Kikuchi-Fujimoto disease associated with hemophagocytic lymphohistiocytosis following the BNT162b2 mRNA COVID-19 vaccination.

Kikuchi-Fujimoto disease (KD) is a self-limiting histiocytic necrotizing lymphadenitis. One case of KD following administration of the BNT162b2 mRNA COVID-19 vaccine was recently reported.[1] Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory state brought on by uncontrolled histiocytes, macrophages and T-cell activation, which have also been occasionally observed after BNT162b2 vaccination.[2] KD and HLH present overlapping pathogenesis and symptoms, and their association has been previously described in children and adult patients.[3,4] Here, we report the first case of KD associated with HLH following the BNT162b2 mRNA COVID-19 vaccination.

A 38-year-old previously healthy woman was admitted to the hospital with a history of a fever of 40°C for more than ten days, associated with chills and fatigue. She presented with a diffuse cutaneous eruption of erythematous papules, which were subsequently confluent (Figure 1, AB). She had previously been treated with antibiotics (amoxicillin and clavulanic acid, followed by teicoplanin and doxycycline), with no improvement. The first dose of the BNT162b2 mRNA COVID-19 vaccine was administered two months after giving birth to a healthy baby. Three weeks before the onset of fever, the patient received a second dose of the vaccine, inoculated in the same left arm as the first dose. At hospital admission, her nasopharyngeal swab for SARS CoV-2 PCR was negative; SARS CoV-2 IgG antibodies were positive (>2.080 BAU/mL; cut-off: 33.8 BAU/mL; LIAISON SARS-CoV-2 TrimericS IgG, Diasorin, Saluggia, Italy).

Figure 1.

Patient’s clinical and radiological findings. A and B) Diffuse maculo-papular skin rash; C and D) CT scan showing left axillary lymph node enlargement.

Her physical exam was normal except for the cutaneous rash and multiple enlarged tender lymph nodes in the left axillary zone. This was confirmed by a contrastenhanced computed tomography (CT) examination (Figure 1, C-D).

Laboratory tests showed bi-cytopenia with leukopenia and anemia (neutrophil count, 0.9 x 109/L; lymphocyte count, 0.3 x 109/L, hemoglobin, 9.8 g/L), increased lactate dehydrogenase and transaminase levels, high serum ferritin levels (500 μg/L), mild hypertriglyceridemia (225 mg/dL) and normal fibrinogen. Her serum soluble interleukin- 2 receptor (IL-2R) level was increased to 2.610 U/mL (normal value 223-710) and her natural killer (NK) cell count was low (<35 cells/μL; normal value 200-400). IL-6, IL-8 and IL-10 levels were normal, but the tumor necrosis factor (TNF) level was increased. The patient underwent a bone marrow aspiration and trephine procedure, which showed hemophagocytosis (Figure 2, A-C). A diagnosis of HLH was confirmed based on the fulfilment of 6/8 HLH-2004 diagnostic criteria.[5] In addition, an excisional lymph node biopsy of the left axillary was performed. Histopathological examination of the lymph node revealed histiocytic necrotizing lymphadenitis, characterized by paracortical, well-circumscribed necrotic areas with karyorrhexis and fibrin deposits. Immunohistochemistry revealed numerous CD68-positive histiocytes as well as several CD3-positive T cells and few CD20-positive B cells. All these features are considered typical of KD (Figure 2, D-F).

Figure 2.

Lymph node and bone marrow histological findings. A) Increased diffusion of histiocytes (brown color) in the bone marrow trephine biopsy; CD68 (PGM1) stain, 10X magnification; B) An histiocyte showing phagocytosis of hemopoietic elements; CD68 (PGM1) stain, 60X magnification; C) Histiocytes showing phagocytosis of red cells, platelets, erythroid precursor cells; hematoxylin-eosin stain, 60X magnification; D) A low power view of the lymph node showing paracortical necrotizing zones (N) in an otherwise preserved architecture; hematoxylin-eosin stain; E) The paracortical necrotizing areas were characterized by many reactive T lymphocytes, as shown by immunohistochemistry for CD3; 10X magnification; F) The immunostaining for CD68 revealed numerous histiocytes within the necrosis; 10X magnification.

Further analysis did not show ongoing infections of HCV, HBV hepatitis virus, HIV, toxoplasma, rubeovirus, brucella, leptospirosis, bartonella, chlamydia, morbillivirus, mycoplasma or yersinia. The tuberculosis Quantiferon test was also negative. Epstein Barr virus (EBV), Parvovirus B19, cytomegalovirus, JC virus and herpes- 6 DNA were also absent. Antinuclear antibodies (ANA), antibodies to double-stranded DNA (antidsDNA), and antibodies to extractable nuclear antigens (anti-ENA) were absent. The rheumatoid factor test was negative and both complement C3 and C4 serum levels were normal.

The patient was promptly initiated on steroids (methylprednisolone 1 mg/kg i.v.), in adherence with the recommended treatment for HLH. Sudden fever lysis was observed and clinical conditions improved. Methyl-prednisone was substituted with prednisone (1 mg/day) at hospital discharge one week later. This schedule was maintained for a further two weeks, reduced to a half dosage for three more weeks, then tapered over the following three weeks. IL-2R levels decreased to 1.170 U/mL and 740 U/mL after two and three weeks of steroid treatment, respectively, and reached normal levels (460 U/mL) after four weeks. NK cells also returned to normal levels. The patient is doing well and follow-up is still ongoing.

To the best of our knowledge, this is the first case of KD associated with HLH following COVID-19 vaccination. HLH is a severe hyperinflammatory syndrome, secondary to aberrant cytokine production and uncontrolled histiocyte activation, following infections, in particular EBV, hematological malignancies, autoimmune diseases, hematopoietic stem cells or organ transplantation. It is characterized by cytopenia, unremitting fever, hepatic dysfunction and a fatal multiple organ failure without early recognition and prompt treatment. The first line of treatment is steroids and/or immunoglobulins, with etoposide added in poor responders.[5] KD is a self-limiting histiocytic necrotizing lymphadenitis that commonly occurs in Asia, although it is present globally.[6] It is characterized by fever, lymphadenopathy and leukopenia, may be associated with a skin rash and is mainly characterized by transient red, millet-sized maculopapules.[7] Since no skin biopsy was carried out, it remains unclear whether the patient’s skin rash was associated with KD or was a possible adverse effect of teicoplanin (Figure 1, A-B). KD pathogenesis is unknown, although it is believed to be a consequence of an aberrant T cells and histiocyte immune response to an immunogenic antigen. An association with organisms such as toxoplasma, cytomegalovirus, varicella-zoster virus, EBV, human herpes virus-6, HIV, and yersinia enterocolitica, has been suggested, although convincing evidence has yet to be presented. Moreover, a possible association with autoimmune disorders, including antiphospholipid antibody syndrome and mixed connective tissue disease, has been reported.[1] Steroids and immunoglobulins treatment may be beneficial. The association between HLH and KD has been described in both children and adult patients and has a potentially fatal outcome if left untreated.[3,4,8] Some authors have reported that that CD8+ T lymphocytes in patients with HLH-KD may be excessively activated, altering the course of the self-limited KD progress and resulting in HLH.[8]

Both HLH and KD following BNT162b2 mRNA COVID-19 vaccination have recently been described.[1,2] Notably, after mass vaccination against COVID-19, a vaccine-associated hypermetabolic lymphadenopathy (VAHL) in the axillary or supraclavicular lymph nodes, ipsilateral to the vaccination site, has been reported.[9,10,11] This is frequently observed after BNT162b2 administration, with higher intensities following the booster dose, and lasting until three weeks after vaccination. We hypothesize that our patient first developed a left-axillary VHAL following two ipsilateral vaccine dose inoculations, followed by a systemic inflammatory response syndrome (SIRS) with KD features in the axillary lymph nodes, and HLH symptoms as a systemic inflammatory reaction. Dermal histiocytes and macrophages represent the first resident antigen-presenting cell (APC) transfected by the mRNA vaccine that presents antigenic peptides on major histocompatibility (MHC) class I and MHC class II molecules of CD4+ and CD8+ cells, resulting in immune response expansion. Additionally, intramuscular vaccine injection leads to a local increase in proinflammatory cytokines, which form an immune-stimulatory environment in draining axillary lymph nodes.[12] It remains unclear whether an alternate arm inoculation in our patient might have been less immune-reactive.

In conclusion, we have described the first case of KD associated with HLH following COVID-19 vaccination. This is a rare event and does not compromise the safety and efficacy of the BNT162b2 mRNA vaccine in the fight against COVID-19. Physicians should be aware of rare systemic inflammatory reactions that require early diagnosis and treatment.