68 results match your criteria: "Medical college of Wisconsin and Children's Wisconsin[Affiliation]"

Background: Immunocompromised patients are at increased risk of SARS-CoV-2 infections. Patients undergoing chimeric antigen receptor (CAR) T-cell therapy for relapsed/refractory B-cell malignancies are uniquely immunosuppressed due to CAR T-mediated B-cell aplasia (BCA). While SARS-CoV-2 mortality rates of 33%-40% are reported in adult CAR T-cell recipients, outcomes in pediatric and young adult CAR T-cell recipients are limited.

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Article Synopsis
  • Histone lysine methyltransferases (KMTs) and demethylases (KDMs) are key enzymes that regulate gene expression and chromatin structure, and their malfunction is linked to congenital regulopathies.
  • The study found damaging genetic variants in KMTs and KDMs in families with developmental eye diseases, indicating a connection to structural eye defects along with other abnormalities.
  • Genetic testing is crucial for accurate diagnosis in affected individuals, as the research identified nine novel variants, many of which may be pathogenic, expanding the understanding of KMT and KDM roles in ocular developmental disorders.
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Background: Pathogenic variants in human MAB21L2 result in microphthalmia, anophthalmia, and coloboma. The exact molecular function of MAB21L2 is currently unknown. We conducted a series of yeast two-hybrid (Y2H) experiments to determine protein interactomes of normal human and zebrafish MAB21L2/mab21l2 as well as human disease-associated variant MAB21L2-p.

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Understanding clinical and biological heterogeneity to advance precision medicine in paediatric acute respiratory distress syndrome.

Lancet Respir Med

February 2023

Division of Neonatology and Paediatric Intensive Care, Department of Paediatrics, University Hospital of Geneva, University of Geneva, Geneva, Switzerland.

Article Synopsis
  • - PARDS is a severe lung condition in children that differs from ARDS in adults due to factors like age, lung growth, and underlying health issues, resulting in higher mortality and long-term health problems.
  • - There is no specific treatment for PARDS; current management focuses on supportive care, highlighting the need for better strategies to identify who might benefit from targeted interventions like specific ventilation techniques or prone positioning.
  • - Improving our understanding of the diverse clinical features of PARDS compared to adult ARDS, and utilizing advanced data analysis techniques, could lead to more personalized and effective treatment approaches in the future.
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  • - ARHGAP35 is important for various cellular processes and has been linked to cancer and developmental issues in both humans and mice, particularly in eye and neural structures.
  • - Researchers found harmful genetic variants of ARHGAP35 in five people from four families with eye disorders such as anophthalmia and microphthalmia, along with other health problems.
  • - The identified genetic variants mainly affected the protein's C-terminus and suggest that ARHGAP35 may play a significant role in eye development, hinting at a shared mechanism for related ocular diseases, but more research is needed.
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TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions.

Am J Hum Genet

December 2022

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA; Texas Children's Hospital, Houston, TX, USA. Electronic address:

An Xq22.2 region upstream of PLP1 has been proposed to underly a neurological disease trait when deleted in 46,XX females. Deletion mapping revealed that heterozygous deletions encompassing the smallest region of overlap (SRO) spanning six Xq22.

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Background: Infants with bronchopulmonary dysplasia (BPD) are often prescribed diuretics before the neonatal intensive care unit (NICU) discharge. It is unknown whether outpatient medication weaning strategies affect the duration of home oxygen therapy.

Methods: This was a secondary cohort analysis of infants born <32 weeks gestational age with BPD from 2015 to 2018 discharged from our NICU or regional NICUs, referred to our pulmonary clinic for home oxygen management.

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HLA Associations in pediatric autoimmune liver diseases: Current state and future research initiatives.

Front Immunol

November 2022

Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology & Nutrition Medical College of Wisconsin and Children's Wisconsin, Milwaukee, WI, United States.

The strongest genetic association with autoimmunity is within chromosome 6p21, where the human leukocyte antigen (HLA) complex resides. This review will focus on the HLA associations within pediatric autoimmune hepatitis, autoimmune sclerosing cholangitis and primary sclerosing cholangitis. In general, there is considerable overlap in HLA genotypes conferring susceptibility to pediatric autoimmune liver diseases, however unique HLA associations and protective HLA genotypes exist.

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Chimeric antigen receptor (CAR) T-cell therapy has demonstrated remarkable clinical responses in hematologic malignancies. Recent advances in CAR T-cell therapy have expanded its application into other populations including older patients and those with central nervous system and solid tumors. Although its clinical efficacy has been excellent for some malignancies, CAR T-cell therapy is associated with severe and even life-threatening immune-mediated toxicities, including cytokine release syndrome and neurotoxicity.

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Background/objectives: Children with cancer have an increased risk for developing a venous thromboembolism (VTE) during their treatment course. Direct oral anticoagulants (DOACs) represent a relatively new class of oral medications to treat VTE; however, data are limited to support use in this patient group. Given the safety and efficacy data from numerous perspective adult studies, providers now consider off-label use in select children.

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A patient suspected of an inborn error of metabolism will commonly have urine organic acid analysis performed as part of their workup. The traditional urine organic acid method involves extraction of the acidic fraction from urine samples using an organic solvent, derivatization of extracted compounds, and identification using gas chromatography-mass spectrometry (GC/MS). Unfortunately, the extraction step results in the loss of many neutral and positively charged compounds which may be of interest to metabolic physicians and biochemical geneticists.

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Imaging recommendations in pediatric lymphoma: A COG Diagnostic Imaging Committee/SPR Oncology Committee White Paper.

Pediatr Blood Cancer

June 2023

Diagnostic Imaging and Pediatrics, Imaging and Radiation Oncology Core, Lincoln, Warren Alpert Medical School, Brown University, Providence, Rhode Island, USA.

Hodgkin lymphoma (HL) and non-Hodgkin lymphoma (NHL) are both malignancies originating in the lymphatic system and both affect children, but many features differ considerably, impacting workup and management. This paper provides consensus-based imaging recommendations for evaluation of patients with HL and NHL at diagnosis and response assessment for both interim and end of therapy (follow-up).

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Purpose: Nonresponse and relapse after CD19-chimeric antigen receptor (CAR) T-cell therapy continue to challenge survival outcomes. Phase II landmark data from the ELIANA trial demonstrated nonresponse and relapse rates of 14.5% and 28%, respectively, whereas use in the real-world setting showed nonresponse and relapse rates of 15% and 37%.

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Background: Hematopoietic stem cell (HSC) harvest apheresis and leukapheresis are performed in the pediatric intensive care unit (PICU) for high-risk pediatric patients who require procedural sedation. Patients need central access either with their own central lines, ports or require apheresis catheter (CVL) placement. Previously, patients were either awake or emerging from sedation on PICU admission.

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Article Synopsis
  • Tisagenlecleucel, a CAR T-cell therapy targeting CD19, has shown remarkable response rates in patients up to age 26 with refractory B-cell acute lymphoblastic leukemia and is FDA approved for this use.
  • * A study analyzed data from 185 patients to determine the effects of different CAR T-cell doses on overall survival (OS), event-free survival (EFS), and relapse-free survival (RFS).
  • * Results indicated that higher doses of tisagenlecleucel improved survival and remission rates without increasing toxicity, suggesting the potential benefits of targeting higher doses within the approved range for better outcomes.
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Secondary Impact of the Coronavirus Disease 19 Pandemic on Patients and the Cellular Therapy Healthcare Ecosystem.

Transplant Cell Ther

November 2022

Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati, College of Medicine, Cincinnati, Ohio.

The Coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has significantly impacted global health and healthcare delivery systems. To characterize the secondary effects of the COVID-19 pandemic and mitigation strategies used in the delivery of hematopoietic stem cell transplantation (HSCT) care, we performed a comprehensive literature search encompassing changes in specific donor collection, processing practices, patient outcomes, and patient-related concerns specific to HSCT and HSCT-related healthcare delivery. In this review, we summarize the available literature on the secondary impacts the COVID-19 pandemic on the fields of HSCT and cellular therapy.

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Novel Genetic Diagnoses in Septo-Optic Dysplasia.

Genes (Basel)

June 2022

Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Wisconsin, Milwaukee, WI 53226, USA.

Septo-optic dysplasia (SOD) is a developmental phenotype characterized by midline neuroradiological anomalies, optic nerve hypoplasia, and pituitary anomalies, with a high degree of variability and additional systemic anomalies present in some cases. While disruption of several transcription factors has been identified in SOD cohorts, most cases lack a genetic diagnosis, with multifactorial risk factors being thought to play a role. Exome sequencing in a cohort of families with a clinical diagnosis of SOD identified a genetic diagnosis in 3/6 families, de novo variants in , , and , and explored variants of uncertain significance in the remaining three.

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Axenfeld-Rieger syndrome: more than meets the eye.

J Med Genet

April 2023

Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Wisconsin, Milwaukee, Wisconsin, USA

Article Synopsis
  • Axenfeld-Rieger syndrome (ARS) is a rare genetic disorder characterized by eye anomalies and potential systemic features, with varying subtypes linked to specific genes that influence the severity and type of symptoms.
  • A study examined 128 individuals with genetic variants related to ARS, revealing a range of ocular anomalies and distinct systemic features for different gene types, including high rates of dental and heart defects.
  • The findings emphasize the importance of gene-specific diagnoses for ARS, as clinical features can significantly differ based on the affected gene, and suggest that the De Hauwere syndrome may be related to the FOXC1 gene.
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The Plain Community (PC) is a medically underserved group found predominantly in the northeastern and midwestern USA. Due to the community's founder population with few converts and infrequent outside marriage, metabolic and genetic disorders are more prevalent. Individuals in the PC experience geographic, financial, and cultural barriers when accessing healthcare.

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Article Synopsis
  • The overview discusses the upcoming 5th edition of the WHO Classification of Haematolymphoid Tumours, specifically focusing on lymphoid neoplasms, while myeloid and histiocytic neoplasms will be covered separately.
  • Key changes from the previous 4th edition include a hierarchical reorganization of entities, modifications in their nomenclature, and revisions to diagnostic criteria and subtypes.
  • The new edition will also see the deletion of certain entities, the introduction of new ones, and the inclusion of tumour-like lesions and germline predisposition syndromes related to lymphoid neoplasms.
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Background: Persistent pulmonary hypertension of the newborn (PPHN) occurs when pulmonary vascular resistance (PVR) fails to decrease at birth. Decreased angiogenesis in the lung contributes to the persistence of high PVR at birth. MicroRNAs (miRNAs) regulate gene expression through transcript binding and degradation.

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Donor cell leukemia is a rare complication following hematopoietic stem cell transplant (HSCT). There are currently few reports in children and only rare, reported cases of donor-derived myelodysplastic syndrome/acute myeloid leukemia in patients with an underlying germline GATA2 mutation. Most reported cases are myeloid in origin and occur following related HSCT.

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Quality improvement and quality assurance form a complementary and independent relationship. Quality assurance measures compliance against industry standards using audits, whereas quality improvement is a continuous process focused on processes and systems that can improve care. The Model for Improvement is a robust quality improvement tool that transplant and cellular therapy teams can use to redesign healthcare processes.

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Background: Diagnosis of invasive candidiasis (IC) relies on insensitive cultures; the relative utility of fungal biomarkers in children is unclear.

Methods: This multinational observational cohort study enrolled patients aged >120 days and <18 years with concern for IC from 1 January 2015 to 26 September 2019 at 25 centers. Blood collected at onset of symptoms was tested using T2Candida, Fungitell (1→3)-β-D-glucan, Platelia Candida Antigen (Ag) Plus, and Platelia Candida Antibody (Ab) Plus assays.

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