Recent advances in antitumor vaccines.

S L Hu, I Hellström, K E Hellström
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引用次数: 4

Abstract

Immunization with anti-idiotypic antibodies can induce cell-mediated and humoral antitumor immunity in animal models. This immunity can sometimes cause tumor destruction. However, more needs to be learned about how best to induce the type of immune response that is responsible for tumor destruction, since the presence of anti-idiotypic antibodies has been shown occasionally to enhance, rather than to inhibit, tumor growth. There is evidence suggesting that immunization of human cancer patients with Ab2 can have therapeutic benefit, and also that patients who mount a vigorous Ab2 response following treatment with an Ab1 may do clinically better than those who do not make any Ab2. Although the generation of Ab2 related to infused antitumor Ab1 does not cause tumor rejection in the majority of patients, and although the clinical data from patients given Ab2 are scarce, the suggestion that Ab2 may cause destruction of human cancers indicates that further work in this area may become rewarding.

抗肿瘤疫苗的最新进展。
在动物模型中,抗独特型抗体免疫可诱导细胞介导和体液性抗肿瘤免疫。这种免疫有时会导致肿瘤的破坏。然而,关于如何最好地诱导负责肿瘤破坏的免疫反应类型,还需要了解更多,因为抗独特型抗体的存在已被证明偶尔会增强而不是抑制肿瘤生长。有证据表明,对携带Ab2的人类癌症患者进行免疫接种可能具有治疗益处,并且在使用Ab1治疗后产生强烈Ab2反应的患者可能比不产生Ab2的患者在临床上表现更好。尽管与输注抗肿瘤Ab1相关的Ab2的产生在大多数患者中不会引起肿瘤排斥反应,尽管来自给予Ab2的患者的临床数据很少,但Ab2可能导致人类癌症破坏的建议表明,在这一领域的进一步工作可能是有益的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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