首页> 外文期刊>The Journal of Experomental Medicine >Human T cell leukemia/lymphoma virus I infection and subsequent cloning of normal human B cells. Direct responsiveness of cloned cells to recombinant interleukin 2 by differentiation in the absence of enhanced proliferation.
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Human T cell leukemia/lymphoma virus I infection and subsequent cloning of normal human B cells. Direct responsiveness of cloned cells to recombinant interleukin 2 by differentiation in the absence of enhanced proliferation.

机译:人T细胞白血病/淋巴瘤病毒I感染以及随后正常人B细胞的克隆。克隆细胞对重组白介素2的直接反应是在不增强增殖的情况下进行分化。

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A human T cell leukemia/lymphoma virus (HTLV)-I-infected B cell clone expressed Tac antigen on its cell surface and responded to recombinant interleukin 2 (IL-2) by increased production of IgM without any increase in proliferation. Anti-Tac antibody completely inhibited the IL-2-induced differentiation of this HTLV-I-infected B cell clone. This study demonstrates that HTLV-I can directly infect normal mature human B cells, and that the Tac antigen, which may be induced by infection with HTLV-I, is the functional receptor for IL-2-induced B cell differentiation. The availability of such cell lines and clones should provide useful tools to delineate precisely the differentiation step in the human B cell cycle.
机译:被人T细胞白血病/淋巴瘤病毒(HTLV)-I感染的B细胞克隆在其细胞表面表达Tac抗原,并通过增加IgM的产生而对重组白介素2(IL-2)作出反应,而增殖没有任何增加。抗Tac抗体完全抑制了被HTLV-1感染的B细胞克隆的IL-2诱导的分化。该研究证明HTLV-1可以直接感染正常的成熟人类B细胞,而可能被HTLV-1感染诱导的Tac抗原是IL-2诱导的B细胞分化的功能性受体。此类细胞系和克隆的可用性应提供有用的工具,以准确描绘人B细胞周期中的分化步骤。

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