Sheet4-表格 1 Flashcards
Define hyperacute transplant rejection.
Antibody-mediated due to the presence of preformed anti-donor antibodies in the transplant recipient. Occurs within minutes after transplantation.
Define Ig allotype.
Ig epitope that differs among members of the same species (on light or heavy chain)
Define Ig idiotype.
Ig epitope determine by the antigen-binging site (specific for a given antigen-binding site)
Define Ig isotype.
Ig epitope common to a single class of Ig (5 classes, determined by the heavy chain)
Give 3 classic examples of bacteria with antigen variation.
(1) Salmonella (2 flagellar variants)
(2) Borrelia (relapsing fever)
(3) Neisseria gonorrhoeae (pilus protein)
Give 3 examples of possibly causes for SCID?
(1) failure to synthesize class II MHC antigens
(2) defective Il-2 receptors
(3) adenosine deaminase deficiency
Goodpasture’s syndrome is associated with what kind of autoantibodies?
anti-basement membrane antibodies.
Helper T cells have CD(?) which binds to class (?) MHC on antigen-presenting cells.
CD4 binds to class II MHC
How does Bruton’s agammaglobulinemia usually present?
as bacterial infections in boys after about 6 months of age, when levels of maternal IgG antibody decline
How is active immunity acquired?
Active immunity is induced after exposure to foreign antigens. There is a slow onset with long-lasting protection.
How is passive immunity acquired?
by receiving preformed antibodies from another host. Antibodies have a short life span, but the immunity has a rapid onset.
IL-4 promotes the growth of B cells and the synthesis of what 2 immunoglobulins?
IgE and IgG
In what immune deficiency do neutrophils fail to respond to chemotactic stimuli?
Job’s syndrome
In what T-cell deficiency do the thymus and parathyroids fail to develop owing to failure of development of the 3rd and 4th pharyngeal
pouches?
Thymic aplasia (DiGeorge syndrome)
Job’s syndrome is associated with high levels of what immunoglobulin?
IgE
MHC I Ag loading occurs in __(1?)__ while MHC II Ag loadingoccurs in __(2?)__?
(1) in rER (viral antigens)
(2) in acidified endosomes.
Primary biliary cirrhosis has what kind of autoantibodies?
anti-mitochondrial antibodies
Role of TH1 cells?
produce IL-2 (activate Tc cells and further stimulate TH1 cell) and g-interferon (activate macrophages)
Role of TH2 cells?
produce IL-4 and IL-5 (help B cells make Ab)
Sensitized T lymphocytes encounter antigen and then release lymphokines which
leads to macrophage activation’ in what hypersensitivity reaction?
Type IV
TB skin test, transplant rejection, and contact
dermatitis are examples of what type of hypersensitivity reaction?
Type IV
The 3 kinds of MHC class I genes are…
A, B, and C
The 3 kinds of MHC class II genes are…
DP, DQ, DR
The Fc portion of immunoglobulins are at the __?__ terminal.
The carboxy terminal
What 2 cytokines are secreted by macrophages?
IL-1 and TNF-a
What 2 kinds of autoantibodies are specific for systemic lupus?
Anti-dsDNA and anti-Smith
What 3 cytokines are classified as ‘acute phase cytokines’?
IL-1, IL-6, and TNF-a
What 3 ways do interferons interfere with viral protein synthesis?
(1) alpha and beta interferons induce production of a second protein that degrades viral mRNA
(2) gamma interferons increase MHC class I expression and antigen presentation in all
cells
(3) activates NK cells to kill virus-infected cells.
What affect do the acute phase cytokines have on fat and muscle?
mobilization of energy reserves to raise body
temperature
What affect do the acute phase cytokines have on the bone marrow?
Incr. Production of Colony stim. Factor (CS) which leads to leukocytosis
What affect do the acute phase cytokines have on the hypothalamus?
increase body temperature
What antibody isotype can cross the placenta?
IgG
What are 3 types of antigen-presenting cells?
macrophages, B cells, and dendritic cells
What are the maim symptoms of serum sickness an at what period of time following Ag exposure?
fever, urticaria, arthralgias, proteinuria, lymphadenopathy 5-10 days after Ag exposure
What are the major symptoms of graft-vs-host disease?M
maculopapular rash, jaundice, hepatosplenomegaly, and diarrhea.
What B- and T- cell deficiency, assoc. with IgA deficiency, presents with
cerebellar problems and spider angiomas?
ataxia-telangiectasia
What causes the tissue damage associated with Serum sickness?
formation of immune complexes of foreign
particles and Abs that deposit in membranes where they fix complement
What class of MHC proteins are the main determinants of organ rejection?
class II MHC
What complement components can cause
anaphylaxis?
C3a and C5a
What components of the alternative complement pathway make the C3
convertase?
C3b, Bb
What components of the alternative complement pathway make the C5
convertase?
C3b, Bb, and 3b
What components of the classic complement pathway make the C3 convertase?
C4b, C2b
What components of the classic complement pathway make the C5 convertase?
C4b, 2b, and 3b
What components of the complement pathway are deficient in Neisseria sepsis?
The MAC complex–(C5b, C6, C7, C8, C9)
What cytokines attract and activate neutrophils?
TNF-a and B
What disease is associated with a X-linked defect in a tyrosine-kinase gene associated with low levels of all classes of immunoglobulins?
Bruton’s agammaglobulinemia
What disease is associated with anti-epithelial cell autoantibodies?
Pemphigus vulgaris
What disease is associated with anti-microsomal autoantibodies?
Hashimoto’s thyroiditis
What does a deficiency of C1 esterase inhibitor cause (in the complement cascade)?
angioedema because of overactive complement
What does a deficiency of C3 cause (in the complement cascade)?
can lead to severe, recurrent pyogenic sinus and respiratory tract infections.
What does deficiency of decay-accelerating factor (DAF) in the complement cascade cause?
leads to paroxysmal nocturnal hemoglobinuria
PNH
What does Job’s syndrome classically present with?
recurrent ‘cold’ (noninflamed) staphylococcal abscesses
What does TNF-a stimulate dendritic cells to do during the acute phase response?
TNF-a stimulates their migration to lymph nodes and their maturation for the initiation of the adaptive immune response.
What elements of the complement cascade made the Membrane Attack Complex (MAC)?
C5b, C6, C7, C8, and C9
What Ig is found in secretions as a monomer or a dimer?
IgA
What Ig is found in secretions as a monomer or a pentamer?
IgM
What immune deficiency disease has an autosomal-recessive defect in phagocytosis that results from microtubular and lysosomal defects of phagocytic cells?
Chediak-Higashi disease
What immune deficiency is associated with elevated IgA levels, normal IgE levels, and
low IgM levels?
Wiskott-Aldrich syndrome
I L U~
I M U~
What immune deficiency presents with tetany owing to hypocalcemia, congenital defects of the heart and great vessels, and recurrent viral, fungal, and protozoal infections?
Thymic aplasia (DiGeorge syndrome)
What immunoglobulin isotype has the lowest concentration in serum?
IgE
What immunoglobulin isotype is involved in type-I hypersensitivity reactions?
IgE
What immunoglobulin isotype is produced in the primary response to an antigen and is
on the surface of B cells?
IgM
What immunoglobulin isotype mediates immunity to worms?
IgE
What immunoglobulin isotype prevents the attachment of bacteria and viruses to mucous membranes?
IgA
What immunoglobulins bind and activate the classic complement pathway?
IgG and IgM (the Fc portion)
What interleukin induces naive helper T-cells to become TH1 cells?
IL-12
What interleukin induces naive helper T-cells to become TH2 cells?
IL-4
What interleukin stimulates the growth of both helper and cytotoxic T-cells?
IL-2
What is Chronic mucocutaneous candidiasis?
T-cell dysfunction specifically against Candida albicans.
What is important about the CD3 complex?
It is a cluster of polypeptides associated with a T-cell receptor and is important in signal transduction.
What is the cellular process that causes type I hypersensitivity?
Ag cross-links IgE on presensitized mast cells and basophils, triggering the release of vasoactive amines.
What is the cellular process that causes type II hypersensitivity?
IgM, IgG bind to Ag on ‘enemy’ cell, leading to lysis (by complement) or phagocytosis (its cytotoxic).
What is the main antibody in the secondary immune response?
IgG
What is the most abundant immunoglobulin isotype?
IgG
What is the most common selective immunoglobulin deficiency?
selective IgA deficiency