Reibnegger G, Fuchs D, Fuith L C, Hausen A, Werner E R, Werner-Felmayer G, Wachter H
Institute for Medical Chemistry and Biochemistry, University of Innsbruck, Austria.
Cancer Detect Prev. 1991;15(6):483-90.
A review is presented on studies concerning neopterin determination in patients with malignant neoplastic diseases. Neopterin is produced chiefly by human macrophages through their activation by T-cell-derived interferon gamma. In vivo, determinationof neopterin in various body fluids provides a convenient way to monitor early events that are involved in cell-mediated immune responses. In malignant neoplasia, elevation of neopterin concentrations in body fluids depends on tumor type. Within a given type of tumor, more advanced stages are generally associated with higher levels than early disease. In a variety of different tumor types and sites, a significantly poorer prognosis was associated with high pretherapeutic neopterin concentrations. This predictive value is independent of several possible confounders such as stage or therapy. During follow-up malignant disease, neopterin elevations may predict deterioration of the clinical status of the patients and thereby provide a valuable additional marker for monitoring such patients. Possible immunobiological implications of the results are discussed.
本文综述了有关恶性肿瘤疾病患者新蝶呤测定的研究。新蝶呤主要由人类巨噬细胞通过T细胞衍生的γ干扰素激活而产生。在体内,测定各种体液中的新蝶呤为监测细胞介导免疫反应中涉及的早期事件提供了一种便捷的方法。在恶性肿瘤中,体液中新蝶呤浓度的升高取决于肿瘤类型。在给定的肿瘤类型中,较晚期通常比较早期疾病的新蝶呤水平更高。在多种不同的肿瘤类型和部位,治疗前新蝶呤浓度高与预后明显较差相关。这种预测价值独立于一些可能的混杂因素,如分期或治疗。在恶性疾病的随访期间,新蝶呤升高可能预示患者临床状况恶化,从而为监测此类患者提供一个有价值的额外标志物。文中还讨论了这些结果可能的免疫生物学意义。