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突尼斯快速进展型乳腺癌病因中细胞免疫和遗传学作用的研究。

Studies on the role of cellular immunity and genetics in the etiology of rapidly progressing breast cancer in Tunisia.

作者信息

Levine P H, Mourali N, Tabbane F, Loon J, Terasaki P, Tsang P, Bekesi J G

出版信息

Int J Cancer. 1981 May 15;27(5):611-5. doi: 10.1002/ijc.2910270507.

Abstract

It has been suggested that poussée évolutive (PEV) or rapidly progressing breast cancer (RPBC) represents a failure in the host immune system to control the proliferation of breast cancer cells. To evaluate this possibility, we have performed in vivo and in vitro assays of cellular immunity in Tunisian patients with breast cancer. Studies of delayed hypersensitivity using microbial antigens and in vitro including lymphocyte transformation tests and measurements of B and T cells indicated that RPBC patients had an immune response comparable to that of breast cancer patients without evidence of rapid progression. Normal Tunisians were more immunocompetent, however, an appeared to have a higher level of immune activity than normal individuals in the United States. In a second, independent series, an increased frequency of blood group A was found in RPBC patients, suggesting a genetic predisposition to this form of breast cancer. However HLA typing for A, B and DRW antigens revealed no specific RPBC-associated HLA antigen. Our studies clearly demonstrate that RPBC, or PEV, is not a reflection of immunodeficiency.

摘要

有人提出,进展性突发(PEV)或快速进展性乳腺癌(RPBC)代表宿主免疫系统在控制乳腺癌细胞增殖方面的失败。为了评估这种可能性,我们对突尼斯乳腺癌患者进行了体内和体外细胞免疫测定。使用微生物抗原进行的迟发型超敏反应研究以及包括淋巴细胞转化试验和B细胞与T细胞测量在内的体外研究表明,RPBC患者的免疫反应与无快速进展证据的乳腺癌患者相当。然而,突尼斯正常人的免疫能力更强,而且似乎比美国的正常人具有更高水平的免疫活性。在第二个独立系列研究中,发现RPBC患者中血型A的频率增加,提示对这种形式的乳腺癌存在遗传易感性。然而,对A、B和DRW抗原进行的HLA分型未发现与RPBC相关的特异性HLA抗原。我们的研究清楚地表明,RPBC或PEV并非免疫缺陷的反映。

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