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Titlebook: Vaccines; New Generation Immun Gregory Gregoriadis,Brenda McCormack,Anthony C. Al Book 1995 Plenum Press, New York 1995 Antigen.Hepatitis.d

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樓主: Goiter
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發(fā)表于 2025-3-23 10:24:13 | 只看該作者
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發(fā)表于 2025-3-24 00:20:47 | 只看該作者
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發(fā)表于 2025-3-24 04:20:25 | 只看該作者
Synthetic Peptide Vaccines: Success at Last,sport. Peptide vaccines have the advantage that they can be produced in a completely reproducible manner, they are cheap compared to subunit or whole protein vaccines and potentially they can be precisely targeted to meet specific demands. For instance, peptide vaccines may be used to break maternal
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發(fā)表于 2025-3-24 07:13:44 | 只看該作者
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發(fā)表于 2025-3-24 13:47:55 | 只看該作者
Genetic Restriction of Responses to Peptide Antigens,ce long term protective immunity in the host. Whilst in most, if not all, cases these will be complex and multifactorial it is clearly necessary to identify the key immunogens required for the vaccine. In the case of peptide vaccines these immunogens will be the B-cell and T-cell epitopes which when
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發(fā)表于 2025-3-24 16:39:27 | 只看該作者
DNA-Based Immunization: Prospects For a Hepatitis B Vaccine,ces in the form of either DNA or RNA. To date, most examples of nucleic acid-based immunization have used DNA encoding a polypeptide sequence, thus the subsequent discussion will be restricted to DNA-based immunization (for an example of an RNA-based vaccine, see Martinon et al., 1993). Administrati
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發(fā)表于 2025-3-24 22:40:07 | 只看該作者
Characterization of Immune Responses Elicited by an Experimental Facilitated-DNA Vaccine for Human operate by inducing immune responses in the host that limit and ultimately clear infections; they typically do not prevent infections from occurring. Vaccine efficacy is therefore, dependent on the induction of appropriate types of immune responses and on the establishment of immunological memory.
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發(fā)表于 2025-3-25 00:03:50 | 只看該作者
Recombinant Self-Replicating RNA Vaccines, reticulum (ER), where they associate with class I molecules of the major histocompatibility complex (MHC) and are then transported to the cell surface for recognition by CD8+ cytotoxic T lymphocytes (CTLs). Extra-cellular antigens such as virus particles or soluble protein subunits are degraded int
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