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聚肌胞苷酸对巨噬细胞诱导的抗原特异性T淋巴细胞增殖的抑制作用:菌株及抗原非依赖性

Inhibition of macrophage-induced antigen-specific T lymphocyte proliferation by poly I:C: strain and antigen independence.

作者信息

Kirschmann D A, Murasko D M

机构信息

Department of Microbiology & Immunology, Medical College of Pennsylvania, Philadelphia 19129.

出版信息

Cell Immunol. 1991 Jun;135(1):16-26. doi: 10.1016/0008-8749(91)90250-f.

Abstract

We have previously demonstrated that IFN-alpha/beta, poly I:C (an inducer of IFN-alpha/beta), and IFN-gamma can inhibit the ability of KLH-pulsed peritoneal macrophages to induce proliferation of syngeneic, KLH immune T lymphocytes in CBA/J mice. In this study, we show that this IFN-induced immunosuppression is not restricted to CBA/J (H-2k) mice but is also seen in BALB/cJ (H-2d) mice. A similar inhibition of proliferation is observed with the KLH-specific T cell hybridoma BDK, 100, which requires KLH-pulsed macrophages for optimum proliferation and IL-2 production. The immunosuppression produced by IFN was also independent of the antigen employed. Inhibition of T lymphocyte proliferation was observed when casein, instead of KLH, was used to immunize T cells and to pulse peritoneal macrophages in vivo. Utilizing KLH and casein, the antigen specificity of the inhibition was demonstrated. Therefore, the inhibition by the IFN-inducer poly I:C of macrophage-induced, antigen-specific T cell proliferation is not limited by H-2 type of the mice or to one antigen.

摘要

我们之前已经证明,干扰素-α/β、聚肌胞苷酸(一种干扰素-α/β诱导剂)和干扰素-γ能够抑制经钥孔血蓝蛋白(KLH)刺激的腹腔巨噬细胞诱导同基因的、对KLH免疫的T淋巴细胞在CBA/J小鼠体内增殖的能力。在本研究中,我们发现这种由干扰素诱导的免疫抑制作用并不局限于CBA/J(H-2k)小鼠,在BALB/cJ(H-2d)小鼠中也能观察到。对于KLH特异性T细胞杂交瘤BDK100也观察到了类似的增殖抑制现象,该杂交瘤需要经KLH刺激的巨噬细胞才能实现最佳增殖和白细胞介素-2的产生。干扰素产生的免疫抑制作用也与所使用的抗原无关。当用酪蛋白而非KLH在体内免疫T细胞并刺激腹腔巨噬细胞时,也观察到了T淋巴细胞增殖受到抑制。利用KLH和酪蛋白,证明了这种抑制作用具有抗原特异性。因此,干扰素诱导剂聚肌胞苷酸对巨噬细胞诱导的、抗原特异性T细胞增殖的抑制作用不受小鼠H-2类型的限制,也不限于一种抗原。

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