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
Q

Individuals lacking spleens–

A
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
Q

Intestinal M cells

A

Lymph tissue integrated into gut tissue
Direct communication with lymphoid tissue and lamen of gut

Follicle (b cell)
T cell
Germinal center

27
Q

Recognition of INNATE immunity

A

Rapid (elements are preformed, coded in DNA)
Fixed (same response for each antigen)
Limited specificites
Constant during response

28
Q

Recognition of ADAPTIVE immunity

A

Slow (memory)
Variable
Numerous selective specificities
Improve during response

29
Q

Innate and adaptive immunity interaction

A

takes place in spleen and lymph node.

APC – innate

30
Q

Innate response to infection

A

infection –> recognition by nonspecific effectors –> removal of infection

31
Q

Primary response

A

infection –> recruitment of effector cells –> recognition, activation of effector cells –> removal

32
Q

Secondary Response

A

infection –> transport of antigen to lymphoid –> recognition by B and T cells –> clonal expansion, differentiation of effector cells –> Removal