Final (Exam 3) Flashcards
What type of tissue includes the GI tract, salivary glands, lacrimal glands (tear ducts), mammary glands, and the genito-urinary tract?
mucosal tissues
What lines the mucosa throughout the body?
lymphatic tissue and epithelial tissue
What is the largest immunological organ in the body?
The intestine
What percentage of all lymphocytes are located at mucosal sites?
70-80 (75)
What are the two important sites within the mucosal immune system?
inductive and effector sites
Which of the two mucosal immune sites is more organized?
the inductive sites
What type of mucosal site is associated with the lamina propria, various mucosae, stroma of exocrine glands, and surface epithelia
effector site
What is the highly vascular layer of connective tissue under the base layer epithelium known as
Lamina propria
What connects effector sites to inductive sites?
mesenteric lymph nodes
Which tissue are Peyer’s patches, the appendix, and isolated lymphoid follicles associated with
GALT (Gut-Associated Lymphoid Tissue)
What tissue is not regularly found in non-immunocompromised adults and usually requires induction by exogenous stimuli
BALT (Bronchus-Associated Lymphoid Tissue)
What is Waldeyer’s Pharyngeal Ring associated with?
NALT (Nasopharynx-Associated Lymphoid Tissue)
How are pathogens entering the body if NALT is responding?
Ingesting or inhaling
What four tonsillar structures make up the pharynx
Adenoids, lingual and palatine tonsils, and adjacent submucosal lymphatics (pharynx)
What is
1. a key site for tolerance induction to food proteins
2. a firewall to prevent live commensal intestinal bacteria from penetrating systemic immune system
3. provides source of memory B & T Cells
4. has precursor sources for intestinal IgA-producing plasma cells
mesenteric lymph nodes
What is the constitutive mucosal tissue adjacent to major airways and is it normally found in humans?
BALT, no
What are small clusters of lymphoid cells located at the bottom of intestinal crypts, which develop into ILF by recruiting B cells
Cryptopatches
what are inductive sites for mucosal b and t cells in GALT
isolated lymphoid follicles
What are lymphatic tissues throughout the ileum region of the small intestine known as
1. between GALT and luminal microenvironment
2. home to many B cells with germinal centers
Peyer’s patches
Most gene defects for primary immunodeficiencies are caused by mutations in genes on what chromosome? who is affected more?
X chromosome; men
What are HIV, cancer, steroids, and malnutrition responsible for causing?
secondary immunodeficiencies
- Bruton’s gammaglobulinemia (XLA – X-linked agammaglobulinemia)
- common variable immunodeficiency (CVID – hypogammaglobulinemia)
- X-linked hyper IgM syndrome
- IgA deficiency
These are all what type of deficiency?
B cell deficiencies
- A child is healthy for the first 1-6 months of life
- Frequent strep and enterovirus infections
- Require stem cell transplantation or IV Ig therapy for their severe antibody deficiency
- B cell arrested in the pre-B cell stage
XLA
- decreased IgG, IgM, and IgA
- diagnosed 10-20 yrs
- Iv IG replacement therapy treatment
- autosomal recessive pattern
- involved in survival and maturation of B cells
CVID
- high levels of IgM
- problem with isotype switching/plasma cell development
- noticeable after baby is 6 months to 1 yr
- frequent pneumonia, sinus infections, and ear infections
X-linked hyper IgM syndrome
- low or no levels of IgA
- most common primary immunodeficiency
- most often asymptomatic but susceptible if there is also an IgG2 deficiency
- increased incidence of allergy and autoimmune diseases
IgA deficiency
DiGeorge syndrome, Wiskott-Aldrich syndrome, and BLS are what type of immunodeficiencies
T Cell Deficiencies (SCID)
- autosomal dominant
- defect in chromosome 22 (CATCH 22)
- cardiac abnormalities, abnormal facies, thymic abnormalities, cleft palate, blue fingers
- cognitive impairments
- profound T cell deficiencies
DiGeorge Syndrome
- reduced T cell numbers
- defective NK cell cytotoxicity
- failure of antibody responses
- reduced ability to form blood clots
- mutations in was gene (WASP protein) involved in actin rearrangement
- only IgM antibodies produced
- rash on face
Wiskott-Aldrich Syndrome
- Failure to express MHC class
- type I if MHC class I or type 2 if MHC class II
- type one involved with open ulcers on skin, face, arms, and legs
- defection in maturation in thymus, poor activation in periphery
BLS
- x linked recessive
- mutations in IL2RG gene (for normal immune system function)
- lack immune cells, recurrent and persistent infections
- common decrease in recruitment/cytokine release
X-linked SCID
- accumulation of toxic purine metabolites in cell synthesizing DNA
- block in T cell maturation
- either gene replacement therapy or stem cell transplant
Adenosine deaminase (ADA) purine nucleotide phosphorylase (PNP) deficiencies
- mutation in gene responsible for skin, hair, nails, and immune system
- problem with formation of thymus
- causes T cell immunodeficiency
- congenital alopecia
Nude (FOXN1 gene mutation)
- virtually no immune system
- impaired AIRE
- problems activating RAG genes
Omenn’s syndrome
What form of protection do live attenuated or killed bacteria vaccines provide
- Antibody response
- Cell-mediated immune response
What form of protection do live attenuated viruses provide?
- Antibody response
- Cell-mediated immune response
What form of protection do subunit (protein) vaccines provide?
- Antibody response
What form of protection do conjugate vaccines provide?
- T helper cell dependent response
- Antibody response to polysaccharide
What form of protection do synthetic vaccines provide?
- Antibody response
- Cytotoxic killer T
What form of protection do viral vectored vaccines provide?
- Antibody response
- CTL
What form of protection do DNA vaccines provide?
- Humoral response
- Cell-mediated response
What phase involves testing in small groups of people (20-80) for the first time and can take months
Phase 1
What phase involves larger groups (100-300) that studies effectiveness as well as safety and can take months to years
Phase 2
What phase involves larger groups (1000-3000) that confirms effectiveness, monitors side effects, compares to standard treatments, and can take years to decades
Phase 3
What phase involves making a vaccine available to the public, involves tracking safety, and is ongoing
Phase 4
What phase occurs during a primary immune response where effector cells decline after first exposure and there is an appearance of memory cells
contraction phase