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Sunday, August 29, 2021
08-29-2021-0222 - Kaposi's sarcoma-associated herpesvirus (KSHV) her 8 hhv-8 HHV-8 hhv geven castleman castle inflammation cytokine syndrome KSHV inflammatory cytokine syndrome AIDS primary effusion lymphoma sarcoma plaqules-meateous-hf-etc. genetic modification deep muscle tissue migration cell migration and recolonization base cells similar bacteria migration way from muscle transform of epidiy radiation oncovirus - virus implantation virus usurpation of ho migrans tunneling reassembly/restructure/reformulation/etc. coagulation haemo base/inf/etc. aids aid blood vessel disease tissue disease inversions STD immunosuppression multicentric dysplasia angiofollicular lymph node hyperplasia hamartoma lymphoproliferative proliferation disorder disease HIV immunosuppressants MCD Human herpesvirus 8 associated multicentric Castleman disease hemangiomas proinflammatory cytokines B cells b plasma plasmablast immune leprosy lupers leupus lups lupus eosilophil chromosomal relocation translocation recombination cytokine sharon petersen Lymphocytic interstitial pneumonitis siboan wade smith cancer Flu-like symptoms ascites pleural effusions edema hepatomegaly spleenomegaly thymomegaly-malacia-condeterior conde terior condeterior detrius decay matter fungus asburgers
Above. lil deucedeuce witch encounter remix
Kaposi's sarcoma-associated herpesvirus (KSHV) is the ninth known human herpesvirus; its formal name according to the International Committee on Taxonomy of Viruses (ICTV) is Human gammaherpesvirus 8, or HHV-8 in short.[1] Like other herpesviruses, its informal names are used interchangeably with its formal ICTV name. This virus causes Kaposi's sarcoma, a cancer commonly occurring in AIDS patients,[2] as well as primary effusion lymphoma,[3] HHV-8-associated multicentric Castleman's disease and KSHV inflammatory cytokine syndrome.[4] It is one of seven currently known human cancer viruses, or oncoviruses.[2] Even after so many years of discovery of KSHV/HHV8, there is no known cure for KSHV associated tumorigenesis.
Virus classificatio
(unranked):VirusRealm:DuplodnaviriaKingdom:HeunggongviraePhylum:PeploviricotaClass:HerviviricetesOrder:HerpesviralesFamily:HerpesviridaeGenus:RhadinovirusSpecies:
Human gammaherpesvirus 8
In 1872, Moritz Kaposi described a blood vessel tumor[5] (originally called "idiopathic multiple pigmented sarcoma of the skin") that has since been eponymously named Kaposi's sarcoma (KS). KS was at first thought to be an uncommon tumor of Jewish and Mediterranean populations until it was later determined to be extremely common throughout sub-Saharan African populations. This led to the first suggestions in the 1950s that this tumor might be caused by a virus. With the onset of the AIDS epidemic in the early 1980s, there was a sudden resurgence of KS affecting primarily gay and bisexual AIDS patients, with up to 50% of reported AIDS patients having this tumor—an extraordinary rate of cancer predisposition.[citation needed]
The pathogen was ultimately identified in 1994 by Yuan Chang and Patrick S. Moore, a wife and husband team at Columbia University, through the isolation of DNA fragments from a herpesvirus found in a KS tumor in an AIDS patient.[7][8][9] Chang and Moore used representational difference analysis, or RDA, to find KSHV by comparing KS tumor tissue from an AIDS patient to his own unaffected tissue. The idea behind this experiment was that if a virus causes KS, the genomic DNA in the two samples should be precisely identical except for DNA belonging to the virus. In their initial RDA experiment, they isolated two small DNA fragments that represented less than 1% of the actual viral genome. These fragments were similar (but still distinct from) the known herpevirus sequences, indicating the presence of a new virus. Starting from these fragments, this research team was then able to sequence the entire genome of the virus less than two years later.[citation needed]
The discovery of this herpesvirus sparked considerable controversy and scientific in-fighting until sufficient data had been collected to show that indeed KSHV was the causative agent of Kaposi's sarcoma.[10] The virus is now known to be a widespread infection of people living in sub-Saharan Africa; intermediate levels of infection occur in Mediterranean populations (including Lebanon, Saudi Arabia, Italy, and Greece) and low levels of infection occur in most Northern European and North American populations. Gay and bisexual men are more susceptible to infection (through still unknown routes of sexual transmission) whereas the virus is transmitted through non-sexual routes in developing countries.[citation needed]
After infection, the virus enters into lymphocytes via macropinosomes where it remains in a latent ("quiet") state. Only a subset of genes that are encoded in KSHV latency associated region (KLAR) are expressed during latency including latency-associated nuclear antigen (LANA), vFLIP, vCyclin and 12 microRNA.
LANA tethers the viral DNA to cellular chromosomes, inhibits p53 and retinoblastoma protein and suppresses viral genes needed for full virus production and assembly ("lytic replication")....
https://en.wikipedia.org/wiki/Kaposi%27s_sarcoma-associated_herpesvirus
Human herpesvirus 8 associated multicentric Castleman disease (HHV-8-associated MCD) is a subtype of Castleman disease (also known as giant lymph node hyperplasia, lymphoid hamartoma, or angiofollicular lymph node hyperplasia), a group of rare lymphoproliferative disorders characterized by lymph node enlargement, characteristic features on microscopic analysis of enlarged lymph node tissue, and a range of symptoms and clinical findings.
People with human herpesvirus 8 associated multicentric Castelman disease (HHV-8-associated MCD) have enlarged lymph nodes in multiple regions and often have flu-like symptoms, abnormal findings on blood tests, and dysfunction of vital organs, such as the liver, kidneys, and bone marrow.
HHV-8-associated MCD is known to be caused by uncontrolled infection with the human herpesvirus 8 virus (HHV-8) and is most frequently diagnosed in patients with human immunodeficiency virus (HIV). HHV-8-associated MCD is treated with a variety of medications, including immunosuppressants, chemotherapy, and antivirals.
Castleman disease is named after Dr. Benjamin Castleman, who first described the disease in 1956. The Castleman Disease Collaborative Network is the largest organization focused on the disease and is involved in research, awareness, and patient support.
rashes such as cherry hemangiomas or Kaposi sarcoma; enlargement of the liver and/or spleen; and extravascular fluid accumulation in the extremities (edema), abdomen (ascites), or lining of the lungs (pleural effusion).[1]
In HHV-8-associated MCD the HHV-8 virus infects B cells and plasmablasts in lymph nodes and causes infected cells to release proinflammatory cytokines, signaling molecules that increase the activity of immune cells. In particular, HHV-8 infection of immune cells leads to increased levels of Interleukin-6 (IL-6), a cytokine known to play a role in other forms of Castleman disease.[citation needed]
The HHV-8 virus contains a gene coding for a viral variant of the IL-6 molecule. Cells infected by HHV-8 produce the viral variant of IL-6 and normal human IL-6, both of which contribute to the increased B cell proliferation and clinical findings seen in HHV-8-associated MCD.[4]
| HHV-8-associated MCD | |
|---|---|
| Other names | Giant lymph node hyperplasia, lymphoid hamartoma, angiofollicular lymph node hyperplasia |
.jpg) | |
| Micrograph of HHV8-associated Castleman's Disease showing LANA-1 positive lymphoblasts in a regressed germinal center and mantle zone. LANA-1 stain. | |
https://en.wikipedia.org/wiki/HHV-8-associated_MCD
Idiopathic multicentric Castleman disease (iMCD) is a subtype of Castleman disease (also known as giant lymph node hyperplasia, lymphoid hamartoma, or angiofollicular lymph node hyperplasia), a group of lymphoproliferative disorders characterized by lymph node enlargement, characteristic features on microscopic analysis of enlarged lymph node tissue, and a range of symptoms and clinical findings.
People with iMCD have enlarged lymph nodes in multiple regions and often have flu-like symptoms, abnormal findings on blood tests, and dysfunction of vital organs, such as the liver, kidneys, and bone marrow.
iMCD has features often found in autoimmune diseases and cancers, but the underlying disease mechanism is unknown. Treatment for iMCD may involve the use of a variety of medications, including immunosuppressants and chemotherapy.
Castleman disease was named after Dr. Benjamin Castleman, who first described the disease in 1956. The Castleman Disease Collaborative Network is the largest organization focused on the disease and is involved in research, awareness, and patient support.
| Idiopathic multicentric Castleman disease | |
|---|---|
| Other names | Giant lymph node hyperplasia, lymphoid hamartoma, angiofollicular lymph node hyperplasia |
 | |
| Micrograph of lymph node biopsy demonstrating hyaline vascular features consistent with Castleman disease | |
| Specialty | Hematology, immunology, rheumatology, pathology |
| Diagnostic method | Based on patient history, physical exam, laboratory testing, medical imaging, histopathology |
| Frequency | approximately 1500-1800 new cases per year in the United States |
Several theoretical mechanisms for iMCD have been proposed based on existing research and observed similarities between iMCD and other diseases that present with similar clinical findings and lymph node histology:[2]
- Autoimmune – The immune system may produce antibodies that target healthy cells in the body instead of bacteria and viruses. Self-directed antibodies are commonly seen in autoimmune diseases such as systemic lupus erythematous and rheumatoid arthritis.
- Autoinflammatory – A mutation in a gene controlling inflammatory systems may contribute to harmful activation of inflammatory pathways in patients with iMCD.
- Neoplastic – Genetic mutations that develop in mature cells (somatic mutations) may cause an overgrowth of abnormal cells as in cancers such as lymphoma.
- Pathogen – Human herpesvirus 8 (HHV-8) is the known causative agent in HHV-8-associated MCD, which has very similar symptoms and findings to iMCD. While iMCD by definition is not caused by HHV-8, an unknown virus may cause the disease.
There have been no reported cases of UCD transforming into iMCD.[citation needed]
Idiopathic multicentric Castleman disease[edit]
iMCD may be further differentiated by the presence of associated diseases, such as polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, skin changes syndrome (POEMS syndrome), or by distinct clinical features, such as thrombocytopenia, anasarca, myelofibrosis, renal dysfunction, and organomegaly syndrome (TAFRO syndrome).[5]
Diagnostic criteria[edit]
Diagnosis of iMCD requires: the presence of both major criteria, multiple regions of enlarged lymph nodes as demonstrated by medical imaging; the presence of at least two minor criteria, at least one of which must be an abnormal laboratory test; and exclusion of diseases that can mimic iMCD.[citation needed]
Major criteria 1: multiple regions of enlarged lymph nodes[edit]
Radiologic imaging must demonstrate enlarged lymph nodes in multiple regions.[5]
Major criteria 2: microscopic analysis of lymph node biopsy consistent with iMCD[edit]
The microscopic appearance (histology) of biopsied tissue from an enlarged lymph node must demonstrate a constellation of features consistent with Castleman disease. There are three patterns of characteristic histologic features associated with iMCD:[5]
- Hypervascular - regressed germinal centers, follicular dendritic cell prominence, hypervascularity in interfollicular regions, and prominent mantle zoneswith an “onion-skin” appearance.
- Plasmacytic – increased number of follicles with large hyperplastic germinal centers and sheet-like plasmacytosis (increased number of plasma cells).
- Mixed – features of both hypervascular and plasmacytic.
iMCD most commonly demonstrates plasmacytic features; however, hypervascular features or a mixture of both hypervascular and plasmacytic features may also be seen in iMCD lymph nodes. The clinical utility of subtyping iMCD by histologic features is uncertain, as histologic subtypes do not consistently predict disease severity or treatment response.[citation needed]
Staining with latency-associated nuclear antigen (LANA-1), a marker of HHV-8 infection, must be negative to diagnose iMCD.[5]
Minor criteria
https://en.wikipedia.org/wiki/Idiopathic_multicentric_Castleman_disease
Cytokines are a broad and loose category of small proteins (~5–20 kDa) important in cell signaling. Cytokines are peptides and cannot cross the lipid bilayer of cells to enter the cytoplasm. Cytokines have been shown to be involved in autocrine, paracrine and endocrine signaling as immunomodulating agents. Their definite distinction from hormones is still part of ongoing research.
Cytokines include chemokines, interferons, interleukins, lymphokines, and tumour necrosis factors, but generally not hormones or growth factors (despite some overlap in the terminology). Cytokines are produced by a broad range of cells, including immune cells like macrophages, B lymphocytes, T lymphocytes and mast cells, as well as endothelial cells, fibroblasts, and various stromal cells; a given cytokine may be produced by more than one type of cell.[1][2] They act through cell surface receptors and are especially important in the immune system; cytokines modulate the balance between humoral and cell-based immune responses, and they regulate the maturation, growth, and responsiveness of particular cell populations. Some cytokines enhance or inhibit the action of other cytokines in complex ways. They are different from hormones, which are also important cell signaling molecules. Hormones circulate in higher concentrations, and tend to be made by specific kinds of cells. Cytokines are important in health and disease, specifically in host immune responsesto infection, inflammation, trauma, sepsis, cancer, and reproduction.
The word comes from the ancient Greek language: cyto, from Greek κύτος, kytos, 'cavity, cell' + kines, from Greek κίνησις, kinēsis, 'movement'.
https://en.wikipedia.org/wiki/Cytokine
08-29-2021-1416 - Duplodnaviria
Duplodnaviria is a realm of viruses that includes all double-stranded DNA viruses that encode the HK97 fold major capsid protein. The HK97 fold major capsid protein (HK97 MCP) is the primary component of the viral capsid, which stores the viral deoxyribonucleic acid (DNA). Viruses in the realm also share a number of other characteristics, such as an icosahedral capsid, an opening in the viral capsid called a portal, a protease enzymethat empties the inside of the capsid prior to DNA packaging, and a terminase enzyme that packages viral DNA into the capsid.
Duplodnaviria was established in 2019 based on the shared characteristics of viruses in the realm. There are two groups of viruses in Duplodnaviria: tailed bacteriophages of the order Caudovirales, which infect prokaryotes, and herpesviruses of the order Herpesvirales, which infect animals. Tailed bacteriophages are very diverse and ubiquitous worldwide, and they may be the oldest lineage of viruses. Herpesviruses either share a common ancestor with tailed bacteriophages or are a breakaway group from within Caudovirales.
Tailed bacteriophages are important in marine ecology by recycling nutrients in organic material from their hosts and are the focus of much research, and herpesviruses are associated with a variety of diseases in animals, including humans. A common feature among viruses in Duplodnaviria is that many are able to persist in their host for long periods of time without replicating while still being able to resurface in the future. Example of this include the herpes simplex virus, which causes recurring infections, and the varicella zoster virus, which initially causes chickenpox early in life then shingles later in life.
| Virus classification | |
|---|---|
| (unranked): | Virus |
| Realm: | Duplodnaviria |
| Kingdom: | Heunggongvirae |
https://en.wikipedia.org/wiki/Duplodnaviria
prion disease,
08-28-2021-2159 - Neurosarcoidosis Neurocystcercosis Parasitic Worm equid infectious her, roseolo, purulent rables ns disease, poxiviridae, molluscum contagium, mollusk shellfish arthropod crustacean birt kermits, etc..roseola, etc.. dirt, damp, mold, fungus, drust dry dusting dust mite dirt are air aerosol aero spore suspension gas environment air breeders etc. bluetongue hand foot mouth disease.
above.
BOB THE DRAG QUEEN - PURSE FIRST (feat. DJ Mitch Ferrino)
08-29-2021-1410 - Percavirus equid mustelid phocid vespertillo HIV + equine squid sea air land etc. gamma hersec5 KHSV kshv HV H V hv
The genus consists of the following six species:[2]
- Equid gammaherpesvirus 2
- Equid gammaherpesvirus 5
- Felid gammaherpesvirus 1
- Mustelid gammaherpesvirus 1
- Phocid gammaherpesvirus 3
- Vespertilionid gammaherpesvirus 1
https://en.wikipedia.org/wiki/Percavirus
above.
Suicide Commando - H.I.V. +
08-29-2021-1407 - alveolar macrophage, pulmonary macrophage dust cell lung respiratory system
An alveolar macrophage, pulmonary macrophage, (or dust cell) is a type of macrophage, a professional phagocyte, found in the airways and at the level of the alveoli in the lungs, but separated from their walls.[1]
Activity of the alveolar macrophage is relatively high, because they are located at one of the major boundaries between the body and the outside world. They are responsible for removing particles such as dust or microorganisms from the respiratory surfaces.
Alveolar macrophages are frequently seen to contain granules of exogenous material such as particulate carbonthat they have picked up from respiratory surfaces. Such black granules may be especially common in smoker's lungs or long-term city dwellers.
The alveolar macrophage is the third cell type in the alveolus, the others are the type I and type II pneumocytes.
Micrograph showing hemosiderin-laden alveolar macrophages, as seen in a pulmonary haemorrhage. H&E stain.
https://en.wikipedia.org/wiki/Alveolar_macrophage
above. combichrist -
This Is My Rifle
08-29-2021-1406 - In the natural environment, Legionella lives within amoebae such as Acanthamoeba spp., Naegleria spp., Vermamoeba vermiformis, or other protozoa such as Tetrahymena pyriformis.[12]
In the natural environment, Legionella lives within amoebae such as Acanthamoeba spp., Naegleria spp., Vermamoeba vermiformis, or other protozoa such as Tetrahymena pyriformis.[12]
A Legionella pneumophila bacterium (green) caught by a Vermamoeba vermiformisamoeba (orange)
https://en.wikipedia.org/wiki/Q_fever
above.
MARILYN MANSON - THIRD DAY OF A SEVEN DAY BINGE
08-29-2021-1401 - Q fever or query fever cox coxiella ella burn burnetti burnetii coxiella burnetii bacteria inhalation cattle sheep goat rodent arthropod crustecean bacteria viri cellular infectivity survival requirements time obligate intracellular pathogenic parasite immunohistochemical immunology histology pathology hematology radiology bruce brucellosis leptospirosis spirochete leprosy lupus HIV molluscum contagium poxiviridae neuro-granulation disseminative granulation non caseous plaque tuberculosis miliary caseous necrosis gangrene fulminant fulminancy bubules purulent bubulant rables; burna cox, cow chicken
C. burnetii, the Q fever-causing agent
Q fever or query fever is a disease caused by infection with Coxiella burnetii,[1][3][4] a bacterium that affects humans and other animals. This organism is uncommon, but may be found in cattle, sheep, goats, and other domestic mammals, including cats and dogs. The infection results from inhalation of a spore-like small-cell variant, and from contact with the milk, urine, feces, vaginal mucus, or semenof infected animals. Rarely, the disease is tick-borne.[5] The incubation period is 9–40 days. Humans are vulnerable to Q fever, and infection can result from even a few organisms.[5] The bacterium is an obligate intracellular pathogenic parasite.
In the natural environment, Legionella lives within amoebae such as Acanthamoeba spp., Naegleria spp., Vermamoeba vermiformis, or other protozoa such as Tetrahymena pyriformis.[12]
Upon inhalation, the bacteria can infect alveolar macrophages, where the bacteria can replicate. This results in Legionnaires' disease and the less severe illness Pontiac fever. Legionella transmission is via inhalation of water droplets from a contaminated source that has allowed the organism to grow and spread (e.g., cooling towers). Transmission also occurs less commonly via aspiration of drinking water from an infected source. Person-to-person transmission has not been demonstrated;[4] though, it could be possible in rare cases.[13]
https://en.wikipedia.org/wiki/Q_fever
American Pie
Q feverOther namesQuery fever, coxiellosis[1][2]
Immunohistochemical detection of C. burnetii in resected cardiac valve of a 60-year-old man with Q fever endocarditis, Cayenne, French Guiana: Monoclonal antibodies against C. burnetii and hematoxylin were used for staining; original magnification is ×50.SpecialtyInfectious disease Typesacute, chronic[1]Risk factorsContact with livestock[2]Differential diagnosispneumonia, influenza, brucellosis, leptospirosis, meningitis, viral hepatitis, dengue fever, malaria, other rickettsial infections[2]
Immunohistochemical detection of C. burnetii in resected cardiac valve of a 60-year-old man with Q fever endocarditis, Cayenne, French Guiana: Monoclonal antibodies against C. burnetii and hematoxylin were used for staining; original magnification is ×50.SpecialtyInfectious disease Typesacute, chronic[1]Risk factorsContact with livestock[2]Differential diagnosispneumonia, influenza, brucellosis, leptospirosis, meningitis, viral hepatitis, dengue fever, malaria, other rickettsial infections[2]
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