Skip to main content
Top
Published in: Journal of Hematology & Oncology 1/2019

Open Access 01-12-2019 | Lymphoma | Research

APRIL and BAFF: novel biomarkers for central nervous system lymphoma

Authors: Matthias Mulazzani, Marion Huber, Sabine Borchard, Sigrid Langer, Barbara Angele, Elisabeth Schuh, Edgar Meinl, Martin Dreyling, Tobias Birnbaum, Andreas Straube, Uwe Koedel, Louisa von Baumgarten

Published in: Journal of Hematology & Oncology | Issue 1/2019

Login to get access

Abstract

Background

Early diagnosis of CNS lymphoma (CNSL) is essential for successful therapy of this rapidly progressing brain tumor. However, in patients presenting with focal brain lesions, fast and reliable diagnosis of PCNSL remains a challenge. A proliferation-inducing ligand (APRIL) and B cell activating factor (BAFF) are important factors in the pathophysiology, diagnosis, and prognosis of systemic B cell malignancies. However, their utility as biomarkers for the diagnosis of CNSL and their effects on CNSL cells remain unclear.

Methods

In this prospective study, we analyzed the levels of APRIL and BAFF in the cerebrospinal fluid (CSF) of 116 patients with suspected focal brain lesions, including 53 CNSL patients. Additionally, we serially measured their levels during chemotherapy and relapse. Furthermore, we analyzed the effect of APRIL and BAFF on two B cell lymphoma cell lines using proliferation, viability, and chemotaxis assays.

Results

CSF levels of APRIL and BAFF reliably differentiated CNSL from other focal brain lesions (including primary and metastatic brain tumors, autoimmune-inflammatory lesions, and neuroinfectious lesions) with a specificity of 93.7% (APRIL, BAFF) and a sensitivity of 62.3% (APRIL) and 47.1% (BAFF). Serial CSF analysis of CNSL patients during chemotherapy and relapse demonstrates a close correlation of APRIL CSF levels and the course of this disease. In vitro, APRIL and BAFF showed anti-apoptotic effects during MTX treatment and mediated chemotaxis of malignant B cells.

Conclusion

This study extends the spectrum of valuable diagnostic biomarkers in CNSL. In patients with focal brain lesions, measurement of APRIL in CSF could help accelerating the diagnosis of CNSL. Moreover, our results highlight an important role of APRIL and BAFF in the pathophysiology of CNSL.
Appendix
Available only for authorised users
Literature
1.
go back to reference Deckert M, Brunn A, Montesinos-Rongen M, Terreni MR, Ponzoni M. Primary lymphoma of the central nervous system--a diagnostic challenge. Hematol Oncol. 2014;32(2):57–67.PubMedCrossRef Deckert M, Brunn A, Montesinos-Rongen M, Terreni MR, Ponzoni M. Primary lymphoma of the central nervous system--a diagnostic challenge. Hematol Oncol. 2014;32(2):57–67.PubMedCrossRef
2.
go back to reference Lim T, et al. Primary CNS lymphoma other than DLBCL: a descriptive analysis of clinical features and treatment outcomes. Ann Hematol. 2011;90(12):1391–8.PubMedPubMedCentralCrossRef Lim T, et al. Primary CNS lymphoma other than DLBCL: a descriptive analysis of clinical features and treatment outcomes. Ann Hematol. 2011;90(12):1391–8.PubMedPubMedCentralCrossRef
3.
go back to reference Deckert M, et al. Modern concepts in the biology, diagnosis, differential diagnosis and treatment of primary central nervous system lymphoma. Leukemia. 2011;25(12):1797–807.PubMedCrossRef Deckert M, et al. Modern concepts in the biology, diagnosis, differential diagnosis and treatment of primary central nervous system lymphoma. Leukemia. 2011;25(12):1797–807.PubMedCrossRef
4.
go back to reference Fischer L, et al. Meningeal dissemination in primary CNS lymphoma: prospective evaluation of 282 patients. Neurology. 2008;71(14):1102–8.PubMedCrossRef Fischer L, et al. Meningeal dissemination in primary CNS lymphoma: prospective evaluation of 282 patients. Neurology. 2008;71(14):1102–8.PubMedCrossRef
5.
go back to reference Louis DN, et al. The 2016 World Health Organization classification of tumors of the central nervous system: a summary. Acta Neuropathol. 2016;131(6):803–20.PubMedCrossRef Louis DN, et al. The 2016 World Health Organization classification of tumors of the central nervous system: a summary. Acta Neuropathol. 2016;131(6):803–20.PubMedCrossRef
6.
go back to reference Dammers R, et al. Safety and efficacy of frameless and frame-based intracranial biopsy techniques. Acta Neurochir. 2008;150(1):23–9.PubMedCrossRef Dammers R, et al. Safety and efficacy of frameless and frame-based intracranial biopsy techniques. Acta Neurochir. 2008;150(1):23–9.PubMedCrossRef
7.
go back to reference Porter AB, et al. Primary central nervous system lymphoma can be histologically diagnosed after previous corticosteroid use: a pilot study to determine whether corticosteroids prevent the diagnosis of primary central nervous system lymphoma. Ann Neurol. 2008;63(5):662–7.PubMedCrossRef Porter AB, et al. Primary central nervous system lymphoma can be histologically diagnosed after previous corticosteroid use: a pilot study to determine whether corticosteroids prevent the diagnosis of primary central nervous system lymphoma. Ann Neurol. 2008;63(5):662–7.PubMedCrossRef
8.
go back to reference Antinori A, et al. Value of combined approach with thallium-201 single-photon emission computed tomography and Epstein-Barr virus DNA polymerase chain reaction in CSF for the diagnosis of AIDS-related primary CNS lymphoma. J Clin Oncol. 1999;17(2):554–60.PubMedCrossRef Antinori A, et al. Value of combined approach with thallium-201 single-photon emission computed tomography and Epstein-Barr virus DNA polymerase chain reaction in CSF for the diagnosis of AIDS-related primary CNS lymphoma. J Clin Oncol. 1999;17(2):554–60.PubMedCrossRef
9.
go back to reference Sasayama T, et al. Cerebrospinal fluid interleukin-10 is a potentially useful biomarker in immunocompetent primary central nervous system lymphoma (PCNSL). Neuro-oncology. 2012;14(3):368–80.PubMedCrossRef Sasayama T, et al. Cerebrospinal fluid interleukin-10 is a potentially useful biomarker in immunocompetent primary central nervous system lymphoma (PCNSL). Neuro-oncology. 2012;14(3):368–80.PubMedCrossRef
10.
go back to reference Sasagawa Y, Akai T, Tachibana O, Iizuka H. Diagnostic value of interleukin-10 in cerebrospinal fluid for diffuse large B-cell lymphoma of the central nervous system. J Neuro-Oncol. 2015;121(1):177–83.CrossRef Sasagawa Y, Akai T, Tachibana O, Iizuka H. Diagnostic value of interleukin-10 in cerebrospinal fluid for diffuse large B-cell lymphoma of the central nervous system. J Neuro-Oncol. 2015;121(1):177–83.CrossRef
12.
go back to reference Song Y, et al. Cerebrospinal fluid IL-10 and IL-10/IL-6 as accurate diagnostic biomarkers for primary central nervous system large B-cell lymphoma. Sci Rep. 2016;6:38671.PubMedPubMedCentralCrossRef Song Y, et al. Cerebrospinal fluid IL-10 and IL-10/IL-6 as accurate diagnostic biomarkers for primary central nervous system large B-cell lymphoma. Sci Rep. 2016;6:38671.PubMedPubMedCentralCrossRef
13.
14.
go back to reference Caudie C, et al. CSF levels and diagnostic utility of cerebrospinal fluid beta2-microglobulin. Ann Biol Clin (Paris). 2005;63(6):631–7. Caudie C, et al. CSF levels and diagnostic utility of cerebrospinal fluid beta2-microglobulin. Ann Biol Clin (Paris). 2005;63(6):631–7.
15.
go back to reference Strehlow F, et al. Osteopontin in cerebrospinal fluid as diagnostic biomarker for central nervous system lymphoma. J Neuro-Oncol. 2016;129(1):165–71.CrossRef Strehlow F, et al. Osteopontin in cerebrospinal fluid as diagnostic biomarker for central nervous system lymphoma. J Neuro-Oncol. 2016;129(1):165–71.CrossRef
16.
go back to reference Kersten MJ, et al. Elevation of cerebrospinal fluid soluble CD27 levels in patients with meningeal localization of lymphoid malignancies. Blood. 1996;87(5):1985–9.PubMedCrossRef Kersten MJ, et al. Elevation of cerebrospinal fluid soluble CD27 levels in patients with meningeal localization of lymphoid malignancies. Blood. 1996;87(5):1985–9.PubMedCrossRef
17.
go back to reference Baraniskin A, et al. Identification of microRNAs in the cerebrospinal fluid as marker for primary diffuse large B-cell lymphoma of the central nervous system. Blood. 2011;117(11):3140–6.PubMedCrossRef Baraniskin A, et al. Identification of microRNAs in the cerebrospinal fluid as marker for primary diffuse large B-cell lymphoma of the central nervous system. Blood. 2011;117(11):3140–6.PubMedCrossRef
18.
19.
go back to reference Robertus JL, et al. Specific expression of miR-17-5p and miR-127 in testicular and central nervous system diffuse large B-cell lymphoma. Mod Pathol. 2009;22(4):547–55.PubMedCrossRef Robertus JL, et al. Specific expression of miR-17-5p and miR-127 in testicular and central nervous system diffuse large B-cell lymphoma. Mod Pathol. 2009;22(4):547–55.PubMedCrossRef
20.
go back to reference Zheng J, et al. Clinicopathological study of gene rearrangement and microRNA expression of primary central nervous system diffuse large B-cell lymphomas. Int J Clin Exp Pathol. 2013;6(10):2048–55.PubMedPubMedCentral Zheng J, et al. Clinicopathological study of gene rearrangement and microRNA expression of primary central nervous system diffuse large B-cell lymphomas. Int J Clin Exp Pathol. 2013;6(10):2048–55.PubMedPubMedCentral
23.
go back to reference Rickert RC, Jellusova J, Miletic AV. Signaling by the tumor necrosis factor receptor superfamily in B-cell biology and disease. Immunol Rev. 2011;244(1):115–33.PubMedPubMedCentralCrossRef Rickert RC, Jellusova J, Miletic AV. Signaling by the tumor necrosis factor receptor superfamily in B-cell biology and disease. Immunol Rev. 2011;244(1):115–33.PubMedPubMedCentralCrossRef
24.
go back to reference Tangye SG, Bryant VL, Cuss AK, Good KL. BAFF, APRIL and human B cell disorders. Semin Immunol. 2006;18(5):305–17.PubMedCrossRef Tangye SG, Bryant VL, Cuss AK, Good KL. BAFF, APRIL and human B cell disorders. Semin Immunol. 2006;18(5):305–17.PubMedCrossRef
25.
go back to reference Mackay F, Silveira PA, Brink R. B cells and the BAFF/APRIL axis: fast-forward on autoimmunity and signaling. Curr Opin Immunol. 2007;19(3):327–36.PubMedCrossRef Mackay F, Silveira PA, Brink R. B cells and the BAFF/APRIL axis: fast-forward on autoimmunity and signaling. Curr Opin Immunol. 2007;19(3):327–36.PubMedCrossRef
26.
go back to reference Krumbholz M, et al. BAFF is produced by astrocytes and up-regulated in multiple sclerosis lesions and primary central nervous system lymphoma. J Exp Med. 2005;201(2):195–200.PubMedPubMedCentralCrossRef Krumbholz M, et al. BAFF is produced by astrocytes and up-regulated in multiple sclerosis lesions and primary central nervous system lymphoma. J Exp Med. 2005;201(2):195–200.PubMedPubMedCentralCrossRef
27.
go back to reference Novak AJ, et al. Expression of BLyS and its receptors in B-cell non-Hodgkin lymphoma: correlation with disease activity and patient outcome. Blood. 2004;104(8):2247–53.PubMedCrossRef Novak AJ, et al. Expression of BLyS and its receptors in B-cell non-Hodgkin lymphoma: correlation with disease activity and patient outcome. Blood. 2004;104(8):2247–53.PubMedCrossRef
28.
go back to reference Kim SJ, et al. Serum BAFF predicts prognosis better than APRIL in diffuse large B-cell lymphoma patients treated with rituximab plus CHOP chemotherapy. Eur J Haematol. 2008;81(3):177–84.PubMedCrossRef Kim SJ, et al. Serum BAFF predicts prognosis better than APRIL in diffuse large B-cell lymphoma patients treated with rituximab plus CHOP chemotherapy. Eur J Haematol. 2008;81(3):177–84.PubMedCrossRef
29.
go back to reference Schwaller J, et al. Neutrophil-derived APRIL concentrated in tumor lesions by proteoglycans correlates with human B-cell lymphoma aggressiveness. Blood. 2007;109(1):331–8.PubMedCrossRef Schwaller J, et al. Neutrophil-derived APRIL concentrated in tumor lesions by proteoglycans correlates with human B-cell lymphoma aggressiveness. Blood. 2007;109(1):331–8.PubMedCrossRef
30.
go back to reference Mizutani H, et al. CSF TACI and BAFF levels in patients with primary CNS lymphoma as novel diagnostic biomarkers. Ann Clin Transl Neurol. 2018;5(12):1611–6.PubMedPubMedCentralCrossRef Mizutani H, et al. CSF TACI and BAFF levels in patients with primary CNS lymphoma as novel diagnostic biomarkers. Ann Clin Transl Neurol. 2018;5(12):1611–6.PubMedPubMedCentralCrossRef
31.
32.
go back to reference Birnbaum T, Langer S, Roeber S, von Baumgarten L, Straube A. Expression of B-cell activating factor, a proliferating inducing ligand and its receptors in primary central nervous system lymphoma. Neurol Int. 2013;5(1):e4.PubMedPubMedCentralCrossRef Birnbaum T, Langer S, Roeber S, von Baumgarten L, Straube A. Expression of B-cell activating factor, a proliferating inducing ligand and its receptors in primary central nervous system lymphoma. Neurol Int. 2013;5(1):e4.PubMedPubMedCentralCrossRef
33.
go back to reference Muta D, et al. Inhibition of eIF4E phosphorylation reduces cell growth and proliferation in primary central nervous system lymphoma cells. J Neuro-Oncol. 2011;101(1):33–9.CrossRef Muta D, et al. Inhibition of eIF4E phosphorylation reduces cell growth and proliferation in primary central nervous system lymphoma cells. J Neuro-Oncol. 2011;101(1):33–9.CrossRef
34.
go back to reference van Westrhenen A, et al. Diagnostic markers for CNS lymphoma in blood and cerebrospinal fluid: a systematic review. Br J Haematol. 2018;182(3):384–403.PubMedPubMedCentralCrossRef van Westrhenen A, et al. Diagnostic markers for CNS lymphoma in blood and cerebrospinal fluid: a systematic review. Br J Haematol. 2018;182(3):384–403.PubMedPubMedCentralCrossRef
35.
go back to reference Baraniskin A, et al. MicroRNAs in cerebrospinal fluid as biomarker for disease course monitoring in primary central nervous system lymphoma. J Neuro-Oncol. 2012;109(2):239–44.CrossRef Baraniskin A, et al. MicroRNAs in cerebrospinal fluid as biomarker for disease course monitoring in primary central nervous system lymphoma. J Neuro-Oncol. 2012;109(2):239–44.CrossRef
36.
go back to reference Baraniskin A, et al. Circulating U2 small nuclear RNA fragments as a novel diagnostic biomarker for primary central nervous system lymphoma. Neuro-oncology. 2016;18(3):361–7.PubMedCrossRef Baraniskin A, et al. Circulating U2 small nuclear RNA fragments as a novel diagnostic biomarker for primary central nervous system lymphoma. Neuro-oncology. 2016;18(3):361–7.PubMedCrossRef
37.
go back to reference Roth P, et al. Differentially regulated miRNAs as prognostic biomarkers in the blood of primary CNS lymphoma patients. Eur J Cancer. 2015;51(3):382–90.PubMedCrossRef Roth P, et al. Differentially regulated miRNAs as prognostic biomarkers in the blood of primary CNS lymphoma patients. Eur J Cancer. 2015;51(3):382–90.PubMedCrossRef
38.
go back to reference Mao X, Sun Y, Tang J. Serum miR-21 is a diagnostic and prognostic marker of primary central nervous system lymphoma. Neurol Sci. 2014;35(2):233–8.PubMedCrossRef Mao X, Sun Y, Tang J. Serum miR-21 is a diagnostic and prognostic marker of primary central nervous system lymphoma. Neurol Sci. 2014;35(2):233–8.PubMedCrossRef
39.
go back to reference Zhao HT, Chen J, Shi SB, Tian J, Tao RJ. Pemetrexed plus rituximab as second-line treatment for primary central nervous system lymphoma. Med Oncol. 2015;32(1):351.PubMedCrossRef Zhao HT, Chen J, Shi SB, Tian J, Tao RJ. Pemetrexed plus rituximab as second-line treatment for primary central nervous system lymphoma. Med Oncol. 2015;32(1):351.PubMedCrossRef
40.
go back to reference Fontanilles M, et al. Non-invasive detection of somatic mutations using next-generation sequencing in primary central nervous system lymphoma. Oncotarget. 2017;8(29):48157–68.PubMedPubMedCentralCrossRef Fontanilles M, et al. Non-invasive detection of somatic mutations using next-generation sequencing in primary central nervous system lymphoma. Oncotarget. 2017;8(29):48157–68.PubMedPubMedCentralCrossRef
41.
go back to reference Hattori K, et al. Clinical significance of disease-specific MYD88 mutations in circulating DNA in primary central nervous system lymphoma. Cancer Sci. 2018;109(1):225–30.PubMedCrossRef Hattori K, et al. Clinical significance of disease-specific MYD88 mutations in circulating DNA in primary central nervous system lymphoma. Cancer Sci. 2018;109(1):225–30.PubMedCrossRef
42.
go back to reference Cani AK, et al. Next generation sequencing of vitreoretinal lymphomas from small-volume intraocular liquid biopsies: new routes to targeted therapies. Oncotarget. 2017;8(5):7989–98.PubMedCrossRef Cani AK, et al. Next generation sequencing of vitreoretinal lymphomas from small-volume intraocular liquid biopsies: new routes to targeted therapies. Oncotarget. 2017;8(5):7989–98.PubMedCrossRef
43.
go back to reference Hiemcke-Jiwa LS, et al. Molecular analysis in liquid biopsies for diagnostics of primary central nervous system lymphoma: review of literature and future opportunities. Crit Rev Oncol Hematol. 2018;127:56–65.PubMedCrossRef Hiemcke-Jiwa LS, et al. Molecular analysis in liquid biopsies for diagnostics of primary central nervous system lymphoma: review of literature and future opportunities. Crit Rev Oncol Hematol. 2018;127:56–65.PubMedCrossRef
44.
go back to reference Varettoni M, et al. Prevalence and clinical significance of the MYD88 (L265P) somatic mutation in Waldenstrom’s macroglobulinemia and related lymphoid neoplasms. Blood. 2013;121(13):2522–8.PubMedCrossRef Varettoni M, et al. Prevalence and clinical significance of the MYD88 (L265P) somatic mutation in Waldenstrom’s macroglobulinemia and related lymphoid neoplasms. Blood. 2013;121(13):2522–8.PubMedCrossRef
45.
go back to reference Kimura A, Yoshikura N, Koumura A, Hayashi Y, Inuzuka T. B-cell-activating factor belonging to the tumor necrosis factor family (BAFF) and a proliferation-inducing ligand (APRIL) levels in cerebrospinal fluid of patients with meningoencephalitis. J Neurol Sci. 2015;352(1–2):79–83.PubMedCrossRef Kimura A, Yoshikura N, Koumura A, Hayashi Y, Inuzuka T. B-cell-activating factor belonging to the tumor necrosis factor family (BAFF) and a proliferation-inducing ligand (APRIL) levels in cerebrospinal fluid of patients with meningoencephalitis. J Neurol Sci. 2015;352(1–2):79–83.PubMedCrossRef
46.
go back to reference Ansell SM, et al. Serum BLyS levels increase after rituximab as initial therapy in patients with follicular Grade 1 non-Hodgkin lymphoma. Am J Hematol. 2009;84(2):71–3.PubMedPubMedCentralCrossRef Ansell SM, et al. Serum BLyS levels increase after rituximab as initial therapy in patients with follicular Grade 1 non-Hodgkin lymphoma. Am J Hematol. 2009;84(2):71–3.PubMedPubMedCentralCrossRef
47.
go back to reference Tobon GJ, Pers JO, Youinou P, Saraux A. B cell-targeted therapies in Sjogren’s syndrome. Autoimmun Rev. 2010;9(4):224–8.PubMedCrossRef Tobon GJ, Pers JO, Youinou P, Saraux A. B cell-targeted therapies in Sjogren’s syndrome. Autoimmun Rev. 2010;9(4):224–8.PubMedCrossRef
48.
go back to reference Lavie F, et al. Increase of B cell-activating factor of the TNF family (BAFF) after rituximab treatment: insights into a new regulating system of BAFF production. Ann Rheum Dis. 2007;66(5):700–3.PubMedCrossRef Lavie F, et al. Increase of B cell-activating factor of the TNF family (BAFF) after rituximab treatment: insights into a new regulating system of BAFF production. Ann Rheum Dis. 2007;66(5):700–3.PubMedCrossRef
49.
go back to reference Ragheb S, et al. Multiple sclerosis: BAFF and CXCL13 in cerebrospinal fluid. Mult Scler. 2011;17(7):819–29.PubMedCrossRef Ragheb S, et al. Multiple sclerosis: BAFF and CXCL13 in cerebrospinal fluid. Mult Scler. 2011;17(7):819–29.PubMedCrossRef
50.
go back to reference Piazza F, et al. Cerebrospinal fluid levels of BAFF and APRIL in untreated multiple sclerosis. J Neuroimmunol. 2010;220(1–2):104–7.PubMedCrossRef Piazza F, et al. Cerebrospinal fluid levels of BAFF and APRIL in untreated multiple sclerosis. J Neuroimmunol. 2010;220(1–2):104–7.PubMedCrossRef
51.
go back to reference Wang H, et al. Cerebrospinal fluid BAFF and APRIL levels in neuromyelitis optica and multiple sclerosis patients during relapse. J Clin Immunol. 2012;32(5):1007–11.PubMedCrossRef Wang H, et al. Cerebrospinal fluid BAFF and APRIL levels in neuromyelitis optica and multiple sclerosis patients during relapse. J Clin Immunol. 2012;32(5):1007–11.PubMedCrossRef
52.
go back to reference Krumbholz M, Derfuss T, Hohlfeld R, Meinl E. B cells and antibodies in multiple sclerosis pathogenesis and therapy. Nat Rev Neurol. 2012;8(11):613–23.PubMedCrossRef Krumbholz M, Derfuss T, Hohlfeld R, Meinl E. B cells and antibodies in multiple sclerosis pathogenesis and therapy. Nat Rev Neurol. 2012;8(11):613–23.PubMedCrossRef
54.
go back to reference Mackay F, Ambrose C. The TNF family members BAFF and APRIL: the growing complexity. Cytokine Growth Factor Rev. 2003;14(3–4):311–24.PubMedCrossRef Mackay F, Ambrose C. The TNF family members BAFF and APRIL: the growing complexity. Cytokine Growth Factor Rev. 2003;14(3–4):311–24.PubMedCrossRef
56.
go back to reference Pelekanou V, et al. BAFF, APRIL, TWEAK, BCMA, TACI and Fn14 proteins are related to human glioma tumor grade: immunohistochemistry and public microarray data meta-analysis. PLoS One. 2013;8(12):e83250.PubMedPubMedCentralCrossRef Pelekanou V, et al. BAFF, APRIL, TWEAK, BCMA, TACI and Fn14 proteins are related to human glioma tumor grade: immunohistochemistry and public microarray data meta-analysis. PLoS One. 2013;8(12):e83250.PubMedPubMedCentralCrossRef
57.
go back to reference Deshayes F, et al. Abnormal production of the TNF-homologue APRIL increases the proliferation of human malignant glioblastoma cell lines via a specific receptor. Oncogene. 2004;23(17):3005–12.PubMedCrossRef Deshayes F, et al. Abnormal production of the TNF-homologue APRIL increases the proliferation of human malignant glioblastoma cell lines via a specific receptor. Oncogene. 2004;23(17):3005–12.PubMedCrossRef
58.
59.
go back to reference Novak AJ, Bram RJ, Kay NE, Jelinek DF. Aberrant expression of B-lymphocyte stimulator by B chronic lymphocytic leukemia cells: a mechanism for survival. Blood. 2002;100(8):2973–9.PubMedCrossRef Novak AJ, Bram RJ, Kay NE, Jelinek DF. Aberrant expression of B-lymphocyte stimulator by B chronic lymphocytic leukemia cells: a mechanism for survival. Blood. 2002;100(8):2973–9.PubMedCrossRef
60.
go back to reference Mackay F, Schneider P, Rennert P, Browning J. BAFF AND APRIL: a tutorial on B cell survival. Annu Rev Immunol. 2003;21:231–64.PubMedCrossRef Mackay F, Schneider P, Rennert P, Browning J. BAFF AND APRIL: a tutorial on B cell survival. Annu Rev Immunol. 2003;21:231–64.PubMedCrossRef
61.
go back to reference Xia XZ, et al. TACI is a TRAF-interacting receptor for TALL-1, a tumor necrosis factor family member involved in B cell regulation. J Exp Med. 2000;192(1):137–43.PubMedPubMedCentralCrossRef Xia XZ, et al. TACI is a TRAF-interacting receptor for TALL-1, a tumor necrosis factor family member involved in B cell regulation. J Exp Med. 2000;192(1):137–43.PubMedPubMedCentralCrossRef
62.
go back to reference Fu L, et al. BAFF-R promotes cell proliferation and survival through interaction with IKKbeta and NF-kappaB/c-Rel in the nucleus of normal and neoplastic B-lymphoid cells. Blood. 2009;113(19):4627–36.PubMedPubMedCentralCrossRef Fu L, et al. BAFF-R promotes cell proliferation and survival through interaction with IKKbeta and NF-kappaB/c-Rel in the nucleus of normal and neoplastic B-lymphoid cells. Blood. 2009;113(19):4627–36.PubMedPubMedCentralCrossRef
63.
go back to reference Kern C, et al. Involvement of BAFF and APRIL in the resistance to apoptosis of B-CLL through an autocrine pathway. Blood. 2004;103(2):679–88.PubMedCrossRef Kern C, et al. Involvement of BAFF and APRIL in the resistance to apoptosis of B-CLL through an autocrine pathway. Blood. 2004;103(2):679–88.PubMedCrossRef
64.
go back to reference He B, et al. Lymphoma B cells evade apoptosis through the TNF family members BAFF/BLyS and APRIL. J Immunol. 2004;172(5):3268–79.PubMedCrossRef He B, et al. Lymphoma B cells evade apoptosis through the TNF family members BAFF/BLyS and APRIL. J Immunol. 2004;172(5):3268–79.PubMedCrossRef
65.
go back to reference Lwin T, et al. Lymphoma cell adhesion-induced expression of B cell-activating factor of the TNF family in bone marrow stromal cells protects non-Hodgkin’s B lymphoma cells from apoptosis. Leukemia. 2009;23(1):170–7.PubMedCrossRef Lwin T, et al. Lymphoma cell adhesion-induced expression of B cell-activating factor of the TNF family in bone marrow stromal cells protects non-Hodgkin’s B lymphoma cells from apoptosis. Leukemia. 2009;23(1):170–7.PubMedCrossRef
66.
go back to reference Hoffmann FS, et al. The immunoregulator soluble TACI is released by ADAM10 and reflects B cell activation in autoimmunity. J Immunol. 2015;194(2):542–52.PubMedCrossRef Hoffmann FS, et al. The immunoregulator soluble TACI is released by ADAM10 and reflects B cell activation in autoimmunity. J Immunol. 2015;194(2):542–52.PubMedCrossRef
67.
go back to reference Laurent SA, et al. gamma-Secretase directly sheds the survival receptor BCMA from plasma cells. Nat Commun. 2015;6:7333.PubMedCrossRef Laurent SA, et al. gamma-Secretase directly sheds the survival receptor BCMA from plasma cells. Nat Commun. 2015;6:7333.PubMedCrossRef
68.
go back to reference Badr G, et al. BAFF enhances chemotaxis of primary human B cells: a particular synergy between BAFF and CXCL13 on memory B cells. Blood. 2008;111(5):2744–54.PubMedCrossRef Badr G, et al. BAFF enhances chemotaxis of primary human B cells: a particular synergy between BAFF and CXCL13 on memory B cells. Blood. 2008;111(5):2744–54.PubMedCrossRef
69.
go back to reference Vincent FB, Morand EF, Schneider P, Mackay F. The BAFF/APRIL system in SLE pathogenesis. Nat Rev Rheumatol. 2014;10(6):365–73.PubMedCrossRef Vincent FB, Morand EF, Schneider P, Mackay F. The BAFF/APRIL system in SLE pathogenesis. Nat Rev Rheumatol. 2014;10(6):365–73.PubMedCrossRef
Metadata
Title
APRIL and BAFF: novel biomarkers for central nervous system lymphoma
Authors
Matthias Mulazzani
Marion Huber
Sabine Borchard
Sigrid Langer
Barbara Angele
Elisabeth Schuh
Edgar Meinl
Martin Dreyling
Tobias Birnbaum
Andreas Straube
Uwe Koedel
Louisa von Baumgarten
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Journal of Hematology & Oncology / Issue 1/2019
Electronic ISSN: 1756-8722
DOI
https://doi.org/10.1186/s13045-019-0796-4

Other articles of this Issue 1/2019

Journal of Hematology & Oncology 1/2019 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine