Marriott J B, Clarke I A, Dredge K, Muller G, Stirling D, Dalgleish A G
Division of Oncology, Department of OGEM, St George's Hospital Medical School, London, UK, and Celgene Corporation, Warren, New Jersey, USA.
Clin Exp Immunol. 2002 Oct;130(1):75-84. doi: 10.1046/j.1365-2249.2002.01954.x.
Thalidomide (Thd) is clinically useful in a number of conditions where its efficacy is probably related to its anti-TNF-alpha activity. More recently, Thd has also been shown to co-stimulate T cells and second generation co-stimulatory (IMiD trade mark ) analogues are currently being assessed in the treatment of cancer patients. However, in contrast to their known suppressive effects during inflammatory stimuli, the effects of Thd/IMiDs on TNF-alpha and TNF receptors (TNFRs) during T cell co-stimulation are not known. We sought to determine the effect of Thd, two clinically relevant IMiDs (CC-4047, ACTIMID trade mark and CC-5013, REVIMID trade mark ) and a non-stimulatory SelCID analogue (CC-3052) on TNF-alpha production and on the expression and shedding of TNFRs during co-stimulation. We found that co-stimulation of PBMC with Thd/IMiDs, but not CC-3052, prevented alphaCD3-induced T cell surface expression of TNFR2 and thereby reduced soluble TNFR2 (sTNFR2) levels. However, there was no effect on total (surface/intracellular) TNFR2 protein expression, suggesting inhibition of trafficking to the cell membrane. The extent of co-stimulation by Thd/IMiDs (assessed by CD69/CD25 expression and IL-2/sIL-2Ralpha production) was similar for CD4+ and CD8+ T lymphocytes and correlated with TNFR2 inhibition. Co-stimulation, but not the early inhibitory effect on TNFR2, was IL-2-dependent and led to increased TNF-alpha production by both CD4+ and CD8+ T lymphocytes. The clinical relevance of this observation was confirmed by the elevation of serum TNF-alpha during REVIMID trade mark treatment of patients with advanced cancer. Together, these results suggest a possible role for TNF-mediated events during co-stimulation and contrast with the TNF inhibitory effects of Thd and its analogues during inflammatory stimuli.
沙利度胺(Thd)在许多疾病的治疗中具有临床应用价值,其疗效可能与其抗肿瘤坏死因子-α(TNF-α)活性有关。最近,Thd还被证明可共刺激T细胞,目前正在评估第二代共刺激(IMiD商标)类似物在癌症患者治疗中的作用。然而,与它们在炎症刺激期间已知的抑制作用相反,Thd/IMiDs在T细胞共刺激过程中对TNF-α和TNF受体(TNFRs)的影响尚不清楚。我们试图确定Thd、两种临床相关的IMiDs(CC-4047,ACTIMID商标和CC-5013,REVIMID商标)以及一种非刺激性的SelCID类似物(CC-3052)在共刺激过程中对TNF-α产生以及TNFRs表达和脱落的影响。我们发现,用Thd/IMiDs而非CC-3052共刺激外周血单核细胞(PBMC)可阻止αCD3诱导的TNFR2在T细胞表面的表达,从而降低可溶性TNFR2(sTNFR2)水平。然而,对总(表面/细胞内)TNFR2蛋白表达没有影响,提示对转运至细胞膜的抑制作用。Thd/IMiDs的共刺激程度(通过CD69/CD25表达和IL-2/sIL-2Rα产生评估)在CD4+和CD8+ T淋巴细胞中相似,且与TNFR2抑制相关。共刺激而非对TNFR2的早期抑制作用依赖于IL-2,并导致CD4+和CD8+ T淋巴细胞产生的TNF-α增加。晚期癌症患者接受REVIMID商标治疗期间血清TNF-α升高证实了这一观察结果的临床相关性。总之,这些结果提示TNF介导的事件在共刺激过程中可能发挥作用,这与Thd及其类似物在炎症刺激期间的TNF抑制作用形成对比。