Wagner T L, Ahonen C L, Couture A M, Gibson S J, Miller R L, Smith R M, Reiter M J, Vasilakos J P, Tomai M A
Department of Pharmacology, 3M Pharmaceuticals, 3M Center, St. Paul, Minnesota, 55144, USA.
Cell Immunol. 1999 Jan 10;191(1):10-9. doi: 10.1006/cimm.1998.1406.
Cytokines produced by antigen-presenting cells are known to affect the development and cytokine profile of T cells. The immune response modifiers imiquimod and R-848 were previously shown to stimulate human and mouse cultures to secrete interferon-alpha. Results from the present study demonstrate that R-848 and imiquimod are capable of inducing interleukin-12 and interferon-gamma in mouse and human cell cultures. Both CD4(+) and CD8(+) T lymphocytes were responsible for producing IFN-gamma following stimulation with R-848. Macrophages were required for induction of interferon-gamma by R-848 and the cytokines IFN-alpha and IL-12 mediated this response. R-848 and imiquimod were also found to inhibit IL-4 and IL-5 production in mouse and human culture systems. The inhibition of IL-5 in response to R-848 is seen in cultures containing CD4(+) lymphocytes and macrophages and is mediated in part by IFN-alpha. These data suggest that imiquimod and R-848 may have clinical utility in diseases where cell-mediated immune responses are important and in diseases associated with overexpression of IL-4 or IL-5 such as atopic disease.
已知抗原呈递细胞产生的细胞因子会影响T细胞的发育和细胞因子谱。免疫反应调节剂咪喹莫特和R - 848先前已被证明能刺激人和小鼠培养物分泌α干扰素。本研究结果表明,R - 848和咪喹莫特能够在小鼠和人类细胞培养物中诱导白细胞介素-12和γ干扰素。在用R - 848刺激后,CD4(+)和CD8(+) T淋巴细胞均负责产生γ干扰素。R - 848诱导γ干扰素需要巨噬细胞,且α干扰素和白细胞介素-12细胞因子介导了这一反应。还发现R - 848和咪喹莫特在小鼠和人类培养系统中抑制白细胞介素-4和白细胞介素-5的产生。在含有CD4(+)淋巴细胞和巨噬细胞的培养物中可见对R - 848反应时白细胞介素-5的抑制,且部分由α干扰素介导。这些数据表明,咪喹莫特和R - 848在细胞介导的免疫反应起重要作用的疾病以及与白细胞介素-4或白细胞介素-5过表达相关的疾病(如特应性疾病)中可能具有临床应用价值。