Publications by authors named "Ileana C Miranda"

Allogeneic hematopoietic stem cell transplantation is an established treatment for hematological malignancies and some genetic diseases. Acute graft-versus-host disease (GVHD) is the most common and debilitating side effect with poor survival rates of 5% to 30% for severe cases. In this manuscript, we describe a tetravalent T-cell-engaging bispecific antibody (BsAb) based on the immunoglobulin G-[L]-single-chain variable fragment (IgG-[L]-scFv) platform, with all 4 binding domains specific for CD3.

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  • Researchers rediscovered the intracellular bacterium Cm, historically linked to severe pneumonia in mice, in research mouse colonies, noting its moderate prevalence.
  • They observed clinical disease in genetically engineered mouse strains with impaired immune responses, presenting symptoms like poor condition and hunched posture, along with histopathological evidence of Cm in various tissues.
  • The study suggests that Cm could negatively impact research validity, underscoring the need to exclude this bacterium from mouse colonies used in scientific studies.
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Vaccination will likely be a key component of strategies to curtail or prevent future sarbecovirus pandemics and to reduce the prevalence of infection and disease by future SARS-CoV-2 variants. A "pan-sarbecovirus" vaccine, that provides maximum possible mitigation of human disease, should elicit neutralizing antibodies with maximum possible breadth. By positioning multiple different receptor binding domain (RBD) antigens in close proximity on a single immunogen, it is postulated that cross-reactive B cell receptors might be selectively engaged.

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Background: Vonoprazan is a new acid-suppressing drug that received FDA approval in 2022. It reversibly inhibits gastric acid secretion by competing with the potassium ions on the luminal surface of the parietal cells (potassium-competitive acid blockers or P-CABs). Vonoprazan has been on the market for a short time and there are many clinical trials to support its clinical application.

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CLN2 disease is a fatal, childhood autosomal recessive disorder caused by mutations in ceroid lipofuscinosis type 2 (CLN2) gene, encoding tripeptidyl peptidase 1 (TPP-1). Loss of TPP-1 activity leads to accumulation of storage material in lysosomes and resultant neuronal cell death with neurodegeneration. Genotype/phenotype comparisons suggest that the phenotype should be ameliorated with increase of TPP-1 levels to 5-10% of normal with wide central nervous system (CNS) distribution.

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  • Feline chronic gingivostomatitis (FCGS) is a painful oral condition in cats, marked by inflammation and ulcers in the mouth, but the exact causes are still unclear.
  • Researchers conducted RNA sequencing on tissue samples from affected and healthy cats to find genes and pathways involved in FCGS for potential treatment options.
  • The study found that certain immune-related genes and pathways, particularly influenced by IL6, are overrepresented in affected tissues, suggesting new avenues for clinical interventions.
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(Cb), the cause of hyperkeratotic dermatitis in various immunocompromised mouse strains, significantly impacts research outcomes if infected mice are used. Although Cb has been isolated from a variety of species, including mice, rats, cows, and humans, little is known about the differences in the infectivity and clinical disease that are associated with specific Cb isolates. The infectious dose that colonized 50% of the exposed population (ID ) and any associated clinical disease was determined in athymic nude mice (Hsd:Athymic Nude-Foxn1 nu ) inoculated with Cb isolates collected from mice ( = 5), rat ( = 1), cow ( = 1), and humans ( = 2) The same parameters were also determined for 2 of the mouse isolates in 2 furred immunocompromised mouse strains (NSG [NOD.

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  • Feline chronic gingivostomatitis (FCGS) is a painful disease in cats that causes sores and inflammation in their mouths.
  • Scientists studied the genes in affected cats' tissues to find out what might be causing the disease and how to help.
  • They discovered that many genes related to the immune system and inflammation were involved, which could help them create better treatments for the disease in the future.
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Nearly half of all pregnancies are unintended; thus, existing family planning options are inadequate. For men, the only choices are condoms and vasectomy, and most current efforts to develop new contraceptives for men impact sperm development, meaning that contraception requires months of continuous pretreatment. Here, we provide proof-of-concept for an innovative strategy for on-demand contraception, where a man would take a birth control pill shortly before sex, only as needed.

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Introduction: The pathogenesis of thymic epithelial tumors remains largely unknown. We previously identified GTF2I L424H as the most frequently recurrent mutation in thymic epithelial tumors. Nevertheless, the precise role of this mutation in tumorigenesis of thymic epithelial cells is unclear.

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  • Angiogenesis plays essential roles in disease, particularly during inflammation and the repair of blood vessel occlusions, but can lead to issues like excessive granulation and vascular overgrowth in conditions such as pulmonary hypertension.
  • The review examines various abnormal vascular growths in the central nervous system of animals, focusing on the complexity of diagnosing similar conditions, including reactive angioendotheliomatosis and various CNS malformations, often leading to confusion among pathologists.
  • Different types of vascular lesions and tumors are discussed, such as benign hamartomas, arteriovenous malformations, and hemangiosarcomas, emphasizing the need for clearer diagnostic criteria and a deeper understanding of these pathologic conditions.
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SOX2 is a major transcriptional regulator of stem cell pluripotency and self-renewability. Its expression in cancer stem cells from several different tumor types in humans and rodent models directly implicates SOX2 in tumorigenicity, metastasis, drug resistance, recurrence, and poor survival. Our objective was to investigate the expression of SOX2 in canine neoplasia.

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Proliferation of ectopic Schwann cells within the central nervous system (CNS) parenchyma (schwannosis) in early life is most commonly associated with human neurofibromatosis type-2 and has been unrecognized in domestic animals. Three foals and a calf, 5 to 11 weeks old, with progressive neurological signs from birth were studied. Histologically, at multiple levels of the spinal cord, all animals had bilateral plaques of proliferative spindle cells, predominantly affecting the white matter adjacent to dorsal and ventral nerve roots and variably extending into the gray matter.

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Mucociliary clearance is a main defense mechanism of the respiratory tract, which can be inherently impaired in primary ciliary dyskinesia (PCD) or reversibly altered in secondary ciliary dyskinesia (SCD). Limited diagnostic test availability likely leads to misdiagnosis or underdiagnosis of PCD in animals. This study evaluated the light and transmission electron microscopy (TEM) changes in the respiratory mucosa of 15 dogs with chronic respiratory disease suspected of PCD.

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