免疫反应中的T区和b区。静脉注射胸腺依赖性(SRBC)和胸腺非依赖性(副伤寒疫苗内毒素)抗原后大鼠脾脏T细胞和B细胞区室的体积变化组织计量学研究。

A J Veerman, H D Vries
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引用次数: 0

摘要

在大鼠脾脏白髓中,研究了静脉注射相当剂量的副伤寒疫苗(PTV,胸腺独立)和绵羊红细胞(SRBC,胸腺依赖)后不同隔室中细胞数量的变化。在小动脉周围淋巴鞘(PALS)中测量细胞浓度和体积。在给抗原后的前5天,仅记录卵泡和边缘带的体积。此外,进行组织学观察。在胸腺依赖区,PTV在给药后12-24小时引起水肿。服用SRBC后,直到第二天淋巴细胞数量增加,可能代表T细胞从循环池流入。两种抗原均引起外周PALS的浆细胞反应(第2 -4天)。在骨髓依赖区,在给予PTV后的最初24小时内,中等大小的淋巴细胞从边缘区大量转移到卵泡。这些细胞随后转化为原细胞。在SRBC(6和12小时)后,只有少数边缘区淋巴细胞似乎迁移到卵泡中。有人认为,PTV中存在的内毒素是在给予抗原后,所有边缘区(B)细胞都有反应的原因。内毒素刺激可能为边缘带细胞的命运提供了一种模型,这种细胞受到其他药物的刺激,如抗原(刺激抗原结合B细胞)或抗原-抗体复合物(刺激fc受体B细胞)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T- and B-areas in immune reactions. Volume changes in T and B cell compartments of the rat spleen following intravenous administration of a thymus-dependent (SRBC) and a thymus-independent (paratyphoid vaccin-endotoxin) antigen. A histometric study.

In the white pulp of rat spleens cell numbers were studied in the different compartments following intravenous administration of comparable doses of paratyphoid vaccine (PTV, thymus-independent) and sheep red blood cells (SRBC, thymus-dependent). In the periarteriolar lymphatic sheaths (PALS) both cell concentration and volume were measured. For the follicles and the marginal zone only volume was recorded in the first 5 days following antigen administration. Additionally, histologic observations were made. In the thymus-dependent area PTV caused oedema 12-24 hours after administration. Following SRBC administration an increase in lymphocyte numbers occurred until the second day, probably representing an influx of T cells from the recirculating pool. Both antigens gave rise to a plasmacellular reaction in the peripheral PALS (2nd-4th day). In the bone marrow-dependent areas a massive shift of medium-sized lymphocytes from the marginal zone to the follicles took place in the first 24 hours following PTV administration. These cells subsequently transformed into blasts. After SRBC (6 and 12 hours) only a few marginal zone lymphocytes seemed to migrate into the follicles. It is aruged that the endotoxin present in PTV is responsible for the fact that, following administration of the antigen, all marginal zone (B) cells responded. Endotoxin stimulation might provide a model for the fate of marginal zone cells stimulated by other agents, such as antigen (stimulating antigen binding B cells) or antigen-antibody complexes (stimulating Fc-receptor B cells).

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