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在双侧大鼠肿瘤内注射免疫刺激剂。

Intra-lesional injection of immunostimulants in bilateral rat tumors.

作者信息

Salomon J C, Galinha A, Lascaux V, Prin J, Puvion F, Lynch N

出版信息

Int J Cancer. 1976 Sep 15;18(3):379-91. doi: 10.1002/ijc.2910180318.

DOI:10.1002/ijc.2910180318
PMID:955748
Abstract

Rats grafted with either two or six fragments of isogenic methylcholanthrene-induced transplantable fibrosarcomas were treated IT1 with living BCG or killed C. parvum or a mixture of both immunostimulants. Various tumor combination and therapeutic agent dosages were compared. When two fragments of the same tumor McFiFi2 (S) were grafted simultaneously, IT treatment of one of these with 2 mg of BCG induced cure of both in 50% of the animals, but IT injection of 2 X 10(9) C. parvum was completely without effect in this situation. The prognosis was however, improved when the dose of immunostimulant was increased. The best results were obtained when each individual tumor in rats with two or six simultaneous identical grafts were treated with a mixture of BCG and C. parvum. The combination of IT immunostimulant treatment and surgical excision of the treated lesion demonstrated a persistence of the curative effect on the remote untreated tumor. Double grafting with isologous non-identical tumors revealed the influence of tumor burden and of the specificity of anti-tumor action of the treatment. The distant specific regression obtained in this system implies a specific immunological mechanism mediated by effector cells and/or antibodies which can circulate, identify the target cell and destroy it. This is in accordance with morphological observations. The intimate contact between BCG and the growing structured tumor is necessary for the therapeutic phenomenon.

摘要

给移植了2个或6个同基因甲基胆蒽诱导的可移植纤维肉瘤片段的大鼠,经腹腔内(IT)注射活卡介苗(BCG)、灭活的微小隐孢子虫(C. parvum)或这两种免疫刺激剂的混合物进行治疗。比较了各种肿瘤组合和治疗剂剂量。当同时移植同一肿瘤McFiFi2(S)的2个片段时,对其中一个经腹腔内注射2毫克卡介苗治疗后,50%的动物中两个肿瘤均治愈,但在此情况下,经腹腔内注射2×10⁹个微小隐孢子虫则完全无效。然而,当免疫刺激剂剂量增加时,预后得到改善。当用卡介苗和微小隐孢子虫的混合物对同时移植2个或6个相同移植物的大鼠中的每个单独肿瘤进行治疗时,获得了最佳结果。经腹腔内免疫刺激剂治疗与对治疗部位进行手术切除相结合,对远处未治疗的肿瘤显示出持续的治愈效果。用异源非同一肿瘤进行双重移植揭示了肿瘤负荷和治疗的抗肿瘤作用特异性的影响。在该系统中获得的远处特异性消退意味着由效应细胞和/或抗体介导的特异性免疫机制,这些效应细胞和/或抗体可以循环、识别靶细胞并将其破坏。这与形态学观察结果一致。卡介苗与生长中的结构化肿瘤之间的密切接触对于治疗现象是必要的。

相似文献

1
Intra-lesional injection of immunostimulants in bilateral rat tumors.在双侧大鼠肿瘤内注射免疫刺激剂。
Int J Cancer. 1976 Sep 15;18(3):379-91. doi: 10.1002/ijc.2910180318.
2
Therapeutic effect of intratumoral injection of bcg and other substances in rats and mice.卡介苗及其他物质瘤内注射对大鼠和小鼠的治疗效果。
Int J Cancer. 1975 Oct 15;16(4):515-25. doi: 10.1002/ijc.2910160402.
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Experimental cancer immunotherapy: comparison of tumor rejection if F344 rats given live Mycobacterium bovis (Strain BCG) and killed Corynebacterium parvum.实验性癌症免疫疗法:给予F344大鼠活牛分枝杆菌(卡介苗菌株)和灭活细小棒状杆菌后肿瘤排斥反应的比较。
J Natl Cancer Inst. 1976 May;56(5):985-9. doi: 10.1093/jnci/56.5.985.
4
Various modalities of local administration of bacterial immunostimulants in transplantable rat tumours and in primitive methylcholanthrene mouse tumours.细菌免疫刺激剂在可移植大鼠肿瘤和原始甲基胆蒽小鼠肿瘤中的各种局部给药方式。
Dev Biol Stand. 1977;38:373-8.
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[Treatment of solid tumours by intratumoral injection of immunostimulants].[通过瘤内注射免疫刺激剂治疗实体瘤]
Ann Immunol (Paris). 1977 Jan-Mar;128(1-2):125-7.
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Comparison of BCG and C. parvum preparations for adjuvant contact therapy of a rat sarcoma.用于大鼠肉瘤辅助接触疗法的卡介苗与微小隐孢子虫制剂的比较。
Dev Biol Stand. 1977;38:39-43.
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Abrogation of antitumor effects of Corynebacterium parvum and BCG by antimacrophage agents: brief communication.抗巨噬细胞药物对短小棒状杆菌和卡介苗抗肿瘤作用的消除:简报
J Natl Cancer Inst. 1977 Dec;59(6):1751-3. doi: 10.1093/jnci/59.6.1751.
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Tumor growth inhibition and potentiation of immunotherapy by indomethacin in mice.吲哚美辛对小鼠肿瘤生长的抑制作用及对免疫疗法的增强作用
J Natl Cancer Inst. 1979 Jan;62(1):117-21.
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Immunotherapy of autochthomous rat methylcholanthrene-induced sarcomas with a mixture of allogeneic tumor cells and BCG-CWS.用同种异体肿瘤细胞与卡介苗细胞壁骨架混合物对大鼠甲基胆蒽诱发的自体肉瘤进行免疫治疗。
Tohoku J Exp Med. 1980 Jan;130(1):49-53. doi: 10.1620/tjem.130.49.
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C. parvum treatment of transplanted rat tumours of spontaneous origin.微小隐孢子虫对自发起源的移植大鼠肿瘤的治疗作用。
Int J Cancer. 1979 Sep 15;24(3):323-8. doi: 10.1002/ijc.2910240309.

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Cancer Immunol Immunother. 1983;15(3):172-7. doi: 10.1007/BF00199160.