Chapter 31 Terms and Ideas Flashcards

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1
Q

Innate immunity

A

nonspecific, used against many organisms:
• Includes barriers, such as skin and molecules toxic to invaders, as first line of defense.
• Second line of innate defenses includes phagocytic cells, which ingest foreign cells and other particles.
• These defenses may be present all the time or activated rapidly

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2
Q

Adaptive immunity

A
  • Distinguishes between substances produced by self and nonself.
  • Involves antibody proteins and others that bind to and destroy pathogens.
  • Slow to develop and long-lasting, found only in vertebrate animals
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3
Q

Phagocytes

A

large cells that engulf pathogens and other substances by phagocytosis (i.e. macrophages)

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4
Q

Lymphocytes

A

involve B cells and T cells, take part in adaptive immunity

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5
Q

Antibodies

A

proteins that bind specifically to substances identified by the immune system. Antibodies are produced by B cells

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6
Q

Major histocompatibility complex (MHC)

A

• MHC I proteins are found on most cell surfaces
• MHC II proteins are found on most immune system cells
MHC proteins are important self-identifying labels

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7
Q

T cell receptors

A

integral membrane proteins on T cells, recognize and bind nonself molecules on other cells

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8
Q

Cytokines

A

soluble signaling proteins that bind to a cell’s surface receptors and alter that cell’s behavior

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9
Q

Normal Flora

A

the bacteria and fungi that usually live on body surfaces

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10
Q

Mucus

A

secreted by mucous membranes. Mucus traps microorganisms so cilia can remove them.
Cilia continuously move the mucus plus debris up towards nose and mouth

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11
Q

Lysozyme

A

an enzyme that attacks bacterial cell walls, is found in tears, nasal mucus, and saliva

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12
Q

Defensins

A

peptides with hydrophobic domains that are toxic to many pathogens (produced by mucous membrane)

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13
Q

Phagocytes

A

recognize pathogenic cells and ingest them by phagocytosis

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14
Q

Natural killer cells

A

a type of lymphocyte that can detect virus-infected cells and some tumor cells:
• Can initiate apoptosis in these cells
• Can interact with the specific defense mechanisms and lyse cells labeled by antibodies

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15
Q

Complement system

A

Proteins act in a cascade—each protein activates the next.
Provide three types of defense:
• Attach to microbes and mark them for phagocytes to engulf
• Activate inflammation response and attract phagocytes to site of infection
• Lyse invading cells

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16
Q

Interferons

A

signaling molecules produced by cells infected by a pathogen.
Interferons increase resistance of neighboring cells to the pathogen by:
• Binding to receptors on noninfected cell membranes—stimulate a signaling pathway that inhibits viral reproduction
• Stimulating cells to hydrolyze pathogen’s proteins to peptides

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17
Q

Inflammation

A

a coordinated response to injury—it isolates damage, recruits cells against pathogens, and promotes healing

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18
Q

Mast cells

A

cells adhering to skin and organ linings; release chemical signals

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19
Q

Mast cells chemical signals released

A
  • Tumor necrosis factor—cytokine that kills target cells and activates immune cells
  • Prostaglandins—initiate inflammation in nearby tissues, dilate blood vessels and interact with nerve endings, increasing sensitivity to pain
  • Histamine—amino acid derivative that increases permeability of blood vessels so white blood cells can act on tissues
20
Q

Puss

A

Mixture of leaked fluid and dead cells

21
Q

Allergic reaction

A

a nonself molecule that is normally harmless binds to mast cells, causing the release of histamine and subsequent inflammation

22
Q

Autoimmune diseases

A

the immune system fails to distinguish between self and nonself, and attacks tissues in the organism’s own body

23
Q

Sepsis

A

the inflammation due to a bacterial infection does not remain local

24
Q

Specificity (Adaptive immunity)

A

T cell receptors and antibodies bind to specific nonself molecules (antigens).
Specific sites on the antigens are called antigenic determinants

25
Q

Diversity (Adaptive immunity)

A

The immune system must respond to a wide variety of pathogens by activating specific lymphocytes from a pool.
Diversity is generated primarily by DNA changes—chromosomal rearrangements and other mutations

26
Q

Clonal selection

A

a particular response is selected after the antigen binds to a specific T or B cell and the lymphocyte generates clones

27
Q

Clonal deletion

A

Any immature B and T cells that show the potential to mount an immune response to self antigens undergo apoptosis (non-working clones)

28
Q

Autoimmunity

A

failure of clonal deletion (destroys its own cells)

29
Q

Immunological memory

A

the immune system “remembers” a pathogen after the first encounter

30
Q

Primary immune response

A

when antigen is first encountered, “naïve” lymphocytes proliferate to produce two types of cells— effector and memory cells

31
Q

Effector cells

A

carry out the attack. Effector B cells (plasma cells) secrete antibodies. Effector T cells secrete cytokines and other molecules

32
Q

Memory cells

A

are long-lived cells that can divide on short notice to produce effector and more memory cells

33
Q

Secondary immune response

A

when antigen is encountered again, memory cells proliferate and launch an army of plasma cells and effector T cells

34
Q

Adaptive immune response phases

A
  • Recognition phase—the organism discriminates between self and nonself to detect a pathogen.
  • Activation phase—the recognition event leads to a mobilization of cells and molecules to fight the invader.
  • Effector phase—the mobilized cells and molecules destroy the invader
35
Q

Humoral immune response

A

involves B cells that make antibodies

36
Q

Antigen-presenting cells

A

antigen is recognized by a T helper cell with a specific binding site

37
Q

Effector phase B cells versus T cells

A

B clone cells produce antibodies that bind to free antigen— results in inactivation and destruction of the antigen.
TC clone cells bind to cells bearing the antigen and destroy them

38
Q

Immunoglobulins

A

or antibodies, which contain a tetramer of four polypeptides
Two light chains and two heavy chains (disulfide bonds)
Each polypeptide has a constant region and a variable region

39
Q

Constant region

A

determines the general structure and function (the class) of an immunoglobulin

40
Q

Variable region

A

different for each specific immunoglobulin—responsible for antibody specificity

41
Q

Five classes of immunoglobulins

A
  • IgG is secreted by B cells and constitutes about 80 percent of circulating antibodies.
  • IgD is the cell surface receptor on a B cell.
  • IgM is the initial surface and circulating antibody released by a B cell.
  • IgA protects mucosa on epithelia exposed to the environment.
  • IgE binds to mast cells and is involved with inflammation
42
Q

Terminal transferase

A

adds nucleotides before DNA is rejoined to create insertion mutations

43
Q

Cellular immune response (two types of T cells)

A
  • T-helper cells (TH)- responds in activation of cellular immune response
  • Cytotoxic T cells (TC)-responds in death of a cell carrying an antigen
44
Q

Class I MHC proteins

A

are present on the surface of every nucleated cell. They present antigens to TC cells

45
Q

Class II MHC proteins

A

on surfaces of macrophages, B cells, and dendritic cells—present antigens to TH cells

46
Q

Regulatory T Cells

A

Tregs recognize self antigens—when activated they release the cytokine interleukin 10.
This blocks T cell activation and leads to apoptosis of TC and TH cells bound to the same antigen