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Titlebook: Combination Therapies 2; Biological Response Enrico Garaci,Allan L. Goldstein Book 1993 Springer Science+Business Media New York 1993 AIDS

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Raj Senani,D. R. Bhaskar,R. K. Sharmact than single treatments (1–4) The rationale of this new approach stems from the observations that immune physiologic responses involve cascades and feedback networks in which the release of one cytokine modulate both cytokine and cytokine-receptor production. Moreover, combination of BRMs could affect different immune effector cells.
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Effect of Thymosin α 1 on Cocaine-Induced Inhibition of T-Cell Dependent Murine Immune Responsen by mitogens.. Phagocitic activity of peritoneal macrophages was inhibited by a single injection of cocaine, while short term administration induced a significant reduction of spleen and thymus weight..
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ans in this area to discuss new and emerging uses for biological response modifiers (BRM‘s) in the treatment of cancer and infectious diseases. The meeting was held during May 1-3, 1992 in Acireale, Sicily (Italy). It was hosted by Professor G. Nicoletti CU. of Catania) and organized by the Institut
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Tumor Immunogenicity Induced by the Local Occurrence of Il-2through the local release of cytokines and chemotactic factors. means that spontaneous tumors are often found to be heavily infiltrated by leukocytes of several kind. It is uncertain, however, whether the reactive infiltrate impedes the growth of a tumor or is of prognostic significance..
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Regulation of Gene Expression by Interferonsticular we will focus on some characteristics of cis-acting DNA elements that are located upstream from the initiation site for RNA transcription and of nuclear transacting factors that are required for modulation of gene expression by IFNs.
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W. Baiker,E. v. Czako,M. Keck,G. NehmizThymosin α., is a 28 amino acid, 3108 molecular weight acidic peptide isolated from thymosin fraction 5 (1). Its amino acid sequence is homologous in murine, bovine and human species (2) and a chemically synthesized version (3) has shown activity similar to the native peptide in modulating T-cell maturation (1).
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