Onah D N, Hopkins J, Luckins A G
University of Edinburgh, Centre for Tropical Veterinary Medicine, Midlothian, Scotland, UK.
Parasitol Res. 1999 Apr;85(4):263-9. doi: 10.1007/s004360050545.
This paper reports on changes in the lymphocyte composition of the peripheral blood in sheep infected with Trypanosoma evansi. In addition, parasite-specific IgG1 and IgM antibody responses were monitored using a double-sandwich enzyme-linked immunosorbent assay (ELISA) technique. Eight sheep were infected with 2 x 10(6) T. evansi TREU 2143. The infection was characterised by chronicity and ended in self-cure in two of the sheep. These two sheep were designated group A, whereas the other six sheep, which remained parasitaemic until treated, were designated group B. Analysis of the peripheral blood lymphocytes (PBLs) by indirect immunofluorescence staining and flow cytometry revealed significant alterations in the numbers of T- and B-cell subsets detected in all infected sheep. In group A, whereas the numbers of CD8+ cells decreased, CD4+ cells showed marginal decreases, remaining at or above pre-infection figures and resulting in increase in the CD4:CD8 ratio. In group B, CD8+ cells showed few marginal decreases, being at or above pre-infection figures most of the time, whereas CD4+ cells decreased significantly from day 26 post infection (p.i.) such that the CD4:CD8 ratio decreased. Infection also resulted in significant increases (P < 0.001) as of day 26 p.i. in circulating B-cells in group B as shown by the numbers of sIg+, CD45R+, CD1+ and major histocompatibility complex (MHC) II+ cells. The increases, however, were moderate and biphasic in group A. T. evansi-specific IgM and IgG1 antibody isotypes were detected in all infected sheep, but their levels were significantly higher in group A than in group B (IgM P < 0.05; IgGI P < 0.01). In addition, although an initially higher level of IgM response was subsequently replaced by a higher level of IgG1 response in group A, this was never the case in group B until after drug treatment.
本文报道了感染伊氏锥虫的绵羊外周血淋巴细胞组成的变化。此外,使用双夹心酶联免疫吸附测定(ELISA)技术监测了寄生虫特异性IgG1和IgM抗体反应。8只绵羊感染了2×10⁶个伊氏锥虫TREU 2143。感染的特征为慢性,其中两只绵羊最终自愈。这两只绵羊被指定为A组,而另外六只绵羊在接受治疗前一直存在寄生虫血症,被指定为B组。通过间接免疫荧光染色和流式细胞术分析外周血淋巴细胞(PBL)发现,所有感染绵羊中检测到的T细胞和B细胞亚群数量有显著变化。在A组中,CD8⁺细胞数量减少,CD4⁺细胞略有减少,仍保持在感染前水平或以上,导致CD4:CD8比值增加。在B组中,CD8⁺细胞略有减少,大多数时间保持在感染前水平或以上,而CD4⁺细胞在感染后第26天(p.i.)显著减少,使得CD4:CD8比值降低。感染还导致B组中循环B细胞从感染后第26天起显著增加(P < 0.001),表现为sIg⁺、CD45R⁺、CD1⁺和主要组织相容性复合体(MHC)II⁺细胞数量增加。然而,A组中的增加是适度的且呈双相性。在所有感染绵羊中均检测到伊氏锥虫特异性IgM和IgG1抗体亚型,但A组中的水平显著高于B组(IgM P < 0.05;IgG1 P < 0.01)。此外,虽然A组中最初较高水平的IgM反应随后被更高水平的IgG1反应所取代,但在B组中直到药物治疗后才出现这种情况。