Yefenof E, Gafanovitch I, Oron E, Bar M, Klein E
Lautenberg Center for General and Tumor Immunology, Hebrew University-Hadassah Medical School, Jerusalem, Israel.
Cancer Immunol Immunother. 1995 Dec;41(6):389-96. doi: 10.1007/BF01526559.
Polysaccharide K (PSK) is a biological response modifier used for adjuvant immunotherapy of malignant diseases. We studied the potential applicability of PSK for preventing tumor progression using an experimental model of murine lymphoma. Mice inoculated with the radiation leukemia virus (RadLV) develop thymic lymphomas after a latency of 3-6 months. However, 2 weeks after virus inoculation, prelymphoma cells can already be detected in the thymus. We found that PSK treatment induced hyperresponsiveness to concanavalin A and heightened production of interleukin-2 (IL-2) and IL-4 in spleen cells of both control and prelymphoma mice. The response was transient and was accompanied with a dominant usage of T cells expressing V beta 8, but other T cell subsets were also stimulated by PSK. T lymphoma cells expressing V beta 8.2 underwent apoptosis when incubated with PSK. Treatment of RadLV-inoculated mice with PSK delayed the onset of overt lymphoma (and mortality) but could not protect the mice from the disease. Combined treatment with PSK and a RadLV-specific immunotoxin prevented synergistically the progression of the prelymphoma cells to frank lymphoma. The results suggest that PSK contains a superantigen-like component that selectively activates V beta 8+ T cells. Its administration prelymphoma mice interfered with the process of lymphoma progression.
多糖K(PSK)是一种用于恶性疾病辅助免疫治疗的生物反应调节剂。我们使用小鼠淋巴瘤实验模型研究了PSK在预防肿瘤进展方面的潜在适用性。接种辐射白血病病毒(RadLV)的小鼠在3 - 6个月的潜伏期后会发生胸腺淋巴瘤。然而,在病毒接种后2周,胸腺中就已经可以检测到淋巴瘤前期细胞。我们发现,PSK处理可诱导对照小鼠和淋巴瘤前期小鼠脾细胞对刀豆球蛋白A的高反应性,并提高白细胞介素-2(IL-2)和IL-4的产生。这种反应是短暂的,并且伴随着表达Vβ8的T细胞的优势使用,但其他T细胞亚群也受到PSK的刺激。与PSK一起孵育时,表达Vβ8.2的T淋巴瘤细胞会发生凋亡。用PSK处理RadLV接种的小鼠可延迟明显淋巴瘤(和死亡)的发生,但不能保护小鼠免于患病。PSK与RadLV特异性免疫毒素联合治疗可协同阻止淋巴瘤前期细胞发展为明显的淋巴瘤。结果表明,PSK含有一种超抗原样成分,可选择性激活Vβ8 + T细胞。在淋巴瘤前期小鼠中给予PSK会干扰淋巴瘤的进展过程。