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Portuguese Journal of Nephrology & Hypertension

versão impressa ISSN 0872-0169

Port J Nephrol Hypert vol.26 no.2 Lisboa abr. 2012

 

Renal transplantation in an HIV-2 positive recipient in Portugal

 

Ana Natário1,2, Bruno Rodrigues2, Patrícia Matias2, Cristina Jorge2, Margarida Bruges2, Rita Birne2, Ana Miranda3, Kamal Mansinho3, Domingos Machado2, André Weigert2

1 Department of Nephrology, Centro Hospitalar Setúbal, Setúbal, Portugal.

2 Department of Nephrology, Hospital Santa Cruz, Carnaxide, Portugal.

3 Department of Infectious Diseases, Hospital Egas Moniz, Lisbon, Portugal.

correspondence to:

 

ABSTRACT

The improvement of combined antiretroviral therapy regimens has made solid organ transplantation a therapeutic option for patients with human immunodeficiency virus (HIV) infection. Generally, HIV-2 infectionpresents a slower clinical progression and immunological degradation than HIV-1. HIV-2 infection treatment can be challenging when a complex immunosuppressive regimen is combined with antiretroviraltherapy. The authors report the first case in Portugal of renal transplantation in an HIV-2 patient.

A 54-year-old man from Guinea-Bissau was diagnosed with HIV-2 infection on starting haemodialysis in Portugal in 1998. At diagnosis, HIV infection staging revealed undetectable plasma HIV- 2 RNA and T-cell CD4 counts of 808 cells/μl, with no need for combined antiretroviral therapy during follow-up.

The patient underwent renal transplantation from a deceased donor in March 2011. He developed delayed graft function and started therapy with methylprednisolone and thymoglobulin. The patient gradually recovered renal function and was discharged after two weeks with serum creatinine of 2.3 mg/dL.

The HIV-2 RNA levels remained undetectable, but T-cell CD4count decreased to less than 200 cells/μl and combined antiretroviral therapy with abacavir, lamivudine and raltegravir was started. Nine months after transplantation, the patient has a serum creatinine of 1.5 mg/dL and a nonreplicating HIV status.

Key-Words: Antiretroviral therapy; HIV-2 infection; immunosuppressive therapy; kidney transplantation.

 

INTRODUCTION

Human immunodeficiency virus type 2 (HIV-2) was first recognised in 19851. Infection with HIV-2 occurs mainly in West Africa but a considerable number of cases have been recognised in Europe, India and the United States2. The transmission routes are the same as those for HIV-1, namely sexual, blood-borne exposure (blood transfusion, shared needles) and vertical3, but HIV-2 has a lower risk of contagion.

HIV-associated nephropathy (HIVAN) occurs in about 7% of patients with HIV- 1infection4, but this complication has been only rarely reported in HIV-2infected individuals5. Since the introduction of effective combined antiretroviral therapy (cART), promoting immunological recovery and replication suppression, the outcome of HIV patients has improved dramatically, and several studies show thatthe mortality rate for HIV end-stage renal disease (ESRD) patients is now similar to those without HIV infection. Given this significant improvement in HIV patients’ morbidity and mortality, kidney transplantation has been increasingly considered an alternative treatment for ESRD in this population6.

CASE REPORT

A 54-year-old hypertensive man from Guinea-Bissau was transferred to Portugal in 1998 due to the need for renal replacement therapy. The presumed cause of ESRD was hypertensive nephropathy.

HIV-2 infection was diagnosed when he started chronic haemodialysis in Portugal. During follow-up HIV-2 RNA plasma levels were persistently undetectable and TCD4 remained > 200 cells/μl, with no need for cART. The patient underwent adequate dialysis, his nutritional status was favourable and no opportunistic infections occurred. He was considered a candidate for a deceased donor kidney and on 23 March 2011 underwent renal transplantation from a 67-year-old deceased donor (death from a cerebrovascular accident). Both the donor and the recipient had the same ABO and Rhesus blood type. The receptor had 4 HLA- mismatches (2 in B and 2 in DR) and a panel reactive antibody (PRA) of 40% with positive anti-MICA (MHC class I- related chain A) antibodies. Cold ischaemia time was 16 hours. There were no episodes of hypotension during or after the surgery. According to our protocol, tacrolimus (0.1-0.15mg/Kg) was given before the surgical procedure, and basiliximab (20mg), mycophenolate mofetil (1g) and methylprednisone (500mg) during surgery. In this case, due to PRA and MICA antibodies, intravenous immunoglobulin (2g/Kg) was used in continuous perfusion during the first 48 hours after the transplantation.

The patient developed severe postoperative oliguria.

Doppler ultrasound showed no obstruction, but a high resistivity index (0.8). It was decided not to perform a graft biopsy since the patient developed symptomatic anaemia (7.4g/dL). Although two days after transplantation the patient had a TCD4 count of 214 cells/μl, it was decided to suspend tacrolimus and to administer a three-day course of methylprednisolone (500mg/day) and a five-day course of thymoglobulin (1.25 mg/Kg/day). After thymoglobulin, HIV-2 RNA plasma levels remained undetectable (< 50 cp/ml), but absolute and percentage of TCD4 count fell to 16 cells/μl (9%). In the week after the transplantation, antiretroviral therapy regimen with two nucleoside reverse transcriptase inhibitors – lamivudine, abacavir – and an integrase inhibitor, raltegravir, were started, with good tolerance.

The patient needed three dialysis sessions, but after one week there was a gradual improvement of urinary output and renal function. Tacrolimus (0.1-0.15 mg/Kg/day) was introduced on the seventh postoperative day. The patient was discharged after two weeks with an improving graft function (serum creatinine of 2.3 mg/dL). Nine months posttransplant, graft function is stable with a serum creatinine of 1.5 mg/dL. Patient is clinically stable and asymptomatic, showing good immunological recovery (TCD4=294 cells/μl) and undetectable HIV-2 viral load.

DISCUSSION

The burden of renal disease in HIV patients living in Africa is adversely influenced by inadequate socioeconomic and health care infrastructures7. The absence of renal replacement therapy in Guinea-Bissau led to the life-saving transfer of the patient to Portugal.

This patient presented with HIV-2 infection since 1998, with long-term nonprogression behaviour, supported by the slow immunological degradation and absence of opportunistic or AIDS-related events. In

March 2011, the patient successfully underwent deceased donor kidney transplant. After the surgery the patient presented delayed graft function (DGF) which was probably due to a combination of several factors, namely, expanded criteria donor (ECD) 8 and a cold ischaemia time of 16 hours. However, he also had a PRA of 40% with positive MICA antibodies, known risk factors for acute rejection. One study of the United Network for Organ Sharing database demonstrated a lower death-censored graft survival at one year in patients with HIV-1 and renal transplants from deceased donors older than 50 years of age and with a cold ischaemia time longer than 16 hours9.

ECD kidneys accounts for about 15% of deceased donor kidneys in the USA and has statistically an estimated graft survival at two years of about 80% compared with a two-year graft survival of 88% in a standard criteria kidney10. In some studies11,12, a trend to higher rejection rates was noted in HIV-1 infected patients. The reason for such rates is unclear, but dysregulation of the immune system or insufficient immunosuppression are two possible causes11.

Although graft biopsy was not performed, the authors consider that acute tubular necrosis best explains the cause of the initial oliguria. The transplantation team decided to avoid calcineurin inhibitors (CNI) during the first week and initiate thymoglobulin, in order to avoid nephrotoxicity and achieve adequate immunosuppression.

In the last few years, several retrospective and prospective small studies have shown encouraging results, suggesting that renal transplantation is feasible in adequately selected HIV-infected patients.

The results of the largest prospective, nonrandomized trial of kidney transplantation in HIV-1 infected patients have recently been published12. The patient and graft survival rates at three years were 88.2 and 73.7% respectively, which were between the reported rates for older-kidney transplant recipients and for all kidney-transplant recipients13.

The first three months after transplantation remain the most critical period for development of significant complications, and one of the most concerning issues in our patient was the need to use immunosuppressive drugs with higher risk of opportunistic infections and interactions with cART. The administration of a complex immunosuppressive regimen in combination with antiretroviral herapy poses a major challenge since drug interactions resulting in altered exposure to immunosuppressants may be associated with rejection13. Contemporary treatment of HIV infection involves the combination of at least three fully active drugs from the currently available classes of antiretroviral medications: nucleoside reverse transcriptase inhibitors (NRTI), nonnucleoside reverse transcriptase inhibitors (NNRTIs), protease inhibitors (PIs), entry inhibitors and integrase inhibitors. The current antiretroviral regimens considered for naïve patients are based on a combination of two nucleoside reverse transcriptase inhibitors and a boosted protease inhibitor, a nonnucleoside reverse transcriptase inhibitor or an integrase inhibitor14. Antiretroviral medications are generally used in normal doses and adjusted to the improved kidney function that occurs after the transplantation.

In comparison to HIV-1, more patients with HIV-2 infection present as long-term nonprogressors or slow progressors. Although this could be used to argue for a later TCD4-driven initiation of cART, it has been demonstrated that immunological recovery on therapy could be slower in HIV-2 than HIV-1 patients15 and excessive delay in initiating cART may carry long-term negative immunological consequences16.

Current therapeutic HIV guidelines recommend the initiation of cART in individuals presenting with less than 350 TCD4 cells/μl or with concurrent morbidities, namely, HIVAN.

Antiretroviral susceptibility can differ significantly between HIV-1 and HIV-2, as HIV-2 is intrinsically resistant to two of the major classes of antiretroviral drugs: NNRTIs and fusion inhibitors. Considering the class of protease inhibitors, indinavir, saquinavir, lopinavir and darunavir are the most efficient molecules in HIV-2 suppression17. This patient started antiretroviral therapy regimen based on a triple combination: two NRTI (abacavir and lamivudine), since he presented anaemia and moderate elevated serum creatinine levels, something that would contraindicate the use of zidovudine or tenofovir respectively; and an integrase inhibitor (raltegravir) trying to minimize drug interactions between protease inhibitors and CNI which are also metabolised by the CYP450 pathway13.

Additionally, abacavir and raltegravir have the advantage of having low urinary excretion, and therefore, no requirement for dose adjustment. Mycophenolate mofetil has inhibitory effects on HIV and is synergistic with abacavir18. Lamivudine has only few interactions with micophenolate mofetil.

There are no current recommendations about how to treat rejection episodes in HIV-positive recipients, but these patients are more likely to receive induction therapy19. The use of antilymphocyte polyclonal antibodies is controversial, and many authors recommend restricting this therapy for patients at very high immunological risk of rejection9,20. Thymoglobulin, an agent frequently used to manage acute rejection, may be associated with marked TCD4 depletion6.

Several studies have reported significant decreases in TCD4 counts in HIV-infected recipients related to the use of thymoglobulin9,12. In a study published by Stock et al., the median change in the TCD4 count from baseline to 1 year was greater in patients who received induction therapy with thymoglobulin than those who did not (-239 versus -135 cells per mm3)12. However, these changes were transient and the median change in TCD4+ count from baseline to three years was not significantly different between these groups (-57 and -52 cells per mm3, respectively). Another study9 also showed that there was no increased risk of opportunistic infections or progression to AIDS or death related to induction therapy. Consistent with this findings, after polyclonal therapy TCD4 count fell to 16 cells/μl in our recipient, but there were no AIDS-defining diseases or opportunistic infections and the patient experienced immunological recover during follow-up (TCD4=294 cells/μl).

Clinical trials of cART in HIV-2 are scarce compared the ones available to HIV-1, possibly related to low prevalence and geographic distribution constraints16. Until there is better evidence from randomised controlled trials, judgement of what constitutes good care in HIV-2 management must therefore rely on data from small cohort studies and case series, theoretical assertions and parallels with HIV-1 therapeutics.

The potential benefits of kidney transplantation in HIV-2 patients must be confirmed by further studies before recommendations can be made for clinical practice.

 

References

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Correspondence to:

Dr Ana Natário

Department of Nephrology

Centro Hospitalar Setúbal

Rua Camilo Castelo Branco

2910-446 Setúbal, Portugal

Email:ananatario@hotmail.com

 

Conflict of interest statement. None declared.

 

Received for publication: 12/02/2012

Accepted in revised form: 23/02/2012

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