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用色甘酸钠特异性抑制同种异体反应。

Specific inhibition of allogeneic reactions with disodium cromoglycate.

作者信息

McIntyre J A, Neerunjun E D, Faulk W P

出版信息

Hum Immunol. 1981 Oct;3(2):163-72. doi: 10.1016/0198-8859(81)90053-7.

Abstract

Milligram amounts of disodium cromoglycate (DSCG) inhibit allogeneic responses in mixed lymphocyte culture (MLC) reactions, but do not affect cell viability or suppress lymphocyte responses to either phytohemagglutinin (PHA) or pokeweed (PKW) mitogens. Preincubation of lymphocytes with DSCG is without effect, indicating that membrane binding is an unlikely explanation for inhibition. The HLA-DR tissue typing of cells in the presence of optimal MLC-inhibitory doses of DSCG is normal suggesting that MLC-reactive lymphocytes are not denied recognition of these antigens. Timed studies demonstrate that DSCG must be present continuously during the induction period, for removal of DSCG after 16 hr culture restores MLC reactivity and addition of the drug after 48 hr is without effect. Both natural killing (NK) and cell mediated lympholysis (CML) assays proceed normally in the presence of optimal MLC-inhibitory concentrations of DSCG; however, CML reactions are eliminated by the addition of drug during cytotoxic T cell priming. Background CML reactivity also disappears when lymphocytes are continuously cocultured in DSCG, implying that such killing cannot be attributed to NK activity. DSCG is said to inhibit allergic reactions by impeding calcium flux across mast cell membranes, thereby preventing degranulation, but other mechanisms are required to explain the selective effects on in vitro lymphocyte reactivity.

摘要

毫克量的色甘酸钠(DSCG)可抑制混合淋巴细胞培养(MLC)反应中的同种异体反应,但不影响细胞活力,也不抑制淋巴细胞对植物血凝素(PHA)或商陆(PKW)有丝分裂原的反应。淋巴细胞与DSCG预孵育无效,这表明膜结合不太可能是抑制作用的原因。在存在最佳MLC抑制剂量的DSCG的情况下,细胞的HLA-DR组织分型正常,这表明MLC反应性淋巴细胞并未被阻止识别这些抗原。定时研究表明,DSCG必须在诱导期持续存在,因为培养16小时后去除DSCG可恢复MLC反应性,而48小时后添加该药物则无效。在存在最佳MLC抑制浓度的DSCG的情况下,自然杀伤(NK)和细胞介导的淋巴细胞溶解(CML)试验均正常进行;然而,在细胞毒性T细胞致敏期间添加药物可消除CML反应。当淋巴细胞在DSCG中持续共培养时,背景CML反应性也会消失,这意味着这种杀伤不能归因于NK活性。据说DSCG通过阻止钙穿过肥大细胞膜的流动来抑制过敏反应,从而防止脱颗粒,但需要其他机制来解释对体外淋巴细胞反应性的选择性作用。

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