Antibody structure and intro Flashcards

1
Q

Definition of immune system

A

Cells and humeral factors dedicated to defend the body against infection

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2
Q

Order of pathogens

A

Bacteria
Viruses
Fungi
Parasites

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3
Q

Physical barriers (innate)

A

Skin (keratinized cells)
Mucus to catch containing lysozymes
ciliated epithelial cells (lungs)

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4
Q

Soluable factors (innate)

A

Lysozymes
phagocytes and H2O2 production
HCL in stomach
Compliment proteins
Interferon cytokines

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5
Q

Compliment proteins

A

Serum glycoproteins that are activated by innate immune response and induce cytotoxicity to pathogen

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6
Q

Interferon cytokines

A

antiviral glycoproteins, get released when a cell is infected by a virus

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7
Q

Five cardinal signs of inflammatory response

A

Rubor (redness)
Calor (heat)
Dolor (pain)
Tumor (swelling)
Functio-laesia (loss of function)

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8
Q

Pluripotent haematopoetic cell lines

A

Lymphoid (forms adaptive immune B and T cells)
Myeloid (becomes polymorphonuclear leukocytes)
Erythroid (makes megakaryocytic then platelets)

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9
Q

Neutrophil

A

From Myeloid precursor
Does phagocytosis to kill pathogens
They die and are degraded by macrophages into pus

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10
Q

Eosinophil

A

From Myeloid precursor
Kills parasites marked by antibodies by releasing granule contents

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11
Q

Basophil

A

From Myeloid precursor
Method unknown

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12
Q

Dendritic cell

A

From Myeloid precursor
Site of communication to activate T cells (has dendrites to increase SA and signal response)

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13
Q

Mast cell

A

Excludes parasites by release of histamine

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14
Q

Monocyte

A

precursor to macrophage

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15
Q

Macrophage

A

Phagocytosis of pathogens and activated T cells and immune response

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16
Q

Leukocyte proportions

A

Neutrophil 40-75
Eosinophil 1-6
Basophil <1
Monocyte 2-10
Lymphocyte 20-50

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17
Q

Primary lymphoid organs

A

Bone marrow
Thymus
Where lymphocytes develop and mature

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18
Q

Secondary lymphoid tissues

A

Spleen
Adenoids
Tonsils
Appendix
Lymph nodes
Peters patches
Mature lymphocytes are stimulated

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19
Q

GALT

A

Gut associated lymphoid tissue
Tonsils, adenoids, appendix, peyers patches

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20
Q

BALT

A

Bronchial associated lymphoid tissue
No fibrous capsule just aggregates

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21
Q

MALT

A

mucosa associated lymphoid tissue
no fibrous capsule just aggregates

22
Q

Lymph nodes

A

Where many lymph vessels join (anastomosing)
Contains mature lymphocytes that filter through the lymph containing pathogens

23
Q

Lymph return to venous

A

Subclavian vein in the neck

24
Q

Mature lymphocyte circulation

A

1 Organs -> blood stream -> 2 organs -> lymphatics to return to blood or tissue `

25
Spleen
2 Organ where RBC are broken down, contains no lymphatic connections but does contain white pulp fill of B cells
26
Antibody, Immunoglobulin, Ig
protein made in B cells on the surface or secreted
27
T-cell receptors
TCR's are found on the surface of T cells to recognize antigen and define the T cell
28
Antigen
Any substance capable of inducing a specific immune response. Bound by immunoglobulin or TCRs
29
Epitope
*Antigenic determinant*, this is where the antibodies paratope binds Most antigens are multivalent with many epitopes bind to all types
30
Adaptive immunity attributes
Specificity (many antibodies) Amplification (once found it grows) Modulation (change of Ig isotypes) Memory (secondary immune response)
31
Draw the primary and secondary immune response curve
Lecture 1 slide 48
32
Overall Aby stucture
4 chains (to heavy and to light) disulfide bonds to connect (covalent) N-terminus in variable region C-terminus in constant region
33
Papain
Fab (fragment antigen binding) x2 Fc (fragment crystallizable)
34
Pepsin
F(ab')2 large 2 arm fragment degraded Fc
35
Heavy chain isotypes
GAMED IgG = Gamma A = Alpha (Dimer or monomer) M = Mew (3 C domains) (pentamer) E = Epsilon (3 C domains) D = Delta
36
Light Chain isotypes
Kappa and Lambda
37
Paratope
Antigen binding site on Aby Has framework regions (FR) hypervariable regions (HV) loops or complementaity determining regions (CDR)
38
Aby isotypes
Have differing Fc regions that cause different responses when they find an epitope to bind. They are *glycosylated* in the SER or Golgi
39
Fragments light chains isotypes
V-Variable, J-Joining, C-constant
40
fragments of heavy chain isotypes
V-Variable, D-diversity, J-joining, C-constant, MC- membrane coding
41
Fragment recombination
Via RAG-1 and RAG-2 Recombination activation gene Cut based off recombination signal sequences of heptameter or nonamer that are separated by 12 and 23 BP spacers (12/23 rule)
42
Allelic exclusion
The idea that once specificity is cut out of the fragment it cannot be changed.
43
Affinity maturation
Once selectivity is chosen only random mutations in the CDRs can increase specificity over time (rapid replication increases the speed of mutation
44
Joining chain
Chain that joins type A or M Aby isotypes
45
Isotope order
Starts with many IgM to capture lots of antigen, then some IgD in primary response. then diversifies into other types
46
IgM
Pentamer, First to be secreated to kickstart immune response, very good at triggering compliment system, Short Half-life
47
IgD
Doesn't really have any standout feature other than it is one of the first secreted along with IgM
48
IgG
The most prominent Aby that is good at everything besides crossing epithelium
49
IgA
Dimer or monomer, is really good at crossing epithelium in its dimer form and getting too mucus membranes
50
IgE
is a bitch and is taken up by mast cells for allergic response, very short half-life
51
12/23 rule
coding sections (V,D,J,C) are flanked by heptameters followed by 12 or 23 BP, 12 and 12 or 23 and 23 can't be recombined so that the order is correct.