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Related Concept Videos

Hypersensitivity Reactions: Immune-Complex Reactions01:19

Hypersensitivity Reactions: Immune-Complex Reactions

Type III hypersensitivity reactions occur when antigen–antibody complexes form and activate the complement system. Normally, these complexes help the clearance of antigens by phagocytes and red blood cells. However, when large numbers of immune complexes are present, they can deposit in tissues—particularly in the walls of blood vessels—leading to inflammation and tissue injury. These deposits trigger complement activation and neutrophil recruitment, resulting in serum sickness, a systemic...
Hypersensitivities01:30

Hypersensitivities

Hypersensitivity, also known as a hypersensitivity reaction or allergic reaction, is a condition where the body's immune system reacts abnormally to a foreign substance. Such substances, that cause hypersensitivity are referred to as an allergen, could be something typically harmless to most people, like pollen or certain foods.
Types of Hypersensitivities
Hypersensitivity reactions are categorized into four types: Type 1, Type 2, Type 3, and Type 4. Each type has a distinct mechanism...
Hypersensitivity Reactions: Delayed Hypersensitivity Reactions01:29

Hypersensitivity Reactions: Delayed Hypersensitivity Reactions

Delayed-Type Hypersensitivity (DTH), or Type IV hypersensitivity, is a cell-mediated immune response. It occurs when T cells, rather than antibodies, mediate a reaction to specific antigens. It is characterized by a delayed onset (1-2 days) and involves the recruitment of macrophages to the inflammation site.The initiation of a DTH response begins with the sensitization of T cells. During this phase, which lasts at least 1-2 weeks, antigen-specific T cells are activated, clonally expanded, and...

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Contact Hypersensitivity as a Murine Model of Allergic Contact Dermatitis
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HISTOLOGICAL AND SEROLOGICAL SEQUENCES IN EXPERIMENTAL HYPERSENSITIVITY.

C V Hawn1, C A Janeway

  • 1Departments of Pathology and Pediatrics, Harvard Medical School, Boston.

The Journal of Experimental Medicine
|October 30, 2009
PubMed
Summary

Foreign protein injections in rabbits caused distinct pathological lesions, primarily in arteries or kidneys, correlating with antigen-antibody reactions and protein type. This research clarifies immune responses to specific bovine proteins.

Keywords:
ANAPHYLAXIS and ALLERGY/experimental

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Area of Science:

  • Immunology and Pathology
  • Experimental Medicine
  • Animal Models in Research

Background:

  • Foreign protein injections can induce immune-mediated pathological changes.
  • Understanding the specific responses to different protein fractions is crucial for predicting and managing adverse reactions.
  • Previous studies noted arterial lesions following foreign serum injection.

Purpose of the Study:

  • To correlate sequential pathological and immunological changes in rabbits after foreign protein injection.
  • To compare the distinct responses to crystallized bovine serum albumin, bovine serum gamma globulin, and whole bovine serum.
  • To investigate the role of antigen-antibody reactions in the development of these lesions.

Main Methods:

  • Normal rabbits received single intravenous injections of bovine serum albumin, bovine serum gamma globulin, or whole bovine serum (1 gm/kg).
  • Animals were bled at intervals for serological studies (antibody detection).
  • Animals were sacrificed at varying times for detailed pathological examination of tissues.

Main Results:

  • Whole bovine serum induced acute, segmental arterial inflammatory lesions, peaking at 2 weeks and healing by 4 weeks.
  • Bovine serum albumin primarily caused arterial lesions, less intense and widespread than whole serum, healing by 4 weeks.
  • Bovine serum gamma globulin primarily induced kidney glomerular and cardiac lesions, peaking at 1 week and healing by 2 weeks; arterial lesions were rare.

Conclusions:

  • Pathological lesions observed were consistent with antigen-antibody reactions occurring in tissues.
  • Lesion development correlated with the presence of circulating antigen and the subsequent appearance of antibodies.
  • Different protein fractions (albumin vs. gamma globulin) elicited distinct pathological patterns and temporal responses.