LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 69

Search options

  1. Article ; Online: FoxP3 associates with enhancer-promoter loops to regulate T

    Ramirez, Ricardo N / Chowdhary, Kaitavjeet / Leon, Juliette / Mathis, Diane / Benoist, Christophe

    Science immunology

    2022  Volume 7, Issue 67, Page(s) eabj9836

    Abstract: Gene expression programs are specified by higher-order chromatin structure and enhancer-promoter loops (EPLs). T regulatory cell ( ... ...

    Abstract Gene expression programs are specified by higher-order chromatin structure and enhancer-promoter loops (EPLs). T regulatory cell (T
    MeSH term(s) Animals ; Forkhead Transcription Factors/genetics ; Forkhead Transcription Factors/immunology ; Gene Expression Regulation/genetics ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Promoter Regions, Genetic/genetics ; T-Lymphocytes, Regulatory/immunology
    Chemical Substances Forkhead Transcription Factors ; Foxp3 protein, mouse
    Language English
    Publishing date 2022-01-14
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ISSN 2470-9468
    ISSN (online) 2470-9468
    DOI 10.1126/sciimmunol.abj9836
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: A perspective into the relationships between amphibian (

    Hossainey, Muhammad Riadul Haque / Hauser, Kelsey A / Garvey, Christina N / Kalia, Namarta / Garvey, Juliette M / Grayfer, Leon

    Philosophical transactions of the Royal Society of London. Series B, Biological sciences

    2023  Volume 378, Issue 1882, Page(s) 20220124

    Abstract: Macrophage ( ... ...

    Abstract Macrophage (M
    MeSH term(s) Animals ; Xenopus laevis ; Myeloid Cells ; Anura ; Macrophages ; Leukocytes ; Mammals
    Chemical Substances 1,4-bis(3-carboxy-4-hydroxyphenylethenyl)-benzene
    Language English
    Publishing date 2023-06-12
    Publishing country England
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 208382-6
    ISSN 1471-2970 ; 0080-4622 ; 0264-3839 ; 0962-8436
    ISSN (online) 1471-2970
    ISSN 0080-4622 ; 0264-3839 ; 0962-8436
    DOI 10.1098/rstb.2022.0124
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Letter: is the AHHS score really useful in clinically severe alcoholic hepatitis?

    Buchard, Benjamin / Sévigné, Luc / Darcha, Claude / Muti, Leon / Joubert, Juliette / Abergel, Armand

    Alimentary pharmacology & therapeutics

    2021  Volume 53, Issue 10, Page(s) 1160–1161

    MeSH term(s) Hepatitis, Alcoholic/diagnosis ; Histological Techniques ; Humans ; Liver Cirrhosis ; Prognosis
    Language English
    Publishing date 2021-04-21
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 639012-2
    ISSN 1365-2036 ; 0269-2813 ; 0953-0673
    ISSN (online) 1365-2036
    ISSN 0269-2813 ; 0953-0673
    DOI 10.1111/apt.16307
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Mutations from patients with IPEX ported to mice reveal different patterns of FoxP3 and Treg dysfunction.

    Leon, Juliette / Chowdhary, Kaitavjeet / Zhang, Wenxiang / Ramirez, Ricardo N / André, Isabelle / Hur, Sun / Mathis, Diane / Benoist, Christophe

    Cell reports

    2023  Volume 42, Issue 8, Page(s) 113018

    Abstract: Mutations of the transcription factor FoxP3 in patients with "IPEX" (immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome) disrupt regulatory T cells (Treg), causing an array of multiorgan autoimmunity. To understand the functional ... ...

    Abstract Mutations of the transcription factor FoxP3 in patients with "IPEX" (immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome) disrupt regulatory T cells (Treg), causing an array of multiorgan autoimmunity. To understand the functional impact of mutations across FoxP3 domains, without genetic and environmental confounders, six human FOXP3 missense mutations are engineered into mice. Two classes of mutations emerge from combined immunologic and genomic analyses. A mutation in the DNA-binding domain shows the same lymphoproliferation and multiorgan infiltration as complete FoxP3 knockouts but delayed by months. Tregs expressing this mutant FoxP3 are destabilized by normal Tregs in heterozygous females compared with hemizygous males. Mutations in other domains affect chromatin opening differently, involving different cofactors and provoking more specific autoimmune pathology (dermatitis, colitis, diabetes), unmasked by immunological challenges or incrossing NOD autoimmune-susceptibility alleles. This work establishes that IPEX disease heterogeneity results from the actual mutations, combined with genetic and environmental perturbations, explaining then the intra-familial variation in IPEX.
    MeSH term(s) Animals ; Female ; Humans ; Male ; Mice ; Alleles ; Forkhead Transcription Factors/genetics ; Mice, Inbred NOD ; Mutation/genetics ; T-Lymphocytes, Regulatory
    Chemical Substances Forkhead Transcription Factors ; FOXP3 protein, human
    Language English
    Publishing date 2023-08-21
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2023.113018
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article: Establishment of an Inactivation Method for Ebola Virus and SARS-CoV-2 Suitable for Downstream Sequencing of Low Cell Numbers.

    Olejnik, Judith / Leon, Juliette / Michelson, Daniel / Chowdhary, Kaitavjeet / Galvan-Pena, Silvia / Benoist, Christophe / Mühlberger, Elke / Hume, Adam J

    Pathogens (Basel, Switzerland)

    2023  Volume 12, Issue 2

    Abstract: Technologies that facilitate the bulk sequencing of small numbers of cells as well as single-cell RNA sequencing (scRNA-seq) have aided greatly in the study of viruses as these analyses can be used to differentiate responses from infected versus ... ...

    Abstract Technologies that facilitate the bulk sequencing of small numbers of cells as well as single-cell RNA sequencing (scRNA-seq) have aided greatly in the study of viruses as these analyses can be used to differentiate responses from infected versus bystander cells in complex systems, including in organoid or animal studies. While protocols for these analyses are typically developed with biosafety level 2 (BSL-2) considerations in mind, such analyses are equally useful for the study of viruses that require higher biosafety containment levels. Many of these workstreams, however, are not directly compatible with the more stringent biosafety regulations of BSL-3 and BSL-4 laboratories ensuring virus inactivation and must therefore be modified. Here we show that TCL buffer (Qiagen), which was developed for bulk sequencing of small numbers of cells and also facilitates scRNA-seq, inactivates both Ebola virus (EBOV) and SARS-CoV-2, BSL-4 and BSL-3 viruses, respectively. We show that additional heat treatment, necessary for the more stringent biosafety concerns for BSL-4-derived samples, was additionally sufficient to inactivate EBOV-containing samples. Critically, this heat treatment had minimal effects on extracted RNA quality and downstream sequencing results.
    Language English
    Publishing date 2023-02-17
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2695572-6
    ISSN 2076-0817
    ISSN 2076-0817
    DOI 10.3390/pathogens12020342
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Complement-driven hemolytic uremic syndrome.

    Leon, Juliette / LeStang, Marie-Bénédicte / Sberro-Soussan, Rebecca / Servais, Aude / Anglicheau, Dany / Frémeaux-Bacchi, Véronique / Zuber, Julien

    American journal of hematology

    2023  Volume 98 Suppl 4, Page(s) S44–S56

    Abstract: Overactivation of the complement alternative pathway drives the pathogenesis of primary atypical hemolytic uremic syndrome (aHUS). Genetically-determined or acquired dysregulation of the complement is frequently identified in patients with aHUS, ... ...

    Abstract Overactivation of the complement alternative pathway drives the pathogenesis of primary atypical hemolytic uremic syndrome (aHUS). Genetically-determined or acquired dysregulation of the complement is frequently identified in patients with aHUS, pregnancy-related hemolytic uremic syndrome (HUS), and severe hypertension-associated HUS. In contrast, it is still unclear whether self-limited complement activation, which frequently occurs in other forms of HUS, provides key mechanistic clues or results from endothelial damage. Development of novel biomarkers is underway to firmly establish complement-driven pathogenesis. C5 blockade therapy has revolutionized the management of aHUS patients, resulting in a halving of the subpopulation under chronic dialysis over the course of a few years. On the other hand, the efficacy of C5 blockade in secondary forms of HUS, as assessed by small and uncontrolled case series, is less compelling and should be investigated through properly designed prospective clinical trials. The increased risk of meningococcal infection, related to C5 inhibition, must be rigorously addressed with suitable prophylaxis. Treatment duration should be determined based on an individualized benefit/risk assessment.
    MeSH term(s) Humans ; Prospective Studies ; Atypical Hemolytic Uremic Syndrome/therapy ; Complement Activation ; Risk Factors ; Biomarkers
    Chemical Substances Biomarkers
    Language English
    Publishing date 2023-01-22
    Publishing country United States
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 196767-8
    ISSN 1096-8652 ; 0361-8609
    ISSN (online) 1096-8652
    ISSN 0361-8609
    DOI 10.1002/ajh.26854
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: Zootoxins and Domestic Animals: A European View.

    Nagy, Andras-Laszlo / Ardelean, Sabrina / Chapuis, Ronan J J / Bouillon, Juliette / Pivariu, Dalma / De Felice, Beatrice / Bertazzo, Mirko / Fossati, Paola / Spicer, Leon J / Dreanca, Alexandra Iulia / Caloni, Francesca

    Toxins

    2024  Volume 16, Issue 1

    Abstract: Zootoxins are produced by venomous and poisonous species and are an important cause of poisoning in companion animals and livestock in Europe. Little information about the incidence of zootoxin poisoning is available in Europe, with only a few case ... ...

    Abstract Zootoxins are produced by venomous and poisonous species and are an important cause of poisoning in companion animals and livestock in Europe. Little information about the incidence of zootoxin poisoning is available in Europe, with only a few case reports and review papers being published. This review presents the most important zootoxins produced by European venomous and poisonous animal species responsible for poisoning episodes in companion animals and livestock. The main zootoxin-producing animal species, components of the toxins/venoms and their clinical effects are presented. The most common zootoxicoses involve terrestrial zootoxins excreted by the common toad, the fire salamander, the pine processionary caterpillar, and vipers. The lack of a centralized reporting/poison control system in Europe makes the evaluation of the epidemiology of zootoxin-induced poisonings extremely difficult. Even if there are many anecdotal reports in the veterinary community about the exposure of domestic animals to terrestrial and marine zootoxins, the number of published papers regarding these toxicoses is low. Climate change and its consequences regarding species distribution and human-mediated transportation are responsible for the emerging nature of some intoxications in which zootoxins are involved. Although new venomous or poisonous animal species have emerged in regions where they were previously unreported, zootoxins produced by native species remain the main concern in Europe. The diversity of poisonous and venomous animal species and the emerging nature of certain poisonings warrant the continuous update to such knowledge by veterinary professionals and animal owners. This review offers an overview about zootoxin-related poisonings in domestic animals in Europe and also provides important information from a health perspective.
    MeSH term(s) Animals ; Humans ; Animals, Domestic ; Climate Change ; Europe/epidemiology ; Livestock
    Language English
    Publishing date 2024-01-16
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2518395-3
    ISSN 2072-6651 ; 2072-6651
    ISSN (online) 2072-6651
    ISSN 2072-6651
    DOI 10.3390/toxins16010048
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article ; Online: De novo posttransplant membranous nephropathy following BNT162b2 mRNA COVID-19 vaccine in a kidney transplant recipient.

    Chavarot, Nathalie / Padden, Michael / Amrouche, Lucile / Malard, Stéphanie / Scemla, Anne / Sberro-Soussan, Rebecca / Léon, Juliette / Legendre, Christophe / Duong, Jean Paul / Zuber, Julien / Anglicheau, Dany / Rabant, Marion / Isnard, Pierre

    American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

    2022  Volume 22, Issue 12, Page(s) 3188–3189

    MeSH term(s) Humans ; BNT162 Vaccine ; COVID-19/epidemiology ; COVID-19/prevention & control ; COVID-19 Vaccines/adverse effects ; Glomerulonephritis, Membranous/etiology ; Kidney Transplantation/adverse effects ; RNA, Messenger
    Chemical Substances BNT162 Vaccine ; COVID-19 Vaccines ; RNA, Messenger
    Language English
    Publishing date 2022-08-24
    Publishing country United States
    Document type Letter
    ZDB-ID 2060594-8
    ISSN 1600-6143 ; 1600-6135
    ISSN (online) 1600-6143
    ISSN 1600-6135
    DOI 10.1111/ajt.17166
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article ; Online: Does Kono-S Anastomosis Reduce Recurrence in Crohn's Disease Compared with Conventional Ileocolonic Anastomosis? A Nationwide Propensity Score-matched Study from GETAID Chirurgie Group [KoCoRICCO Study].

    Alibert, Line / Betton, Louis / Falcoz, Antoine / Manceau, Gilles / Benoist, Stéphane / Zerbib, Philippe / Podevin, Juliette / Maggiori, Léon / Brouquet, Antoine / Tyrode, Gaëlle / Vuitton, Lucine / Vernerey, Dewi / Lefevre, Jérémie H / Lakkis, Zaher

    Journal of Crohn's & colitis

    2023  Volume 18, Issue 4, Page(s) 525–532

    Abstract: Background and aims: Postoperative recurrence is a major concern in Crohn's disease. The Kono-S anastomosis has been described to reduce the rate of recurrence. However, the level of evidence for its effectiveness remains low. The KoCoRICCO study aimed ... ...

    Abstract Background and aims: Postoperative recurrence is a major concern in Crohn's disease. The Kono-S anastomosis has been described to reduce the rate of recurrence. However, the level of evidence for its effectiveness remains low. The KoCoRICCO study aimed to compare outcomes between Kono-S anastomosis and conventional anastomosis in two nationwide, prospective cohorts.
    Methods: Adult patients with Crohn's disease, who underwent ileocolonic resection with Kono-S anastomosis, were prospectively included in seven referral centres between 2020 and 2022. Patients with conventional side-to-side anastomosis were enrolled from a previously published cohort. A propensity score analysis was performed to compare recurrence at first endoscopy in a matched 1:2 ratio population.
    Results: A total of 433 patients with ileocolonic anastomosis were enrolled, of whom 155 had a Kono-S anastomosis. Before matching, both groups were unbalanced for preoperative, intraoperative, and postoperative characteristics. After matching patients with available endoscopic follow-up, endoscopic recurrence ≥i2 was found in 47.5% of the Kono-S group and 44.3% of the conventional side-to-side group [p = 0.6745].
    Conclusions: The KoCoRICCO study suggests that Kono-S anastomosis does not reduce the risk of endoscopic recurrence in Crohn's disease compared with conventional side-to-side anastomosis. Further research with a longer follow-up is necessary to determine whether there is a potential benefit on surgical recurrence.
    MeSH term(s) Humans ; Crohn Disease/surgery ; Anastomosis, Surgical/methods ; Male ; Female ; Propensity Score ; Adult ; Ileum/surgery ; Recurrence ; Colon/surgery ; Colon/pathology ; Prospective Studies ; Middle Aged
    Language English
    Publishing date 2023-10-18
    Publishing country England
    Document type Journal Article ; Comparative Study ; Multicenter Study
    ZDB-ID 2390120-2
    ISSN 1876-4479 ; 1873-9946
    ISSN (online) 1876-4479
    ISSN 1873-9946
    DOI 10.1093/ecco-jcc/jjad176
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article ; Online: Design and Biochemical Characterization of Peptidic Inhibitors of the Myb/p300 Interaction.

    Jones, Matthew / Grosche, Philipp / Floersheimer, Andreas / André, Jérome / Gattlen, Raphael / Oser, Dieter / Tinchant, Juliette / Wille, Roman / Chie-Leon, Barbara / Gerspacher, Marc / Ertl, Peter / Ostermann, Nils / Altmann, Eva / Manchado, Eusebio / Vorherr, Thomas / Chène, Patrick

    Biochemistry

    2023  Volume 62, Issue 7, Page(s) 1321–1329

    Abstract: The Myb transcription factor is involved in the proliferation of hematopoietic cells, and deregulation of its expression can lead to cancers such as leukemia. Myb interacts with various proteins, including the histone acetyltransferases p300 and CBP. Myb ...

    Abstract The Myb transcription factor is involved in the proliferation of hematopoietic cells, and deregulation of its expression can lead to cancers such as leukemia. Myb interacts with various proteins, including the histone acetyltransferases p300 and CBP. Myb binds to a small domain of p300, the KIX domain (p300
    MeSH term(s) Peptides/pharmacology ; Protein Binding ; Proto-Oncogene Proteins c-myb/antagonists & inhibitors ; Proto-Oncogene Proteins c-myb/chemistry ; E1A-Associated p300 Protein/antagonists & inhibitors ; E1A-Associated p300 Protein/chemistry
    Chemical Substances Peptides ; Proto-Oncogene Proteins c-myb ; E1A-Associated p300 Protein (EC 2.3.1.48)
    Language English
    Publishing date 2023-03-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1108-3
    ISSN 1520-4995 ; 0006-2960
    ISSN (online) 1520-4995
    ISSN 0006-2960
    DOI 10.1021/acs.biochem.2c00690
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top