Flow Cytometric Analysis of T Cells in Hemophagocytic Lymphohistiocytosis
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Background: T cell immunophenotypes in patients with hemophagocytic lymphohistiocytosis (HLH) have been described. Downregulation of CD5 or CD7 on T cells has been reported in patients with Epstein-Barr virus (EBV)-positive HLH. As the utility of T cell immunophenotypes as an adjunctive diagnostic or a prognostic marker for HLH has not been evaluated, we analyzed T cell immunophenotypes in HLH patients for this purpose. Methods: We classified 45 HLH patients into three subgroups: EBV-positive HLH (N=27), EBV-negative secondary HLH (N=15), and familial HLH (N=3). We retrospectively characterized downregulation patterns of CD5 or CD7 on activated T cells, using flow cytometry. Overall survival was estimated using Kaplan-Meier curves and compared using the log-rank test. Results: An aberrant immunophenotype, including CD5 and/or CD7 downregulation on T cells, was observed in 55.6% (15/27) of the EBV-positive HLH patients and 100% of the familial HLH (3/3). Only one (1/15, 6.7%) patient with EBV-negative secondary HLH showed an aberrant loss of CD7 antigen on CD8+ T cells. The presence of an aberrant T cell immunophenotype was not related to overall survival in EBV-positive HLH and EBV-negative secondary HLH patients. Conclusions: An aberrant T cell immunophenotype may assist in discriminating EBV-negative secondary HLH and EBV-positive HLH. However, it may not be useful as a prognostic marker.
Abstract
Background: T cell immunophenotypes in patients with hemophagocytic lymphohistiocytosis (HLH) have been described. Downregulation of CD5 or CD7 on T cells has been reported in patients with Epstein-Barr virus (EBV)-positive HLH. As the utility of T cell immunophenotypes as an adjunctive diagnostic or a prognostic marker for HLH has not been evaluated, we analyzed T cell immunophenotypes in HLH patients for this purpose. Methods: We classified 45 HLH patients into three subgroups: EBV-positive HLH (N=27), EBV-negative secondary HLH (N=15), and familial HLH (N=3). We retrospectively characterized downregulation patterns of CD5 or CD7 on activated T cells, using flow cytometry. Overall survival was estimated using Kaplan-Meier curves and compared using the log-rank test. Results: An aberrant immunophenotype, including CD5 and/or CD7 downregulation on T cells, was observed in 55.6% (15/27) of the EBV-positive HLH patients and 100% of the familial HLH (3/3). Only one (1/15, 6.7%) patient with EBV-negative secondary HLH showed an aberrant loss of CD7 antigen on CD8+ T cells. The presence of an aberrant T cell immunophenotype was not related to overall survival in EBV-positive HLH and EBV-negative secondary HLH patients. Conclusions: An aberrant T cell immunophenotype may assist in discriminating EBV-negative secondary HLH and EBV-positive HLH. However, it may not be useful as a prognostic marker.
참고문헌 (30)
- Otrock ZK, "Clinical characteristics, prognostic factors, and outcomes of adult patients with hemophagocytic lymphohistiocytosis", Am J Hematol, 90, pp.220~224 (2015)
- McCall CM, "Flow cytometric findings in hemophagocytic lymphohistiocytosis", Am J Clin Pathol, 137, pp.786~794 (2012)
- 신상용, "First Report on Familial Hemophagocytic Lymphohistiocytosis with an Abnormal Immunophenotype and T Cell Monoclonality in Korea", Annals of Laboratory Medicine, 35(1), pp.155~158 (2015), 대한진단검사의학회
- Wada T, "Down-regulation of CD5 expression on activated CD8+ T cells in familial hemophagocytic lymphohistiocytosis with perforin gene mutations", Hum Immunol, 74, pp.1579~1585 (2013)
- Henter JI, "HLH-2004 : Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis", Pediatr Blood Cancer, 48, pp.124~131 (2007)
- Stevens SJ, "Toward standardization of Epstein-Barr virus DNA load monitoring : unfractionated whole blood as preferred clinical specimen", J Clin Microbiol, 39, pp.1211~1216 (2001)
- Jamal S, "Immunophenotypic analysis of peripheral T-cell neoplasms. A multiparameter flow cytometric approach", Am J Clin Pathol, 116, pp.512~526 (2001)
- Brisse E, "Advances in the pathogenesis of primary and secondary haemophagocytic lymphohistiocytosis : differences and similarities", Br J Haematol, 174, pp.203~217 (2016)
- Ishii E, "Hemophagocytic lymphohistiocytosis in children : pathogenesis and treatment", Front Pediatr, 4, pp.47~ (2016)
- Sieni E, "Familial hemophagocytic lymphohistiocytosis : a model for understanding the human machinery of cellular cytotoxicity", Cell Mol Life Sci, 69, pp.29~40 (2012)
- Sieni E, "Familial hemophagocytic lymphohistiocytosis : when rare diseases shed light on immune system functioning", Front Immunol, 5, pp.167~ (2014)
- Yoon HS, "UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis", Haematologica, 95, pp.622~626 (2010)
- Koh KN, "Clinical features, genetics, and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in Korea : report of a nationwide survey from Korea Histiocytosis Working Party", Eur J Haematol, 94, pp.51~59 (2015)
- Manji F, "Acute HIV infection presenting as hemophagocytic lymphohistiocytosis : case report and review of the literature", BMC Infect Dis, 17, pp.633~ (2017)
- Brisse E, "How viruses contribute to the pathogenesis of hemophagocytic lymphohistiocytosis", Front Immunol, 8, pp.1102~ (2017)
- Marsh RA, "Epstein-Barr virus and hemophagocytic lymphohistiocytosis", Front Immunol, 8, pp.1902~ (2017)
- Ishii E, "Nationwide survey of hemophagocytic lymphohistiocytosis in Japan", Int J Hematol, 86, pp.58~65 (2007)
- Imashuku S, "Clinical features and treatment strategies of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis", Crit Rev Oncol Hematol, 44, pp.259~272 (2002)
- Kawa K, "Epstein-Barr virus--associated diseases in humans", Int J Hematol, 71, pp.108~117 (2000)
- Dojcinov SD, "EBV-positive lymphoproliferations of B- T- and NK-cell derivation in non-immunocompromised hosts", Pathogens, 7 (2018)
- Lin MT, "Massive expansion of EBV+ monoclonal T cells with CD5 down regulation in EBV-associated haemophagocytic lymphohistiocytosis", J Clin Pathol, 60, pp.101~103 (2007)
- Weisberger J, "Down-regulation of pan-T-cell antigens, particularly CD7, in acute infectious mononucleosis", Am J Clin Pathol, 120, pp.49~55 (2003)
- Wada T, "Immunophenotypic analysis of Epstein-Barr virus(EBV)-infected CD8(+)T cells in a patient with EBV-associated hemophagocytic lymphohistiocytosis", Eur J Haematol, 79, pp.72~75 (2007)
- Karandikar NJ, "Unusual immunophenotype of CD8+ T cells in familial hemophagocytic lymphohistiocytosis", Blood, 104, pp.2007~2009 (2004)
- Toga A, "Clinical significance of cloned expansion and CD5 down-regulation in Epstein-Barr Virus(EBV)-infected CD8+ T lymphocytes in EBV-associated hemophagocytic lymphohistiocytosis", J Infect Dis, 201, pp.1923~1932 (2010)
- Manno EC, "Familial hemophagocytic lymphohistiocytosis type 3 diagnosed at school age : a case report", J Pediatr Hematol Oncol, 36, pp.e128~e130 (2014)
- Tembhare P, "Flow cytometric immunophenotypic assessment of T-cell clonality by Vbeta repertoire analysis : detection of T-cell clonality at diagnosis and monitoring of minimal residual disease following therapy", Am J Clin Pathol, 135, pp.890~900 (2011)
- Mehta RS, "Hemophagocytic lymphohistiocytosis(HLH) : a review of literature", Medical Oncology, 30, pp.740~ (2013)
- Imashuku S, "Longitudinal follow-up of patients with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis", Haematologica, 89, pp.183~188 (2004)
- Ohga S, "Hematopoietic stem cell transplantation for familial hemophagocytic lymphohistiocytosis and Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in Japan", Pediatr Blood Cancer, 54, pp.299~306 (2010)
