Publications by authors named "Sblattero D"

Background: Drug delivery strategies using chitosan nanobubbles (CS-NBs) could be used to reduce drug side effects and improve outcomes in hepatocellular carcinoma (HCC) treatment. To enhance their action, a targeting agent, such as the humanized anti-GPC3 antibody GC33 (condrituzumab), could be attached to their surface. Here, we investigated the use of idarubicin-loaded CS-NBs for HCC treatment and a GC33-derived minibody (that we named 4A1) to enhance CS-NB delivery.

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Purpose: In the bloodstream, nanoparticles (NPs) interact with serum proteins to form the protein corona, which includes both opsonins, promoting NP recognition and elimination, and dysopsonins, which can inhibit opsonin activity. Albumin, the most abundant serum protein, is part of this corona and can act as a dysopsonin, potentially hiding NPs from the immune system. This study aims to investigate how a covalently bound layer of human serum albumin (HSA) on polymeric NPs affects the protein corona and their behavior in the immune system.

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Background: Recently, we developed AT101, an IgM-class mouse monoclonal antibody directed against glypican-1 (GPC1), a proteoglycan that can be considered as useful target for glioblastoma multiforme (GBM) treatment being specifically and highly expressed on GBM cell surface. Here, we proposed the use of AT101 as targeting agent in a drug delivery nanoplatfom to effectively deliver chitosan nanobubbles (NBs) for GBM treatment.

Methods: Chitosan NBs were prepared and conjugated with AT101 or left unconjugated as control.

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Background: Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive cancers with a very low survival rate at 5 years. The use of chemotherapeutic agents results in only modest prolongation of survival and is generally associated with the occurrence of toxicity effects. Antibody-based immunotherapy has been proposed for the treatment of PDAC, but its efficacy has so far proved limited.

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Article Synopsis
  • Transglutaminase 2 (TG2) is a multifunctional protein found throughout various tissues, but its role in biological processes can vary based on factors like cell type and localization.
  • Researchers studied three zebrafish genes related to human TG2 (zTGs2), confirming their expression and function during embryonic development, and found that zTGs2 functions similarly to the human enzyme.
  • The study demonstrated that zTGs2 can facilitate cell adhesion and has comparable effects in apoptotic processes to human TG2, laying the groundwork for further research on TG2 functions using zebrafish as a model organism.
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Activated T cells express the inducible T-cell co-stimulator (ICOS) that, upon binding to its ubiquitously expressed ligand (ICOSL), regulates the immune response and tissue repair. We sought to determine the effect of ICOS:ICOSL interaction on human M1 and M2 macrophages. M1 and M2 macrophages were polarized from monocyte-derived macrophages, and the effect of a soluble recombinant form of ICOS (ICOS-CH3) was assessed on cytokine production and cell migration.

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  • The study investigates whether the CagY antigen plays a role in the proliferation of malignant B cells in low-grade gastric MALT lymphoma.
  • Researchers compared T cell clones from patients with MALT lymphoma to those with chronic gastritis, focusing on their response to CagY and their ability to help B cell proliferation.
  • Findings reveal that CagY significantly stimulates B cell proliferation and activates T cells in MALT lymphomas, suggesting its importance in this type of cancer.
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  • Biologic drugs, particularly anti-TNF therapies, are the primary treatment for rheumatoid arthritis, but they face challenges like inconsistent effectiveness, risk of infections, and high costs.
  • A new bispecific antibody (BsAb) was created to target the inflamed joint tissues specifically while neutralizing TNFα, demonstrating effectiveness similar to the existing adalimumab drug.
  • This BsAb showed improved tissue targeting and maintained high drug levels in the affected area for longer periods, resulting in better therapeutic outcomes and potential benefits for other biologic treatments.
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Background: Recently published paediatric guidelines for diagnosing coeliac disease do not include recommendations on the follow-up of coeliac disease patients.

Goal: The aim of this study was to assess the management practices and experience of coeliac disease patients with their follow-up appointments in Central Europe.

Study: Gastroenterologists and coeliac disease patients in five Central European countries were asked to complete the web-based questionnaire focusing on coeliac disease management practices.

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Objectives: Celiac disease (CD) remains undiagnosed for a long time in many adult and pediatric patients. We assessed the knowledge about CD among healthcare professionals (HCPs) and CD patients in Central Europe (CE).

Methods: HCPs and CD patients from 5 CE countries were asked to complete the web-based questionnaire about CD.

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Objectives: During the past decades, there has been a shift in the clinical presentation of coeliac disease (CD) to nonclassical, oligosymptomatic, and asymptomatic forms. We assessed clinical presentation of CD in children and adolescents in Central Europe.

Methods: Paediatric gastroenterologists in 5 countries retrospectively reported data of their patients diagnosed with CD.

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Biofilms are aggregates of microbial cells encased in a highly hydrated matrix made up of self-produced extracellular polymeric substances (EPS) which consist of polysaccharides, proteins, nucleic acids, and lipids. While biofilm matrix polysaccharides are unraveled, there is still poor knowledge about the identity and function of matrix-associated proteins. With this work, we performed a comprehensive proteomic approach to disclose the identity of proteins associated with the matrix of biofilm-growing C1576 reference strain, a cystic fibrosis clinical isolate.

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Article Synopsis
  • The interaction between Helicobacter pylori (HP) and the host is crucial for understanding the long-term persistence of the bacterium and its role in diseases like gastric cancer and autoimmune gastritis.
  • Circulating antibodies can provide a "disease signature," which is valuable for early diagnostics, as symptoms often appear late in the disease's progression.
  • A new approach using "phage display" and deep sequencing was employed to identify specific HP antigens recognized during immune response, leading to the discovery of unique patterns of these antigens related to different HP-related diseases.
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  • High-Throughput Sequencing technologies are revolutionizing research, especially in analyzing phage display libraries, by replacing tedious methods with automated sequencing.
  • The InteractomeSeq web server provides a specialized tool for analyzing raw sequencing data, allowing users to define parameters for characterizing protein domains or epitopes effectively.
  • This tool is significant for advancing large-scale biomarker profiling, vaccine development, and gene annotation, offering valuable resources for both scientific and clinical communities.
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West Nile virus is a widespread mosquito-borne human and animal pathogenic virus of increasing importance. The E protein of the viral envelope is critical for attachment and entry into the host cell and has been the target for vaccine design and small molecule inhibitors. Furthermore, the detection of anti-E IgM and IgG antibodies is widely used in serology to diagnose these infections.

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  • The study evaluated the usage of a "no-biopsy" diagnostic approach for coeliac disease (CD) among pediatric gastroenterologists in Central Europe, in light of new ESPGHAN guidelines that allow diagnosis without duodenal biopsy if specific criteria are met.
  • Medical records from 653 children diagnosed with CD in 2016 showed that only 20.6% of symptomatic patients used the "no-biopsy" method, despite approximately 60% being eligible for it based on high transglutaminase antibody levels (TGA).
  • The study found that children diagnosed without biopsies experienced more signs of malabsorption, but there were no significant delays in diagnosis compared to those who underwent biopsies
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Transposable elements (TEs) compose about half of the mammalian genome and, as embedded sequences, up to 40% of long noncoding RNA (lncRNA) transcripts. Embedded TEs may represent functional domains within lncRNAs, providing a structured RNA platform for protein interaction. Here we show the interactome profile of the mouse inverted short interspersed nuclear element (SINE) of subfamily B2 (invSINEB2) alone and embedded in antisense (AS) ubiquitin C-terminal hydrolase L1 (Uchl1), an lncRNA that is AS to Uchl1 gene.

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The identification of effective biomarkers for early diagnosis, prognosis, and response to treatments remains a challenge in ovarian cancer (OC) research. Here, we present an unbiased high-throughput approach to profile ascitic fluid autoantibodies in order to obtain a tumor-specific antigen signature in OC. We first reported the reactivity of immunoglobulins (Igs) purified from OC patient ascites towards two different OC cell lines.

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Objectives: Coeliac disease (CD) is a systemic autoimmune disorder affecting about 1% of the population. Many patients remain undiagnosed or are diagnosed with substantial delay. We assessed diagnostic delays in symptomatic CD children in Central Europe (CE).

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Despite the advances in the treatment of rheumatoid arthritis (RA) achieved in the last few years, several patients are diagnosed late, do not respond to or have to stop therapy because of inefficacy and/or toxicity, leaving still a huge unmet need. Tissue-specific strategies have the potential to address some of these issues. The aim of the study is the development of a safe nanotechnology approach for tissue-specific delivery of drugs and diagnostic probes.

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Tick-borne encephalitis virus (TBEV) is a member of the Flavivirus genus and is the main pathogenic arbovirus circulating in Europe, Russia and China. The envelope (E) protein is exposed on the viral surface and is the main antigen that is employed in diagnostic tests based on the detection of protein-specific antibodies from serum samples of infected individuals. The high degree of similarity among the E proteins of flaviviruses can, in some cases, lead to cross-reactivity and false-positive results in serological tests.

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An unbalance between Abs that recognize an autoantigen (idiotypes; IDs) and Igs that bind such Abs (anti-IDs) is considered a functional event in autoimmune disorders. We investigated the presence of an ID/anti-ID network in celiac disease (CD), a condition in which antitissue transglutaminase 2 (TG2) Abs are suspected to contribute to CD pathogenesis. To characterize the ID side, we reproduced by in vitro yeast display the intestine-resident Abs from CD and control patients.

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In vitro display technologies have put together the generation of large antibody libraries with selection and screening procedures to identify lead candidates. Phage display antibody libraries allow selecting and identifying binders for a variety of antigens. Nonetheless, the procedure is limited by the possibility to quantitatively follow the enrichment during selection cycles and tune up the clones for specific binding proprieties (i.

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During the last 20 years in vitro technologies opened powerful routes to combine the generation of large libraries together with fast selection and screening procedures to identify lead candidates. One of the most successful methods is based on the use of filamentous phages. Functional Antibodies (Abs) fragments can be displayed on the surface of phages by fusing the coding sequence of the antibody variable (V) regions to the phage minor coat protein pIII.

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