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本文引用的文献

1
THE PREPARATION OF I-131-LABELLED HUMAN GROWTH HORMONE OF HIGH SPECIFIC RADIOACTIVITY.高比放射性碘-131标记人生长激素的制备
Biochem J. 1963 Oct;89(1):114-23. doi: 10.1042/bj0890114.
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A nonlinear least squares program based on differential equations, MULTI (RUNGE), for microcomputers.基于微分方程的非线性最小二乘程序MULTI(RUNGE),用于微型计算机。
J Pharmacobiodyn. 1983 Aug;6(8):595-606. doi: 10.1248/bpb1978.6.595.
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IgG2a monoclonal antibodies inhibit human tumor growth through interaction with effector cells.IgG2a单克隆抗体通过与效应细胞相互作用抑制人类肿瘤生长。
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Specific and nonspecific macromolecule-drug conjugates for the improvement of cancer chemotherapy.用于改善癌症化疗的特异性和非特异性大分子 - 药物偶联物。
Biopolymers. 1983 Jan;22(1):557-67. doi: 10.1002/bip.360220168.
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Response of cutaneous T cell lymphoma to therapy with hybridoma monoclonal antibody.皮肤T细胞淋巴瘤对杂交瘤单克隆抗体治疗的反应
Lancet. 1981 Aug 1;2(8240):226-30. doi: 10.1016/s0140-6736(81)90475-x.
6
Cytotoxic effect of anti-Mr 67,000 protein immunotoxins on human tumors in a nude mouse model.抗67,000道尔顿蛋白免疫毒素对裸鼠模型中人类肿瘤的细胞毒性作用。
Cancer Res. 1985 Mar;45(3):1328-36.
7
Human immune response to multiple injections of murine monoclonal IgG.人类对多次注射鼠源单克隆IgG的免疫反应。
J Immunol. 1985 Aug;135(2):1530-5.
8
Pharmacokinetics of monoclonal immunoglobulin G1, F(ab')2, and Fab' in mice.小鼠体内单克隆免疫球蛋白G1、F(ab')2和Fab'的药代动力学
Cancer Res. 1986 Aug;46(8):3969-78.
9
A monoclonal antibody against human colon cancers.一种针对人类结肠癌的单克隆抗体。
Tohoku J Exp Med. 1986 Apr;148(4):353-60. doi: 10.1620/tjem.148.353.
10
Biodistribution of methotrexate-monoclonal antibody conjugates and complexes: experimental and clinical studies.甲氨蝶呤-单克隆抗体缀合物与复合物的生物分布:实验与临床研究
Cancer Treat Rev. 1987 Dec;14(3-4):411-20. doi: 10.1016/0305-7372(87)90039-9.

一种单克隆抗体 - 药物偶联物瘤内注射化疗的疗效与特异性

Efficacy and specificity of a monoclonal antibody-drug conjugate in chemotherapy by intratumoral injection.

作者信息

Kitamura K, Takahashi T, Miyagaki T, Yamaoka N, Tsurumi H, Ohtsuji E, Kamiguchi M, Noguchi A, Yamaguchi T

机构信息

First Department of Surgery, Kyoto Prefectural University of Medicine.

出版信息

Jpn J Cancer Res. 1992 Jul;83(7):769-74. doi: 10.1111/j.1349-7006.1992.tb01978.x.

DOI:10.1111/j.1349-7006.1992.tb01978.x
PMID:1387634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5918930/
Abstract

The murine monoclonal antibody (Mab) A7 conjugated to neocarzinostatin (A7-NCS) was injected intratumorally (IT) into tumor bearing nude mice. Its pharmacokinetics and tumoricidal effects were compared in the high, moderate and low antigen expressing xenograft for SW1116, WiDr and KB tumor-bearing nude mice, respectively. When injected IT into nude mice, [125I]A7-NCS was retained in the tumors according to the degree of antigen expression; it was also disseminated into the blood inverse proportion to the antigen expression. Addition of an excess amount of Mab A7 reduced [125I]-A7-NCS accumulation in SW1116 xenograft and elevated the [125I]A7-NCS concentration in the circulation. Complete tumor reduction was found in all 5 mice with SW1116 tumor, and 2 of 5 mice with WiDr tumor. However, only incomplete tumor suppression was observed in mice with the KB tumor. The significant tumor reduction in SW1116 bearing nude mice was attenuated when excess of Mab A7 was simultaneously administered with A7-NCS. These findings indicate that A7-NCS was localized in the target tumors and exerted its tumoricidal effects depending on the degree of antigen-antibody interaction when administered IT. Thus, A7-NCS can be used successfully in vivo for local therapy, auguring new and promising applications for local cancer therapy.

摘要

将与新制癌菌素(A7-NCS)偶联的鼠单克隆抗体(Mab)A7瘤内注射(IT)到荷瘤裸鼠体内。分别在高、中、低抗原表达的SW1116、WiDr和KB荷瘤裸鼠异种移植模型中比较其药代动力学和杀瘤效果。当瘤内注射到裸鼠体内时,[125I]A7-NCS根据抗原表达程度保留在肿瘤中;它也与抗原表达成反比地扩散到血液中。加入过量的单克隆抗体A7可减少[125I]-A7-NCS在SW1116异种移植瘤中的蓄积,并提高循环中[125I]A7-NCS的浓度。在所有5只携带SW1116肿瘤的小鼠和5只携带WiDr肿瘤的小鼠中有2只发现肿瘤完全消退。然而,在携带KB肿瘤的小鼠中仅观察到不完全的肿瘤抑制。当过量的单克隆抗体A7与A7-NCS同时给药时,携带SW1116的裸鼠中显著的肿瘤消退减弱。这些发现表明,A7-NCS在瘤内给药时定位于靶肿瘤,并根据抗原-抗体相互作用程度发挥其杀瘤作用。因此,A7-NCS可成功用于体内局部治疗,为局部癌症治疗带来新的、有前景的应用。