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Journal of Cellular Immunology
ISSN: 2689-2812
Human Gray and White Matter Metabolomics to Differentiate APOE and Stage Dependent Changes in Alzheimer’s Disease
Alzheimer’s disease (AD) is a leading cause of death and morbidity in the United States [1]. The hallmarks of AD are β-amyloid (Aβ) and tau. However, studies have indicated that metabolic dysfunction may play a more pivotal role in the progression of AD [2]. Glucose hypometabolism and mitochondrial dysfunction are well-known features of AD [2].
J Cell Immunol, 2021, Volume 3, Issue 6, p397-412 | DOI: 10.33696/immunology.3.123Inulin Supplementation Mitigates Gut Dysbiosis and Brain Impairment Induced by Mild Traumatic Brain Injury during Chronic Phase
Approximately 1.6-3.8 million people sustain a mild traumatic brain injury (mTBI) in the US annually. This amounts to the hospitalization of 100-300 per 100,000 young adults. The Centers for Disease Control and Prevention reports that around 5.3 million people live with a permanent disability after mTBI, and there are currently no known restorative therapies.
J Cell Immunol, 2022, Volume 4, Issue 2, p50-64 | DOI: 10.33696/immunology.4.132Glucose Metabolism is a Better Marker for Predicting Clinical Alzheimer’s Disease than Amyloid or Tau
Alzheimer’s disease (AD) research has long been dominated with communications regarding the amyloid hypothesis and targeting amyloid clearance through pharmacological therapies from the brain [1].
J Cell Immunol, 2022, Volume 4, Issue 1, p15-18 | DOI: 10.33696/immunology.4.128The Role of Myeloid Populations during Perinatal Liver Injury and Repair
The maturation of the immune system is a complex process that undergoes major transitions during fetal and neonatal development [1]. Throughout this developmental window, the response to liver injury is dependent on the nature and timing of the insult [2].
J Cell Immunol, 2021, Volume 3, Issue 1, p42-45 | DOI: 10.33696/immunology.3.076Exploring and Targeting the Tumor Immune Microenvironment of Neuroblastoma
Neuroblastoma is derived from the developing sympathetic nervous system and is the most common extracranial solid tumor of childhood.
J Cell Immunol, 2021, Volume 3, Issue 5, p305-316 | DOI: 10.33696/immunology.3.111The Interplay between Transcription Factor SALL4 and Histone Modifiers in Hematopoietic Stem and Progenitor Cells
Currently, there is a growing need for culturing hematopoietic stem/progenitor cells (HSPCs) ex vivo for various clinical applications such as HSPC transplantation and gene therapy. For many patients with hematologic, genetic, and immune diseases, HSPC transplants can be a life-saving treatment. There are over 20,000 patients in the US receiving HSPC transplantation yearly [1].
J Cell Immunol, 2021, Volume 3, Issue 1, p26-30 | DOI: 10.33696/immunology.3.073A Review of the Possibility of Nafamostat Mesylate in COVID-19 Treatment
Coronavirus disease 2019 (COVID-19), which started in Wuhan in December 2019, is a pandemic caused by the newly emerged severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (genus Betacoronavirus, family Coronaviridae).
J Cell Immunol, 2021, Volume 3, Issue 1, p1-7 | DOI: 10.33696/immunology.3.069Hypomagnesemia and Outcomes in Hematologic Malignancies
Magnesium is an essential mineral and cofactor for hundreds of enzymes and reactions. Magnesium is essential for the regulation of cell growth, division, and differentiation as well as protein synthesis, cell signaling and structural functions.
J Cell Immunol, 2020, Volume 2, Issue 5, p245-249 | DOI: 10.33696/immunology.2.050Updates of Recent Vinpocetine Research in Treating Cardiovascular Diseases
Vinpocetine was originally discovered and marketed under the trade name Cavinton around 1978. Vinpocetine is a synthetic derivative of the vincamine molecule which is an alkaloid extracted from the periwinkle plant, Vinca minor [1]. It has been clinically used in many Asian and Europe countries for preventing and treating neurological
J Cell Immunol, 2020, Volume 2, Issue 5, p211-219 | DOI: 10.33696/immunology.2.045M1 and M2 Macrophages Polarization via mTORC1 Influences Innate Immunity and Outcome of Ehrlichia Infection
Macrophages are innate immune cells that play a key role in regulation of innate and adaptive immune responses against infections with several pathogens as they respond to pathogens and tissue injury, serve as antigen presenting cells priming the adaptive immune response, drive inflammation and host defense as well as repairing
J Cell Immunol, 2020, Volume 2, Issue 3, p108-115 | DOI: 10.33696/immunology.2.029Scientific Archives is a global publisher initiated with the mission of ensuring equal opportunity for accessing science to research community all over the world. Spreading research findings with great relevance to all channels without any barrier is our goal. We want to overcome the challenges of Open Access with ensured quality and transparency.