Acquired hemophagocytic syndrome: comment to the case report.

Hemophagocytosis represents the peculiar pathological feature of activated macrophages engulfing hematopoietic cells as a result of an immune dysregulatory disorder. This finding is the hallmark of a rare hyperinflammatory disease known as hemo phagocytic ly mphohistiocytosis (HLH). HLH is a severe condition characterized by an abnormal ineffective immune response caused by an uncontrolled activation and proliferation of macrophages, natural killer (NK) cells and T-helper lymphocytes, leading to excessive cytokine production, subsequent amplification of pathologic immune stimulation, increased phagocytic activity and tissue damage [1]. Typically, heat shock proteins (HSP) are associated with a peculiar combination of clinical and biochemical features, including prolonged high fever, pancytopenia, hepatosplenomegaly, hypertriglyceridemia, hyperferritinemia and hemophagocytosis in the bone marrow. If undiagnosed or not promptly treated, HLH almost inevitably results in death. First described in 1939 by Scott and Robb-Smith [2] as a life-threatening disorder characterized by histiocytic proliferation with erytrophagocytosis in the lymphoreticular system, it was named ‘histiocytic medullary reticulosis’ (HMR) and ascribed among malignant histiocytosis. In the following years, HSP were considered a hereditary immune dysregulatory disorder, called ‘familial hemophagocytic reticulosis’ [3], until Risdall described a viral association with HLH, highlighting a possible acquired etiology and therefore referring to it as ‘reactive hemophagocytic syndrome’ [4]. Subsequently, several cases have been involved in the genesis of sporadic HLH, including infections, malignancies, autoimmune diseases and metabolic co nditions. Therefore, HLH can be etiologically classified into a primary (genetic) or a secondary (acquired) disorder. All forms of HLH share hereditary or acquired immune defects characterized by impaired function of NK cells and cytotoxic T cells. Primary HLH includes two groups: first, the familial hemophagocytic lymphohistiocytosis syndromes (FHLH1–5), in which HLH is the sole manifestation of the disease, and second, immunodeficiency syndromes associated with albinism (Chediak Higashi syndrome, Griscelli syndrome type II, Hermansky-Pudlak syndrome type II) or other primary immunodeficiencies (i.e., X-linked lymphoproliferative disorder type I or II), where the hemophagocytosis is a part of a complex landscape of clinical manifestations [5]. Although not yet entirely identified, the known genetic abnormalities cause defect in proteins (like perforin, MUNC13.4, syntaxin-11 and STXBP2) that play a key role in granule-dependent lymphocyte cytotoxicity, impairing the maturation or the secretion cytotoxic granules during target cell killing, thus prejudicing the immune response [6]. Hereditary HLH usually occurs in infants or young children, with clear familial inheritance, is associated with high risk of recurrence and short life expectancy without hematopoietic cell transplantation. Commentary

Hemophagocytosis represents the peculiar pathological feature of activated macrophages engulfing hematopoietic cells as a result of an immune dysregulatory disorder. This finding is the hallmark of a rare hyperinflammatory disease known as hemo phagocytic ly mphohistiocytosis (HLH).
HLH is a severe condition characterized by an abnormal ineffective immune response caused by an uncontrolled activation and proliferation of macrophages, natural killer (NK) cells and T-helper lymphocytes, leading to excessive cytokine production, subsequent amplification of pathologic immune stimulation, increased phagocytic activity and tissue damage [1]. Typically, heat shock proteins (HSP) are associated with a peculiar combination of clinical and biochemical features, including prolonged high fever, pancytopenia, hepatosplenomegaly, hypertriglyceridemia, hyperferritinemia and hemophagocytosis in the bone marrow. If undiagnosed or not promptly treated, HLH almost inevitably results in death.
First described in 1939 by Scott and Robb-Smith [2] as a life-threatening disorder characterized by histiocytic proliferation with erytrophagocytosis in the lymphoreticular system, it was named 'histiocytic medullary reticulosis' (HMR) and ascribed among malignant histiocytosis. In the following years, HSP were considered a hereditary immune dysregulatory disorder, called 'familial hemophagocytic reticulosis' [3], until Risdall described a viral association with HLH, highlighting a possible acquired etiology and therefore referring to it as 'reac-tive hemophagocytic syndrome' [4]. Subsequently, several cases have been involved in the genesis of sporadic HLH, including infections, malignancies, autoimmune diseases and metabolic co nditions.
Therefore, HLH can be etiologically classified into a primary (genetic) or a secondary (acquired) disorder. All forms of HLH share hereditary or acquired immune defects characterized by impaired function of NK cells and cytotoxic T cells.
Primary HLH includes two groups: first, the familial hemophagocytic lymphohistiocytosis syndromes (FHLH1-5), in which HLH is the sole manifestation of the disease, and second, immunodeficiency syndromes associated with albinism (Chédiak Higashi syndrome, Griscelli syndrome type II, Hermansky-Pudlak syndrome type II) or other primary immunodeficiencies (i.e., X-linked lymphoproliferative disorder type I or II), where the hemophagocytosis is a part of a complex landscape of clinical manifestations [5].
Although not yet entirely identified, the known genetic abnormalities cause defect in proteins (like perforin, MUNC13.4, syntaxin-11 and STXBP2) that play a key role in granule-dependent lymphocyte cytotoxicity, impairing the maturation or the secretion cytotoxic granules during target cell killing, thus prejudicing the immune response [6]. Hereditary HLH usually occurs in infants or young children, with clear familial inheritance, is associated with high risk of recurrence and short life expectancy without hematopoietic cell transplantation. Secondary HLH, currently more common than primary forms, affects older children or adults without known genetic cause. Several pathological conditions may act as a trigger for the development of acquired HLH.
Infections, mainly viral and Epstein-Barr virus (EBV) associated, but also caused by bacterial, fungal and parasitic organisms, play a crucial role. However, infections may also represent the stimulus responsible for an acute exacerbation of primary forms of HLH; moreover, there is often an overlap between HLH secondary to infection and a septic process, whose di fferential diagnosis is extremely complex [7].
HLH is associated with several disorders of the immune system, including autoimmune disorders, being lupus erythematosus the most frequently reported one, acquired immune deficiencies (such as AIDS) or immune disorders after hematopoietic stem cell transplantation. Macrophage activation syndrome can be considered as a variant of HLH developing in autoinflammatory diseases, principally in systemic juvenile idiopathic arthritis. Interestingly, also various metabolic disorders, including lysinuric protein intolerance, multiple sulphatase deficiency and alterations of propionate metabolism are known to be potential triggers for HLH [8].
HLH is known to develop in patients with malignancies, mainly lymphoproliferative disorders. Often, infections promote HLH in the context of a compromised immune system due to chemotherapy or cytokines produced by the tumor cells or infected T lymphocytes [9]. Among hematological malignancies, lymphomas or leukemias of T or NK cell lines, which are frequently related to EBV infection, are the most frequently associated with HLH [5,10].
HLH is the result of uncontrolled hyperinflammatory reaction to various types of triggers. The main physiopathological mechanism is an abnormal activation and proliferation of macrophages and CD8 + lymphocytes, and prominent cytokines production (including IFN-γ, sIL-2R, IL-1, TNF-α, IL-6 and IL-18) induced by T-helper lymphocytes [19,20]. This hypercytokinemia leads to an autoamplification loop of macrophages and cytotoxic lymphocyte activation resulting in tissue damages. While the pathogenesis of primary HLH is largely understood, the mechanisms underly-ing acquired HLH are not yet fully reco gnized [21,22].
In genetic HLH, hereditary mutations affect the transport, release and/or activity of cytolytic granules in NK cells and cytotoxic T lymphocytes (CTL). Cytotoxic granules contain perforin and granzymes that induce apoptosis of target cells. Moreover perforin is important for the down-regulation of the immune response. As a result, despite NK and CTL granule-dependent cytotoxic activity is impaired, they can still activate and secrete cytokines, supporting a persistent activation of the immune response with tissue damage [22].
Different pathogenetic mechanisms can support acquired HLH. In most cases, there is not an impairment of lymphocyte cytotoxic activity, although some heterozygous mutations in genes that regulate the innate immune response and the NK function have been correlated with secondary HLH [23]. In case of infections, mainly by intracellular microorganism, the pathogenesis lies in a direct activation of Toll-like receptors with disproportionate activation of normal macrophage and T cells, leading to a detrimental Th1 cytotoxic response. The inability to deal with infections in immunocompromised patients can be a trigger for HLH development: cells of the innate immune response are continuously activated via pattern recognition receptors (such as Toll-like receptors) that respond to components of opportunistic bacteria, mycoplasma, fungi, and viruses, sustaining an uncontrolled immune response. In autoimmune disorders, non-antigen-specific triggering of innate immunity may represent the precipitating factor [21]. Several cytokines released by malignancies may induce HLH [5]. HLC can be an extremely rare consequence of the cytotoxic effects of chemotherapy, whose massive tumor cell destruction results in a pathological immune response, leading to excessive cytokine production [14,17,24].
Given the poor prognosis, timely diagnosis is crucial. There is no single feature that is pathognomonic for HLH, including hemophagocytosis. To facilitate the diagnosis, the HLH Study Group of the Histiocyte Society has established a panel of eight diagnostic criteria, five of which are required for HLH. The utility of these criteria is questionable because they lack specificity. Therefore, it is the coexistence of different clinical features (especially the triad of prolonged fever, hepatospleno-megaly-and cyto-penias) to become relevant [25].
Each clinical and laboratory finding is strictly related to the hyper-inflammation state of the disease. Macrophage and T-lymphocyte proliferation results in hepatosplenomegaly and peripheral lymphadenopathy. Fever is secondary to high concentrations of IL-2 and IL-1. Cytopenias is ascribable to TNF-α and IFN-γ overproduction that suppress hematopoiesis and direct hemophagocytosis. Coagulopathy is often reported, and www.future-science.com future science group future science group Acquired hemophagocytic syndrome: comment to the case report Commentary due to macrophage secretion of plasminogen activators resulting in an accelerated conversion of plasminogen to plasmin and consequent hypofibrinogenemia. Disseminated intravascular coagulation can be a rare manifestation of elevated levels of TNF-α and IFN-γ. Serum ferritin elevation induced by IL-1β is highly sensitive and specific for HLH. Hyper triglyceridemia is the consequence of lipoprotein lipase inhibition by TNF-α.
As a severe condition, there should be no delay in starting therapy. The goal of treatment is to regulate the immune system dysfunction, suppressing the hyperinflammatory state. It is also important to treat the cause responsible for acquired HLH. Cortico steroids alone, or in association with intravenous immunoglobulin, represents the main therapy in patients with rheumatologyassociated HLH (macrophage activation syndrome), but may be also active for others secondary forms of HLH. In the latter case, however, the lack of a quick response should result in the promptly set up of full therapy, consisting in immune-suppressive agents, cytotoxic drugs, biological response modifiers, and stem-cell transplantation as suggested by the HLH-94 protocol. Unfortunately, about 25% of patients fail to achieve complete remission with standard therapy. At the moment, there are no standard salvage therapies. No conclusive results are reported with the use of infliximab, daclizumab, alemtuzumab, anakinra and other agents [26].
Refractory patients generally have dismal prognosis, encouraging research aimed at a better understanding of disease pathogenesis so as to develop more effective therapies.
Financial & competing interests disclosure The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
No writing assistance was utilized in the production of this manuscript.

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