Ngu V A, Titanji V P, Muna D, Nyoth J, Lekeuagni C, Yaoundé C
J Natl Med Assoc. 1981 Oct;73(10):927-37.
It has been proposed that the elimination of excess scar tissue from the body is achieved by specialized killer cells, which are activated by vascular changes in the scar tissue. The malignant tumor is, according to this theory, considered to be a special type of excess scar tissue of fetal or near fetal age, the fetal blood supply of which prevents the activation of those specialized killer cells which were believed to eliminate excess scar tissue. Therefore, it is assumed that if the specialized killer cells of a malignant tumor patient are activated artificially, they would cause malignant tumor regression in vivo. This method of treatment is called autobiotherapy because it utilizes biological products from the patient to treat his own malignant tumor. Preliminary evidence is presented in support of autobiotherapy of malignant tumor disease.The peripheral leucocytes of 27 malignant tumor patients were activated separately by incubation in a serum-free medium containing the respective tumor cells or material. The effect of the injection of the activated leucocytes or their products, termed tumor leucocyte cultures (TLC), was studied in five patients with Kaposi sarcoma, five with carcinoma of the breast, four with carcinoma of the cervix, three with soft tissue sarcoma, two with carcinoma of the lung, two with carcinoma of the maxillary antrium, and a miscellaneous group of six patients. In 52 percent of cases, there was significant tumor regression. Tumor regression was most marked in patients with Kaposi sarcoma, carcinoma of the cervix, pharynx, and pancreas, one patient with a slow growing fibrosarcoma, one patient with a metastatic breast carcinoma, and also in one patient with myelogenous leukemia. However, not all the types of tumor studied responded satisfactorily to autobiotherapy. The reasons for the differences in response to autobiotherapy remain to be determined. Even so, the positive results obtained indicate that autobiotherapy is worthy of further research as an alternative in controlling malignant tumor disease.
有人提出,身体中多余瘢痕组织的清除是由特殊的杀伤细胞完成的,这些细胞被瘢痕组织中的血管变化激活。根据这一理论,恶性肿瘤被认为是胎儿期或接近胎儿期的一种特殊类型的多余瘢痕组织,其胎儿血液供应阻止了那些被认为能清除多余瘢痕组织的特殊杀伤细胞的激活。因此,假定如果人工激活恶性肿瘤患者的特殊杀伤细胞,它们将在体内导致恶性肿瘤消退。这种治疗方法被称为自体疗法,因为它利用患者自身的生物制品来治疗其自身的恶性肿瘤。文中给出了支持恶性肿瘤疾病自体疗法的初步证据。27例恶性肿瘤患者的外周血白细胞分别在含有相应肿瘤细胞或物质的无血清培养基中孵育而被激活。对5例卡波西肉瘤患者、5例乳腺癌患者、4例宫颈癌患者、3例软组织肉瘤患者、2例肺癌患者、2例上颌窦癌患者以及6例其他类型患者组成的混合组,研究了注射激活的白细胞或其产物(称为肿瘤白细胞培养物,TLC)的效果。在52%的病例中,出现了明显的肿瘤消退。肿瘤消退在卡波西肉瘤、宫颈癌、咽癌和胰腺癌患者中最为显著,在1例生长缓慢的纤维肉瘤患者、1例转移性乳腺癌患者以及1例骨髓性白血病患者中也很明显。然而,并非所有研究的肿瘤类型对自体疗法都有令人满意的反应。对自体疗法反应差异的原因尚待确定。即便如此,所获得的阳性结果表明,自体疗法作为控制恶性肿瘤疾病的一种替代方法值得进一步研究。