Semipurified saline extracts of seeds from Crotolaria juncea, Cassia marginata, Ficus racemosa, Cicer arietinum (L-532), Gossipium indicum (G-27), Melia composita, Acacia lenticularis, Meletia ovalifolia, Acacia catechu and Peltophorum ferrenginium were tested for leukoagglutinating activity against whole leukocytes and mononuclear cells from patients with chronic myeloid leukaemia (34), acute myeloblastic leukaemia (5), acute lymphoblastic leukaemia (7), chronic lymphocytic leukaemia (3), various lymphoproliferative/haematologic disorders (54), and normal healthy subjects (50). In addition, bone marrow cells from three patients undergoing diagnostic bone marrow aspiration and activated lymphocytes from mixed lymphocyte cultures (MLC) were also tested. All the seed extracts agglutinated white blood cells from patients with different types of leukaemia. But none of them reacted with peripheral blood cells of normal individuals, patients with various lymphoproliferative/haematologic disorders or cells from MLC. Leukoagglutination of leukaemic cells with each of the seed extracts was inhibited by simple sugars. Only in one instance, cells from bone marrow of an individual who had undergone diagnostic bone marrow aspiration for a non-malignant condition were agglutinated. It is felt that purification of these seed extracts may yield leukaemia-specific lectins.
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Clin Cancer Res
January 2025
Bristol-Myers Squibb (United States), Summit, New Jersey, United States.
Purpose: Orvacabtagene autoleucel (orva-cel; JCARH125), a CAR T-cell therapy targeting B-cell maturation antigen (BCMA), was evaluated in relapsed/refractory multiple myeloma (RRMM) patients in the EVOLVE phase 1/2 study (NCT03430011). We applied a modified piecewise model to characterize orva-cel transgene kinetics and assessed the impact of various covariates on its pharmacokinetics (PK).
Experimental Design: The population PK analysis included 159 patients from the EVOLVE study.
Stem Cell Rev Rep
January 2025
Institute for Cellular and Molecular Medicine, Department of Immunology, SAMRC Extramural Unit for Stem Cell Research and Therapy, University of Pretoria, Pretoria, 0084, South Africa.
Histochem Cell Biol
January 2025
Department of Histology and Embryology, Faculty of Medicine, Ankara Yildirim Beyazit University, 06800, Ankara, Turkey.
Bone marrow mesenchymal stromal cells (BM-MSCs) are integral components of the bone marrow microenvironment, playing a crucial role in supporting hematopoiesis. Recent studies have investigated the potential involvement of BM-MSCs in the pathophysiology of acute lymphoblastic leukemia (ALL). However, the exact contribution of BM-MSCs to leukemia progression remains unclear because of conflicting findings and limited characterization.
View Article and Find Full Text PDFRadiologie (Heidelb)
January 2025
Department of Radiology, The Affiliated Hospital of Wuhan Sports University, 430079, Wuhan, China.
Objective: This study aimed to explore and evaluate a novel method for diagnosing patellar chondromalacia using radiomic features from patellar sagittal T2-weighted images (T2WI).
Methods: The experimental data included sagittal T2WI images of the patella from 40 patients with patellar chondromalacia and 40 healthy volunteers. The training set comprised 30 cases of chondromalacia and 30 healthy volunteers, while the test set included 10 cases of each.
ACS Appl Mater Interfaces
January 2025
Department of Chemical Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
The innate immune system is tightly regulated by a complex network of chemical signals triggered by pathogens, cellular damage, and environmental stimuli. While it is well-established that changes in the extracellular environment can significantly influence the immune response to pathogens and damage-associated molecules, there remains a limited understanding of how changes in environmental stimuli specifically impact the activation of the NLRP3 inflammasome, a key component of innate immunity. Here, we demonstrated how shear stress can act as Signal 2 in the NLRP3 inflammasome activation pathway by treating LPS-primed immortalized bone marrow-derived macrophages (iBMDMs) with several physiologically relevant magnitudes of shear stress to induce inflammasome activation.
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