This observation is especially intriguing in patients with “warm” immunoglobulin G (IgG)–mediated AHA that is not primarily complement-mediated. Almost all patients with “warm” IgG-mediated AHA also show a brisk reticulocytosis, unlike ITP in which ineffective platelet production contributes to thrombocytopenia. Perhaps the size and rigidity of the antibody, complement in the case of “cold,” IgM-coated red blood cells, and the location and developmental expression of antigens on red cell precursors and on mature red cell surface permits more efficient clearance by tissue macrophages than comparably opsonized platelets. Clinical disease might develop at lower antibody density more rapidly after autoantibodies form, when they might be more susceptible to immunosuppression.1 Lower rates of spontaneous or treatment-derived responses may also relate to the site of the underlying immune defect as AHA or Evans syndrome is more common in patients with constitutive defects, such as the autoimmune lymphoproliferative syndrome.2
This conundrum brings us to the observations of Barcellini et al in their article in this issue of Blood.3 They report that each of 14 patients with primary warm AHA and 5 of 9 patients with primary cold AHA responded to 4 weekly intravenous injections of low-dose rituximab (100 mg/wk × 4), which they substituted for conventional dosing (375 mg/m2/wk × 4). The choice of a lower dose was based on the reasoning that less drug would be needed to ablate a smaller number of autoreactive B cells in AHA than is required to induce remission in B-cell lymphoma. Similar findings of efficacy in ITP have been reported in single-arm studies, but only 20% of patients appear to maintain a complete response more than 3 years after low or conventional doses of rituximab.4 The results of Barcellini et al compare very favorably to other series of adults with warm AHA treated with rituximab using conventional dosing.4 However, more time will need to elapse to determine whether patients with AHA treated with “low-dose” rituximab relapse at the same rate as those with ITP. Likewise, it will be important to see whether the reduced dosage leads to better preservation of pretreatment B- and T-cell repertoires and preserves response to vaccination5 and lowers risk of infection. In addition, paraproteins (if present) may serve as useful surrogate markers of efficacy and mechanism of effect.
Why does ITP or AHA recur despite prolonged and virtually complete B-cell depletion in the peripheral blood? Potential reasons include down-regulation, internalization or proteolytic shedding of CD20, failure to ablate “CD20 low”-expressing early B-cell progenitors, plasma cells and long-lived memory cells, and cell sanctuaries in the bone marrow, spleen, and lymphoid organs where the effect on B cell–T cell cooperation and induction of T-regulatory suppressor cells may be incomplete.6 The mechanism of action of rituximab is complex, incompletely understood, and may even involve induction of an idiotype-specific T-cell response that sustains remission.7 It is possible that low-dose rituximab invokes an immunomodulatory response that does not require complete B-cell depletion.
The article by Barcellini et al also reminds us that we know frightfully little as to how red cell or platelet autoantibodies arise, how rituximab works, or how it should be administered and monitored. The premise underlying immunosuppression for AHA and ITP is that the responsible autoreactive B and T cells are more susceptible to eradication or are simply less abundant in the immune repertoire than those responsible for normal host responses and therefore more likely to be eliminated on a sensitivity or stoichastic basis, permitting a normal underlying immune system to re-emerge. But we also know that AHA and ITP are common and refractory to intervention in patients with inherited or acquired disruptions in immune regulation, for example, APLS or CVID, so more immunosuppression is not necessarily more effective.2
It is possible that the dose of anti-CD20 that impairs B-cell proliferation, antibody production, and T-cell education differs among patients and autoimmune disorders. Are even higher doses (eg, 1000 mg) used to treat rheumatoid arthritis more efficacious in the long run? What is the optimal agent(s) to combine with rituximab and in which patients? Anti-CD20 antibodies re-engineered to enhance effector functions are in development; synergy with other immunosuppressive agents has been demonstrated,8 and sensitization to anti-CD209 has been reported in the setting of B-cell malignancy. In addition, patients with chronic lymphocytic leukemia previously treated with rituximab may show a significant response to a second type I antibody, ofatumumab, that recognizes a different epitope on CD20.10 Such combination or sequential therapy with different anti-CD20s has not been reported in AHA or ITP. Moreover, recent studies indicate that type I and type II anti-CD20 antibodies differ in their distribution in lipid rafts in the plasma membrane and in their capacity to cause complement-dependent cytotoxicity versus programmed cell death.7 The implications of these findings in the treatment of AHA and ITP are unknown.
Thus, we are left with many unanswered questions but also potential opportunities to improve outcome. However, unless we can identify and track the B- and possibly T-cell clones that cause AHA and ITP, we are doomed to human trials based on empiricism rather than controlled trials based on rational principles.
Conflict-of-interest disclosure: The authors declare no competing financial interests. ■
- © 2012 by The American Society of Hematology