Chehimi J, Starr S E, Frank I, Rengaraju M, Jackson S J, Llanes C, Kobayashi M, Perussia B, Young D, Nickbarg E
Division of Infectious Diseases and Immunology, Children's Hospital of Philadelphia, Pennsylvania.
J Exp Med. 1992 Mar 1;175(3):789-96. doi: 10.1084/jem.175.3.789.
Natural killer cell stimulatory factor (NKSF), or interleukin 12 (IL-12), is a heterodimeric lymphokine produced by B cells that has multiple effects on T and NK cell functions. NKSF at concentrations as low as 0.4 pM enhances the spontaneous cytotoxic activity of peripheral blood lymphocytes (PBL) against a variety of tumor-derived target cell lines and virus-infected target cells. The combined treatment of PBL with NKSF and IL-2 results in a less than additive enhancement of cytotoxicity. NKSF enhances the cytotoxic activity of spontaneously cytotoxic CD16+CD5- NK cells and does not confer cytotoxic activity to CD16-CD5+ T cells. PBL from patients infected with human immunodeficiency virus (HIV) have significantly lower cytotoxic activity against tumor-derived target cells and virus-infected target cells than PBL from control healthy donors. Treatment of PBL from HIV-infected patients with NKSF and/or IL-2 results in an increase of NK cell cytotoxicity against both types of target cells to levels similar to or higher than those of untreated PBL from healthy donors. PBL from HIV-infected patients produce interferon gamma in response to NKSF and/or IL-2, although at levels 5- or 10-fold lower than those produced by PBL from healthy donors. The multiple biological effects of NKSF, its activity at very low molar concentrations, and its ability to synergize with other physiological stimuli suggest that NKSF/IL-12 is a lymphokine likely to have physiological importance and considerable therapeutic potential.
自然杀伤细胞刺激因子(NKSF),即白细胞介素12(IL - 12),是一种由B细胞产生的异二聚体淋巴因子,对T细胞和NK细胞的功能具有多种作用。低至0.4 pM浓度的NKSF可增强外周血淋巴细胞(PBL)对多种肿瘤来源的靶细胞系和病毒感染靶细胞的自发细胞毒活性。PBL与NKSF和IL - 2联合处理导致细胞毒性增强程度小于相加效应。NKSF增强自发细胞毒性的CD16 + CD5 - NK细胞的细胞毒活性,而不赋予CD16 - CD5 + T细胞细胞毒活性。感染人类免疫缺陷病毒(HIV)患者的PBL对肿瘤来源的靶细胞和病毒感染靶细胞的细胞毒活性明显低于健康对照供体的PBL。用NKSF和/或IL - 2处理HIV感染患者的PBL可使NK细胞对两种靶细胞的细胞毒性增加至与健康供体未处理的PBL相似或更高的水平。HIV感染患者的PBL对NKSF和/或IL - 2有反应而产生γ干扰素,尽管其水平比健康供体的PBL产生的低5至10倍。NKSF的多种生物学效应、其在极低摩尔浓度下的活性以及与其他生理刺激协同作用的能力表明,NKSF/IL - 12是一种可能具有生理重要性和相当大治疗潜力的淋巴因子。