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乙内酰脲免疫抑制作用与致癌作用。

Hydantoin immunosuppression and carcinogenesis.

作者信息

Levo Y, Markowitz O, Trainin N

出版信息

Clin Exp Immunol. 1975 Mar;19(3):521-7.

Abstract

The immunological response of mice submitted to hydantoin treatment was determined. Hydantoin reduced the absolute number of spleen cells in treated animals and did not modify spleen cells reactivity to concanavalin A, although the response to SRBC challenge, as measured by the Jerne plaque-forming cell technique, was significantly decreased. Following these findings, the influence of hydantoin on carcinogenesis was evaluated by using the model of urethane-induced lung adenomas in SWR mice. Treatment with hydantoin significantly reduced the incidence of the induced adenomas. We confirmed that hydantoin modifies the immune response of the host mainly by depressing its humoral function and we have shown that this effect was associated with an inhibitory effect on tumour induction.

摘要

测定了接受乙内酰脲治疗的小鼠的免疫反应。乙内酰脲减少了经治疗动物脾脏细胞的绝对数量,且未改变脾脏细胞对刀豆球蛋白A的反应性,不过通过耶尔恩空斑形成细胞技术测定,对SRBC攻击的反应显著降低。基于这些发现,利用SWR小鼠中尿烷诱导的肺腺瘤模型评估了乙内酰脲对致癌作用的影响。乙内酰脲治疗显著降低了诱导腺瘤的发生率。我们证实乙内酰脲主要通过抑制宿主的体液功能来改变其免疫反应,并且我们已经表明这种作用与对肿瘤诱导的抑制作用有关。

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1
IMMUNOLOGICAL FACTORS IN THE PROCESS OF CARCINOGENESIS.致癌过程中的免疫因素
Br Med Bull. 1964 May;20:154-8. doi: 10.1093/oxfordjournals.bmb.a070310.
4
Immunological abnormalities and hydantoins.免疫异常与乙内酰脲类药物
Br Med J. 1972 Jun 3;2(5813):561-3. doi: 10.1136/bmj.2.5813.561.
5
The immune reaction as a stimulator of tumor growth.作为肿瘤生长刺激因素的免疫反应。
Science. 1972 Apr 14;176(4031):170-1. doi: 10.1126/science.176.4031.170.
6
Hydantoin-induced pseudo-pseudolymphoma.
Ann Intern Med. 1968 Sep;69(3):557-68. doi: 10.7326/0003-4819-69-3-557.
8
Immunological enhancement as studied by cell culture techniques.通过细胞培养技术研究免疫增强作用。
Annu Rev Microbiol. 1970;24:373-98. doi: 10.1146/annurev.mi.24.100170.002105.
9
Cellular immunity against tumor antigens.针对肿瘤抗原的细胞免疫。
Adv Cancer Res. 1969;12:167-223. doi: 10.1016/s0065-230x(08)60331-0.
10
Potential hazards of hydantoin use.
Ann Intern Med. 1972 Dec;77(6):998-9. doi: 10.7326/0003-4819-77-6-998.

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