Kariya Y, Inoue N, Kihara T, Okamoto N, Sugie K, Mori T, Uchida A
Department of Late Effect Studies, Kyoto University, Japan.
Immunol Lett. 1992 Feb 15;31(3):241-5. doi: 10.1016/0165-2478(92)90121-4.
The protein-bound polysaccharide PSK was tested for the ability to activate human natural killer (NK) cells. When blood lymphocytes and purified CD3-CD16+ large granular lymphocytes (LGL) were treated in vitro overnight with PSK, they demonstrated enhanced NK cell activity against K562. The PSK-activated killer cells also lysed NK-resistant targets and freshly isolated autologous and allogeneic tumor cells. The PSK effect was observed with concentrations that could be obtained in the blood of cancer patients receiving oral administration of PSK. PSK-induced enhancement of NK activity was not abrogated by monoclonal antibodies (mAb) that neutralized interferon (IFN) alpha, IFN gamma, or interleukin-2 (IL-2). In addition, mAb reactive with p55 (alpha chain) or p75 (beta chain) glycoproteins of IL-2 receptors had no effects on PSK-enhanced NK activity even when used simultaneously. These results indicate that the PSK could activate human NK cells independently of IFN and IL-2/IL-2R systems.
对蛋白结合多糖PSK激活人类自然杀伤(NK)细胞的能力进行了测试。当血液淋巴细胞和纯化的CD3-CD16+大颗粒淋巴细胞(LGL)在体外与PSK一起处理过夜时,它们对K562的NK细胞活性增强。PSK激活的杀伤细胞也能裂解NK抗性靶标以及新鲜分离的自体和同种异体肿瘤细胞。在接受口服PSK的癌症患者血液中可达到的浓度下观察到了PSK的作用。PSK诱导的NK活性增强不会被中和干扰素(IFN)α、IFNγ或白细胞介素-2(IL-2)的单克隆抗体(mAb)消除。此外,与IL-2受体的p55(α链)或p75(β链)糖蛋白反应的mAb即使同时使用也对PSK增强的NK活性没有影响。这些结果表明,PSK可以独立于IFN和IL-2/IL-2R系统激活人类NK细胞。