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肿瘤生长与免疫破坏逃逸:以紫外线诱导的肿瘤为模型

Tumor growth and evasion of immune destruction: UV-induced tumors as a model.

作者信息

Mullen C A, Schreiber H

出版信息

Surv Immunol Res. 1985;4(4):264-70. doi: 10.1007/BF02918734.

Abstract

A number of complex interrelating mechanisms contributing to progressive growth of an immunogenic tumor and its evasion of immune destruction are exemplified in the model of the UV-induced tumor 1591 (fig. 3). The effects of (i) carcinogen-induced immune suppression, (ii) age-related changes in immune competence, (iii) generation and immunoselection of tumor cell variants which do not express target tumor antigen and (iv) tumor-induced immune suppression have been documented. The findings may help to assess the problems and the possibilities of immunotherapy of cancer. The problems reside in the many avenues of escape available to the tumor. The possibilities for immunotherapy derive from the fact that progressively growing tumors may still retain immunogenic antigens and therefore be susceptible to immune attack.

摘要

在紫外线诱导的肿瘤1591模型中(图3),有许多复杂的相互关联机制促成了免疫原性肿瘤的渐进性生长及其对免疫破坏的逃避。已记录到以下几种效应:(i)致癌物诱导的免疫抑制;(ii)免疫能力的年龄相关变化;(iii)不表达靶肿瘤抗原的肿瘤细胞变体的产生和免疫选择;(iv)肿瘤诱导的免疫抑制。这些发现可能有助于评估癌症免疫治疗的问题和可能性。问题在于肿瘤有多种逃避途径。免疫治疗的可能性源于这样一个事实,即逐渐生长的肿瘤可能仍保留免疫原性抗原,因此易受免疫攻击。

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