4.7 Article

CXCL13 plus interleukin 10 is highly specific for the diagnosis of CNS lymphoma

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BLOOD
卷 121, 期 23, 页码 4740-4748

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AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2013-01-476333

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资金

  1. National Institutes of Health [R01CA139-83-01A1]
  2. University of California San Francisco-Gladstone Institute of Virology & Immunology Center for AIDS Research [P30 AI027763]
  3. University of California, San Francisco Brain Tumor Specialized Program of Research Excellence [P50CA097257]
  4. Leukemia & Lymphoma Society

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Establishing the diagnosis of focal brain lesions in patients with unexplained neurologic symptoms represents a challenge. The goal of this study is to provide evidence supporting functional roles for CXC chemokine ligand (CXCL) 13 and interleukin (IL)-10 in central nervous system (CNS) lymphomas and to evaluate the utility of each as prognostic and diagnostic biomarkers. We demonstrate for the first time that elevated CXCL13 concentration in cerebrospinal fluid (CSF) is prognostic and that CXCL13 and CXCL12 mediate chemotaxis of lymphoma cells isolated from CNS lymphoma lesions. Expression of the activated form of Janus kinase 1 supported a role for IL-10 in prosurvival signaling. We determined the concentration of CXCL13 and IL-10 in CSF of CNS lymphoma patients and control cohorts including inflammatory and degenerative neurologic disease in a multicenter study involving 220 patients. Bivariate elevated CXCL13 plus IL-10 was 99.3% specific for primary and secondary CNS lymphoma, with sensitivity significantly greater than reference standard CSF tests. These results identify CXCL13 and IL-10 as potentially important biomarkers of CNS lymphoma that merit further evaluation and support incorporation of CXCL13 and IL-10 into diagnostic algorithms for the workup of focal brain lesions in which lymphoma is a consideration.

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