Abstract
There is no information about XCL1 in patients with acute lymphoblastic leukemia (ALL). The objective of this study was to correlate the serum levels of XCL1 and survival in ALL patients. Only ALL patients older than 12 months were considered to participate. Serum XCL1 was measured at diagnosis, end of remission induction, and end of consolidation. Thirty-three ALL patients with median age of 21 years (1–78) were included. Higher XCL1 level (above 50 pg/mL) at ALL diagnosis correlated with higher survival (p = 0.038), whereas XCL1 level at end of induction and consolidation had no significant correlation. Concerning the behavior of serum XCL1 during treatment, higher survival at 5 years was observed in the group with progressively decreased levels of XCL1 (70%) than those with progressively increasing (29%) or no detectable XCL1 (14%). In conclusion, higher serum XCL1 levels at diagnosis and their progressive decline throughout chemotherapy could be correlated with higher survival.
Similar content being viewed by others
References
Gökbuget N, Stanze D, Beck J et al (2012) Outcome of relapsed adult lymphoblastic leukemia depends on response to salvage chemotherapy, prognostic factors, and performance of stem cell transplantation. Blood 120:2032–2041
Rowe J (2010) Prognostic factors in adult acute lymphoblastic leukaemia. Brit J Haematol 150:389–405
Mazuri B, Mertas A, Sónta-Jakimczy K et al (2004) Concentration of IL-2, IL-6, IL-8, IL-10 and TNF-alpha in children with acute lymphoblastic leukemia after cessation of chemotherapy. Hematol Oncol 22:27–34
Bruserud O, Ulvestad E (2003) Human acute lymphoblastic leukemia (ALL) blasts as accessory cells during T-cell activation: differences between patients in costimulatory capacity affect proliferative responsiveness and cytokine release by activated T cells. Cancer Immunol Immunother 52:215–225
Lei Y, Takahama Y (2012) XCL1 and XCR1 in the immune system. Microbes Infect 14:262–267
Rossi D, Zlotnik A (2000) The biology of chemokines and their receptors. Annu Rev Immunol 18:217–242
Rollins B (1997) Chemokines. Blood 90:909–928
Ordway D, Higgins D, Sanchez-Campillo J et al (2007) XCL1 (lymphotactin) chemokine produced by activated CD8 T cells during the chronic stage of infection with Mycobacterium tuberculosis negatively affects production of IFN-γ by CD4 T cells and participates in granuloma stability. J Leukoc Biol 82:1221–1229
Dong C, Chua A, Ganguly B et al (2005) Glycosylated recombinant human XCL1/lymphotactin exhibits enhanced biologic activity. J Immunol Methods 302:136–144
Visentini M, Carbonari M, Ghia E, De Propriis S et al (2006) A lymphotactin-producing monoclonal T-cell lymphoproliferative disorder with extreme lymphocytopenia and progressive leukoencephalopathy. Leuk Lymphoma 47:1421–1423
Stievano L, Tosello V, Marcato N et al (2003) CD8þ alpha betaþ T cells that lack surface CD5 antigen expression are a major lymphotactin (XCL1) source in peripheral blood lymphocytes. J Immunol 171:4528–4538
Volkman B, Liu T, Peterson F (2009) Lymphotactin structural dynamics. Methods Enzymol 461:51–70
Huang H, Li F, Cairns F et al (2001) Neutrophilis and B cells express XCR1 receptor and chemotactically respond to lymphotactin. Biochem Biophys Res Commun 281:378–382
Rosas-Taraco A, Higgins D, Sánchez-Campillo J et al (2009) Intrapulmonary delivery of XCL1-targeting small interfering RNA in mice chronically infected with Mycobacterium tuberculosis. Am J Respir Cell Mol Biol 41:136–145
Endres M, Andreas K, Kalwitz G et al (2010) Chemokine profile of synovial fluid from normal, osteoarthritis and rheumatoid arthritis patients: CCL25, CXCL10 and XCL1 recruit human subchondral mesenchymal progenitor cells. Osteoarthr Cartil 18:1458–1466
Emtage P, Wan Y, Hitt M et al (1999) Adenoviral vectors expressing lymphotactin and interleukin-12 synergize to facilitate tumor regression in murine breast cancer models. Hum Gene Ther 10:697–709
Cairns CM, Gordon JR, Li F et al (2001) Lymphotactin expression by engineered myeloma cells drives tumor regression: mediation by CD4+ and CD8+ T cells and neutrophils expressing XCR1 receptor. J Immunol 167:57–65
Kelner GS, Kennedy J, Bacon KB et al (1994) Lymphotactin: a cytokine that represents a new class of chemokine. Science 266:1395–1399
Cerdan C, Devilard E, Xerri L et al (2001) The C-class chemokine lymphotactin costimulates the apoptosis of human CD4(+) T cells. Blood 97:2205–2212
Hedrick JA, Saylor V, Figueroa D et al (1997) Lymphotactin is produced by NK cells and attracts both NK cells and T cells in vivo. J Immunol 158:1533–1540
Reikvam H, Fredly H, Kittang OA et al (2013) The possible diagnostic and prognostic use of systemic chemokine profiles in clinical medicine—the experience in acute myeloid leukemia from disease development and diagnosis via conventional chemotherapy to allogeneic stem cell transplantation. Toxins 5:336–362
Kornblau SM, McCue D, Singh N et al (2010) Recurrent expression signatures of cytokines and chemokines are present and are independently prognostic in acute myelogenous leukemia and myelodysplasia. Blood 116:4251–4261
Bradley LM, Asensio VC, Schioetz LK, Harbertson J et al (1999) Islet-specific Th1, but not Th2, cells secrete multiple chemokines and promote rapid induction of autoimmune diabetes. J Immunol 162(5):2511–2520
Klein M, Paul R, Angele B et al (2006) Protein expression pattern in experimental pneumococcal meningitis. Microbes Infect 8:974–983
Dorner BG, Smith HR, French AR et al (2004) Coordinate expression of cytokines and chemokines by NK cells during murine cytomegalovirus infection. J Immunol 172:3119–3131
Cerdan C, Serfling E, Olive D (2000) The C-class chemokine, lymphotactin, impairs the induction of Th1-type lymphokines in human CD4(+) T cells. Blood 96:420–428
Van Dongen J, Van der Velden V, Brüggemann M et al (2015) Minimal residual disease diagnostics in acute lymphoblastic leukemia: need for sensitive, fast, and standardized technologies. Blood 125:3996–4009
Pérez-Figueroa E, Sánchez-Cuaxospa M, Martínez-Soto KA et al (2016) Strong inflammatory response and Th1-polarization profile in children with acute lymphoblastic leukemia without apparent infection. Oncol Rep 35:2699–2706
Gómez AM, Martínez C, González M et al (2015) Chemokines and relapses in childhood acute lymphoblastic leukemia: a role in migration and in resistance to antileukemic drugs. Blood Cell Mol Dis 55:220–227
Funding
The present investigation was sponsored with own resources of the Service of Hematology.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
All procedures performed in the study were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Conflict of interest
The authors declare that they have no conflict of interest.
Rights and permissions
About this article
Cite this article
Gutiérrez-Aguirre, C.H., Flores-Jiménez, J.A., Alatorre-Ricardo, J. et al. The prognostic significance of serum XCL1 concentration in patients with acute lymphoblastic leukemia: a pilot study. Ann Hematol 96, 2015–2024 (2017). https://doi.org/10.1007/s00277-017-3142-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00277-017-3142-3