Immune Hemolysis: Diagnosis and Treatment Recommendations

Wilma Barcellini
Seminars in hematology · 2015 · vol. 52(4) , pp. 304–312 · doi:10.1053/j.seminhematol.2015.05.001 · PMID:26404442 · W2153815562
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This paper reviews current diagnostic strategies and offers treatment recommendations for immune-mediated hemolytic anemia.

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Abstract

Autoimmune hemolytic anemia (AIHA) is a heterogeneous disease usually classified as warm, cold [cold agglutinin disease (CAD)] or mixed, according to the thermal range of the autoantibody. Diagnosis is based on the direct antiglobulin test (DAT), typically positive with anti-IgG antisera in warm AIHA and anti-C3d in CAD. Diagnostic pitfalls are due to IgA autoantibodies, warm IgM, low-affinity IgG, or IgG below the threshold of sensitivity, and about 5% of AIHA remains DAT-negative. The treatment of AIHA is still not evidence-based. Corticosteroids are the first-line therapy for warm AIHA. For refractory/relapsed cases, the choice is between splenectomy (effective in ~70% cases but with a presumed cure rate of 20%) and rituximab (effective in ~70%-80% of cases), which is becoming the preferred second-line treatment, and thereafter any of the immunosuppressive drugs (azathioprine, cyclophosphamide, cyclosporine, mycophenolate mofetil). Rituximab is now recommended as first-line treatment for CAD. Additional therapies are intravenous immunoglobulins, danazol, and plasma exchange, with alemtuzumab and high-dose cyclophosphamide as the last options.

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MeSH descriptors

Anemia, Hemolytic, Autoimmune Anemia, Hemolytic, Autoimmune Anemia, Hemolytic, Autoimmune Antibodies, Anti-Idiotypic Antibodies, Anti-Idiotypic Autoantibodies Autoantibodies Humans Splenectomy Treatment Outcome

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