Publications by authors named "J. Stary"

Alzheimer's disease, the most common form of dementia, is characterized by the deposition of amyloid plaques and neurofibrillary tangles in the brain, leading to the loss of neurons and a decline in a person's memory and cognitive function. As a multifactorial disease, Alzheimer's involves multiple pathogenic mechanisms, making its treatment particularly challenging. Current drugs approved for the treatment of Alzheimer's disease only alleviate symptoms but cannot stop the progression.

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The taurine transporter (TauT, SLC6A6) is a member of the solute carrier 6 (SLC6) family, which plays multiple physiological roles. The SLC6 family is divided into four subfamilies: GABA (γ-aminobutyric acid), monoamine, glycine and neutral amino acid transporters. Proteins from the GABA group, including the taurine transporter, are primarily considered therapeutic targets for treating central nervous system disorders.

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  • Acute lymphoblastic leukemia (γδ T-ALL) is a rare and complex condition in children, prompting a study of 200 pediatric cases to identify its clinical and genetic characteristics.
  • The research revealed that very young children (under 3 years) with γδ T-ALL face a significantly high risk and display specific genetic changes, particularly involving STAG2 inactivation and LMO2 activation.
  • Importantly, their findings suggest that targeting DNA repair pathways linked to STAG2 inactivation with specific drugs could offer new treatment options and help classify patients based on their risk levels.
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  • Inotuzumab ozogamicin is an approved treatment for relapsed/refractory B-cell precursor acute lymphoblastic leukemia (BCP-ALL) in adults, but its pharmacokinetics in children have not been studied until now.
  • This research analyzed serum concentrations from a diverse patient group, utilizing a modified adult pharmacokinetic model to understand how the drug behaves in pediatric patients with BCP-ALL.
  • Results indicated that older pediatric patients showed a different drug clearance pattern, with higher drug exposure correlating to better treatment responses among those with relapsed/refractory BCP-ALL.
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  • * Three new recurring KMT2A-rearranged groups were identified, and a significant variation in 5-year event-free survival rates was observed across 13 different groups, highlighting the impact of genetic factors on patient outcomes.
  • * The research suggests incorporating five specific adverse-risk KMT2A fusions into current risk stratification models and calls for further studies to confirm the associations
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Chronic sarcoidosis is a complex granulomatous disease with limited treatment options that can progress over time. Understanding the molecular pathways contributing to disease would aid in new therapeutic development. To understand whether macrophages from patients with nonresolving chronic sarcoidosis are predisposed to macrophage aggregation and granuloma formation and whether modulation of the underlying molecular pathways influence sarcoidosis granuloma formation.

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  • Serovar L1-L3 of Chlamydia trachomatis causes lymphogranuloma venereum (LGV), with rising cases among HIV-positive men who have sex with men (MSM), making differentiation between LGV and other CT infections crucial for treatment.
  • A study analyzed 2,083 CT infections from 1,479 patients in Austria between 2014 and 2021, revealing that LGV was found in 15% of cases and accounted for 23% of rectal CT infections in MSM.
  • Most LGV cases were among MSM, often HIV-positive, and frequently included concurrent syphilis; interestingly, 45% of LGV cases were asymptomatic, indicating the need
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Purpose: The AIEOP-BFM ALL 2009 protocol included, at the end of the induction phase, a randomized study of patients with high-risk (HR) ALL to investigate if an intensive exposure to pegylated L-asparaginase (PEG-ASNASE, 2,500 IU/sqm once a week × 4) on top of BFM consolidation phase IB allowed us to decrease minimal residual disease (MRD) and improve outcome.

Patients And Methods: A total of 1,097 patients presented, from June 2010 to February 2017, with one or more of the following HR criteria: rearrangement, hypodiploidy, prednisone poor response, poor bone marrow response at day 15 (Flow MRD ≥10%), or no complete remission (CR) at the end of induction. Of them, 809 (85.

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Background: Graft-versus-host disease (GvHD) is a major life-threatening complication of allogeneic haematopoietic stem cell transplantation (HSCT), limiting the broad application of HSCT for haematological malignancies. Cutaneous GvHD is described as a post-transplant inflammatory reaction by skin-infiltrating donor T cells and remaining recipient tissue-resident memory T cells. Despite the major influence of lymphocytes on GvHD pathogenesis, the complex role of mononuclear phagocytes (MNPs) in tissues affected by GvHD is increasingly appreciated.

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Purpose: Gamma delta T-cell receptor-positive acute lymphoblastic leukemia (γδ T-ALL) is a high-risk but poorly characterized disease.

Methods: We studied clinical features of 200 pediatric γδ T-ALL, and compared the prognosis of 93 cases to 1,067 protocol-matched non-γδ T-ALL. Genomic features were defined by transcriptome and genome sequencing.

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  • Juvenile myelomonocytic leukaemia (JMML) is a type of cancer that occurs in children and is linked to problems with certain genes in the RAS pathway.
  • Kids with a condition called neurofibromatosis type 1 (NF-1) are more likely to get JMML because of a faulty NF1 gene they inherit.
  • The study looked at 25 JMML patients, finding different types of NF1 gene problems and suggesting that testing for NF1 gene issues is important even if patients don’t show signs of NF-1.
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A highly efficient, bio-ecofriendly, and transparent flame retardant (FR) for cotton fabric was developed and deposited onto the cellulose skeletal structure of cotton fabric through a one-pot sol-gel process. The flame retardant functional coating is composed of ammonium polyphosphate (APP), guar gum (GG), citric acid (CA), and a negligible amount of catalyst. Cotton fabrics were impregnated with different concentrations of ammonium polyphosphate and guar gum, with citric acid as a crosslinking agent.

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The prognostic impact of PICALM::MLLT10 status in childhood leukaemia is not well described. Ten International Berlin Frankfurt Münster-affiliated study groups and the Children's Oncology Group collaborated in this multicentre retrospective study. The presence of the PICALM::MLLT10 fusion gene was confirmed by fluorescence in situ hybridization and/or RNA sequencing at participating sites.

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In patients infected with severe acute respiratory syndrome coronavirus 2, vasculopathic changes of the skin are associated with a severe prognosis. However, the pathogenesis of this vasculopathy is not conclusively clarified. In this study, 25 prospectively collected skin samples from patients with COVID-19-related skin lesions were examined for vasculopathic changes and, in case of vasculitis, were further analyzed with electron microscopy and immunohistochemistry.

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Purpose: Historically, patients with T-cell acute lymphoblastic leukemia (T-ALL) who fail to achieve remission at the end of induction (EOI) have had poor long-term survival. The goal of this study was to examine the efficacy of contemporary therapy, including allogeneic hematopoietic stem cell transplantation (HSCT) in first remission (CR1).

Methods: Induction failure (IF) was defined as the persistence of at least 5% bone marrow (BM) lymphoblasts and/or extramedullary disease after 4-6 weeks of induction chemotherapy.

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Syphilis.

J Dtsch Dermatol Ges

May 2023

Syphilis is a curable systemic infectious disease with a clear increase in incidence in recent years. The disease presents with a broad clinical spectrum and challenges clinicians due to the long incubation period and the sometimes complex interpretation of serological test results. Penicillin G remains the treatment of choice in all stages of syphilis.

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In , two genes ( and ) have been found to be associated with the invasion of the amniotic cavity, and a single gene () to be associated with intra-amniotic infections and a high risk of preterm birth. The syntopic presence of spp. in the same patient has been shown to correlate with the absence of in .

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Article Synopsis
  • - The study analyzed 6,187 pediatric patients with acute lymphoblastic leukemia (ALL), focusing on minimal residual disease (MRD) assessment through flow cytometry (FCM) and the effects of different methotrexate (MTX) doses on survival rates.
  • - Key findings revealed that 5-year event-free survival (EFS) rates were 75.2%, with variations based on risk groups: standard risk (90.7%), intermediate risk (77.9%), and high risk (60.8%).
  • - Results indicated that MRD could be effectively assessed with FCM, and that while both MTX doses tested were similarly effective, the augmented treatment protocol showed no significant survival benefits over the standard
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