Sophisticated cell targeting systems such as the gene therapy approach developed for senescent cell clearance by Oisin Biotechnologies could also be turned to stem cell or
immune cell destruction, given suitable markers of cell chemistry.
Not exact matches
A molecule that helps cancer
cells evade programmed self -
destruction, an internal source of death, might also help malignant
cells hide from the
immune system, an external source of death.
The researchers showed that the synapse - eating process requires a protein in the complement system — a part of the
immune response that helps «tag» unwanted
cells and other debris for
destruction.
Checkpoint inhibitors block that handshake, which alerts
immune cells to cancer
cells and target them for
destruction.
Type 1 diabetes, formerly known as juvenile diabetes, is characterized by the
immune system's
destruction of the beta
cells in the pancreas.
In particular, it has evolved to show itself three to nine months after infection, allowing its own
destruction by displaying antigens on its
cell surfaces so the dog's
immune system can destroy it.
This is an illustration of how the engineered protein facilitates
destruction of latently HIV - infected
immune cells.
This is characterised by the targeted strengthening of the body's own
immune cells, unlike in chemotherapy, in which the aim is direct
destruction of the cancer
cells.
Slusher teamed up with Johns Hopkins Kimmel Cancer Center immunologist Jonathan Powell, M.D., Ph.D., who has studied how cancer
cells use different metabolic pathways to evade
destruction by
immune cells.
Among the protagonists are B
cells, which produce antibody molecules able to neutralize pathogens or mark them for
destruction, and T
cells, which prompt infected
cells to kill themselves or secrete chemicals that direct the activities of other
immune players.
Therefore, these «self - reactive» T
cells survive
destruction within an organ called the thymus, the central
immune organ in which T -
cells mature, and attack healthy
cells and tissues, including melanocytes.
«Not only did we confirm that the presence of blood in the brain recruits peripheral
immune cells to the area, which is sufficient to cause myelin
destruction, we also identified fibrinogen as the critical protein driving this process.»
If the T -
cells miss their target or if they mistakenly order the
destruction of a healthy
cell, the result will be disease in the form of infection, cancer, allergies or auto -
immune conditions.
Such neoantigens are foreign to the
immune system, and thus, the cancer
cell is flagged for
destruction, usually with the help of immunotherapy drugs.
By attaching to the myeloma
cells, it marks them for
destruction, and by attaching to NK
cells, it primes the
immune cells to search for and attack the myeloma
cells
The selective pressure of the competent
immune system «edits» the tumor by selecting for
cells that can avoid
immune destruction.
Further, they present two new hallmarks — reprogramming of energy metabolism and evasion of
immune destruction — that have emerged as critical capabilities of cancer
cells.
This draws the innate
immune system's natural killer (NK)
cells into the fray, promotes the antibody - mediated
destruction of malignant
cells and, ultimately, supports the activation of T
cells that specifically target the cancer.
«The
destruction of red blood
cells outside of vessels by
immune cells in PNH has long been speculative due to limited experimental evidence.»
This enhances the
immune response through multiple mechanisms: by attaching to the myeloma
cells, it marks them for
destruction, and by attaching to the NK
cells, it primes the
immune cells to search for and attack the myeloma
cells.
Researchers have discovered that a subset of human antibodies have catalytic activity against a particular antigen, breaking it down into smaller and less harmful fragments instead of trapping it for removal or
destruction by other
immune cells.
Interestingly, when parental d42m1 sarcoma
cells were transplanted into wild - type mice, around 20 % of recipients developed «escape» tumors which evaded
immune destruction and progressed (escape clones).
These «surface proteins» are easily recognized by the
immune cells and targeted for
destruction.
The high doses of therapy lead to the
destruction of a patient's own marrow and
immune system, which is then replaced by marrow from a donor or from peripheral blood stem
cells that have been harvested before therapy.
Specifically, some tumor
cells appeared to express PD - L1, essentially «wrapping» themselves in it to avoid
immune recognition and
destruction.
When implanted, PEC - 01
cells are expected to differentiate into pancreatic islet
cells that produce insulin and other hormones that regulate blood sugar, while the Encaptra device is designed to protect the
cells from
immune destruction.
One of the main reasons cancer remains difficult to treat is that cancer
cells have developed a multitude of mechanisms that allow them to evade
destruction by the
immune system.
Another potential mechanism through which iodine exacerbates or induces Hashimoto's is by up - regulating Th17
cells, the
immune cell subset responsible for tissue
destruction in autoimmune disease, and by suppressing development of regulatory T
cells, the population that invokes oral tolerance to arrest autoimmune responses (31).
The
cells in the
immune system responsible for this auto -
destruction are called TH - 17
cells.
The common identifying factor in most autoimmune diseases is a destructive processes called inflammation which will eventually cause the
destruction of
cells and tissues specific to the type of auto -
immune disease he person has.
While dogs tend to develop diabetes mellitus secondary to either
immune destruction of the pancreatic beta
cells or severe pancreatitis, cats tend to develop diabetes mellitus secondary to pancreatitis or amyloidosis.
The third stage of the infection results from a progressive
destruction of the white blood
cells and dysfunction of the
immune system.
IDDM can also be triggered by infectious virus diseases,
immune deficiencies that result in
destruction of the insulin - producing
cells in the pancreas, pancreatic infections, steroids and reproductive hormones, and Cushing's disease.
There are a few less - often used: Valbazen (albendazole) is about 90 % effective in removing cysts but has been implicated in birth defects, suppression of the
immune system, and
destruction of red blood
cells.
Along with myasthenia gravis, other canine diseases that can be treated with plasmapheresis include lupus and
immune - mediated hemolytic anemia, which causes the premature
destruction of oxygen - carrying red blood
cells.
There are a number of causes of anemia in dogs, such as excessive internal bleeding or
destruction of red blood
cells arising from infections or exposure to toxins (medicines and household products metals such as zinc), but the most common cause is a disease called
immune mediated hemolytic anemia (IMHA).
This discoloration is the result of excessive bilirubin in the bloodstream, which can be the result of either backed up liver circulation due to disease, or as the result of excessive accumulation of bilirubin due to the
destruction of red blood
cells caused by a disruption in red blood
cell metabolism, a defective
immune system, or both.
At least 50 % of diabetic dogs have type 1 diabetes based on present evidence of
immune destruction of β -
cells.
The etiology of β -
cell destruction in diabetic dogs is often unknown, although there is evidence that it is frequently caused by
immune - mediated processes similar to human type 1 diabetes (70 — 72,82 — 84).
We will identify an ITP disease profile by measuring
immune cells and proteins that may be involved platelet
destruction.
Our project aims to investigate the specific causes of ITP by identifying an ITP disease profile by measuring
immune cells and proteins that may be involved platelet
destruction.
In dogs, Diabetes is thought to be an
immune mediate disease process causing
destruction of the
cells in the pancreas responsible for the production of insulin [3].
ACT - activated clotting time (bleeding disorders) ACTH - adrenocorticotropic hormone (adrenal gland function) Ag - antigen test for proteins specific to a disease causing organism or virus Alb - albumin (liver, kidney and intestinal disorders) Alk - Phos, ALP alkaline phosphatase (liver and adrenal disorders) Allergy Testing intradermal or blood antibody test for allergen hypersensitivity ALT - alanine aminotransferase (liver disorder) Amyl - amylase enzyme — non specific (pancreatitis) ANA - antinuclear antibody (systemic lupus erythematosus) Anaplasmosis Anaplasma spp. (tick - borne rickettsial disease) APTT - activated partial thromboplastin time (blood clotting ability) AST - aspartate aminotransferase (muscle and liver disorders) Band band
cell — type of white blood
cell Baso basophil — type of white blood
cell Bile Acids digestive acids produced in the liver and stored in the gall bladder (liver function) Bili bilirubin (bile pigment responsible for jaundice from liver disease or RBC
destruction) BP - blood pressure measurement BUN - blood urea nitrogen (kidney and liver function) Bx biopsy C & S aerobic / anaerobic bacterial culture and antibiotic sensitivity test (infection, drug selection) Ca +2 calcium ion — unbound calcium (parathyroid gland function) CBC - complete blood count (all circulating
cells) Chol cholesterol (liver, thyroid disorders) CK, CPK creatine [phospho] kinase (muscle disease, heart disease) Cl - chloride ion — unbound chloride (hydration, blood pH) CO2 - carbon dioxide (blood pH) Contrast Radiograph x-ray image using injected radiopaque contrast media Cortisol hormone produced by the adrenal glands (adrenal gland function) Coomb's anti- red blood
cell antibody test (
immune - mediated hemolytic anemia) Crea creatinine (kidney function) CRT - capillary refill time (blood pressure, tissue perfusion) DTM - dermatophyte test medium (ringworm — dermatophytosis) EEG - electroencephalogram (brain function, epilepsy) Ehrlichia Ehrlichia spp. (tick - borne rickettsial disease) EKG, ECG - electrok [c] ardiogram (electrical heart activity, heart arryhthmia) Eos eosinophil — type of white blood
cell Fecal, flotation, direct intestinal parasite exam FeLV Feline Leukemia Virus test FIA Feline Infectious Anemia: aka Feline Hemotrophic Mycoplasma, Haemobartonella felis test FIV Feline Immunodeficiency Virus test Fluorescein Stain fluorescein stain uptake of cornea (corneal ulceration) fT4, fT4ed, freeT4ed thyroxine hormone unbound by protein measured by equilibrium dialysis (thyroid function) GGT gamma - glutamyltranferase (liver disorders) Glob globulin (liver,
immune system) Glu blood or urine glucose (diabetes mellitus) Gran granulocytes — subgroup of white blood
cells Hb, Hgb hemoglobin — iron rich protein bound to red blood
cells that carries oxygen (anemia, red
cell mass) HCO3 - bicarbonate ion (blood pH) HCT, PCV, MHCT hematocrit, packed -
cell volume, microhematocrit (hemoconcentration, dehydration, anemia) K + potassium ion — unbound potassium (kidney disorders, adrenal gland disorders) Lipa lipase enzyme — non specific (pancreatitis) LYME Borrelia spp. (tick - borne rickettsial disease) Lymph lymphocyte — type of white blood
cell MCHC mean corpuscular hemoglobin concentration (anemia, iron deficiency) MCV mean corpuscular volume — average red
cell size (anemia, iron deficiency) Mg +2 magnesium ion — unbound magnesium (diabetes, parathyroid function, malnutrition) MHCT, HCT, PCV microhematocrit, hematocrit, packed -
cell volume (hemoconcentration, dehydration, anemia) MIC minimum inhibitory concentration — part of the C&S that determines antimicrobial selection Mono monocyte — type of white blood
cell MRI magnetic resonance imaging (advanced tissue imaging) Na + sodium ion — unbound sodium (dehydration, adrenal gland disease) nRBC nucleated red blood
cell — immature red blood
cell (bone marrow damage, lead toxicity) PCV, HCT, MHCT packed -
cell volume, hematocrit, microhematocrit (hemoconcentration, dehydration, anemia) PE physical examination pH urine pH (urinary tract infection, urolithiasis) Phos phosphorus (kidney disorders, ketoacidosis, parathyroid function) PLI pancreatic lipase immunoreactivity (pancreatitis) PLT platelet —
cells involved in clotting (bleeding disorders) PT prothrombin time (bleeding disorders) PTH parathyroid hormone, parathormone (parathyroid function) Radiograph x-ray image RBC red blood
cell count (anemia) REL Rocky Mountain Spotted Fever / Ehrlichia / Lyme combination test Retic reticulocyte — immature red blood
cell (regenerative vs. non-regenerative anemia) RMSF Rocky Mountain Spotted Fever SAP serum alkaline phosphatase (liver disorders) Schirmer Tear Test tear production test (keratoconjunctivitis sicca — dry eye,) Seg segmented neutrophil — type of white blood
cell USG Urine specific gravity (urine concentration, kidney function) spec cPL specific canine pancreatic lipase (pancreatitis)-- replaces the PLI test spec fPL specific feline pancreatic lipase (pancreatitis)-- replaces the PLI test T4 thyroxine hormone — total (thyroid gland function) TLI trypsin - like immunoreactivity (exocrine pancreatic insufficiency) TP total protein (hydration, liver disorders) TPR temperature / pulse / respirations (physical exam vital signs) Trig triglycerides (fat metabolism, liver disorders) TSH thyroid stimulating hormone (thyroid gland function) UA urinalysis (kidney function, urinary tract infection, diabetes) Urine Cortisol - Crea Ratio urine cortisol - creatine ratio (screening test for adrenal gland disease) Urine Protein - Crea Ratio urine protein - creatinine ratio (kidney disorders) VWF VonWillebrands factor (bleeding disorder) WBC white blood
cell count (infection, inflammation, bone marrow suppression)
Lymphocytic thyroiditis, probably
immune - mediated, is characterized histologically by a diffuse infiltration of the gland by lymphocytes, plasma
cells, and macrophages and results in progressive
destruction of follicles and secondary fibrosis.
In addition to affecting the GI tract, parvovirus also attacks your dog's
immune system, resulting in panleukopenia, or
destruction of disease - fighting white blood
cells.
The pathogenic mechanisms responsible for decreased insulin production and secretion are multiple, but usually they are related to
destruction of islet
cells, secondary to either
immune destruction or severe pancreatitis (dogs) or amyloidosis (cats).