Mytar B, Wołoszyn M, Ruggiero I, Pryjma J, Zembala M
Department of Clinical Immunology, Polish-American Institute of Paediatrics, Jagiellonian University Medical College, Cracow, Poland.
Immunol Invest. 1995 Nov;24(6):897-906. doi: 10.3109/08820139509060716.
The question was asked whether tumour necrosis factor alpha (TNF) is involved in regulation of interferon gamma (IFN gamma) production by T cells. Monocytes were exposed to exogenous TNF or to TNF synthesis inhibitors (pentoxifylline, PTX and adriamycin, ADR) and then used as antigen (PPD) presenting cells for autologous T cells. The ability of T lymphocytes to release IFN gamma was assessed after 3 days of culture. Preincubation of monocytes with rTNF enhanced their ability to induce IFN gamma production while TNF synthesis inhibitors decreased it. Anti-TNF and anti-TNF-R2 monoclonal antibodies (mAbs) inhibited monocyte ability to present PPD for IFN gamma production which suggested that endogenously produced TNF by monocytes had to be released and acted on TNF-R2 on the monocyte surface. The enhancing effect of exogenous TNF was also abrogated by anti-TNF-R2 mAb. Pretreatment of monocytes with rTNF enhanced, while pretreatment with PTX decreased, PPD-induced IL-6 production. An increased production of IL-4 was found in cultures of PTX-treated, PPD-pulsed monocytes with T cells. This may indicate that in the relative absence of monocyte costimulatory signal(s), probably IL-6, Th2 cells are stimulated. These results indicate that TNF is involved in control of monocyte-mediated regulation of cytokine production by T cells.
有人提出问题,即肿瘤坏死因子α(TNF)是否参与T细胞对γ干扰素(IFNγ)产生的调节。将单核细胞暴露于外源性TNF或TNF合成抑制剂(己酮可可碱,PTX和阿霉素,ADR),然后用作自体T细胞的抗原(PPD)呈递细胞。培养3天后评估T淋巴细胞释放IFNγ的能力。用rTNF预孵育单核细胞可增强其诱导IFNγ产生的能力,而TNF合成抑制剂则降低该能力。抗TNF和抗TNF-R2单克隆抗体(mAb)抑制单核细胞呈递PPD以产生IFNγ的能力,这表明单核细胞内源性产生的TNF必须释放并作用于单核细胞表面的TNF-R2。抗TNF-R2 mAb也消除了外源性TNF的增强作用。用rTNF预处理单核细胞可增强PPD诱导的IL-6产生,而用PTX预处理则降低该产生。在用PTX处理、PPD刺激的单核细胞与T细胞的培养物中发现IL-4产生增加。这可能表明在相对缺乏单核细胞共刺激信号(可能是IL-6)的情况下,Th2细胞受到刺激。这些结果表明TNF参与了单核细胞介导的T细胞细胞因子产生调节的控制。