Immune response functions

Briefly, lactotransferrin has been shown to be involved in numerous inflammatory events (for reviews, see refs. [179,180]) and in immune response functions such as regulation of granulocyte monocyte colony stimulating factor synthesis with suppression of myelopoiesis by inhibition of the production of IL-1 (for a review, see ref [181]),... 

Adjuvants are substances which can modify the immune response of an antigen (139,140). With better understanding of the functions of different arms of the immune system, it is possible to explore the effects of an adjuvant, such that the protective efficacy of a vaccine can be improved. At present, aluminum salt is the only adjuvant approved for use in human vaccines. New adjuvants such as QS-21, 3D-MPL, MF-59, and other liposome preparations are being evaluated. Several of these adjuvants have been in clinical trial, but none have been approved for human use. IL-12 has been proposed as an adjuvant which can specifically promote T-helper 1 ceU response, and can be a very promising adjuvant for future vaccine development. 

Insufficient zinc results in slowed growth, delayed wound healing, poor appetite, mental lethargy, and sexual immaturity and it interferes with the immune response. The main function of zinc in metaboHsm is enzymatic and there is evidence of other physiologic roles, eg, in stabilization of membrane stmcture (57). 

Erythrocyte Entrapment of Enzymes. Erythrocytes have been used as carriers for therapeutic enzymes in the treatment of inborn errors (249). Exogenous enzymes encapsulated in erythrocytes may be useful both for dehvery of a given enzyme to the site of its intended function and for the degradation of pathologically elevated, diffusible substances in the plasma. In the use of this approach, it is important to determine that the enzyme is completely internalized without adsorption to the erythrocyte membrane. Since exposed protein on the erythrocyte surface may ehcit an immune response following repeated sensitization with enzyme loaded erythrocytes, an immunologic assessment of each potential system in animal models is required prior to human trials (250). 

The mammalian and avian immune systems function similarly both incorporate humoral and cell-mediated cytotoxic mechanisms, " and are thought to share a 160m year old relationship with the reptilian immune system. The immune system of mammals shows sexual dimorphism " a greater immune response is normally observed in females, which has been attributed to differences in steroid hormone concentration. In the toad Bufo regularis, sexual dimorphism of the immune system is also apparent. ... 

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. 

Birds. In avian populations, organochlorine-associated suppression of T-cell mediated immune response has been found in herring gull and Caspian tern colonies adjacent to the Great Lakes in Northern America.In the most severe cases, immune response was suppressed by up to 50%. Similarly, seabirds exposed to petrochemicals from oil spills have been found to have suppressed immune function. " ... 

However, not all EDs with a high log possess or require the ability to bioaccnmulate in order to be biologically active. For example, phthalate plasticisers, chlorophenols from Kraft mill effluents and natural or synthetic hormones can influence an organism s hormone profile and affect reproductive function and immune response without exhibiting bioaccnmiilation. ... 

Cellular cytokines (interferons, G-CSF) and immune response modifiers originally produced from human cells, most often leukocytes, have now been replaced with recombinant products with well-defined structure/function. Futuristic advances in experimental hematology portend development of human blood cells produced from the hemopoetic stem cells. Yet for the foreseeable future, homologous blood donated by healthy, altruistic voluntary blood donors remains the principal source of safe and adequate supply of blood and blood products for transfusion therapy. 

Originally described in the immune system, NFAT proteins comprise a family of transcriptional factors that play key roles in many cellular processes that control not only immune responses but also the development, regulation, and differentiation of many other tissues. Activation of NFAT proteins results in the expression of specific sets of genes that regulate multiple cell functions [1,2]. 

NF-kB regulates both innate and adaptive immune responses ( immune defense) [2]. Understanding the function of NF-kB in the development, maintenance, and activation of cells from the immune system (including hematopoietic cells, macrophages, dendritic cells, B and T lymphocytes) has greatly benefited from the analysis of knockout mice in which individual NF-kB family members were defective. 

The glucocorticoids influence or regulate functions such as the immune response system, the regulation of glucose, fat and protein metabolism, and control of the anti-inflammatory response. Table 50-1 describes the activity of the glucocorticoids within the body. 

Immimological Effects—Functional changes in the immune response. 

Immunotoxicity. Limited information is available regarding the effects of endosulfan on the human immune system. However, specially designed studies using rats indicate that both humoral and cellular immune responses are depressed by ingested endosulfan at doses that do not induce any overt signs of toxicity (Banerjee and Hussain 1986,1987). In vitro studies support the possibility that endosulfan affects immune system function (Das et al. 1988). These results demonstrate that immunotoxicity may be a more sensitive end point of endosulfan-induced toxicity than other end points, and humans may be at risk for adverse immune effects following exposure to endosulfan. An intermediate-duration oral MRL was derived based on the observation of depressed immune responses (Banerjee and Hussain 1987). 

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