Racioppi L, Moscarella A, Ruggiero G, Manzo C, Ferrone S, Fontana S, Zappacosta S
Dipartimento di Biologia e Patologia Cellulare e Molecolare, Università di Napoli, Italy.
J Immunol. 1990 Dec 1;145(11):3635-40.
mAb to monomorphic determinants of HLA class II Ag have been shown to inhibit monocyte-dependent OKT3-induced T cell proliferation, indicating that MHC class II molecules play a regulatory role also in Ag nonrestricted, CD3-induced T cell proliferation. This effect involves several steps in the process of T cell activation and proliferation, including IL-1 beta, IL-6, and IL-2 secretion and IL-2R alpha expression. In the present study, we analyzed the effect of an anti-HLA class II mAb (Q5/6) on the mRNA expression of genes related to monocyte and T cell activation. mRNA levels for early (early c-myc, c-fos) and late (late c-myc, N-ras, c-myb) genes involved in T cell activation were determined as well as mRNA levels for IL-1 beta, IL-6, IFN-gamma, IL-2, and IL-2R alpha. The kinetics of mRNA induction for ICAM-1 was also investigated. The results show that in T lymphocytes the expression of c-fos and early c-myc mRNA was unaffected by mAb Q5/6, whereas the c-myb and N-ras mRNA levels were strongly diminished as well as those of IL-2, IL-2R alpha, and IFN-gamma mRNA. An early increase of ICAM-1 mRNA was partially inhibited. In monocytes, a marked reduction of IL-1 beta and IL-6 mRNA was found. It is concluded that the HLA class II determinant involved in the inhibition mechanism can be engaged in the control of IL-1 beta and IL-6 mRNA levels and constitute an accessory signal up-regulating IL-2 and IL-2R alpha gene activation, through a pathway not affecting c-myc and c-fos expression.
已证明针对人白细胞抗原(HLA)Ⅱ类抗原单态决定簇的单克隆抗体(mAb)可抑制单核细胞依赖性OKT3诱导的T细胞增殖,这表明MHCⅡ类分子在抗原非限制性、CD3诱导的T细胞增殖中也发挥调节作用。这种效应涉及T细胞活化和增殖过程中的几个步骤,包括白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和白细胞介素-2(IL-2)的分泌以及IL-2受体α链(IL-2Rα)的表达。在本研究中,我们分析了一种抗HLAⅡ类mAb(Q5/6)对与单核细胞和T细胞活化相关基因mRNA表达的影响。测定了参与T细胞活化的早期(早期c-myc、c-fos)和晚期(晚期c-myc、N-ras、c-myb)基因的mRNA水平以及IL-1β、IL-6、γ干扰素(IFN-γ)、IL-2和IL-2Rα的mRNA水平。还研究了细胞间黏附分子-1(ICAM-1)mRNA诱导的动力学。结果显示,在T淋巴细胞中,c-fos和早期c-myc mRNA的表达不受mAb Q5/6的影响,而c-myb和N-ras mRNA水平以及IL-2、IL-2Rα和IFN-γ mRNA水平则显著降低。ICAM-1 mRNA的早期增加受到部分抑制。在单核细胞中,发现IL-1β和IL-6 mRNA明显减少。得出的结论是,参与抑制机制的HLAⅡ类决定簇可参与控制IL-1β和IL-6 mRNA水平,并通过一条不影响c-myc和c-fos表达的途径构成上调IL-2和IL-2Rα基因活化的辅助信号。