2017 - IPITA


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Pancreas Transplantation - Outcomes & Complications 3

36.7 - Long term follow up of HIV infected patients after pancreas transplantation

Presenter: GR, Roll, San Francisco, United States
Authors: Garrett Roll, Lyle Burdine, Andrew Posselt, Chris Freise, SangMo Kang, Giulia Conte, Ryutaro Hirose, Sandy Feng, Peter Stock

Long term follow up of HIV infected patients after pancreas transplantation

G. Roll1, L. Burdine1, A. Posselt1, C. Freise1, S. Kang1, G. Conte1, R. Hirose1, S. Feng1, P. Stock1.

1Surgery, Division of Transplant, University of California San Francisco, San Francisco, USA,

Introduction: The approach to transplantation in HIV+ patients has been conservative due to fear of exacerbating an immunocompromised condition. As a result, HIV+ patients with diabetes have been excluded from pancreas transplantation due to the intense immune suppression required to prevent rejection. We report long term follow up of a pilot trial with pancreas transplant in HIV+ Type I diabetic patients. 
Methods: HIV+ patients with CD4 counts >200 cells/ml, with undetectable HIV viral load on a stable anti-retroviral regimen underwent simultaneous pancreas-kidney transplant (SPK) or pancreas after kidney (PAK). Thymoglobulin (Thymo) induction (6 mg/kg) was used for all. Maintenance immunosuppression included Cyclosporine or Tacrolimus, Mycophenolate mofetil, and Pred. 
Results: The average follow up period was 60.3 mo. Thymo induction resulted in profound lymphocyte depeletion, with CD4 counts recovering to baseline after one year. Three patients were treated for pancreas rejection. There were three opportunistic infections, all BK viremia, one of which occurred in an SPK recipient following a second round of thymo for pancreas rejection. All three patients who had an opportunistic infection are still alive, and BK viremia has not had an identifiable effect on kidney function to date in these patients. Two patients died, both with functioning grafts, at 48 mo and 55 mo after transplantation. Neither death was known to be related to an infection in the recipient. One patient has restarted insulin 90 months after transplant. No surviving patients are on dialysis. 
Conclusions: Type I diabetic transplant recipients with well controlled HIV tolerate the intensive lymphocyte depleting induction therapy required for beta cell replacement. Although there have been three opportunistic infections with BK viremia, adequate prophylaxis against opportunistic infections has been largely successful in providing protection until the CD4+ counts return to baseline. Long term follow up supports well controlled HIV+ Type I diabetic patients with renal failure are good candidates for pancreas transplant.

Table 1. Pilot patient cohort

Pt

Type   of TX

Induction

Last   follow up

Pancreas   rejection

OI

Currently   alive

1

SPK

Thymo

48 mo

No

None

No

2

SPK

Thymo

107 mo

Yes

BK viremia

Yes

3

SPK

Thymo

70 mo

No

None

Yes

4

SPK

Thymo

55 mo

No

None

No

5

PAK

Thymo

65 mo

Yes

BK viremia

Yes

6

SPK

Thymo

17 mo

No

BK viremia

Yes

 Table 2. Patient and organ survival

Survival

1 year

3 years

5 years

Patient survival

100 %

100 %

67 %

Death censored kidney survival

100 %

100 %

100 %

Death censored pancreas survival

100 %

100%

100 %

Kidney survival

100 %

100 %

67 %

Pancreas survival

100 %

100%

67%


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