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Titlebook: Anti-Idiotypic Vaccines; P.-A. Cazenave Book 1991 Springer-Verlag New York Inc. 1991 Antigen.cell.genes.parasite.parasites.research.vaccin

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樓主: lumbar-puncture
21#
發(fā)表于 2025-3-25 03:47:07 | 只看該作者
22#
發(fā)表于 2025-3-25 09:16:00 | 只看該作者
Einführung in die Kryptographiestimulation of the lymphocyte clones, which have the potential to mount a response to tumor-associated antigens (TAAs) (1) or due to suppression of cytotoxic T lymphocyte activity by progressive tumor growth (2). A common explanation for the absence of antitumor immunity is that the immune system ha
23#
發(fā)表于 2025-3-25 11:55:45 | 只看該作者
Einführung in die Kryptographie, there are still instances in which suitable vaccines are lacking. For example, the inability to culture large quantities of numerous protozoal pathogens in vitro has prevented the development of conventional vaccines for these organisms. Other obstacles to the development of conventional vaccines
24#
發(fā)表于 2025-3-25 16:06:36 | 只看該作者
Einführung in die Kryptographieathology. We will describe our work in two different viral systems. First we review our studies of the reovirus type 3 system. We have utilized the reovirus type 3—cellular receptor interaction as a model system to develop such a strategy. We demonstrate the utility of monoclonal anti-idiotypic (ant
25#
發(fā)表于 2025-3-25 21:07:39 | 只看該作者
26#
發(fā)表于 2025-3-26 03:02:15 | 只看該作者
https://doi.org/10.1007/978-3-540-74452-8d is based on the property that antibodies can be immunogenic (3). This has been demonstrated in heterologous (4), homologous (3), syngeneic (5), and autologous (6) systems. Historically, the existence of immunoglobulin molecules related to antigenic determinants, not by fitting them but rather by r
27#
發(fā)表于 2025-3-26 07:51:41 | 只看該作者
Progress in Vaccinologyhttp://image.papertrans.cn/a/image/158337.jpg
28#
發(fā)表于 2025-3-26 11:15:40 | 只看該作者
29#
發(fā)表于 2025-3-26 15:55:39 | 只看該作者
30#
發(fā)表于 2025-3-26 18:25:12 | 只看該作者
Einführung in die Kryptographieis method may be effective in breaking tumor antigen-induced tolerance by presenting the critical TAA epitope in a different molecular environment to the tolerized host (8) and may thus break tolerance in tumor-specific immunity. Furthermore, the anti-Id antibodies, the so-called . (7), are the most
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