Publications by authors named "Marie-Christine Moal"

Mycophenolic acid (MPA) targets the inosine 5'-monophosphate dehydrogenase (IMPDH) of human lymphocytes. It is widely used as an immunosuppressant to prevent rejection in solid organ transplant (SOT) recipients who, incidentally, are at risk for pneumonia (PCP). We hypothesized that MPA exerts selective pressure on microorganisms considering its in vitro antifungal activity on other fungi.

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Pulmonary specimen pairs from five patients who presented with pulmonary colonization and later developed Pneumocystis Pneumonia (PcP) were retrospectively examined for P. jirovecii genotyping. A match of genotypes in pulmonary specimen pairs of three patients was observed, whereas a partial match and a mismatch were observed in the fourth and fifth patients, respectively.

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Background: In previous analyses of BENEFIT, a phase 3 study, belatacept-based immunosuppression, as compared with cyclosporine-based immunosuppression, was associated with similar patient and graft survival and significantly improved renal function in kidney-transplant recipients. Here we present the final results from this study.

Methods: We randomly assigned kidney-transplant recipients to a more-intensive belatacept regimen, a less-intensive belatacept regimen, or a cyclosporine regimen.

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Background: Kidney recipients maintaining a prolonged allograft survival in the absence of immunosuppressive drugs and without evidence of rejection are supposed to be exceptional. The ERA-EDTA-DESCARTES working group together with Nantes University launched a European-wide survey to identify new patients, describe them and estimate their frequency for the first time.

Methods: Seventeen coordinators distributed a questionnaire in 256 transplant centres and 28 countries in order to report as many 'operationally tolerant' patients (TOL; defined as having a serum creatinine <1.

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The course of autosomal dominant polycystic kidney disease (ADPKD) varies among individuals, with some reaching ESRD before 40 years of age and others never requiring RRT. In this study, we developed a prognostic model to predict renal outcomes in patients with ADPKD on the basis of genetic and clinical data. We conducted a cross-sectional study of 1341 patients from the Genkyst cohort and evaluated the influence of clinical and genetic factors on renal survival.

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Article Synopsis
  • This study examines post-transplantation lymphoproliferative disorder (PTLD) in kidney transplant recipients in France over a 10-year period, highlighting its serious impact on patient survival.
  • A total of 500 cases of PTLD were analyzed, revealing a 5-year survival rate of 53% and a 10-year rate of 45%, with factors like age, serum creatinine level, and PTLD characteristics affecting survival.
  • The researchers developed a prognostic score based on five variables at diagnosis to classify patients' risk levels, aiming to improve treatment strategies for PTLD in kidney transplant recipients.
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  • This study investigates the impact of switching from a low-exposure calcineurin inhibitor (CNI) to mycophenolate sodium in kidney transplant patients taking everolimus and corticosteroids after one year of surgery.
  • Results showed a small improvement in kidney function (measured by mGFR) for the CNI-free group compared to those who continued with CNI, although the difference wasn't statistically significant.
  • The findings suggest that eliminating CNI might maintain efficacy and could be beneficial, but the small sample size means larger studies are needed to confirm these results.
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Background: Eighteen renal transplant recipients (RTRs) developed Pneumocystis jirovecii infections at the renal transplantation unit of Brest University Hospital (Brest, Brittany, France) from May 2008 through April 2010, whereas no cases of P. jirovecii infection had been diagnosed in this unit since 2002. This outbreak was investigated by identifying P.

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Mycophenolic acid (MPA) dose is frequently reduced in tacrolimus-treated kidney transplant patients, but alternatively the recommended MPA dose can be maintained with reduced tacrolimus exposure. In a 6-month, multicenter, randomized, openlabel study, maintenance kidney transplant patients receiving MPA (mycophenolate mofetil 1g/d or enteric-coated mycophenolate sodium (EC-MPS) 720 mg/d) and tacrolimus were randomized to convert to EC-MPS 1,440 mg/d with reduced tacrolimus (n = 46), or receive EC-MPS 720 mg/d with unchanged tacrolimus (n = 48). Mean estimated GFR (eGFR, aMDRD) at Month 6 was 49.

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In a multicenter trial, renal transplant recipients were randomized to tacrolimus with fixed-dose sirolimus (Tac/SRL, N = 318) or tacrolimus with MMF (Tac/MMF, N = 316). Targeted tacrolimus trough levels were lower in the Tac/SRL group after day 14. The primary endpoint was renal function at 6 months using creatinine clearance (Cockcroft-Gault) and was comparable at 66.

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Article Synopsis
  • Immediate use of everolimus (mTOR inhibitor) post-kidney transplant can limit the need for calcineurin inhibitors while posing risks of delayed graft function (DGF) and impaired wound healing.
  • The CALLISTO study involved 139 deceased-donor kidney transplant patients split into immediate (IE) and delayed (DE) everolimus groups, showing similar outcomes in primary endpoints after 12 months.
  • Both groups had comparable rates of acute rejection and renal function, indicating no significant benefit in delaying everolimus initiation for patients at risk of DGF.
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  • There are concerns that starting sirolimus too soon after kidney transplantation may lead to delayed graft function (DGF) and wound healing issues, prompting the idea to delay everolimus administration instead.
  • A study was conducted to assess the effects of starting everolimus immediately after transplantation versus delaying it for five weeks in patients at risk for DGF.
  • The results showed no significant differences in kidney function recovery, wound healing, or overall treatment tolerance between the immediate and delayed everolimus groups at the 3-month mark.
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Toxoplasmosis is an infrequent, often difficult to diagnose and potentially lethal disease in kidney transplant recipients. Among reported cases, a few were associated with hemophagocytic syndrome (HPS), a rare condition characterized by widespread proliferation of macrophages phagocytizing blood elements, accompanied by fever and pancytopenia. We report here the case of a patient who received a Toxoplasma gondii positive kidney allograft and developed invasive toxoplasmosis 10 days after surgery, with high fever, skin rash, arthralgias, and renal failure, followed by pneumonia, anemia, thrombocytopenia, liver dysfunction, and encephalitis.

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