00:00 / 00:00
Type I hypersensitivity
Type II hypersensitivity
Immune thrombocytopenic purpura
Autoimmune hemolytic anemia
Hemolytic disease of the newborn
Rheumatic heart disease
Type III hypersensitivity
Systemic lupus erythematosus
Type IV hypersensitivity
Cytomegalovirus infection after transplant (NORD)
Post-transplant lymphoproliferative disorders (NORD)
Selective immunoglobulin A deficiency
Common variable immunodeficiency
IgG subclass deficiency
Hyperimmunoglobulin E syndrome
Isolated primary immunoglobulin M deficiency
Severe combined immunodeficiency
Adenosine deaminase deficiency
Hyper IgM syndrome
Leukocyte adhesion deficiency
Chronic granulomatous disease
Blood transfusion reactions and transplant rejection: Pathology review
Immunodeficiencies: T-cell and B-cell disorders: Pathology review
Immunodeficiencies: Combined T-cell and B-cell disorders: Pathology review
Immunodeficiencies: Phagocyte and complement dysfunction: Pathology review
0 / 12 complete
autoantibody p. 113
HLA-DR2 p. 98
labs/findings p. 723
restrictive lung disease p. 700
type II hypersensitivity reactions p. 110
Tanner Marshall, MSVincent Waldman, PhD
Goodpasture syndrome is an autoimmune disease that primarily affects two organs - the lungs and the kidneys.
It causes inflammation and eventually bleeding in the lungs which leads to ‘hemoptysis’ or coughing up of blood, and hematuria or blood in the urine, a pattern first recognized by the pathologist - Dr. Ernest Goodpasture.
To understand Goodpasture syndrome, let’s start by thinking about the basement membrane which is a thin, sheet-like layer of tissue made of protein that keeps the epithelium stuck firmly to actual organ - a bit like double-sided tape which keeps gift wrapping paper stuck to the gift.
The basement membrane is made up of various proteins, but the major one is collagen, and since basement membrane exists throughout every organ system, it’s no wonder that collagen is the most abundant protein in the human body.
As far as proteins go, collagen is a pretty awesome looking one, with a triple-helix structure composed of three separate chains that are intertwined like braided hair.
Each of the chains can be one of six types, named α1 through α6, and the most common form of collagen found in the basement membrane is collagen type IV, which is made by mixing and matching these six α-chains.
One version of type IV collagen combines the α3, α4, and α5 chains. Another combines two α1’s and an α2. A third version has two α5’s and an α6. And so on.
So it turns out that the α3/α4/α5 variant is most common in the glomerular basement membrane of the kidneys and the alveolar basement membrane of the lungs.
In Goodpasture syndrome, autoantibodies bind to a specific part of the α3 chain that is usually hidden deep within the folded chains.
This is an example of a type II hypersensitivity reaction, because once these autoantibodies, usually IgG but rarely IgM or IgA, bind to the the α3 chain, they activate the complement system. The complement system is a series of small proteins present in the blood that act like an enzymatic cascade to fight off bacterial and other pathogenic invasions.
Copyright © 2023 Elsevier, except certain content provided by third parties
Cookies are used by this site.
USMLE® is a joint program of the Federation of State Medical Boards (FSMB) and the National Board of Medical Examiners (NBME). COMLEX-USA® is a registered trademark of The National Board of Osteopathic Medical Examiners, Inc. NCLEX-RN® is a registered trademark of the National Council of State Boards of Nursing, Inc. Test names and other trademarks are the property of the respective trademark holders. None of the trademark holders are endorsed by nor affiliated with Osmosis or this website.