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单克隆抗Ia抗体可抑制小鼠抗原诱导性关节炎的突发反应。

Monoclonal anti-Ia antibodies suppress the flare up reaction of antigen induced arthritis in mice.

作者信息

van den Broek M F, van den Berg W B, van de Putte L B

出版信息

Clin Exp Immunol. 1986 Nov;66(2):320-30.

Abstract

Intravenous injection of methylated bovine serum albumin (mBSA) in mice with a unilateral antigen-induced arthritis induced with mBSA causes a flare up of the inflammation in the arthritic but not in the contralateral joint. To study whether this phenomenon is dependent on class II antigens, we treated C57Bl/10 (H-2b) and C3H (H-2k) mice with monoclonal anti-Iab (HB26) and anti-Iak (2-2-1) antibodies on days -3, -2, -1 and 0 before induction of the flare up. Another group was treated only once on day 0 before antigen challenge. Four injections with HB26 completely suppressed the flare up reaction in C57Bl/10 mice; the same results were seen with 2-2-1 in C3H mice. One injection only partly suppressed the flare up reaction in both strains, whereas four injections with the haplotype-nonspecific antibodies did not affect the flare up. Injections with HB26 appeared to be able to completely suppress a delayed type hypersensitivity reaction but not a reversed passive Arthus reaction in C57B1/10 mice, indicating that anti-Ia antibodies have an effect on lymphocyte-dependent but not on antigen-antibody-dependent inflammatory phenomena. These results demonstrate that the flare up of antigen induced arthritis is dependent on the presence of Ia antigens, suggesting that the interaction between antigen-presenting cells and T lymphocytes plays an important role in this process.

摘要

给用甲基化牛血清白蛋白(mBSA)诱导产生单侧抗原诱导性关节炎的小鼠静脉注射mBSA,会导致关节炎关节炎症加剧,但对侧关节则不会。为了研究这种现象是否依赖于Ⅱ类抗原,我们在诱发炎症加剧前的第-3、-2、-1和0天,用单克隆抗Iab(HB26)和抗Iak(2-2-1)抗体处理C57Bl/10(H-2b)和C3H(H-2k)小鼠。另一组仅在抗原攻击前的第0天接受一次处理。用HB26进行四次注射可完全抑制C57Bl/10小鼠的炎症加剧反应;在C3H小鼠中用2-2-1也得到了相同结果。一次注射仅部分抑制了两种品系的炎症加剧反应,而用单倍型非特异性抗体进行四次注射则不影响炎症加剧反应。在C57B1/10小鼠中,注射HB26似乎能够完全抑制迟发型超敏反应,但不能抑制反向被动Arthus反应,这表明抗Ia抗体对淋巴细胞依赖性炎症现象有作用,但对抗抗原抗体依赖性炎症现象无作用。这些结果表明,抗原诱导性关节炎的炎症加剧依赖于Ia抗原的存在,提示抗原呈递细胞与T淋巴细胞之间的相互作用在这一过程中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/1542525/d0ed7ec3800c/clinexpimmunol00116-0073-a.jpg

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