Lack of functionally active Melan-A(26-35)-specific T cells in the blood of HLA-A2+ vitiligo patients.

Vitiligo, a skin disorder characterized by the spontaneous destruction of melanocytes, is believed to be of autoimmune origin. We investigated the presence and functionality of CD8(+) T-cells specific for the melanocyte-associated antigens Melan-A, gp100, tyrosinase, and TRP-2 in the blood of HLA-A2(+) vitiligo patients. We enumerated antigen-specific CD8(+) T cells by major histocompatibility complex multimer staining directly ex vivo, as well as after 9 days of in vitro stimulation and assessed IFN-gamma secretion by enzyme-linked immunospot (Elispot) assay. Tyrosinase-, gp100-, or TRP-2-specific CD8(+) T cells could not be identified in the peripheral blood of individuals with vitiligo. Although Melan-A-specific T cells were detectable at levels comparable to Flu-MP-specific T cells by multimer staining, these lymphocytes did not express the skin-homing receptor cutaneous lymphocyte antigen, were phenotypically naïve (CD45RA(+)), and were unresponsive in the IFN-gamma Elispot assay, suggesting that they are unlikely to be involved in the etiopathogenesis of vitiligo.

Novel Macrocyclic Amidinoureas: Potent Non-Azole Antifungals Active against Wild-Type and Resistant Candida Species.

Novel macrocyclic amidinourea derivatives 11, 18, and 25 were synthesized and evaluated as antifungal agents against wild-type and fluconazole resistant Candida species. Macrocyclic compounds 11 and 18 were synthesized through a convergent approach using as a key step a ring-closing metathesis macrocyclization reaction, whereas compounds 25 were obtained by our previously reported synthetic pathway. All the macrocyclic amidinoureas showed antifungal activity toward different Candida species higher or comparable to fluconazole and resulted highly active against fluconazole resistant Candida strains showing in many cases minimum inhibitory concentration values lower than voriconazole.

Rôle des pharmacies dans la prise en charge des consommateurs de drogue: 3e vague d'enquête, 2011

Les enquêtes menées auprès des officines vaudoises en 1994 et 2003 avaient montré que les pharmacies étaient des partenaires importants dans le réseau de prise en charge des usagers de drogue par injection (UDI), en particulier en ce qui concerne la dispensation et le suivi des cures de méthadone. Elles avaient aussi mis en évidence les besoins de formation/information des pharmaciens et de leur personnel. La troisième vague de l'enquête pharmacie 2011 avait pour objectif : o de mesurer l'évolution de la remise de seringues par les pharmacies aux UDI o de repérer les lacunes éventuelles dans l'accès au matériel stérile du point de vue géographique o d'apprécier le rôle des pharmacies dans la remise de traitements de méthadone o d'identifier d'éventuels problèmes rencontrés dans ces deux activités (vente de seringues et dispensation de méthadone) o d'identifier les besoins en formation des pharmaciens et du personnel des pharmacies o d'identifier les actions qui favoriseraient une meilleure intégration des pharmacies dans le dispositif de prise en charge des personnes toxicodépendantes o de recueillir l'avis des pharmaciens sur la pose d'automates de distribution de seringues et sur la nécessité d'une extension de la remise de matériel stérile. Méthode L'enquête pharmacie 2011 comprend deux volets. Un premier volet quantitatif, sous la forme d'un questionnaire adressé à toutes les pharmacies du canton (n=248). Le taux de participation de 92% (n=227) est remarquable. Les analyses portent sur 220 questionnaires valides. Un second volet, qualitatif, permet de compléter les données statistiques. Parmi les pharmaciens disposés à s'exprimer dans le cadre d'un entretien (n=90), nous en avons échantillonné [...] [Auteurs, p. 5]

Activation of the NLRP3 inflammasome by Mycobacterium tuberculosis is uncoupled from susceptibility to active tuberculosis.

As a hallmark of tuberculosis (TB), Mycobacterium tuberculosis (MTB) induces granulomatous lung lesions and systemic inflammatory responses during active disease. Molecular regulation of inflammation is associated with inflammasome assembly. We determined the extent to which MTB triggers inflammasome activation and how this impacts on the severity of TB in a mouse model. MTB stimulated release of mature IL-1β in macrophages while attenuated M. bovis BCG failed to do so. Tubercle bacilli specifically activated the NLRP3 inflammasome and this propensity was strictly controlled by the virulence-associated RD1 locus of MTB. However, Nlrp3-deficient mice controlled pulmonary TB, a feature correlated with NLRP3-independent production of IL-1β in infected lungs. Our studies demonstrate that MTB activates the NLRP3 inflammasome in macrophages in an ESX-1-dependent manner. However, during TB, MTB promotes NLRP3- and caspase-1-independent IL-1β release in myeloid cells recruited to lung parenchyma and thus overcomes NLRP3 deficiency in vivo in experimental models.