Boumpas D T, Hooks J J, Popovic M, Tsokos G C, Mann D L
J Clin Immunol. 1985 Sep;5(5):340-4. doi: 10.1007/BF00918253.
B-cell lines were established as spontaneous outgrowths of cell cultures from patients with adult T-cell leukemia (ATL). Three such lines were shown to have integrated human T-cell leukemia/lymphoma virus 1 (HTLV-I) proviral sequences as well as Epstein-Barr virus (EBV) infection. Supernatant fluids from these cultured cells were assayed for interferon (IFN) production. Acid-stable alpha-IFN was found to be produced by one cell line (CF), and acid-labile alpha-IFN by the other two (HS, MJB). In contrast, HTLV-I-infected T-cell lines did not produce IFN. Some EBV-infected B-cell lines produce acid-labile alpha-IFN, while others do not. Since alpha-IFN, both acid stable and acid labile, is found in sera from patients with the polyclonal activation of B cells as a constitutive part of the disease, the above observations suggest a possible role of polyclonal B-cell activation in alpha-IFN production in these diseases.
B细胞系是从成人T细胞白血病(ATL)患者的细胞培养物中自发生长建立的。已证明三个这样的细胞系整合了人类T细胞白血病/淋巴瘤病毒1(HTLV-I)前病毒序列以及爱泼斯坦-巴尔病毒(EBV)感染。对这些培养细胞的上清液进行了干扰素(IFN)产生检测。发现一个细胞系(CF)产生酸稳定的α-干扰素,另外两个细胞系(HS、MJB)产生酸不稳定的α-干扰素。相比之下,HTLV-I感染的T细胞系不产生干扰素。一些EBV感染的B细胞系产生酸不稳定的α-干扰素,而其他细胞系则不产生。由于在B细胞多克隆激活患者的血清中发现了酸稳定和酸不稳定的α-干扰素,作为疾病的一个组成部分,上述观察结果提示多克隆B细胞激活在这些疾病的α-干扰素产生中可能起作用。