immunoped Flashcards

(49 cards)

1
Q

organ that develops and maintains peripheral lymphoid tissues

A

thymus

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2
Q

2 major functions of thymus

A

maturation of precursor T-lymphocytes; induction of immunocompetence

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3
Q

when are T cells first detected in the thymus

A

7th-8th week AOG

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4
Q

site of immune response generation

A

lymph nodes

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5
Q

organ vital for immune responses to blood-borne antigens and acts as waste disposal system

A

spleen

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6
Q

where is MALT found

A

Peyer’s patches in the SI; lymphoid follicles in the appendix; tonsils in the pharynx; submucosal lymphoid tissue throughout the upper airways and bronchi

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7
Q

T-cell that kill microorganism by direct action on their surfaces

A

CD8+ or suppressor/cytotoxic cells

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8
Q

nonphagocytic cells that perform antibody dependent cell cytotoxicity

A

NK cells

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9
Q

protein that creates pores on cell membranes of target cells resulting in lysis

A

cytolysin

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10
Q

first line of defense against neonatal herpes virus infection

A

NK cells

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11
Q

time it takes for a PMN to mature from a myeloblast

A

14 days

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12
Q

term for migration toward site of microbial invasion

A

chemotaxis

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13
Q

contains granules with major basic protein that are toxic for helminths

A

eosinophils

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14
Q

effectors of immediate hypersensitivity that carry Fc receptors for IgE

A

mast cells and basophils

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15
Q

humoral elements

A

Ig; complement; cytokines; ab produced by B cells and plasma cells

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16
Q

largest Ig; earliest antibody in response to an Ag

A

IgM

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17
Q

most abundant Ig; can traverse the placental barrier

A

IgG

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18
Q

Ig synthesized in the submucosa of the respiratory GIT and exretory glands

A

IgA

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19
Q

Ig predominantly found on the human B lymphocytes like IgM; responsible for differentiation of B cell

A

IgD

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20
Q

Ig less than 10% of the serum; role in parasitic infxn and allergic rxn

21
Q

main fxn is to mediate inflammatory processes and facilitate ingestion of opsonizing pathogens for phagocytosis

22
Q

complements common to both to classical and alternative pathways

23
Q

main anaphylatoxins that provoke inflammation

24
Q

complement that has a role in opsonization

25
acts as binding sites and signal transducers for interacting cells; aka phenotypic markers/MHC
Human Leukocyte antigens
26
cell surface proteins that identifiy a particular cell lineage; transduce signals that lead to ymphocyte activation; recognized by monoclonal antibodies; promote cell to cell interaction and adhesion
cluster differentiation(CD) antigen
27
due to release of mediators like histamine leukotriene serotonin after activation by allegens of specific cells(mast and basophils)
Type I (immediate hypersensitivity)
28
Type I rxns
asthma; allergic rhinitis; anaphylaxis
29
Ab bind to Ag and the immune complex formed activates complement leading to formation of MAC eventually leading to cell lysis
Type II (cytotoxic rxn)
30
Type II rxns
hemolytic dse; eryhtroblastosis fetalis; graft rejection; chronic keratitis; Goodpastures; blood transfusion rxn; ITP
31
Type III (immune-complex mediated) rxns
PSGN; serum sickness; RA; SLE; SJS; PAN
32
Ag deposited at local site initiate rxn from sensitized T-cells capable of destroying tissues or target cells
Type IV (delayed hypersensitivity)
33
Type IV rxns
PPD test; contact allergic dermatitis; syphilis; leprosy
34
dse characterized by a block in the dev't of pre-B cell to B cell due to a defect in the heavy chain gene rearrangement; low or absent Ig's; few or abseB cells
X-linked/Bruton's dse agammaglobulinemia
35
increased susceptibility to viral; fungal; and protozal infxn; aberrant thymus; low lymphocyte count; abnormal facies; hypothyroidism; congenital heart dse
DiGeorge Syndrome (CATCH-22)
36
selective defect in cell mediated immunity with susceptibility to chronic candida infection of the skin and mucous membranes; 50% are due to deficiency of adenosine deaminase
Severe Combine Immunodeficiency Disorder
37
when to suspect immunodeficiency
1 or more systemic bacterial infxn(sepsis; meningitis); 2 or more resp or documented bac infxn w/in 1 year; serious infxns occurring at unusual sites(liver; brain abscess); infxns with unusual pathogens; infxns with common childhood pathogens but of unusual severity
38
defect in X linked hyper-IgM syndrome
deficiency of CD40L on activated T cell
39
defect in transient agammaglobulinemia
delayed onset of maturation of normal IgG
40
defective response in bacterial polysaccharide and depressed IgM; gradual loss of humoral and immune response; thrombocytopenia and eczema
Wiskott-Aldrich Syndrome
41
deficiency in NADPH oxidase; recurrent infxn with CATALASE POSITIVE bacteria
chronic granulomatous disease
42
absence of CD18(common B chain of leukocyte integrin); Leukocytosis; failure to form pus; delay in umbilical cord sloughing
Leukocyte adhesion defect
43
granule structural defect; recurrent bacterial infxn; partial albinism
Chediak-Higashi Syndrome
44
deficiency in TNF-gamma; coarse facies; cold abscess; inc IgE
Job's Syndrome
45
screening tests for humoral diseases
serum IgA; antibody titers to vaccines
46
screening test for cell mediated diseases
candida skin test
47
screening test for macrophage diseases
nitroblue tetrazolium test; respiratory burst array
48
screening test for complement disease
CH50
49
allergic rhinitis that follows sensitization to wind-borne pollens of trees grasses &weeds; prevalence increases with age
seasonal AR