Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal disease

In this report, we evaluate the hypothesis that hemophagocytic lymphohistiocytosis in patients with defects of lymphocyte cytotoxicity is usually triggered by infections. We show that in the majority of patients, extensive virus PCR panels performed in addition to routine microbiological investigations remain negative and summarize 25 patients with onset of hemophagocytic lymphohistiocytosis in utero or within the first 10 days of life, in none of which an associated bacterial or viral infection was reported. These observations, even though preliminary, invite to consider a key role of lymphocyte cytotoxicity in controlling T‐cell homeostasis also in the absence of apparent infectious stimuli.

[1]  Scott Montgomery,et al.  Confirmed efficacy of etoposide and dexamethasone in HLH treatment: long-term results of the cooperative HLH-2004 study. , 2017, Blood.

[2]  G. de Saint Basile,et al.  Hemophagocytic syndrome: primary forms and predisposing conditions. , 2017, Current opinion in immunology.

[3]  S. Ehl,et al.  Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis , 2017, Journal of Clinical Immunology.

[4]  S. Ehl,et al.  Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T‐cell activation, differentiation and repertoire , 2017, European journal of immunology.

[5]  G. Mihăescu,et al.  Human anelloviruses: an update of molecular, epidemiological and clinical aspects , 2015, Archives of Virology.

[6]  S. Esposito,et al.  Debate around infection-dependent hemophagocytic syndrome in paediatrics , 2013, BMC Infectious Diseases.

[7]  A. Ramanan,et al.  Review of haemophagocytic lymphohistiocytosis , 2010, Archives of Disease in Childhood.

[8]  K. Weinberg,et al.  Pre‐ and post‐natal treatment of hemophagocytic lymphohistiocytosis , 2009, Pediatric blood & cancer.

[9]  P. Marrack,et al.  An animal model of hemophagocytic lymphohistiocytosis (HLH): CD8+ T cells and interferon gamma are essential for the disorder. , 2004, Blood.

[10]  L. Sung,et al.  The role of infections in primary hemophagocytic lymphohistiocytosis: a case series and review of the literature. , 2001, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[11]  J. Altman,et al.  Counting antigen-specific CD8 T cells: a reevaluation of bystander activation during viral infection. , 1998, Immunity.

[12]  A. Fischer,et al.  Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry. FHL Study Group of the Histiocyte Society. , 1996, Leukemia.

[13]  J. Andersson,et al.  Familial hemophagocytic lymphohistiocytosis and viral infections , 1993, Acta paediatrica.

[14]  M. Uppin,et al.  Hemophagocytic Lymphohistiocytosis , 2012, Indian Journal of Hematology and Blood Transfusion.

[15]  R. Clementi,et al.  Familial hemophagocytic lymphohistiocytosis: how late can the onset be? , 2001, Haematologica.