Macrophage activation syndrome in a newborn: report of a case associated with neonatal lupus erythematosus and a summary of the literature
Pediatric Rheumatology volume 19, Article number: 13 (2021)
Macrophage activation syndrome (MAS) is a life-threatening hyperinflammatory syndrome and is caused by a severely dysregulated immune response. It has rarely been associated with neonatal lupus.
We present a female neonate with MAS born to a mother who had cutaneous lupus erythematosus with circulating anti-nuclear antibodies (ANA), anti-SSA, anti-SSB and anti-extractable nuclear antigen (anti-ENA) antibodies.
Because of neonatal lupus (NLE) with a total atrioventricular block, epicardial pacemaker implantation was required on the sixth day of life. Following surgery she developed non-remitting fever and disseminated erythematous skin lesions. A diagnosis of MAS was made based on these symptoms, with hyperferritinemia, elevated transaminases, hypertriglyceridemia, and a skin biopsy that showed hemophagocytosis. Our patient was treated with steroids for 3 months with good effect. No relapse has occurred.
MAS is a rare complication of neonatal lupus that may be difficult to diagnose, but needs to be treated promptly. In this article, pathogenesis and overlap of MAS and hemophagocytic lymphohistiocytosis (HLH) has been described.
Diagnosis of MAS can be difficult. Different diagnostic criteria are used in both diagnosing MAS and HLH. Validated criteria for diagnosis of MAS in other disease than systemic onset JIA have not been validated yet. In NLE, diagnosing MAS is even more difficult, since skin lesions are already common in NLE. We show the potential additional value of skin biopsy in diagnosing MAS.
Neonatal lupus erythematosus (NLE) is an auto-immune disease caused by transplacental transfer of maternal auto-antibodies anti-SSA (anti-Ro) and anti-SSB (anti-La) . The risk of NLE in maternal auto-immune disease with these antibodies is approximately 2 % . Severity of disease in the mother is not associated with severity of disease in the child. Mothers may have Systemic Lupus Erythematosus (SLE), subacute cutaneous lupus erythematosus, Sjögren syndrome or may not have any signs of auto-immune disease.
A well-known clinical presentation of NLE is neonatal cutaneous lupus and congenital complete heart block; NLE can also present with hepatitis, cytopenias and neurological abnormalities . Macrophage activation syndrome (MAS) is a life-threatening hyperinflammatory syndrome and is caused by a severely dysregulated immune response. It has rarely been associated with neonatal lupus. So far, only four patients have been reported in the literature (Table 1) [6,7,8,9].
Although MAS is a well-known complication of systemic-onset juvenile idiopathic arthritis (soJIA) it less frequently occurs associated with other autoimmune diseases such as Kawasaki disease, systemic lupus erythematosus, polyarticular juvenile idiopathic arthritis, juvenile dermatomyositis, anti-phospholipid syndrome and mixed connective tissue disease [10,11,12,13]. MAS is considered to represent a secondary form of hemophagocytic lymphohistiocytosis (HLH). Diagnosing MAS in diseases other then soJIA is challenging, because diagnostic criteria are only validated in soJIA. Skin findings are not included in the diagnostic criteria for (primary) hemophagocytic lymphohistiocytosis (HLH) or in MAS . However, skin eruption can be an important clinical finding in patients with HLH.
Primary HLH is a group of autosomal recessive immune disorders, all leading to a life-threatening hyperinflammatory state. It is linked to various genetic defects, mostly affecting the perforin-mediated cytolytic pathway [10, 11]. Perforin is a protein, necessary for inducing apoptosis of target cells (viruses, tumors) .
It has been suggested that MAS, primary and secondary forms of HLH are a spectrum of the same disease rather than single entities [10, 16], and steps have been made to think of MAS as ‘reactive’ HLH. Genetic studies confirm overlap between these entities.
In this case report, we show a case of MAS as a complication of NLE, potentially triggered by infection and maybe surgery as well , without a known HLH-susceptibility gene mutation. Additionally, we present a review of the literature of the pathophysiology of MAS and HLH in NLE patients.
A 29-year old, secondary gravida female was referred to the obstetrics department. She was diagnosed with cutaneous lupus erythematosus several years before pregnancy. She had positive anti-nuclear antibodies (ANA), anti-extractable nuclear antigen (anti-ENA), anti-SSA and anti-SSB. Treatment before pregnancy consisted of topical steroids. Before pregnancy, she was never treated with systemic therapy. During gestation she was asymptomatic without medication. Pregnancy was followed carefully at our obstetrics department because of her condition. A structural ultrasound examination at 20 2/7 weeks of gestation showed a fetal bradycardia (50 beats per minute (bpm)), based on a complete atrioventricular (AV) block in absence of a structural heart disease. No other structural abnormalities were found and no hydrops was present. Although controversial and a matter of debate [2, 18], mother was treated after diagnosis of the AV block with dexamethasone in order to suppress a potential ongoing inflammation to prevent fibrotic replacement in the AV node. No improvement of the fetal heart block was observed during close follow-up.
At 37 2/7 weeks of gestation, a female infant was born, birth weight was 2330 g (p5) and APGAR scores 9/10. Complete AV block was confirmed and there was a junctional escape rhythm of 50 bpm (Fig. 1a). The child was admitted to our neonatal intensive care unit for clinical observation. Due to circulatory insufficiency caused by the total AV block with a junction escape rhythm of 50 bpm, isoprenalin was started. Implantation of an epicardial VVI pacemaker system in abdominal position (Microny™, St Jude Medical) was inevitable on day 6.
Two days later, the patient developed fever and the pacemaker implantation wound appeared erythematous and inflamed. Blood- and wound cultures acquired before and during antibiotic treatment remained sterile. C-reactive protein (CRP) was maximum 80 mg/L on day 9 post-birth (ref < 5 mg/L). She was treated for a suspected wound infection with flucloxacillin and gentamycin intravenously. Furthermore, she was treated for perianal candidiasis with topical application of miconazole cream. Despite antibiotic therapy, there was an ongoing redness around the pacemaker pocket with cloudy, purulent fluid draining from the wound and fever persisted, one week after pacemaker implantation.
Surgical wound exploration was performed showing infiltrates with pus, for which antibiotic treatment was switched to ceftazidime. The pacemaker system was left inside and the wound was left open. In the days after exploration the redness slightly diminished around the elevated wound edges with granulation tissue appearing in the wound bed (Fig. 1b). CRP values remained low; varying between 6 and 13 mg/L. In between, fever persisted. The patient developed a generalized non-pruritic skin eruption on the 22nd day of life. Numerous round to oval and partly confluent erythematous papules and plaques, located on the forehead and eyebrows, as well as on the trunk and extremities were noted (Fig. 1c). Some papular lesions had an erosive center. The oral mucosa, palms and soles were not affected. There was no hepatosplenomegaly or lymphadenopathy.
Persistent fever, despite antibiotic treatment, and the atypical extensive skin lesions prompted us to think of other diagnosis like MAS. Our differential diagnosis consisted of persistent infection (systemic candidiasis, CMV, EBV varicella, (perianal skin culture positive for Candida albicans. CMV and EBV both (maternal) IgG positive, IgM negative)); auto-immune (complex neonatal lupus) or auto-inflammatory disease (MAS, primary HLH) or a primary immunodeficiency.
Additional blood tests showed a ferritin level of 4162 mug/L (ref. 10–150 mug/L), a mild anemia (Hb 7.1 mmol/L; 114.4 g/L; ref. 8.5–12.5 mmol/L), leukocytes and thrombocyte counts remained normal. Fibrinogen was 3.6 g/L (ref. 2.1–3.8 g/L), D-dimer 3996 ng/ml; ref. < 500 ng/ml). Furthermore, mildly elevated aminotransferase levels (ASAT 84 U/L (ref. < 31 U/L), ALAT 33 U/L (ref. < 34 U/L), LDH 909 U/L (ref. < 600 U/L) and elevated triglyceride levels, (343.7 mg/dl; ref. < 77.3 mg/dl) were reported. Similar to her mother, she had positive antibodies: ANA, anti-ENA, anti-SSA and B. Soluble IL-2 receptor level was 21,803 pg/ml (< 2500 pg/ml). These results are shown in Table 2.
Because of the non-remitting high-grade fever, extensive skin rash, in combination with liver enzyme abnormalities, elevated ferritin and proven NLE, MAS complicating NLE was suspected and a skin biopsy was taken to exclude other diseases as mentioned previously. Histological examination of a skin biopsy from a lesion on the trunk revealed a dermal interstitial and perivascular infiltrate, mainly consisting of histiocytes. The most notable finding was the presence of hematophagocytosis in the dermis (Fig. 1d). No pathological alterations were found in the epidermis and there was no histopathological evidence of an interface dermatitis and scantly periadnexal infiltration, as can be observed in cutaneous lupus erythematosus. In the skin biopsy sample we studied there was no evidence of involvement of the subcutis, as can be observed in cytophagic histiocytic panniculitis.. Hemophagocytosis describes the histopathological finding of phagocytosis of erythrocytes, platelets, leukocytes and their precursors by histiocytes. Hemophagocytosis in this skin biopsy strongly supports the diagnosis of MAS complicating NLE.
With a presumptive diagnosis of MAS complicating NLE, potentially triggered by wound infection and a pro-inflammatory state after surgery, treatment with prednisolone (2 mg/kg) was started, with vitamin D suppletion. Within 24 h after prednisolone was started, fever subsided. In 2 weeks, ferritin levels dropped and normalized within 2 months. Skin lesions resolved (Fig. 1e) and the pacemaker pocket wound healed completely in 4 weeks. Prednisolone was tapered slowly in 6 weeks and stopped after 3 months of treatment. At that moment, ferritin level was normalized, ANA and anti-ENA remained positive, but anti SSA/B titers were undetectable.
Follow up after 6 months demonstrated a positive ANA, but negative anti ENA, negative anti SSA and negative anti SSB. ANA became negative after 8 months. Genetic tests (next generation sequencing, gene panel) were performed to differentiate between primary HLH or MAS and secondary HLH. No mutations in nine HLH susceptibility genes (PRF1, UNC13D, STX11, STXBP, SH2D1A, XIAP, LYST, RAB27A, AP3B)  were detected.
It has been suggested that MAS, primary and secondary forms of HLH are a spectrum of the same disease rather than single entities [10, 16], and steps have been made to think of MAS as ‘reactive’ HLH . In the spectrum of MAS/HLH, due to genetic susceptibility, a trigger (infection, auto-immune disease, malignancy) results in excessive activation and expansion of monocytes and macrophages; with high levels of circulating cytokines (IFN-gamma/type II interferon-response); IL-2; IL-1, IL-6, IL-18 and TNF-alpha; and also cytokine inhibitors such as soluble TNF-receptors . IL-18 seems to be particular relevant in MAS, since strikingly high levels have been observed in patients with MAS in soJIA. IL-18 is believed to drive the action of CD8+ T-cells and their production of IFN-g, enhancing the cytokine storm [4, 10]. In MAS, IL-1 and IL-18 are upregulated .
In a pro-inflammatory state, cytolytic cells are important in termination of immune responses by inducing apoptosis. The following mechanism of the cytokine storm in MAS and HLH is suspected: the failure of the apoptosis induction of target cells by cytolytic cells might delay the contraction stage of the immune response, leading to persistent expansion of activated T-lymphocytes, macrophages and excessive and persistent cytokine release . Failure to induce apoptosis, due to cytotoxic dysfunction leads to the cytokine storm. In such cytokine storm, clinical findings are non-remitting fever, cytopenias, hepatosplenomegaly and coagulation disorders with extremely high levels of ferritin and hypertriglyceridemia.
In primary HLH, several genetic defects have been described. Most predisposing genetic defects (15–40%) are in the perforin-mediated cytolytic pathway [15, 20]. In about 10–30% of primary HLH, the disease is caused by mutations in MUNC13–4 gene [15, 20]. With this mutation, the function of cytolytic cells is diminished, although the production of perforin is normal. Other genetic mutations related to primary HLH are STXBP2 (syntaxin binding protein 2) and syntaxin 11 . These genes are necessary in the pathway of the release of perforin.
In secondary HLH or MAS, different mutations have been found in previously mentioned genes (Perforin 1, MUNC13–14, STXBP2, Syntaxin 11). Heterozygous mutations have been found in up to 76% of individuals with secondary HLH and MAS [21, 22] as well as mutations in non-coding regions and splice-site mutations of HLH genes, which correlates with a less severe disease course and a later age of onset .
A threshold model has been proposed in MAS, in which combinations of genetic predisposition, underlying inflammatory state and triggering infectious agents, results in a clinically relevant cytokine storm syndrome and MAS [10, 21, 23].
Skin lesions are not included in the diagnostic criteria for (primary) hemophagocytic lymphohistiocytosis (HLH) or in MAS . However, skin eruption can be an important clinical feature in patients with HLH. According to the literature, 6–65% of patients with HLH have skin involvement during the course of disease [3, 5, 24]. Also in MAS/HLH, skin findings have been reported [7, 25, 26]. Cutaneous manifestations of MAS/HLH are however aspecific as most patients present with a transient generalized maculopapular eruption. Patients may also develop skin eruptions that are related to the additional effects of the MAS/HLH (e.g. thrombocytopenic purpura) [3, 27].
In general, skin lesions in neonatal lupus appear after exposition to natural UV-light, in the first 2 months after birth. Skin abnormalities earlier in life, even directly after birth, have been described as well . The pathology of the skin biopsy in our case did not show mononuclear cell infiltration and immunoglobulin deposition, as is expected in neonatal lupus skin abnormalities. Although performing bone marrow aspirate and biopsy is part of the diagnostic work-up of MAS/HLH, less is known about the clinical relevance of skin biopsy in the work-up for MAS/HLH. The classical histopathological skin findings of MAS/HLH include a lymphohistiocytic (perivascular) infiltrate in the dermis without epidermal abnormalities. The most important finding is the presence of hemophagocytosis. This term describes the histopathological finding of phagocytosis of erythrocytes, platelets, leukocytes and their precursors by histiocytes . Data on the presence of hemophagocytosis in a skin biopsy in MAS are lacking, but it has been described before in case reports, with one case with cutaneous hemophagocytosis in NLE [29, 30]. The presence of hemophagocytosis is one of the key features of MAS, as can be seen in bone marrow biopsy in up to 60% of patients with MAS secondary to soJIA . In our case, skin biopsy instead of bone marrow aspirate confirmed the diagnosis of MAS in NLE.
Diagnosis of MAS/HLH
In general, it can be challenging to diagnose MAS/HLH in either primary or secondary forms. Clinical and laboratory features of MAS include sustained fever, hyperferritinemia, pancytopenia, fibrinolytic consumptive coagulopathy and liver dysfunction. There is no diagnostic test or a set of disease uniform diagnostic criteria to differentiate MAS from the underlying systemic inflammatory condition. An expert consensus panel published validated diagnostic criteria for MAS complicating soJIA in 2016 : persistent fever in a patient with soJIA with serum ferritin level > 684 ng/ml plus any of the following: platelet count < 181*10^9/l, ASAT > 48 units/l, triglyceride concentration > 156 mg/dl or fibrinogen < 360 mg/dl .
For secondary HLH, with similar clinical spectrum as MAS, more validated diagnostic criteria are noted in the HLH-2004 diagnostic guidelines . At least five of the following eight criteria are required for the diagnosis: fever, splenomegaly, cytopenias (> 2 of 3 cellines), hypertriglyceridemia (> 265 mg/dl) and/or hypofibrinogenemia (< 1.5 g/l), hemophagocytosis in bone marrow or spleen or lymph nodes, low or absent natural killer cell activity, ferritin > 500 μg/L and sCD25 > 2400 units/ml. The HLH-2004 criteria may delay diagnosis in patients with a less severe initial presentation, since three of eight criteria for diagnosis (sCD25, NK cell function, evidence of hemophagocytosis on bone marrow biopsy) are not fast and easily available.
Our patient fulfilled the diagnostic criteria of MAS secondary to soJIA  but did not meet the criteria for the HLH-2004 criteria: only 4 out of 8 criteria were present (i.e. fever, hyperferritinemia, hypertriglyceridemia. Skin biopsy confirming hemophagocytosis instead of bone marrow biopsy; of note: NK-cell activity was not evaluated).
Levels of IL-18, reflecting inflammasome activation , have been reported to be markedly increased in MAS and only moderately elevated in other rheumatic disease and in familial HLH [4, 33]. It possibly reflects the extent of macrophage activation, given that macrophages seem to be the main source of IL-18. Levels of IL-18 correlate with levels of ferritin . Currently, it can be measured but it is not widely available yet and was not measured in our patient [4, 10, 12]. High levels of IL-18 have been found in neonates born to a mother with adult onset Stills disease .
Next to their antiviral effects, growing evidence suggests that type I and II interferons have immunoregulatory functions that are critical for dampening immunopathogenic mechanisms and minimizing collateral damage from the infection .
For example, the type I interferon family has a central role in the pathogenesis of several autoimmune diseases as in SLE and RA . MAS and HLH are known as type II interferonopathies  (ref dual nature). The type I and II interferon response are closely related and the type I interferon response is capable of suppressing the type II response .
In our patient; we hypothesize primary activation of the type I response (because of maternal auto-antibodies anti SSA, anti SSB). Wound infection and possibly (yet unproven) genetic susceptibility leaded to a type II interferon response.
It would have been informative to measure these interferon responses but has not been done in our patient since it was not available yet at that time.
MAS/HLH secondary to NLE has been treated with steroids as monotherapy in the few cases that has been reported (Table 1). In two neonates, a relapse occurred when steroids were tapered and stopped after 4 weeks of treatment. Longer treatment, around three to 6 months seems to be necessary. This might be related to the disappearance of maternal antibodies in children within the first 3 months after birth.
There are no validated treatment guidelines on MAS in soJIA, nor in other rheumatological disease. First-line treatment is often started with high-dose corticosteroid therapy. Cyclosporine A (an immunosuppressive drug which acts in lowering T-lymphocytes) is also reported to induce remission, as monotherapy or as part of a combination regimen. Etoposide has been given as well, as it is part of the HLH-2004 protocol. IL-receptor antagonists, such as Anakinra, are increasingly used in the treatment of MAS in soJIA, especially in steroid-resistant MAS [10, 12, 36, 37]. Since IL-18 seems to play an important role in the development of MAS, IL-18 blockage may be an important therapeutic target in future therapy, as is currently under study in NLRC4-MAS inflammasomopathies (ClinicalTrials.gov Identifier: 113760). Recently, promising results in the treatment of primary HLH have been shown in a phase 2–3 trial, in which emapalumab (a human anti-interferon-y antibody); administered with dexamethasone, showed to be effective in the treatment of primary HLH . This monoclonal antibody binds interferon-y and neutralizes its biologic activity,controlling hyperinflammation.
MAS/HLH in rheumatic disease (soJIA, Kawasaki, SLE) has a more favourable outcome than in primary HLH, which relies on more treatable factors. When the auto-immune/inflammatory disease is treated properly, the trigger for cytokine storm will be gone . Primary HLH needs to be treated following intensive HLH-2004 guidelines , this is outside the scope of this article to address in further detail.
Our patient has been followed for the first 3 years. She had a growth restriction; her development is normal. The complete AV block persisted and the implanted pacemaker device is working properly. The trigger for MAS/HLH is gone, autoantibodies have become negative. Although long-term effects of NLE complicated by HLH/MAS are not known, no important sequellae have been observed so far.
In children with NLE or in children born from mothers who are SSA- and/or SSB-positive, every condition with persistent fever, abnormal wound healing, atypical skin eruption, should raise awareness of the possible diagnosis of MAS/HLH complicating NLE.
Recent diagnostic criteria of MAS in soJIA seem to be useful in more rheumatological diseases, for instance NLE, but have not been validated yet. A lesional skin biopsy can be taken to assess the presence of hemophagocytosis in the dermal compartment. The results of a skin biopsy may add in the diagnostic work-up and may lead to treatment at an earlier stage.
Availability of data and materials
Anti-extractable nuclear antigen
Anti-Sjögren-syndrome-related antigen A / also called anti-Ro
Anti-Sjögren-syndrome-related antigen B / also called anti-La
- AV block:
- AV node:
Juvenile idiopathic arthritis
Macrophage activation syndrome
Neonatal lupus erythematosus
Systemic-onset juvenile idiopathic arthritis
Systemic lupus erythematosus
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Heijstek, V., Habib, M., van der Palen, R. et al. Macrophage activation syndrome in a newborn: report of a case associated with neonatal lupus erythematosus and a summary of the literature. Pediatr Rheumatol 19, 13 (2021). https://doi.org/10.1186/s12969-021-00500-w