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源自爱泼斯坦-巴尔病毒相关移植后淋巴细胞增生性疾病的B淋巴细胞的体外培养:细胞因子产生及α干扰素的作用

In vitro culture of B-lymphocytes derived from Epstein-Barr-virus-associated posttransplant lymphoproliferative disease: cytokine production and effect of interferon-alpha.

作者信息

Randhawa P, Whiteside T, Zeevi A, Nalesnik M, Alvares C, Gollin S M, Demetris J, Locker J

机构信息

Division of Transplantation Pathology, University of Pittsburgh School of Medicine, Pennsylvania 15213, USA.

出版信息

In Vitro Cell Dev Biol Anim. 1997 Nov-Dec;33(10):803-8. doi: 10.1007/s11626-997-0160-9.

Abstract

Epstein-Barr-virus-associated posttransplant lymphoproliferative disease ranges from transient lymphadenitis to aggressive lymphoma. This study characterizes an in vitro model to study the pathogenesis of this disease with a cell culture system. Five B-cell lines derived from posttransplant lymphoproliferative disease tissue were characterized with regard to immunophenotype, karyotype, molecular genetics, cytokine production, and growth regulation. All cell lines expressed CD19, CD21, CD22, CD43, and CD77, but not CD10 antigens. Immunoglobulin light chain restriction was seen in four of five cell lines, and cytogenetic abnormalities were demonstrable in three of the five. Cells proliferating in culture contained multiple Epstein-Barr virus episomes and showed lytic viral replication. All cell lines produced tumor necrosis factor-beta and interleukin-10 without evidence of autocrine growth regulatory loops involving these cytokines. No evidence of IL-1 alpha, IL-2, IL-4, IL-5 or IL-6 production was found by reverse transcriptase polymerase chain reaction. Adding 500 U IFN-alpha/ml to the culture medium resulted in 30% inhibition of [3H]thymidine incorporation.

摘要

爱泼斯坦-巴尔病毒相关的移植后淋巴细胞增生性疾病范围从短暂性淋巴结炎到侵袭性淋巴瘤。本研究利用细胞培养系统建立了一种体外模型来研究该疾病的发病机制。对源自移植后淋巴细胞增生性疾病组织的5个B细胞系进行了免疫表型、核型、分子遗传学、细胞因子产生及生长调控方面的特征分析。所有细胞系均表达CD19、CD21、CD22、CD43和CD77,但不表达CD10抗原。5个细胞系中有4个出现免疫球蛋白轻链限制,5个中有3个存在细胞遗传学异常。培养中增殖的细胞含有多个爱泼斯坦-巴尔病毒附加体,并显示出裂解性病毒复制。所有细胞系均产生肿瘤坏死因子-β和白细胞介素-10,未发现涉及这些细胞因子的自分泌生长调节环。逆转录聚合酶链反应未发现白细胞介素-1α、白细胞介素-2、白细胞介素-4、白细胞介素-5或白细胞介素-6产生的证据。向培养基中添加500 U干扰素-α/毫升可导致[3H]胸腺嘧啶核苷掺入受到30%的抑制。

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