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Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
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Type II hypersensitivity involves IgG and IgM antibodies targeting cell surface antigens, leading to cell destruction. This can occur through complement activation, antibody-dependent cell-mediated cytotoxicity (ADCC), or acting as opsonins for phagocytosis. When excessive, these reactions cause significant tissue damage.Drug-induced hemolytic anemia is a common example, where drugs like penicillin or cephalosporins bind to red blood cells, forming drug-protein complexes. These complexes...
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Drug-related allergies are immune-mediated responses triggered by the administration of pharmacological agents. These hypersensitivity reactions are classified based on the immune mechanisms involved. The four primary types—Type I, II, III, and IV—are mediated by different immunological pathways and exhibit distinct clinical manifestations.Type I Hypersensitivity/ IgE-Mediated Reactions: Immunoglobulin E (IgE) immediately mediates Type I hypersensitivity reactions. Upon initial...
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Immunotherapy-associated autoimmune hemolytic anemia.

Uqba Khan1,2, Farman Ali1, Muhammad Siddique Khurram1

  • 1Graduate Medical Education, St. John Hospital and Medical Center, Detroit, MI USA.

Journal for Immunotherapy of Cancer
|February 28, 2017
PubMed
Summary

Combined immunotherapy with ipilimumab and nivolumab can cause severe autoimmune hemolytic anemia. Early recognition and treatment with steroids and rituximab are crucial for managing this rare but serious side effect in melanoma patients.

Keywords:
Autoimmune hemolytic anemiaImmunotherapyIpilimumabNivolumab

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Area of Science:

  • Oncology
  • Immunology
  • Hematology

Background:

  • Cancer immunotherapy, particularly with checkpoint inhibitors targeting CTLA-4 and PD-1 pathways, has transformed malignancy treatment.
  • Combined CTLA-4 and PD-1 inhibition offers synergistic efficacy but increases the risk of toxicity.
  • Metastatic melanoma is a key indication for these advanced immunotherapeutic strategies.

Observation:

  • A 43-year-old woman with metastatic melanoma developed severe autoimmune hemolytic anemia after two cycles of ipilimumab and nivolumab.
  • Clinical presentation included severe anemia, elevated lactate dehydrogenase, absent haptoglobin, and a positive direct Coombs test.
  • The patient's symptoms manifested three weeks after her last immunotherapy administration.

Findings:

  • The patient was diagnosed with severe autoimmune hemolytic anemia directly linked to ipilimumab and nivolumab treatment.
  • Successful management was achieved using high-dose steroids and rituximab.
  • This case highlights an unusual and severe adverse event associated with combined immunotherapy.

Implications:

  • Healthcare professionals must be aware of rare but potentially lethal adverse effects of cancer immunotherapies.
  • Early identification and prompt management of immunotherapy-induced autoimmune hemolytic anemia are critical for patient outcomes.
  • Understanding these side effects is essential for the safe and effective application of revolutionary cancer treatments.