Publications by authors named "Brugiere Olivier"

Background: Circulating extracellular vesicles (EVs) have shown promising results as noninvasive biomarkers for predicting disease outcomes in solid organ transplantation. Because in situ graft cell expression of the tolerogenic molecule HLA-G is associated with acceptance after lung transplantation (LTx), we hypothesized that plasma EV-bound HLA-G (HLA-GEV) levels could predict chronic lung allograft dysfunction (CLAD) development.

Methods: We analyzed 78 LTx recipients from the Cohort-for-Lung-Transplantation cohort, all in a stable (STA) state within the first year post-LTx.

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Pulmonary alveolar proteinosis (PAP) results from the accumulation of lipoproteinaceous material in the alveoli and alveolar macrophages, and can be associated with pulmonary fibrosis, with a need for lung transplantation (LTx). Causes of PAP are autoimmune (90%-95%), secondary (5%), or hereditary (<1%). Patients with hereditary PAP are generally not considered for isolated LTx, due to the high probability of recurrence after LTx, and only a challenging scenario with sequential LTx followed by hematopoietic stem cell transplantation (HSCT) was reported as successful.

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We report 3 cases of successful treatment of Microascus spp. bronchopulmonary infection in a multiple-traumatized patient and 2 lung transplant recipients in France. We emphasize the promising use of olorofim antifungal therapy in a rising context of intrinsically less-susceptible respiratory infections caused by mold.

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Lung transplantation is limited by the shortage of suitable donors. Many programs have begun to use extended criteria donors. Donors over 65 years old are rarely reported, especially for young cystic fibrosis recipients.

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Article Synopsis
  • Chronic lung allograft dysfunction (CLAD) is a significant concern for lung transplant patients, prompting the creation of SysCLAD to help predict its onset.
  • Research involved analyzing various factors, including patient health (clinicome), airway microbiota (exposome), and immune responses (immunome), to understand their roles in CLAD development.
  • Findings suggest that exposure to air pollution negatively affects lung function in transplant recipients and highlight potential biomarkers (like MMP-9 and certain immune cells) that could help predict CLAD and improve long-term survival.
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Background: Calcineurin inhibitors (CNIs) remain the cornerstone of maintenance immunosuppression (IS) after lung transplantation (LTx), although CNI-related life-threatening toxic effects may occur. Belatacept, a novel immunosuppressant that blocks a T-cell co-stimulation pathway, is a non-nephrotoxic drug indicated as an alternative to CNIs in kidney Tx. In LTx, there are only a few reports of belatacept conversion as a CNI-free or CNI-sparing IS treatment.

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Article Synopsis
  • * Traditional desensitization methods for these patients often have limitations, making it difficult to find suitable donors.
  • * The presented case is the first successful use of imlifidase for a highly sensitized lung transplant candidate, leading to a successful bilateral lung transplant.
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Lung transplantation (LTx) is a steadily expanding field. The considerable developments have been driven over the years by indefatigable work conducted at LTx centers to improve donor and recipient selection, combined with multifaceted efforts to overcome challenges raised by the surgical procedure, perioperative care, and long-term medical complications. One consequence has been a pruning away of contraindications over time, which has, in some ways, complicated the patient selection process.

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Article Synopsis
  • The study explores how recipient B cells produce donor-specific antibodies after organ transplantation, traditionally thought to require help from the recipient's own CD4 T cells.
  • Researchers found that even without these T cells, recipient mice after heart transplantation produced antibodies against donor MHC I molecules due to help from donor CD4 T cells present in the graft.
  • Similar mechanisms were observed in human kidney and lung transplants, suggesting that a new form of T cell interaction may explain early antibody responses and potentially worse transplant outcomes.
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Background: Survival after lung transplantation (LTx) still remains limited by chronic lung allograft dysfunction (CLAD), thought to represent a form of chronic rejection. We investigated whether the immune checkpoint HLA-G/ILT2 expressed by peripheral T-cell subpopulations could predict CLAD.

Methods: We used data for 150 LTx recipients from COLT (Cohort-For-Lung-Transplantation) cohort with ≥1 available blood sample at 1-, 6-, or 12-months post-Tx.

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Article Synopsis
  • Chronic Lung Allograft Dysfunction (CLAD) presents a significant challenge for lung transplant recipients, with various phenotypes like restrictive allograft syndrome (RAS) and mixed phenotype, highlighting the need for trials to address these conditions.
  • A retrospective study analyzed 70 bilateral lung transplant recipients diagnosed with RAS and mixed phenotype, assessing their functional outcomes and survival rates up to 12 months, revealing concerning mortality and graft survival rates.
  • The findings indicate a critical need for future randomized therapeutic trials, emphasizing the importance of utilizing survival as a clinical endpoint and addressing the high number of missing data points typically linked to patient mortality.
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Article Synopsis
  • - The study aimed to determine if intraoperative blood lactate levels can predict grade-3 primary graft dysfunction (PGD3-T72) after double-lung transplantation, contrasting with previously known factors.
  • - Analyzing data from 449 patients, researchers found that blood lactate levels increased during surgery, with higher levels associated with PGD3-T72. The critical threshold identified was 2.6 mmol/L, which could effectively predict the risk of PGD3-T72.
  • - Ultimately, patients who maintained blood lactate levels below this threshold after surgery were less likely to experience severe graft dysfunction, indicating the potential usefulness of monitoring lactate levels in clinical settings.
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Rational: Pending the authorization of new anti-CMV drugs with fewer adverse effects, exploring the possibilities offered by CMV immunoglobulins (CMVIG) seems necessary. In France, access to CMVIG requires official authorization by the national Health authority and is restricted to second line rescue therapy for CMV infection/disease. The aim of this multicenter retrospective study is to describe the indications and clinical situations that justified its use in France.

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Acute respiratory distress syndrome remains the main cause of death among people with COVID-19. Although many immunomodulatory and antiviral drug therapies have been tested, the only effective therapy against severe COVID-19 pneumonia among the general population is a regimen of high-dose corticosteroids for cases of severe associated inflammation. In solid-organ transplant recipients with long-term immunosuppression, data on disease presentation and evolution are scarce, and the benefit of high-dose corticosteroids remains uncertain for cases of severe COVID-19 pneumonia.

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Background: Pre-formed donor-specific antibodies (DSAs) are associated with worse outcome after lung transplantation (LTx) and might limit access to LTx. A virtual crossmatch-based strategy for perioperative desensitisation protocol has been used for immunised LTx candidates since 2012 at Foch Hospital (Suresnes, France). We compared the outcome of desensitised LTx candidates with high DSA mean fluorescence intensity and those with low or no pre-formed DSAs, not desensitised.

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Background: Lung transplantation (LT) is an identified risk factor for Pneumocystis pneumonia (PCP). However, PCP management and outcomes remain poorly described in LT recipients and PCP incidence is rarely documented in this population.

Methods: PCP episodes that occurred in 9 French LT centers between January 2010 and October 2017 were included in this analysis.

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Background: Restrictive allograft syndrome (RAS) after lung transplantation (LTx) is associated with the poorer graft survival in patients with chronic lung allograft dysfunction (CLAD). Nevertheless, its diagnostic criteria have not been clearly defined after single-LTx (SLTx). Hence, we studied an SLTx cohort with CLAD to investigate the utility of both computed tomography (CT)-score/volume measures and functional spirometric criteria for the early identification of RAS in this population.

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Bronchiolitis obliterans syndrome is the main limitation for long-term survival after lung transplantation. Some specific B cell populations are associated with long-term graft acceptance. We aimed to monitor the B cell profile during early development of bronchiolitis obliterans syndrome after lung transplantation.

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Aims: Antibody-mediated rejection (AMR) is an emerging and challenging issue in transplantation. Endothelial deposition of C4d and microvascular inflammation (MI) are reliable markers of AMR in renal and cardiac transplantation, but remain controversial in the lung. Our aim was to assess C4d immunohistochemistry and histological patterns for the diagnosis of lung AMR.

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Presence of anti-human leukocyte antigen donor-specific antibodies (DSAs) is associated with poor outcome after lung transplantation. Currently, DSAs are detected using the Luminex technique, which may be overly sensitive. The new C1q assay allows for the exclusive detection of complement (C1q)-binding antibodies, involved in antibody-mediated rejection.

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Background: Due to its multisystemic nature, scleroderma is considered a relative contraindication to lung transplantation at many centers. However, recent studies suggest similar post-transplant outcomes in patients with scleroderma compared to those with other causes of interstitial lung disease (ILD). Furthermore, it remains unknown whether scleroderma-associated pulmonary arterial hypertension (PAH) influences post-transplant outcomes.

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Article Synopsis
  • Chronic bronchiolitis obliterans syndrome (BOS) significantly affects long-term survival in lung transplant patients, but the immune mechanisms and predictive biomarkers remain unclear.
  • This study aimed to analyze blood T-lymphocyte profiles to see if they could predict BOS development in lung transplant recipients by assessing CD4 and CD8 T cells at various time points.
  • The results showed a notably higher percentage of CD4CD25FoxP3 T cells in patients who developed BOS, suggesting it could serve as an effective biomarker for predicting BOS in post-transplant patients.
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