Ono A, Mochizuki M, Yamaguchi K, Miyata N, Watanabe T
Department of Pathology, University of Tokyo, Japan.
Br J Ophthalmol. 1995 Mar;79(3):270-6. doi: 10.1136/bjo.79.3.270.
This study aimed to characterise the status of viral infection in patients with HTLV-1 uveitis (HU) by quantifying the circulating HTLV-1 infected cells in the peripheral blood.
Genomic DNA samples of peripheral blood mononuclear cells (PBMC) were obtained from 25 patients with HU, 14 patients with tropical spastic paraparesis/HTLV-1 associated myelopathy (TSP/HAM), and 21 asymptomatic carriers of HTLV-1. Quantitative polymerase chain reaction (PCR) of the gag region of HTLV-1 provirus DNA was performed on these DNA samples. To confirm the PCR, genomic Southern blot hybridisation was performed to identify integrated HTLV-1 provirus. This procedure detected a few percent of HTLV-1 infected cells in the PBMC.
Most of the HU patients had a significantly increased number of circulating HTLV-1 infected cells (mean (SD) 3.84% (4.45%) of the PBMC), whereas the percentage of infected cells in most asymptomatic carriers was less than 1% (0.54% (1.11%)). Most of the TSP/HAM patients also had a relatively high percentage (11.63% (7.67%)). The differences among these three groups were highly significant by the Mann-Whitney U test.
The results suggested that the increase in the number of HTLV-1 infected cells is one base for the development of inflammatory HU lesions, as it is for TSP/HAM.
本研究旨在通过定量外周血中感染人嗜T淋巴细胞病毒1型(HTLV-1)的细胞,来描述HTLV-1葡萄膜炎(HU)患者的病毒感染状况。
从25例HU患者、14例热带痉挛性截瘫/HTLV-1相关脊髓病(TSP/HAM)患者和21例HTLV-1无症状携带者中获取外周血单个核细胞(PBMC)的基因组DNA样本。对这些DNA样本进行HTLV-1前病毒DNA gag区域的定量聚合酶链反应(PCR)。为了确认PCR结果,进行基因组Southern印迹杂交以鉴定整合的HTLV-1前病毒。该方法检测到PBMC中百分之几的HTLV-1感染细胞。
大多数HU患者循环中感染HTLV-1的细胞数量显著增加(平均(标准差)为PBMC的3.84%(4.45%)),而大多数无症状携带者中感染细胞的百分比小于1%(0.54%(1.11%))。大多数TSP/HAM患者也有相对较高的百分比(11.63%(7.67%))。通过Mann-Whitney U检验,这三组之间的差异具有高度显著性。
结果表明,HTLV-1感染细胞数量的增加是炎性HU病变发生的一个基础,就像它是TSP/HAM的发病基础一样。