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首页> 外文期刊>British Journal of Cancer >Cellular Immunity to Encephalitogenic Factor in Man as Measured by the Macrophage Migration Inhibition Test: The Effects of Serum
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Cellular Immunity to Encephalitogenic Factor in Man as Measured by the Macrophage Migration Inhibition Test: The Effects of Serum

机译:巨噬细胞迁移抑制试验测量的人体对脑致病因子的细胞免疫:血清的影响

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摘要

Sensitivity to human encephalitogenic factor (EF) was measured in 70 cancer patients, in 34 patients with various non-malignant diseases and in 18 healthy volunteers, using the macrophage migration inhibition (MMI) test. Sensitization was demonstrated in 44/70 (63%) of the cancer patients, in 11/34 (32%) of the patients with non-malignant conditions and in one (5%) of the healthy individuals. No significant difference was seen in the frequency of demonstrable sensitivity with clinical stage of disease in cancer patients.Autologous serum from cancer patients had the ability to abrogate EF-mediated migration inhibition in 22/30 sensitized individuals. This blocking occurred with a similar frequency in all 3 clinical stages of cancer. Autologous serum from patients with non-malignant disease caused abrogation of EF-mediated migration inhibition in 4/11 sensitized individuals, whilst none of the healthy control individuals showed any significant change in the migration index in the presence of autologous serum. Homologous serum from patients with carcinoma of the breast or lung with and without autologous blocking activity and serum from a healthy individual were tested against lymphocytes from patients with various tumour types with the MMI test. Of 11 patients tested in the absence of serum, 8 (73%) showed significant migration inhibition with EF, whilst serum from patients with carcinoma of the lung or breast with autologous blocking activity abolished migration inhibition with EF in all 8 individuals with the former and in 6 with the latter, regardless of the tumour type from which the lymphocytes under test were derived. Homologous serum from both a carcinoma of the lung and breast without autologous blocking activity did not abolish migration inhibition with EF, except with the latter in one patient with a carcinoma of the lung.
机译:使用巨噬细胞迁移抑制(MMI)测试,在70位癌症患者,34位患有各种非恶性疾病的患者以及18位健康志愿者中测量了对人脑致病因子(EF)的敏感性。在44/70(63%)的癌症患者,11/34(32%)的非恶性疾病患者和一(5%)的健康个体中证实了致敏作用。在癌症患者中,可证明的敏感性与临床分期的频率没有显着差异。来自癌症患者的自体血清具有消除22/30致敏个体中EF介导的迁移抑制的能力。在所有3个临床阶段中,这种阻断的发生频率均相似。来自非恶性疾病患者的自体血清在4/11致敏个体中导致EF介导的迁移抑制被取消,而在存在自体血清的情况下,没有健康对照个体的迁移指数发生任何显着变化。通过MMI测试,对来自具有或没有自体阻断活性的乳腺癌或肺癌患者的同源血清和健康个体的血清进行了抗多种肿瘤类型患者淋巴细胞的检测。在没有血清的情况下测试的11位患者中,有8位(73%)表现出了EF的显着迁移抑制作用,而来自具有自体阻断活性的肺癌或乳癌患者的血清则消除了所有8位前者和EF个体的EF迁移抑制作用。在第6款中,无论后者来自哪种肿瘤,都与受试淋巴细胞的来源无关。来自肺和乳腺的无自体阻断活性的同源血清均不能消除EF对迁移的抑制作用,除非在一名患有肺癌的患者中具有后者。

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