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抗小鼠白细胞介素-6受体抗体对小鼠免疫反应的影响。

Influences of anti-mouse interleukin-6 receptor antibody on immune responses in mice.

作者信息

Mihara Masahiko, Nishimoto Norihiro, Yoshizaki Kazuyuki, Suzuki Takashi

机构信息

Fuji-Gotemba Research Laboratories, Chugai Pharmaceutical Co. Ltd., 135, Komakado 1-chome, Gotemba-shi, Shizuoka 412-8513, Japan.

出版信息

Immunol Lett. 2002 Dec 3;84(3):223-9. doi: 10.1016/s0165-2478(02)00201-8.

Abstract

In the present study, we examined the effect of anti-IL-6 receptor antibody (MR16-1) on humoral and cellular immune responses in mice. MR16-1 did not affect antigen-specific antibody production in either the primary or secondary response in mice immunized with dinitro-phenyl (DNP)-keyhole limpet haemocyanin (KLH) in saline. DNP-KLH immunization with complete Freund's adjuvant (CFA) markedly augmented anti-DNP antibody production and induced interleukin 6 (IL-6) production in serum. In this case, MR16-1 significantly suppressed antibody production and further increased serum IL-6 levels. Regarding the cellular response, we studied the effect on the delayed-type hypersensitivity (DTH) response. DTH response was induced in mice by the immunization with Mycobacterium butyricum with incomplete Freund's adjuvant and following antigen challenge into the footpad 14 days after immunization. When MR16-1 was injected immediately after immunization, the DTH response was significantly suppressed and enlargement of the spleen was also suppressed. This suppressive effect was observed, when MR16-1 was administered on day 0, but not on days 5 and 10. Again, serum IL-6 levels were much higher in MR16-1-treated mice compared with controls. Furthermore, spleen cells from control mice released IL-2 and INFgamma by the stimulation of antigen in vitro. In contrast, spleen cells from MR16-1-treated mice produced these cytokines at a marginal level. In contrast, MR16-1 did not suppress the DTH response, when it was injected immediately after antigen challenge. Our results suggest that IL-6 does not always involve antibody production, although IL-6 augments antibody production, and that IL-6 is essential for the induction of Th1 cells.

摘要

在本研究中,我们检测了抗白细胞介素-6受体抗体(MR16-1)对小鼠体液免疫和细胞免疫反应的影响。在用二硝基苯基(DNP)-钥孔戚血蓝蛋白(KLH)于盐水中免疫的小鼠中,MR16-1对初次或二次反应中的抗原特异性抗体产生均无影响。用完全弗氏佐剂(CFA)进行DNP-KLH免疫显著增强了抗DNP抗体的产生,并诱导血清中白细胞介素6(IL-6)的产生。在这种情况下,MR16-1显著抑制了抗体产生,并进一步提高了血清IL-6水平。关于细胞反应,我们研究了其对迟发型超敏反应(DTH)的影响。通过用丁酸分枝杆菌与不完全弗氏佐剂免疫小鼠,并在免疫后14天对足垫进行抗原攻击来诱导DTH反应。当在免疫后立即注射MR16-1时,DTH反应被显著抑制,脾脏肿大也受到抑制。当在第0天给予MR16-1时观察到这种抑制作用,但在第5天和第10天则未观察到。同样,与对照组相比,经MR16-1处理的小鼠血清IL-6水平要高得多。此外,来自对照小鼠的脾细胞在体外受到抗原刺激时会释放IL-2和干扰素γ。相比之下,来自经MR16-1处理的小鼠的脾细胞产生这些细胞因子的水平很低。相反,当在抗原攻击后立即注射MR16-1时,它并未抑制DTH反应。我们的结果表明,尽管IL-6可增强抗体产生,但IL-6并不总是参与抗体产生,并且IL-6对于Th1细胞的诱导至关重要。

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