16 results match your criteria: "Laboratoire Universitaire de Médecine du Travail-Université Lille 2[Affiliation]"

Compatibility at amino acid position 98 of MICB reduces the incidence of graft-versus-host disease in conjunction with the CMV status.

Bone Marrow Transplant

July 2020

Laboratoire d'ImmunoRhumatologie Moléculaire, INSERM UMR_S1109, Plateforme GENOMAX, Faculté de Médecine, Fédération Hospitalo-Universitaire OMICARE, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg, France.

Graft-versus-host disease (GVHD) and cytomegalovirus (CMV)-related complications are leading causes of mortality after unrelated-donor hematopoietic cell transplantation (UD-HCT). The non-conventional MHC class I gene MICB, alike MICA, encodes a stress-induced polymorphic NKG2D ligand. However, unlike MICA, MICB interacts with the CMV-encoded UL16, which sequestrates MICB intracellularly, leading to immune evasion.

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The extraordinary and unexpected success of cellular immunotherapy using genetically engineered T-cells to express a chimeric antigen receptor (CAR) targeting CD19, in the treatment of refractory or relapsing B-hematological malignancies, has provided a real therapeutic hope. Indeed, remission rates reach more than 80 % in patients at a stage, without any other possibilities of treatment, notably in the child's acute lymphoblastic leukemia. These results, initially resulting from academic research, led to Food and Drug accreditation for market access of two innovative autologous therapy drugs, Kimryah® and Yescarta®.

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[Donor Lymphocyte Infusions (DLI): Guidelines from the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC)].

Bull Cancer

January 2019

CHU de Nantes, Hôtel-Dieu, service d'hématologie, 1, place Ricordeau, 44000 Nantes, France. Electronic address:

Donor lymphocyte infusion (DLI) can be proposed to treat or prevent the relapse of malignant hemopathies following allogeneic stem cell transplantation. The efficiency has been mainly reported in the treatment of CML and low-grade lymphomas while the anti-tumoral activity is less in forms of acute leukemia and myelodysplastic syndromes. The GVL benefit should always be compared to the possible toxic effects of GVHD.

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Article Synopsis
  • * A second allo-HSCT can be a good treatment option, particularly for patients with favorable conditions like good performance status and low co-morbidity scores.
  • * Recommendations include using matched related donors for better outcomes and immunoablative regimens in cases of graft dysfunction; switching donors may also be a viable option if there's no graft-versus-host disease.
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Patient acceptable symptom state and minimal clinically important difference for patient-reported outcomes in systemic sclerosis: A secondary analysis of a randomized controlled trial comparing personalized physical therapy to usual care.

Semin Arthritis Rheum

February 2019

AP-HP, Service de Rééducation et de Réadaptation de l'Appareil Locomoteur et des Pathologies du Rachis, Hôpitaux Universitaires Paris Centre-Groupe Hospitalier Cochin, Paris, France; Sorbonne Paris Cité, Université Paris Descartes, Faculté de Médecine, Paris, France; INSERM UMR 1124, Laboratoire de Pharmacologie, Toxicologie et Signalisation Cellulaire, Faculté des Sciences Fondamentales et Biomédicales, Centre Universitaire des Saints-Pères, Paris, France. Electronic address:

Article Synopsis
  • The study aimed to estimate the patient acceptable symptom state (PASS) and minimal clinically important difference (MCID) for individuals with systemic sclerosis (SSc).
  • A secondary analysis of the SCLEREDUC trial was conducted, which involved 220 SSc patients over 12 months, assessing self-reported health changes and symptom relief.
  • The findings provided the first-ever estimates of PASS and MCID for pain and activity limitations in SSc patients, detailing specific numerical values for various health outcome measures.
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[Prerequisite for hematopoietic cellular therapy programs to set up chimeric antigen receptor T-cell therapy (CAR T-cells): Guidelines from the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC)].

Bull Cancer

December 2017

Aix-Marseille université, Inserm CBT-1409, institut Paoli-Calmettes, centre de thérapie cellulaire, unité de transplantation et de thérapie cellulaire, département de biologie du cancer, 13273 Marseille cedex 9, France; EBMT cell therapy & immunobiology working party (CTIWP), 08005 Barcelone, Espagne. Electronic address:

CAR T-cells are autologous or allogeneic human lymphocytes that are genetically engineered to express a chimeric antigen receptor targeting an antigen expressed on tumor cells such as CD19. CAR T-cells represent a new class of medicinal products, and belong to the broad category of Advanced Therapy Medicinal Products (ATMPs), as defined by EC Regulation 2007-1394. Specifically, they are categorized as gene therapy medicinal products.

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Despite its high prevalence and mortality, little is known about the pathogenesis of rheumatoid arthritis-associated interstitial lung disease (RA-ILD). Given that familial pulmonary fibrosis (FPF) and RA-ILD frequently share the usual pattern of interstitial pneumonia and common environmental risk factors, we hypothesised that the two diseases might share additional risk factors, including FPF-linked genes. Our aim was to identify coding mutations of FPF-risk genes associated with RA-ILD.

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Rituximab treatment circumvents the prognostic impact of tumor-infiltrating T-cells in follicular lymphoma patients.

Hum Pathol

June 2017

INSERM1052, CNRS 5286, Centre de Recherche en Cancerologie de Lyon, Faculté de Médecine Lyon-Sud Charles Mérieux, Hospices Civils De Lyon, Laboratoire d'hématologie, F-69495 Pierre Bénite cedex.

Previous immunohistochemical (IHC) studies showed controversial data about the prognostic value of tumor-infiltrating lymphocytes (TILs) in follicular lymphoma (FL). To clarify this issue, a large series of FL samples from rituximab-treated patients enrolled in the randomized PRIMA trial was examined. IHC was quantified using automated image analysis in 417, 287, 418, 406, 379, and 369 patients for CD3, CD4, CD8, PD1, ICOS, and FOXP3, respectively.

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[Haploidentical hematopoietic stem cell transplantation: Guidelines from the Francophone society of marrow transplantation and cellular therapy (SFGM-TC)].

Bull Cancer

November 2016

Hôpital Brabois, service d'hématologie et de médecine interne, rue du Morvan, 54500 Vandœuvre-les-Nancy, France; CHRU Nancy, université de Lorraine, CNRS UMR 7365, 54500 Vandœuvre-les-Nancy, France.

Haploidentical hematopoietic stem cell transplantation (HSCT) is being increasingly used due to improvement of the transplantation procedures allowing a reduction of graft-versus-host-disease (GVHD) and of transplant-related mortality (TRM). Such improvements have been particularly observed after administration of T-replete HSCT graft associated to an in vivo T cell depletion by the administration of high-doses of cyclophosphamide (HD-Cy) after transplantation. Here, we have analyzed the results of haplo-identical T replete HSC transplants, in particular, when performed with post-transplant HD-Cy in order to provide recommendations for the clinical practice.

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To date, despite an existing regulatory framework and standards, there are no true technical recommendations. A survey of 23 cell processing facilities (France, Belgium and Switzerland) has allowed to overview current practices according to cellular products specifications upon arrival at the facility, with modalities for their preparation prior to cryopreservation, storage, thawing and finally for infusion to patient. Data analysis shows great variability of collected volumes and cell concentrations in cellular products.

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Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHD.

Blood

October 2016

Laboratoire d'ImmunoRhumatologie Moléculaire, INSERM Unité Mixte de Recherche (UMR)_S1109, Plateforme GENOMAX, Faculté de Médecine, Fédération Hospitalo-Universitaire OMICARE, Fédération de Médecine Translationnelle de Strasbourg, and LabEx TRANSPLANTEX, Faculté de Médecine, Université de Strasbourg, Strasbourg, France; INSERM Franco-Japanese Nextgen HLA laboratory, Nagano, Japan and Strasbourg, France; Laboratoire d'Immunologie, Plateau Technique de Biologie, Pôle de Biologie, Nouvel Hôpital Civil, Strasbourg, France.

Article Synopsis
  • Graft-versus-host disease (GVHD) is a serious complication in unrelated donor hematopoietic cell transplantation (HCT), impacted by mismatches in the MICA gene that plays a role in immune responses.
  • A study of 922 HCT pairs found that mismatches in MICA increased the risk of severe acute GVHD and chronic GVHD, along with higher nonrelapse mortality rates, while also showing a lower risk for cancer relapse.
  • Selecting donors that are MICA-matched can improve patient outcomes significantly, as the close genetic link between MICA and HLA-B aids in identifying suitable donors easily.
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Microparticle phenotypes are associated with driver mutations and distinct thrombotic risks in essential thrombocythemia.

Haematologica

September 2016

Centre Hospitalier Universitaire de Lille, Laboratoire d'Hématologie-transfusion, France INSERM UMR 1011, Université de Lille 2, Faculté de Médecine, France; EGID, Institut Pasteur de Lille, France

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Biological and radiological exploration and management of non-functioning pituitary adenoma.

Ann Endocrinol (Paris)

July 2015

Unité fonctionnelle d'hormonologie, pôle biologie, CHU de Pontchaillou, rue Henri-Le-Guilloux, 35043 Rennes, France; Inserm 1414, centre d'investigation clinique, université de Rennes 1, 35033 Rennes, France.

Non-functioning pituitary adenoma may be totally asymptomatic and discovered "incidentally" during radiological examination for some other indication, or else induce tumoral signs with compression of the optic chiasm and pituitary dysfunction. Non-functioning adenomas are mainly gonadotroph, but may also be "silent". Treatment strategy depends on initial clinical, biological, ophthalmological and radiological findings.

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Freezing and storage at -20 °C provides adequate preservation of Toxoplasma gondii DNA for retrospective molecular analysis.

Diagn Microbiol Infect Dis

November 2014

Pôle "Biologie Moléculaire" du Centre National de Référence de la Toxoplasmose, Montpellier, France; CHRU/Université Montpellier 1, Département de Parasitologie-Mycologie, Montpellier, France; CNRS UMR5290/IRD 224/UM1/UM2 ("MiVEGEC"), Montpellier, France. Electronic address:

Nucleic acid-based testing has become crucial for toxoplasmosis diagnosis. For retrospective (forensic or scientific) studies, optimal methods must be employed for DNA long-term storage. We compared Toxoplasma gondii detection before and after DNA storage using real-time PCR.

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Objective: Studies of fractional exhaled NO (FeNO) or induced sputum are now well standardized and the exponential increase in publications about exhaled breath condensate reflects growing interest in a noninvasive diagnosis of pulmonary diseases in occupational medicine.

Methods: This review describes current techniques (FeNO, induced sputum, and exhaled breath condensate) for the study of inflammation and oxidative stress biomarkers.

Results: These biomarkers are FeNO, cytokines, H2O2, 8-isoprostane, malondialdehyde, and nitrogen oxides.

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Background: Cryptosporidiosis represents a major public health problem. This infection has been reported worldwide as a frequent cause of diarrhoea. Particularly, it remains a clinically significant opportunistic infection among immunocompromised patients, causing potentially life-threatening diarrhoea in HIV-infected persons.

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