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Levels of Murine but Not Human CXCL13 Are Greatly Elevated in NOD-SCID Mice Bearing the AIDS-Associated Burkitt Lymphoma Cell Line 2F7

机译:在携带与艾滋病相关的伯基特淋巴瘤细胞系2F7的NOD-SCID小鼠中小鼠而非人类CXCL13的水平大大提高

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摘要

Currently, few rodent models of AIDS-associated non-Hodgkin’s lymphoma (AIDS-NHL) exist. In these studies, a novel mouse/human xenograft model of AIDS-associated Burkitt lymphoma (AIDS-BL) was created by injecting cells of the human AIDS-BL cell line, 2F7, intraperitoneally into NOD-SCID mice. Mice developed tumors in the peritoneal cavity, with metastases to the spleen, thymus, and mesenteric lymph nodes. Expression of the chemokine receptor, CXCR5, was greatly elevated in vivo on BL tumor cells in this model, as shown by flow cytometry. CXCL13 is the ligand for CXCR5, and serum and ascites levels of murine, but not human, CXCL13 showed a striking elevation in tumor-bearing mice, with levels as high as 200,000 pg/ml in ascites, as measured by ELISA. As shown by immunohistochemistry, murine CXCL13 was associated with macrophage-like tumor-infiltrating cells that appeared to be histiocytes. Blocking CXCR5 on 2F7 cells with neutralizing antibodies prior to injection into the mice substantially delayed tumor formation. The marked elevations in tumor cell CXCR5 expression and in murine CXCL13 levels seen in the model may potentially identify an important link between tumor-interacting histiocytes and tumor cells in AIDS-BL. These results also identify CXCL13 as a potential biomarker for this disease, which is consistent with previous studies showing that serum levels of CXCL13 were elevated in human subjects who developed AIDS-lymphoma. This mouse model may be useful for future studies on the interactions of the innate immune system and AIDS-BL tumor cells, as well as for the assessment of potential tumor biomarkers for this disease.
机译:目前,与艾滋病相关的非霍奇金淋巴瘤(AIDS-NHL)的啮齿动物模型很少。在这些研究中,通过将人AIDS-BL细胞系2F7的细胞腹膜内注射到NOD-SCID小鼠中,创建了一种与艾滋病相关的伯基特淋巴瘤(AIDS-BL)的新型小鼠/人异种移植模型。小鼠在腹膜腔内发生肿瘤,转移至脾脏,胸腺和肠系膜淋巴结。流式细胞术表明,在该模型中,趋化因子受体CXCR5的表达在体内在BL肿瘤细胞上大大提高。 CXCL13是CXCR5的配体,鼠类(而非人类)的血清和腹水含量很高,CXCL13在荷瘤小鼠中显示出惊人的升高,通过ELISA测定,腹水中的含量高达200,000 pg / ml。如免疫组织化学所示,鼠CXCL13与似乎是组织细胞的巨噬细胞样肿瘤浸润细胞有关。在注射入小鼠之前,用中和抗体在2F7细胞上阻断CXCR5会大大延迟肿瘤的形成。在模型中看到的肿瘤细胞CXCR5表达和鼠CXCL13水平的明显升高可能潜在地确定了与肿瘤相互作用的组织细胞与AIDS-BL中肿瘤细胞之间的重要联系。这些结果还将CXCL13鉴定为该疾病的潜在生物标志物,这与先前的研究一致,该研究表明在患有AIDS淋巴瘤的人类受试者中CXCL13的血清水平升高。该小鼠模型可用于进一步研究先天免疫系统与AIDS-BL肿瘤细胞之间的相互作用,以及评估该疾病的潜在肿瘤生物标志物。

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