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Bienvenue dans la collection HAL Infinity
Recherche en Immunologie, Inflammation et Maladies Infectieuses : du fondamental au translationnel
L’Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity), créé au 1er janvier 2021, résulte de la fusion de deux unités de recherche localisées sur le campus Purpan, le Centre de Physiopathologie Toulouse Purpan (CPTP) et l’Unité de Différenciation Epithéliale et Autoimmunité Rhumatoïde (UDEAR).
Nombre de fichiers déposés
984
Dernières publications
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Sébastien Lhomme, Cyril Garrouste, Nassim Kamar, Karine Sandres-Sauné, Florence Abravanel, et al.. Influence of Polyproline Region and Macro Domain Genetic Heterogeneity on HEV Persistence in Immunocompromised Patients. Journal of Infectious Diseases, 2025, 209 (2), pp.300-303. ⟨10.1093/infdis/jit438⟩. ⟨hal-04889860⟩
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Julie Noguerol, Karl Laviolette, Margot Zahm, Adeline Chaubet, Ambrine Sahal, et al.. Heterochromatic gene silencing controls CD4+ T cell susceptibility to regulatory T cell-mediated suppression in a murine allograft model. Nature Communications, 2025, 16 (1), pp.566. ⟨10.1038/s41467-025-55848-4⟩. ⟨hal-04893300⟩
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Sarah Soueges, Emmanuel Faure, Perrine Parize, Fanny Lanternier-Dessap, Hervé Lecuyer, et al.. Real-world multicentre study of cefiderocol treatment of immunocompromised patients with infections caused by multidrug-resistant Gram-negative bacteria: CEFI-ID.. Journal of Infection, 2025, 90 (1), pp.106376. ⟨10.1016/j.jinf.2024.106376⟩. ⟨hal-04885304⟩
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Steffi Rocchi, Emeline Scherer, P. Lewis White, Audrey Guitton, Alexandre Alanio, et al.. Interlaboratory assays from the fungal PCR Initiative and the Modimucor Study Group to improve qPCR detection of Mucorales DNA in serum: one more step toward standardization. Journal of Clinical Microbiology, In press, pp.e0152524. ⟨10.1128/jcm.01525-24⟩. ⟨hal-04862485⟩
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Carlo Chizzolini, Jean-Charles Guery, Fanny Noulet, Lyssia Gruaz, Claire Cenac, et al.. Extrafollicular CD19lowCXCR5−CD11c− double negative 3 (DN3) B cells are significantly associated with disease activity in females with systemic lupus erythematosus. Journal of Translational Autoimmunity, 2024, 9, pp.100252. ⟨10.1016/j.jtauto.2024.100252⟩. ⟨hal-04828927⟩
Nombre de notices déposée
1 007
Taux d'open access
76 %
Sujets
Human
T lymphocytes
Autoimmunity
Public health
Pain
Lipids
Metabolism
Congenital infection
Female
Antigen presentation
Male
Kidney transplantation
IgE
Escherichia coli
Biomarkers
Allergy
Inflammation
Therapeutics
France
Prader-Willi syndrome
Liver transplantation
Oxidative stress
Immunotherapy
Prevention
HIV-1
Toxoplasma gondii
Mast cells
Tolerance
Children
Lymphocytes
Multiple sclerosis
B cells
Plasmodium falciparum
Placenta
Organ transplantation
Asthma
Differentiation
NK cells
Immunology
Regulatory T cells
Vaccination
Immune response
Cancer
Hepatitis E virus
Autoimmune diseases
Cytomegalovirus
Chronic kidney disease
Psoriasis
Central nervous system
SARS-CoV-2
Pregnancy
T cells
Rheumatoid arthritis
Risk factors
Treatment
Autoantibodies
Malaria
Infectious disease
Diagnosis
Skin
Frailty
AIDS
Thymus
Ribavirin
Filaggrin
Apoptosis
Macrophages
Anophthalmia
Extracellular vesicles
Transplantation
HIV
Macrophage
COVID-19
Dog
Innate immunity
Omicron
Dupilumab
Cytokines
Lymphocytes T
Immunological synapse
Epidermis
Monocyte
Cameroon
Signaling
Epidemiology
Dendritic cells
Encephalitis
Humans
Atopic dermatitis
Immunosuppression
Vaccine
Dendrimer
Age
Prevalence
Systemic lupus erythematosus
Infection
Anaphylaxis
Cholesterol
Obesity
Hepatitis E