de Wit R, Bakker P J, Reiss P, Hoek F J, Lange J M, Goudsmit J, Veenhof K H
Department of Medicine, Academic Medical Center, Amsterdam, The Netherlands.
AIDS. 1990 May;4(5):459-62. doi: 10.1097/00002030-199005000-00013.
Beta 2-microglobulin (beta 2-M) levels were determined in the serum of 24 patients treated with high-dose human recombinant interferon-alpha (IFN alpha) for AIDS-associated Kaposi's sarcoma. There was a significant increase in serum beta 2-M levels, irrespective of the response to treatment. However, the increase of serum beta 2-M levels in responders appeared to be more pronounced than in those with progressive disease, but this difference was not significant. The increase was only found during the initial 8 weeks; thereafter, beta 2-M levels declined in patients with continuing clinical improvement during ongoing treatment with IFN alpha. This may have been related to IFN alpha dose modification at 8 weeks for all patients. The initial rise in serum beta 2-M might be related to the immunomodulation properties of IFN alpha. Because serum beta 2-M levels were also enhanced in non-responders, this rise does not demonstrate that immunomodulation by IFN alpha is a mechanism of anti-tumour activity in AIDS-associated Kaposi's sarcoma.
测定了24例接受大剂量重组人α干扰素(IFNα)治疗艾滋病相关卡波西肉瘤患者血清中的β2微球蛋白(β2-M)水平。无论治疗反应如何,血清β2-M水平均显著升高。然而,反应者血清β2-M水平的升高似乎比疾病进展者更为明显,但这种差异并不显著。升高仅在最初8周内出现;此后,在持续使用IFNα治疗期间临床持续改善的患者中,β2-M水平下降。这可能与所有患者在8周时调整IFNα剂量有关。血清β2-M最初的升高可能与IFNα的免疫调节特性有关。由于无反应者的血清β2-M水平也升高,因此这种升高并不能证明IFNα的免疫调节是艾滋病相关卡波西肉瘤抗肿瘤活性的一种机制。