Relapsing Lupus Nephritis and Cutaneous Vasculitis: A Race to Contain B Cells

Diane Zisa, MD; Kyriakos A. Kirou, MD, DSc

Disclosures

April 28, 2021

This article originally appeared on the Hospital for Special Surgery's website.

Case Report

A 45-year-old woman with a history of systemic lupus erythematosus (SLE) since 2006 came to the Hospital for Special Surgery in 2014 for continued management of SLE. Disease manifestations included arthritis, alopecia, Raynaud phenomenon, lymphadenopathy, pericarditis, and mononeuritis multiplex. She also had a recurrent erythematous, tender rash on her lower legs; biopsy revealed leukocytoclastic vasculitis with deposits of immunoglobulin M (IgM) and to a lesser extent IgA and C4d within the microvasculature, consistent with an SLE-associated immune complex–mediated vasculitis.

Positive serology results included antinuclear antibody, anti-Smith, anti-Ro, anti-La, and anti-RNP antibodies; low levels of serum complement C3 and C4 were found. Results were negative for anti-dsDNA antibodies, antiphospholipid antibodies, antineutrophil cytoplasmic antibodies, rheumatoid factor, and cryoglobulins.

She was treated with corticosteroids, hydroxychloroquine, azathioprine, tacrolimus, and belimumab. Severe flares of the disease required high-dose corticosteroid therapy.


 

Despite this treatment, she developed progressive disease in 2018, with palpable purpura extending to her proximal legs, arms, and trunk (Figure 1). In the following months, she developed new nephrotic-range proteinuria and microscopic hematuria. A kidney biopsy showed diffuse class IV glomerulonephritis with prominent intracapillary hyaline thrombi and IgM and IgG mesangial and subendothelial deposits. She received pulse-dose and high-dose oral corticosteroids and mycophenolate mofetil 3000 mg/d, with partial improvement in kidney function and proteinuria.


 

However, the rash remained active, causing severe pain and ulceration (Figure 2A) despite treatment with mycophenolate mofetil, corticosteroids, diuretics, and wound care. Two doses of rituximab 1000 mg separated by 2 weeks were added to her regimen, resulting in marked improvement in skin lesions and proteinuria and successful tapering of corticosteroids. Unfortunately, the nephritis and cutaneous vasculitis flared again 5 months later, coinciding with B-cell repletion and a decrease in C3/C4 levels, just before her next scheduled dose of rituximab. This pattern continued (Figure 3) despite addition of weekly belimumab. The refractory left leg skin ulcer eventually healed (Figure 2B).


 

Discussion

Vasculitis occurs in 11%-20% of patients with SLE, most frequently as a small-vessel leukocytoclastic vasculitis manifesting as cutaneous lesions. The development of cutaneous vasculitis in patients with SLE has been demonstrated to correlate with increased SLE activity overall, therefore warranting additional therapy for disease control.

This case highlights the role of B-cell–targeted therapies for both cutaneous vasculitis in SLE and lupus nephritis. The presence of immune complexes in the skin and kidney biopsies, as well as the profound decrease in the serum C3/C4 level coinciding with vasculitic and nephritic flares, suggested a dominant role of the autoimmune B-cell pathway in causing these manifestations. The therapeutic approach thus shifted to B-cell–targeted agents with complementary mechanisms of action: an anti-CD20 antibody (rituximab) and an antibody against soluble B-lymphocyte stimulator (belimumab).

The patient's condition improved with this combination, but the disease predictably flared when CD19/CD20 B-cell subsets repopulated just before the next dose of rituximab. Efforts to preempt flares now involve accelerated dosing of rituximab to every 4 months.

We are unsure why this patient's disease remained refractory. Transient and/or incomplete B-cell depletion is thought to contribute to resistant disease by selecting for potentially more pathogenic B-cell clones. In addition, whereas rituximab results in near complete depletion of circulating B-cells, those in tissues remain relatively unaffected.

Thus, future therapeutic considerations for refractory cases may include achieving a more durable B-cell depletion in peripheral blood and tissue with alternative anti-CD20 antibodies, such as obinutuzumab, which is currently under investigation for use in patients with lupus nephritis. Other therapies for refractory SLE under investigation include Bruton tyrosine kinase inhibitors and plasma cell–targeted agents, such as proteasome inhibitors.

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