Licence S T, Binns R M
Department of Immunology, Babraham Institute, Cambridge, UK.
Immunology. 1995 Jun;85(2):276-84.
Blood leucocyte subsets in neonatally (20-day-old) thymectomized (Tx) and sham-thymectomized (STx) pigs were analysed 13 times over nearly 2 years. Tx piglets showed a persistent selective leucopenia, due mainly to a approximately 95% reduction in gamma delta null T cells which fell, with a circulating half-life of approximately 2 weeks, to approximately 0.3 x 10(6)/ml. This residual population was extrathymic in origin since it increased numerically at least approximately eightfold as the Tx pigs grew. Changes in other subsets were complex and affected by antigenic experience associated with weaning and with a change of accommodation at approximately 4 months postoperation (p.o.). Most major populations were increased long-term after thymectomy, especially after 3 months p.o. [i.e. surface (s)IgM+ B cells and CD2+, CD8+, major histocompatibility complex (MHC) class II+, CD4+ and double-positive CD4+ CD8+ T-cell subsets]. However, during the first 3 months, thymectomy caused a significant delay in development of CD8high and CD4+ T cells and, after 4 months p.o., a continuing lack of CD4only (single-positive) T cells. Fortuitous environmental antigenic stimulation caused a major transient lymphocytosis, with counts increasing 1.2-fold in STx and 3.5-fold in Tx pigs. This was largely due to an increase in CD2+ CD8+ MHC class II+ T cells, particularly in Tx pigs. The small residual thymus-independent gamma delta null subset also increased, while gamma delta T cells in STx pigs actually decreased. Evolving changes in expression of CD45, CD45R, CD44, CD18 and very late antigen type-4 (VLA-4) also occurred following thymectomy. Thus, the most persistent long-term effect of thymectomy, other than the lack of gamma delta null T cells, was the markedly increased numbers of double-positive (CD4+ CD8low) T cells, most of which expressed MHC class II and higher levels of adhesion molecules.
在近2年的时间里,对新生期(20日龄)进行胸腺切除(Tx)和假胸腺切除(STx)的猪的血液白细胞亚群进行了13次分析。Tx仔猪表现出持续性选择性白细胞减少,主要是由于γδ无T细胞减少了约95%,其数量下降至约0.3×10⁶/ml,循环半衰期约为2周。这个残余群体起源于胸腺外,因为随着Tx猪的生长,其数量至少增加了约8倍。其他亚群的变化很复杂,并且受到与断奶以及术后约4个月(p.o.)饲养环境变化相关的抗原经历的影响。大多数主要群体在胸腺切除术后长期增加,尤其是术后3个月后[即表面(s)IgM⁺ B细胞以及CD2⁺、CD8⁺、主要组织相容性复合体(MHC)II类⁺、CD4⁺和双阳性CD4⁺ CD8⁺ T细胞亚群]。然而,在最初3个月内,胸腺切除导致CD8高和CD4⁺ T细胞发育明显延迟,并且在术后4个月后,持续缺乏仅CD4(单阳性)T细胞。偶然的环境抗原刺激导致主要的短暂淋巴细胞增多,STx猪的细胞计数增加1.2倍,Tx猪增加3.5倍。这主要是由于CD2⁺ CD8⁺ MHC II类⁺ T细胞增加,特别是在Tx猪中。小的残余胸腺非依赖性γδ无亚群也增加,而STx猪中的γδ T细胞实际上减少。胸腺切除术后,CD45、CD45R、CD44、CD18和极晚期抗原4型(VLA - 4)的表达也发生了不断演变的变化。因此,胸腺切除术后除了缺乏γδ无T细胞外,最持久的长期影响是双阳性(CD4⁺ CD8低)T细胞数量明显增加,其中大多数表达MHC II类和更高水平的黏附分子。