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Infection Mediator

DNA vimses can regulate the activity of cellular acetyltransferases and to effect cell cycle progression in support of virus replication. Viral infection mediated... [Pg.200]

Malmborg A-C, Soderlind E, Frost L, Borrebaeck CAK, Selective phage infection mediated by epitope expression on F pilus, J. Mol. Biol., 273 544-551, 1997. [Pg.465]

Arita, M., Horie, H., Arita, M., and Nomoto, A. (1999). Interaction of poliovirus with its receptor affords a high level of infectivity to the virion in poliovirus infections mediated by the Fc receptor. J. Virol. 73, 1066-1074. [Pg.446]

Interest in the adhesion of dosage forms to epithelial surfaces has heen aroused hy the possihility of deliberate contact between oral dosage forms and the gut wall to retard the rate of transit down the gastrointestinal tract, but also by the possibility of dosage forms accidentally adhering to the oesophagus or other epithelial surfaces. Adhesive preparations have been formulated for diverse tasks such as the topical treatment of stomatitis and the administration of insulin. The adhesive nature of transdermal patches is important, as is the adhesion of film coats to tablet surfaces. Adhesion of erythrocytes and bacterial cells to polymer surfaces is also of importance in the understanding, respectively, of blood compatibility of polymers and bacterial infection mediated by catheters. [Pg.472]

One more item to consider is that the dysfunctional HPA axis can lead to the decrease in plasma levels of DHEA and DHEA sulfate, DHEAS. Such conditions are associated with the above described mental states. Conversely, increased levels of DHEA, by antagonizing glucocorticoid s antiimmunosuppressivo properties, provides the body with protection against viral or infection-mediated degenerative diseases. In general, high levels of cortisol and depressed serum concentrations of DHEAS are associated with serious illnesses. [Pg.384]

The CXCR4 molecules of the mouse (90% amino acid identity with human CXCR4), rat (>90% identity), cat (94.9% identity), and rhesus macaque (98.3% identity) have all been shown to support fusion or infection mediated by at least some T-tropic HIV strains (13,46-52). Brelot et al. (46) further showed that, in the context of a rat CXCR4 chimera. [Pg.283]

Pneumogstis carini pneumonia (PCP), the most common of the opportunistic infections, occurs in more than 80% of AIDS patients (13). Toxoplasmosis, a proto2oan infection of the central nervous system, is activated in AIDS patients when the 004 count drops and severe impairment of ceU-mediated immunity occurs. Typically, patients have a mass lesion(s) in the brain. These mass lesions usually respond well to therapy and can disappear completely. Fungal infections, such as CTyptococcalmeningitis, are extremely common in AIDS patients, and Histop/asma capsulatum appears when ceU-mediated immunity has been destroyed by the HIV vims, leading to widespread infection of the lungs, Hver, spleen, lymph nodes, and bone marrow. AIDS patients are particularly susceptible to bacteremia caused by nontyphoidal strains of Salmonella. Bacteremia may be cleared by using antibiotic therapy. [Pg.33]

Interferons (lENs) (52,53), a family of species-specific vertebrate proteins, confer nonspecific resistance to a broad range of viral infections, affect cell proliferation, and modulate immune responses. AH three principal interferons, a-interferon (lEN-a) produced by blood leucocytes, P-interferon (lEN-P) by fibroblasts, and y-interferon (lEN-y) by lymphocytes, also have antiviral activity. The abiUty of interferons to inhibit growth of transplantable and carcinogen-induced tumor led to research showing the direct antiproliferative and indirect immune-mediated antitumor activities (see Chemotherapeutics, anticancer). IENs have been found to be efficacious in certain malignancies and viral infections, eg, hairy cell leukemia (85% response) and basal cell carcinoma (86% response). However, the interferons do have adverse side effects (54). [Pg.40]

The deterrnination of the presence of reverse transcriptase in vims-infected cells can be done using labeled nucleotide triphosphates. Reverse transcriptase is an enzyme capable of synthesizing DNA from RNA and it is thought to play an important role in vims-mediated cell modification. This enzyme is also a marker enzyme for HIV, the vims impHcated in causing acquired immunodeficiency syndrome (AIDS). The procedure utilizes radiolabeled nucleotides with nonlabeled substrates to synthesize tagged DNA. The degree of radioactive incorporation reflects the reverse transcriptase activity. [Pg.440]

Chemical-mediated immune suppression has been identified from the experimental study of several wildlife species. Harbour seals fed either chemically contaminated fish from the Wadden Sea or imcontaminated fish were found to have differing immune responses, with the exposed group showing lowered immune response to microbial infections and certain types of cancer. "" Mink fed fish taken from below a discharge point for bleached Kraft pulp mill effluent have also shown impaired immune function, " showing that the non-accnmillative chemicals in this effluent can actively disrupt endocrine associated functions. [Pg.74]

Human bodies are constantly exposed to a plethora of bacteria, viruses, and other inflammatory substances. To combat these infections and toxic agents, the body has developed a carefully regulated inflammatory response system. Part of that response is the orderly migration of leukocytes to sites of inflammation. Leukocytes literally roll along the vascular wall and into the tissue site of inflammation. This rolling movement is mediated by reversible adhesive interactions between the leukocytes and the vascular surface. [Pg.283]

Table 2 summarizes current ASON-mediated therapies against viral infections. [Pg.188]

Parallel to orchestrating acute inflammatory processes by providing an optimal milieu of cytokines, mediators, and adhesion molecules in order to recruit and activate effector cells to the site of infection, dendritic cells also setve as professional antigen-presenting cells for cells of the adaptive immune system ( antigen presentation ... [Pg.614]


See other pages where Infection Mediator is mentioned: [Pg.342]    [Pg.183]    [Pg.247]    [Pg.581]    [Pg.1398]    [Pg.366]    [Pg.274]    [Pg.369]    [Pg.342]    [Pg.183]    [Pg.247]    [Pg.581]    [Pg.1398]    [Pg.366]    [Pg.274]    [Pg.369]    [Pg.33]    [Pg.427]    [Pg.430]    [Pg.496]    [Pg.360]    [Pg.9]    [Pg.62]    [Pg.182]    [Pg.73]    [Pg.421]    [Pg.422]    [Pg.6]    [Pg.196]    [Pg.265]    [Pg.267]    [Pg.331]    [Pg.345]    [Pg.404]    [Pg.531]    [Pg.612]    [Pg.627]    [Pg.639]    [Pg.640]    [Pg.641]    [Pg.643]    [Pg.643]    [Pg.644]    [Pg.974]   
See also in sourсe #XX -- [ Pg.45 ]




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