Titlebook: Immunobiology of Proteins and Peptides V; Vaccines Mechanisms, M. Zouhair Atassi Book 1989 Springer Science+Business Media New York 1989 an

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Stable Recombinant Avirulent , Vaccine Strains,l techniques , it is possible to elucidate these mechanisms in biochemical terms as well as to understand the biology by which pathogens accomplish these feats . Once these mechanisms are understood, the information can be used to design novel strategies to immunize the host to prevent infection and

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Cytotoxic and Helper T-Lymphocyte Responses to Antibody Recognition Regions on Influenza Virus Hemaexposed surface areas in the 3-D structure of HA. Using intact X31 virus as the i mmnunogen, we have determined the recognition of these synthetic peptides by proliferative T-helper lymphocytes (ThL) , delayed type hypersensitivity (DTH) , and cytotoxic T-lymphocytes (CTL) responses. The responses t

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The Application of Molecular Biology to the Development of Novel Vaccines,d disease agents, killed organisms, or biochemically isolated subcomponents or subfractions of the disease causing agent. The fact that these classical vaccines are natural products ensured that, if sufficient care were taken (during attenuation, inactivation, or subunit isolation), the important pr

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Studies on the Clonality of the Antibody Response to a Protein Epitope,deed, the field of “vaccinology” has experienced a dramatic surge. Yet, while many preparations, such as hepatis B immunogens, constitute effective vaccines, attempts to prepare effective vaccines against other diseases, such as malaria or AIDS, have encountered formidable difficulties.

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A VH Region Synthetic Peptide Induces Antibodies Which Bind Native Immunoglobulins and Augment an Ibody has been shown to crossreact idiotypically with the phosphorylcholine-binding BALB/c myeloma protein MOPC167 whose Vh shares homology with A48 from residues 32–44. We have synthesized a peptide corresponding to residues 32–44 of the Vh encoded by a germline gene of the VhX24 family. Anti-peptid

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