Intro to Immunology Flashcards

1
Q

Who was Edward Jenner?

A

First immunologist

* disovered vaccines by experimenting with small pox

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2
Q

The first vaccine proved ______ and demonstrated consequences of ______ epitopes

A

memory

shared

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3
Q

Shared epitope

A

antigenic determinant - most pox viruses were detected similarly by the immune system. But showed different pathogenetics

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4
Q

Different pathogenesis in different hosts because:

A

evolved to infect a broader range of hosts - don’t want to damage the only host

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5
Q

Since vaccines the number of occurrences have greatly decreased - diphtheria, measles, mumps….

A

use of preservatives in the vaccines were thought to cause autism but have been disproven – need to educate

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6
Q

Who dictates the immune response?

A

Cells and cell products

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7
Q

What lines arise from the hematopoietic stem cell?

A

Lymphoid
Myloid
Erythroid/Megakaryocyte

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8
Q

What is innate immunity?

A
most basic form in the immune response
* myeloid cell line (granulocytes)
* Natural Killer cell
Inflammation -- Mast Cell, Eosinophil, Basophil (tissues)
Complement
Epithelial barriers
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9
Q

Natural killer cell

A

arises from lymphoid line
antiviral response
protect against mutogenesis

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10
Q

What is adaptive immunity

A

Lymphoid cell line
* B and T cell
B cells –> Plasma Cells (produce antibodies)
* NOT natural killer cell

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11
Q

What is the main target of a neutrophil?

A

BACTERIAL INFECTION

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12
Q

B and T cells are normally ________

A

Dormant

* only activated when presented with antigen (adaptive immunity)

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13
Q

What is an antigen presenting cell?

A

Macrophage
Dendritic Cell

** contain TOLL RECEPTORS - recognize LPS or peptidoglycan layer. Engulf antigen.

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14
Q

Where are lymphocytes found?

A

Primarily in lymphoid tissues

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15
Q

Primary Lymphoid Tissues

A

Bone Marrow

  • Stem Cells
  • B cell maturation

Thymus

  • T cell devlopment and maturation
  • T cells enter thymus via chemokinesis
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16
Q

Secondary Lymphoid Tissue

A
Spleen
Lymph Nodes
Adenoids
Tonsils
Appendix
GI tract (peyers patches)
17
Q

Lymph Node

A

MAJOR SITE of lymphocyte activation

  • afferent lymphatic vessel - brings lymph in
  • efferent lymphatic vessel - takes lymph out
  • Lymphoid follicle:
    * Mostly B cells (outer region)
    * T cells (inner)
  • Germinal Center - where lymphocytes interact (antibody production)
18
Q

Lymph node antigen activation

A

Naive T cell enters lymph node via High Endothelial Venule
Can move from lymph node to lymph node
When comes in contact with APC becomes Active T Cell
Enters back into blood stream via thoracic duct leave blood vessel into tissues to target infection

19
Q

Lymphocyte Recirculation

A

Lymphocytes move from lymph node to the next

20
Q

Spleen

A

White Pulp - lymphocytes
Red Pulp - RBC, blood filtration
Germinal Centers

21
Q

White pulp

A
B cell zone
T cell zone
PALS
Central artery 
Germinal Center
22
Q

Marginal zone

A

Found between red pulp and white pulp

Contains specialized marcophages - will move antigens from red pulp to white pulp (germinal center)

23
Q

Spleen Open Circulation

A

Filtrations through pulp reticulum

24
Q

Spleen closed circulation

A

Blood goes directly to sinuses

25
Individuals lacking spleens--
``` more susceptible to infection * especially encapsulated bacteria S. pneumoniae meningitis E. coli Slmonella ``` The spleen generates antibodies against polysaccharide antigens (bacterial capsule) -- no spleen encapsulated bacteria will not be targets for immune response
26
Intestinal M cells
Lymph tissue integrated into gut tissue Direct communication with lymphoid tissue and lamen of gut Follicle (b cell) T cell Germinal center
27
Recognition of INNATE immunity
Rapid (elements are preformed, coded in DNA) Fixed (same response for each antigen) Limited specificites Constant during response
28
Recognition of ADAPTIVE immunity
Slow (memory) Variable Numerous selective specificities Improve during response
29
Innate and adaptive immunity interaction
takes place in spleen and lymph node. | APC -- innate
30
Innate response to infection
infection --> recognition by nonspecific effectors --> removal of infection
31
Primary response
infection --> recruitment of effector cells --> recognition, activation of effector cells --> removal
32
Secondary Response
infection --> transport of antigen to lymphoid --> recognition by B and T cells --> clonal expansion, differentiation of effector cells --> Removal