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Kidney transplantation in HIV-positive patients: a report of 14 cases
The HAART reduces the risk of HIV-related renal disease but the incidence of end-stage renal disease (ESRD). Therefore, efficacy and safety of renal transplantation (Tx) is an important resource in the HIV-infected population. We reported the results of kidney Tx in HIV+patients from deceased donors...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International AIDS Society
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512470/ http://dx.doi.org/10.7448/IAS.15.6.18111 |
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author | Casari, S Bossini, N Albini, L Setti, G Valerio, F Izzo, I Costarelli, S Sandrini, S Cancarini, G Castelli, F |
author_facet | Casari, S Bossini, N Albini, L Setti, G Valerio, F Izzo, I Costarelli, S Sandrini, S Cancarini, G Castelli, F |
author_sort | Casari, S |
collection | PubMed |
description | The HAART reduces the risk of HIV-related renal disease but the incidence of end-stage renal disease (ESRD). Therefore, efficacy and safety of renal transplantation (Tx) is an important resource in the HIV-infected population. We reported the results of kidney Tx in HIV+patients from deceased donors from June 2007 to March 2012 at our institution. The patients had to have CD4+T-cell counts≥200/mm(3) and undetectable plasma HIV-RNA if on HAART. The induction immunosuppressive therapy consisted of metilprednisolone and basilixmab; tacrolimus and/or mycofenolic acid were used for maintenance therapy. The therapeutic drug monitoring (TDM) has been performed for the adjusting of both their doses [1]. A total of 14 patients underwent kidney Tx. They were on dialysis (haemodialysis=13, 92.9%; peritoneal=1, 7.1%) for 5±3.1 years and they were included on the Tx waiting list for 10±8 months. The baseline characteristics are showed in Table 1. At the last available point of follow-up (median=42.8 months, IQR=8.5–55.2), 8 out of the 13 patients (61.6%) without steroid had at least one acute rejection episode, but only 1 patient lost the graft, after 43 months (7.1%) due to chronic rejection associated with infectious and vascular complications. After Tx the median CD4+T-cell count increased from 382.5 (IQR range=233–415) to 434 (IQR range=282–605) cells/mm(3) (p=0.055). In Figure 1 are reported the CD4+trends of 9 patients with a follow-up of at least 6 months. HIV infection was well controlled, with only 2 (14.3%) cases of virological failure which were promptly resolved after HAART regimen modification. Table 1 shows the observed infectious complications. The skin Kaposi sarcoma has been resolved by switching to immunosuppressive therapy with sirolimus [2]. Kidney Tx appears to be safe in HIV-positive patients undergoing HAART. The viro-immunological parameters remained well controlled with no increases in infectious complications or neoplasm and a satisfactory control of HIV infection. However, the high rejection rate is a serious concern and suggests to consider a steroid-containing immunosuppressive regimen also in these patients. |
format | Online Article Text |
id | pubmed-3512470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International AIDS Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-35124702012-12-03 Kidney transplantation in HIV-positive patients: a report of 14 cases Casari, S Bossini, N Albini, L Setti, G Valerio, F Izzo, I Costarelli, S Sandrini, S Cancarini, G Castelli, F J Int AIDS Soc Poster Abstract – P158 The HAART reduces the risk of HIV-related renal disease but the incidence of end-stage renal disease (ESRD). Therefore, efficacy and safety of renal transplantation (Tx) is an important resource in the HIV-infected population. We reported the results of kidney Tx in HIV+patients from deceased donors from June 2007 to March 2012 at our institution. The patients had to have CD4+T-cell counts≥200/mm(3) and undetectable plasma HIV-RNA if on HAART. The induction immunosuppressive therapy consisted of metilprednisolone and basilixmab; tacrolimus and/or mycofenolic acid were used for maintenance therapy. The therapeutic drug monitoring (TDM) has been performed for the adjusting of both their doses [1]. A total of 14 patients underwent kidney Tx. They were on dialysis (haemodialysis=13, 92.9%; peritoneal=1, 7.1%) for 5±3.1 years and they were included on the Tx waiting list for 10±8 months. The baseline characteristics are showed in Table 1. At the last available point of follow-up (median=42.8 months, IQR=8.5–55.2), 8 out of the 13 patients (61.6%) without steroid had at least one acute rejection episode, but only 1 patient lost the graft, after 43 months (7.1%) due to chronic rejection associated with infectious and vascular complications. After Tx the median CD4+T-cell count increased from 382.5 (IQR range=233–415) to 434 (IQR range=282–605) cells/mm(3) (p=0.055). In Figure 1 are reported the CD4+trends of 9 patients with a follow-up of at least 6 months. HIV infection was well controlled, with only 2 (14.3%) cases of virological failure which were promptly resolved after HAART regimen modification. Table 1 shows the observed infectious complications. The skin Kaposi sarcoma has been resolved by switching to immunosuppressive therapy with sirolimus [2]. Kidney Tx appears to be safe in HIV-positive patients undergoing HAART. The viro-immunological parameters remained well controlled with no increases in infectious complications or neoplasm and a satisfactory control of HIV infection. However, the high rejection rate is a serious concern and suggests to consider a steroid-containing immunosuppressive regimen also in these patients. International AIDS Society 2012-11-11 /pmc/articles/PMC3512470/ http://dx.doi.org/10.7448/IAS.15.6.18111 Text en © 2012 Casari S et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Poster Abstract – P158 Casari, S Bossini, N Albini, L Setti, G Valerio, F Izzo, I Costarelli, S Sandrini, S Cancarini, G Castelli, F Kidney transplantation in HIV-positive patients: a report of 14 cases |
title | Kidney transplantation in HIV-positive patients: a report of 14 cases |
title_full | Kidney transplantation in HIV-positive patients: a report of 14 cases |
title_fullStr | Kidney transplantation in HIV-positive patients: a report of 14 cases |
title_full_unstemmed | Kidney transplantation in HIV-positive patients: a report of 14 cases |
title_short | Kidney transplantation in HIV-positive patients: a report of 14 cases |
title_sort | kidney transplantation in hiv-positive patients: a report of 14 cases |
topic | Poster Abstract – P158 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512470/ http://dx.doi.org/10.7448/IAS.15.6.18111 |
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