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Topic Review
CAR Therapy
Among the many oncology therapies, few have generated as much excitement as CAR-T. The success of CAR therapy would not have been possible without the many discoveries that preceded it, most notably, the Nobel Prize-winning breakthroughs in cellular immunity. However, despite the fact that CAR-T already offers not only hope for development, but measurable results in the treatment of hematological malignancies, CAR-T still cannot be safely applied to solid tumors. The reason for this is, among other things, the lack of tumor-specific antigens which, in therapy, threatens to cause a lethal attack of lymphocytes on healthy cells. In the case of hematological malignancies, dangerous complications such as cytokine release syndrome may occur. Scientists have responded to these clinical challenges with molecular switches.
  • 966
  • 29 Jun 2022
Topic Review
Psoriasis and Its Clinical Implications
Psoriasis is the result of uncontrolled keratinocyte proliferation, and its pathogenesis involves the dysregulation of the immune system. The interplay among cytokines released by dendritic, Th1, Th2, and Th17 cells leads to the phenotypical manifestations seen in psoriasis. Biological therapies target the cytokine-mediated pathogenesis of psoriasis and have improved patient quality of life.
  • 965
  • 05 May 2022
Topic Review
Immunomodulatory Properties of Bioactive Products
Bioactive products have an effect on the molecular and biochemical functions of a living organism, causing a physiological response of the given tissue. Such a products are biologically active. Depending on the active component and amount, the effects of such products can be positive or negative. Bioactive products can be food ingredients or dietary supplements, and while they are not required for survival, they are responsible for changes in the body’s health.
  • 965
  • 24 Mar 2022
Topic Review
S100 Proteins in Psoriasis and Other Autoimmune Diseases
Very well-known AMP-family members are S100 proteins that constitute the largest, multigenic, and calcium-binding protein family in vertebrates. Over 20 types of these proteins have been identified, of which 13 are expressed in the normal or diseased human epidermis. The name of the S100 proteins is due to their biochemical characteristics, namely, they are 100% soluble in saturated ammonium sulfate at neutral pH. S100 proteins are small, acidic proteins with a molecular weight of 9–13 kDa. They are produced as monomers, but exist in cells as anti-parallel homo- and heterodimers, in which monomers are held together by non-covalent bonds and are oriented by a two-fold axis of rotation. Dimers can further associate to form higher-order multimers. Each S100 monomer consists of two helix–loop–helix structural motifs that are Ca2+-binding domains termed EF-hands. 
  • 964
  • 21 Oct 2022
Topic Review
Mechano-Immunomodulation in Space
The gravity environment in space is termed “microgravity” (μG) and is defined as approximately 10−6 of Earth’s surface gravity (G), as there is never truly a complete absence of gravity. The effects of μG on various cell types have been documented in bone, cartilage, and endothelial cells, to name a few, and immune cells are no exception. Among the various microgravity-induced side effects, a compromised or altered immune response can have serious consequences and jeopardize the survival of humans in space.
  • 963
  • 28 Oct 2021
Topic Review
Ketogenic Diet Mediated Immune Regulation in Different Diseases
Ketogenic diets (KD) encompass a lower consumption of carbohydrates, adequate protein, and a high fat regimen which induces ketone body production via mimicking the metabolism of the fasting state without significant calorie deprivation. Herein, several facets of ketogenic diet as an immunomodulator with respect to its expansive clinical applications are presented.
  • 963
  • 10 Jan 2023
Topic Review
Cytokine Profile with Multiple Sclerosis Following Exercise
Multiple sclerosis (MS) is defined as an immune-mediated inflammatory, neurodegenerative, and demyelinating disease that impacts the central nervous system (CNS) in young individuals. 
  • 961
  • 18 Aug 2022
Topic Review
Extracellular Vesicles in Osteoarthritis
Along with cytokines, extracellular vesicles (EVs) released by immune cells in the joint contribute to osteoarthritis (OA) pathogenesis. By high-resolution flow cytometry, we characterized 18 surface markers and 4 proinflammatory cytokines carried by EVs of various sizes in plasma and synovial fluid (SF) from individuals with knee OA, with a primary focus on immune cells that play a major role in OA pathogenesis.
  • 960
  • 09 Sep 2021
Topic Review
Epithelial-Mesenchymal Transition Phenotype and Immune System
Carcinoma cells that undergo an epithelial-mesenchymal transition (EMT) and display a predominantly mesenchymal phenotype (hereafter EMT tumor cells) are associated with immune exclusion and immune deviation in the tumor microenvironment (TME). A large body of evidence has shown that EMT tumor cells and immune cells can reciprocally influence each other, with EMT cells promoting immune exclusion and deviation and immune cells promoting, under certain circumstances, the induction of EMT in tumor cells. This cross-talk between EMT tumor cells and immune cells can occur both between EMT tumor cells and cells of either the native or adaptive immune system.
  • 959
  • 22 Apr 2022
Topic Review
Immunomodulation Potential of Probiotics
The use of probiotics in livestock has been suggested to significantly improve their health, immunity, growth performance, nutritional digestibility, and intestinal microbial balance. Furthermore, it was reported that the use of probiotics in animals was helpful in equilibrating their beneficial microbial population and microbial turnover via stimulating the host immune response through specific secretions and competitive exclusion of potentially pathogenic bacteria in the digestive tract.
  • 958
  • 11 Mar 2022
Topic Review
SARS-CoV-2 Dysregulates Neutrophil Degranulation and Reduces Lymphocyte Counts
SARS-CoV-2, the virus that causes COVID-19, has given rise to one of the largest pandemics, affecting millions worldwide. High neutrophil-to-lymphocyte ratios have been identified as an important correlate to poor recovery rates in severe COVID-19 patients. However, the mechanisms underlying this clinical outcome and the reasons for its correlation to poor prognosis are unclear. Furthermore, the mechanisms involved in healthy neutrophils acquiring a SARS-CoV-2-mediated detrimental role are yet to be fully understood. 
  • 958
  • 14 Mar 2022
Topic Review
Innate Immunity of the Small Intestine
The small intestine has a huge surface area that is further enhanced by villi and microvilli to facilitate the digestion and absorption of nutrients. The expanded surface area of the small intestine increases the likelihood of exposure to pathogens in the lumen. The small intestine must balance the need for nutrient absorption with the ability to ward off pathogens. The majority of the immune cells in the body reside in the mucosa-associated tissues and the mesenchymal tissues of the gastrointestinal tract (GIT). The gut-associated lymphoid tissues (GALT) play a vital role in the development of the immunity of the entire body, as most of the antigens that get into the body are transported to the GIT for processing by its innate immunity before being delivered to the adaptive immunity.
  • 958
  • 08 Jun 2023
Topic Review
Infectious complications in AIHA
Autoimmune hemolytic anemia (AIHA) may be frequently challenged by infectious complications, mainly as a result of immunosuppressive treatments administered. Furthermore, infectious agents are known triggers of AIHA onset and relapse. Although being risk factors for mortality, infec-tions are an underestimated issue in AIHA.
  • 957
  • 21 Jan 2021
Topic Review
NOD1, NOD2, and NLRC5 Receptors
The innate immune system recognizes pathogen-associated molecular motifs through pattern recognition receptors (PRRs) that induce inflammasome assembly in macrophages and trigger signal transduction pathways, thereby leading to the transcription of inflammatory cytokine genes. Nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs) represent a family of cytosolic PRRs involved in the detection of intracellular pathogens such as mycobacteria or viruses.
  • 957
  • 23 Sep 2022
Topic Review
Mining the Immunopeptidome for Antigenic Peptides in Cancer
Harnessing the immune system for cancer therapy has shown success, however the response to immunotherapy has been limited. Deciphering the immunopeptidome repertoire of cancer cells is crucial for identifying neoantigens. To date the emphasis has been on mutations. However, there is more to neoantigens than mutations. Thus, there is a need to identify other types of neoantigens that are commonly expressed in a cancer type that are presented by MHC class I and class II, to induce a cytotoxic CD8+ T and CD4+ T response, respectively. The immunopeptidome encompasses protein post-translation modifications (PTMs), which are overlooked by genome or transcriptome profiling. This entry covers how the immunopeptidome can yield novel cancer-specific antigens, focusing on PTMs and their applications.
  • 955
  • 26 Oct 2022
Topic Review
Innate Immune Receptor Stimulation
Immunometabolism is a relatively new field of research that aims at understanding interconnections between the immune system and cellular metabolism. This is now well-documented for innate immune cells of the myeloid lineage such as macrophages and myeloid dendritic cells (DCs) when they engage their differentiation or activation programs. Several studies have shown that stimulation of DCs or macrophages by the binding of pathogen-associated molecular patterns (PAMPs) to pattern recognition receptors (PRRs) leads to increased glycolytic activity and rewiring of central carbon metabolism. These metabolic modulations are essential to support and settle immunological functions by providing energy and immunoregulatory metabolites. As the understanding of molecular mechanisms progressed, significant differences between cell types and species have also been discovered. Pathways leading to the regulation of central carbon metabolism in macrophages and DCs by PRR signaling and consequences on cellular functions are reviewed here.
  • 954
  • 08 Feb 2021
Topic Review
Immunotherapy with Checkpoint-Inhibitors for HCC
Immune checkpoint inhibitors (ICIs) are beginning to show promise in the clinical management of hepatocellular carcinoma (HCC). Most recently, the anti-programmed death protein-1 (PD-1) agent atezolizumab combined with bevacizumab demonstrated superiority to sorafenib in a Phase 3 randomised clinical trial in the frontline setting. Other ongoing trials of immunotherapy for HCC are exploring different drug combinations, such as a double checkpoint blockade with PD-1 and anti-Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) agents or with tyrosine kinase inhibitors. Moreover, ICIs are being tested in the adjuvant and neoadjuvant settings trying to resolve long-time unmet needs in HCC. The results of the ongoing trials will be critical to understanding the extent of the therapeutic role of ICIs in the complex and multifaceted clinical scenario of HCC. Still, there are some critical points which need further attention to clarify the best use of ICIs in HCC patients. For instance, the actual eligibility rate of patients in the real-life scenario, the prompt identification and correct management of immune-mediated adverse events, the identification of biomarkers predicting response or resistance, and strategies to prevent the tumour escape from ICI effect.  Deatail review paper about the current therapeutic scenario of immune checkpoint inhibitors (in particular nivolumab, ipilimumab, atezolizumab, pembrolizumab, durvalumab) for the treatment of hepatocellular carcinoma. The first part of this review is dedicated to the concluded and ongoing clinical trials. The second part deals with the hot topics in the field of immunotherapy borrowing concepts from other cancers and adapting them to the specific scenario of hepatocellular carcinoma.
  • 951
  • 25 Oct 2020
Topic Review
Mast Cells in Unconventional Immunotherapy
Mast cells are long-lived, granular, myeloid-derived leukocytes that have significant protective and repair functions in tissues. Mast cells sense disruptions in the local microenvironment and are first responders to physical, chemical and biological insults. When activated, mast cells release growth factors, proteases, chemotactic proteins and cytokines thereby mobilizing and amplifying the reactions of the innate and adaptive immune system. Mast cells are therefore significant regulators of homeostatic functions and may be essential in microenvironmental changes during pathogen invasion and disease. During infection by helminths, bacteria and viruses, mast cells release antimicrobial factors to facilitate pathogen expulsion and eradication. Mast cell-derived proteases and growth factors protect tissues from insect/snake bites and exposure to ultraviolet radiation. Finally, mast cells release mediators that promote wound healing in the inflammatory, proliferative and remodelling stages. Since mast cells have such a powerful repertoire of functions, targeting mast cells may be an effective new strategy for immunotherapy of disease and design of novel vaccine adjuvants.
  • 950
  • 22 Apr 2021
Topic Review
Immune Cell Trafficking across the Different CNS Barriers
Multiple sclerosis (MS) is an inflammatory disease of the central nervous system (CNS) known for the manifestation of demyelinated lesions throughout the CNS, leading to neurodegeneration. To date, not all pathological mechanisms that drive disease progression are known, but the clinical benefits of anti-CD20 therapies have put B cells in the spotlight of MS research.
  • 949
  • 24 Jun 2022
Topic Review
A Mycobacteriophage-Based Vaccine Platform for SARS-CoV-2
Bacteriophage-based vaccines can generate a protective immune response by safely introducing foreign antigens displayed on, encapsidated within, or genetically encoded by phage. Here authors describe recombinants of mycobacteriophage Bxb1 (a phage infecting Mycobacterium smegmatis) that covalently display and express antigenic peptides of the SARS-CoV-2 Spike protein. Several of these vaccine candidates produced Spike-specific antibodies in immunized mice, but the responses were not neutralizing. This mycobacteriophage-based vaccine platform can likely be improved if delivery of larger antigens is achieved. 
  • 948
  • 06 Dec 2021
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