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Antigene therapy

Aside from the fact that chemical substances make them sick, some MCS patients also develop allergies and food intolerances. It s best to let yourself be treated by a therapist or doctor who can test for such things. Here, too, avoidance is the best medicine, as opposed to using all sorts of medications intended to suppress the allergic reactions (although in cases of anaphylactic shock, medicine is a matter of life and death ). Allergy and food intolerance treatment now includes a number of methods, such as low-dose antigen therapy (LDA), enzyme-potentiated desensitization (EPD neutralization injections) and the provocation/neutralization method (injections). [Pg.125]

Peptide nucleic acid (PNA) is another analogue of RNA and DNA that has been considered as a potential ancestor of present day nucleic acids. In this molecule the natural sugar-phosphate backbone has been replaced by peptide-like linkages [218]. In recent years, novel syntheses of PNA have been reported mainly focused on their application for antisense and antigene therapies [219]. The physical-chemical properties of PNA make it both... [Pg.58]

Deoxyribonucleotides, deoxyribonucleotide phosphorothioates, modified DNA, and analogs have wide applications in molecular biology, antisense applications, antigene therapy, etc. Three methods are available for the synthesis of oligonucleoside phosphorothioates phosphoramidite, H-phosphonate, and phospho-... [Pg.272]

Cellular therapies in transplantation and cancer are based on specific cells separated or sorted from human blood, bone marrow, or cord blood by means of their specific cell surface markers or cell differentiation antigens, e.g., CD3, CD4, CD8, CD 14, CD 19, and CD34. For example, the CD34+ stem cells, especially those derived from human embryos, have the capacity to differentiate in culture to generate different somatic cells, e.g., liver cells, heart cells, neurons, etc. This exploding field of research is now termed regenerative medicine. [Pg.265]

HBV infection remains a major worldwide public health problem. The World Health Organization estimates that there are still 350 million chronic carriers of the vims, who are at risk of developing chronic hepatitis, liver cirrhosis, and hepatocellular carcinoma. The success of IFN-a treatment - mainly performed as combined treatment with adenine-arabinoside - has been measured by the normalization of liver enzymes, loss of HBe antigen and of detectable viral DNA in the serum of patients. It has been estimated from several clinical trials that as many as 40% of treated HBV patients would respond to therapy with IFN-a or combined treatment with nucleoside analogues and IFN-a. [Pg.645]

Besides the hormone therapy, the notion of targeted cancer therapy is not so new and can be traced back to the 1940 s [2]. Early approaches included the largely unsuccessful use of antibodies, often conjugated with radioisotopes or toxins, directed against tumor-associated antigens. [Pg.1192]

Ferrara N, Damico L, Shams N, et al (2006) Developmemt of Ranibizumab, an anti-vascular endothelial growth factor antigen binding fragment, as therapy for neovascular age-related macular degeneration. Retina 26 859-870... [Pg.1272]

Enomoto M, Tamori A, Kohmoto MT, Hayashi T, Jomura H, Habu D, Sakaguchi H, Takeda T, Kawada N, Seki S, Shiomi S, Koh N, Nishiguchi S (2007) Lamivudine and IFN-beta sequential therapy in HBe antigen-positive patients with chronic hepatitis B virus genotype C infection. J Interferon Cytokine Res 27 201-207... [Pg.232]

Wolters LM, van Nunen AB, Honkoop P, Vossen AC, Niesters HG, Zondervan PE, de Man RA (2000) Lamivudine-high dose interferon combination therapy for chronic hepatitis B patients co-infected with the hepatitis D virus. J Viral Hepat 7 428 34 Wong DK, Cheung AM, O Rourke K, Naylor CD, Detsky AS, Heathcote J (1993) Effect of alpha-interferon treatment in patients with hepatitis B e antigen-positive chronic hepatitis B. A metaanalysis. Ann Intern Med 119 312-323... [Pg.242]

In oncology, to study the relationship between the normal and the tumour cell, to detect tumour-associated antigens (CEA, carcino-embryonic antigen, and AFP, a-fetoprotein) and subsequently to enable cancer therapy to be monitored, to locate tumour metastases, and to deliver cytotoxic drugs, toxins, radionuclides, or liposomes to tumour cells. [Pg.289]


See other pages where Antigene therapy is mentioned: [Pg.487]    [Pg.687]    [Pg.3200]    [Pg.152]    [Pg.487]    [Pg.687]    [Pg.3200]    [Pg.152]    [Pg.524]    [Pg.33]    [Pg.442]    [Pg.171]    [Pg.394]    [Pg.445]    [Pg.226]    [Pg.309]    [Pg.310]    [Pg.313]    [Pg.200]    [Pg.248]    [Pg.433]    [Pg.601]    [Pg.602]    [Pg.11]    [Pg.144]    [Pg.220]    [Pg.235]    [Pg.236]    [Pg.268]    [Pg.268]    [Pg.269]    [Pg.342]    [Pg.343]    [Pg.304]    [Pg.107]    [Pg.130]    [Pg.308]    [Pg.829]    [Pg.137]    [Pg.433]    [Pg.665]   
See also in sourсe #XX -- [ Pg.324 ]




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