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USMLE - Chapter 2 - Immunology

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  1. Primary Lymphoid Organs to Lymph Node Structural Diagram
    7Topics
  2. Introduction to Lymphatic Drainage to Lymph Node Palpability and Right Lymphatic Duct
    6Topics
  3. Spleen Structure Overview to Thymus-Related Conditions
    6Topics
  4. Components and Mechanism of Immunity to Understanding Immune Privilege
    4Topics
  5. MHC I and II: Introduction and Loci to DQ8, DR3, DR4
    9Topics
  6. Functions of Natural Killer Cells to Major Functions of T Cells
    3Topics
  7. T Cell Development: Bone Marrow & Thymus to Regulatory T Cells and Autoimmunity
    6Topics
  8. T-cell Activation: Antigen Presentation to B-cell Activation: Co-stimulation, Class Switching, and Maturation
    4Topics
  9. Antibody Structure and Function to Antibody Diversity and Specificity
    4Topics
  10. Introduction to Immunoglobulin Isotypes to Thymus-Dependent Antigens
    7Topics
  11. Introduction to Complement System to Convergence and MAC Formation
    9Topics
  12. Early Complement Deficiencies to PNH: Hemolysis & Thrombosis
    4Topics
  13. Interleukin-1: Macrophage Secretion and Acute Response to IL-10 and IL-13: Immune Regulation and IgE Production
    7Topics
  14. Respiratory Burst Introduction to Interferons Clinical Use & Side Effects
    5Topics
  15. T Cell Surface Proteins to Examples of Passive and Active Immunity
    4Topics
  16. Live Attenuated Vaccines: Description to mRNA Vaccine
    8Topics
  17. Overview of Hypersensitivity Types to Type II: Cellular Dysfunction & Clinical Examples
    6Topics
  18. Type III Hypersensitivity: Mechanism & Examples to Type IV Hypersensitivity: Examples & Tests
    5Topics
  19. Allergic and Anaphylactic Transfusion Reactions to Delayed Hemolytic Transfusion Reaction
    5Topics
  20. Autoantibodies in Neuromuscular and Systemic Diseases to Autoantibodies in Metabolic, Hematologic, and Renal Disorders
    5Topics
  21. Bruton's Agammaglobulinemia to Chronic Mucocutaneous Candidiasis
    7Topics
  22. Severe Combined Immunodeficiency (SCID) to Chronic Granulomatous Disease
    7Topics
  23. Intro to Immunodeficiency & T-Cell Bacterial Infections to Parasitic Infections & Key Deficiency Note
    5Topics
  24. Hyperacute Transplant Rejection to Histology of Transplant Rejection
    5Topics
  25. Immunosuppressants: Definition and Risks to Sirolimus & Basiliximab: Clinical Aspects
    5Topics
  26. Azathioprine to Immunotherapy: Interleukin-2 and Interferons
    6Topics
  27. TNF-α Inhibitors: Adalimumab & Infliximab to Omalizumab & Palivizumab: Allergic & Viral
    7Topics
Lesson 19 of27
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Allergic and Anaphylactic Transfusion Reactions to Delayed Hemolytic Transfusion Reaction

Content August 26, 2025

Immunologic blood transfusion reactions

TYPE PATHOGENESIS TIMING CLINICAL PRESENTATION DONOR BLOOD HOST BLOOD
Allergic/anaphylactic reaction Type I hypersensitivity reaction against plasma proteins in transfused blood. IgA-deficient individuals should receive blood products without IgA. Within minutes to 2-3 hr (due to release of preformed inflammatory mediators in degranulating mast cells) Allergies: urticaria, pruritus. Anaphylaxis: wheezing, hypotension, respiratory arrest, shock Donor plasma proteins, including IgA. Host mast cell with IgE (anti-IgA).

TYPE PATHOGENESIS TIMING CLINICAL PRESENTATION DONOR BLOOD HOST BLOOD
Acute hemolytic transfusion reaction Type II hypersensitivity reaction. Typically causes intravascular hemolysis (ABO blood group incompatibility) During transfusion or within 24 hr (due to preformed antibodies) Fever, hypotension, tachypnea, tachycardia, flank pain, hemoglobinuria (intravascular), jaundice (extravascular) Donor RBC with A and/or B group antigens. Host anti-A, anti-B IgG, IgM.

TYPE PATHOGENESIS TIMING CLINICAL PRESENTATION DONOR BLOOD HOST BLOOD
Febrile nonhemolytic transfusion reaction Cytokines created by donor WBCs accumulate during storage of blood products. Reactions prevented by leukoreduction of blood products. Within 1-6 hr (due to preformed cytokines) Fever, headaches, chills, flushing. More common in children. Donor WBC releases preformed cytokines.

TYPE PATHOGENESIS TIMING CLINICAL PRESENTATION DONOR BLOOD HOST BLOOD
Transfusion-related acute lung injury Two-hit mechanism: Neutrophils are sequestered and primed in pulmonary vasculature due to recipient risk factors. Neutrophils are activated by a product (eg, antileukocyte antibodies) in the transfused blood and release inflammatory mediators → capillary permeability → pulmonary edema Within minutes to 6 hr Respiratory distress, noncardiogenic pulmonary edema Donor antileukocyte antibody. Host neutrophil and lungs.

TYPE PATHOGENESIS TIMING CLINICAL PRESENTATION DONOR BLOOD HOST BLOOD
Delayed hemolytic transfusion reaction Anamnestic response to a foreign antigen on donor RBCs (Rh [D] or other minor blood group antigens) previously encountered by recipient. Typically causes extravascular hemolysis. Onset over 24 hr. Usually presents within 1-2 wk (due to slow destruction by reticuloendothelial system) Generally self limited and clinically silent. Mild fever, hyperbilirubinemia.

Topics Covered:

  • Allergic and Anaphylactic Transfusion Reactions
  • Acute Hemolytic Transfusion Reaction
  • Febrile Nonhemolytic Transfusion Reaction
  • Transfusion-Related Acute Lung Injury (TRALI)
  • Delayed Hemolytic Transfusion Reaction