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淋巴细胞减少状态下的抗原定位。I. 慢性胸导管引流后的定位模式。

Antigen localization in lymphopenic states. I. Localization pattern following chronic thoracic duct drainage.

作者信息

Williams G M

出版信息

Immunology. 1966 Nov;11(5):467-74.

Abstract

Adult rats, depleted of thoracic duct lymph for 5–7 days, were tested for their ability to localize I-labelled polymerized flagellin from . Labelled antigen was injected into both hind footpads 6–12 hours after completion of drainage, and the regional nodes were excised 24 hours later. Grain counts on identically exposed autoradiographic sections from regional nodes were used to assess differences in antigen distribution between depleted and nondepleted rats. The uptake of antigen by medullary macrophages was no different in the two groups. However, the uptake of antigen by primary lymphoid follicles was reduced by thoracic duct drainage to levels one-fourth that observed in normal rats. Two procedures were found capable of improving follicular antigen uptake in the chronically depleted rat: (1) regional inoculations of 0.01 ml of specific antiflagellar immune serum at a titre of 1:400 1 hour prior to antigen injection, and (2) daily return by intravenous infusion of washed autogenous thoracic duct lymphocytes collected during drainage. Regional injections of both viable and non-viable lymphocytes were ineffective in improving follicular antigen uptake in the depleted animal. The results show that depleted rats lack a serum factor, presumably an opsonin, important in determining antigen distribution patterns. It seems likely that this factor is normally manufactured by small lymphocytes.

摘要

将成年大鼠的胸导管淋巴排空5至7天,然后测试它们定位来自[具体来源未提及]的I标记聚合鞭毛蛋白的能力。在引流完成后6至12小时,将标记抗原注射到双侧后足垫中,24小时后切除局部淋巴结。对来自局部淋巴结的相同曝光放射自显影片段进行颗粒计数,以评估排空组和未排空组大鼠之间抗原分布的差异。两组中髓质巨噬细胞对抗原的摄取没有差异。然而,胸导管引流使初级淋巴滤泡对抗原的摄取减少至正常大鼠观察值的四分之一。发现两种方法能够改善长期排空大鼠的滤泡抗原摄取:(1)在注射抗原前1小时,局部接种0.01 ml效价为1:400的特异性抗鞭毛免疫血清;(2)每天通过静脉输注在引流期间收集的洗涤自体胸导管淋巴细胞。在排空动物中,注射活淋巴细胞和死淋巴细胞对改善滤泡抗原摄取均无效。结果表明,排空大鼠缺乏一种血清因子,推测为调理素,这一因子在决定抗原分布模式方面很重要。这种因子似乎通常由小淋巴细胞产生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bed4/1423809/0dc499abff0b/immunology00418-0060-a.jpg

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