CHAPTER 15 Flashcards

1
Q

What are the four main body defenses?

A

BCII

BARRIER DEFENSES
CELLULAR DEFENSES
INFLAMMATORY RESPONSE
IMMUNE RESPONSE - to maintain homeostasis and prevent disease.

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2
Q

Acts as 1st physical barrier; secretes chemicals that repel pathogens; constantly renews to prevent colonization; hosts beneficial bacteria.

A

Skin

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3
Q

Line exposed body areas (respiratory, GIT, & GUT); traps and inactivates invaders; uses cilia in the respiratory tract to remove pathogens; protects GIT from erosion & traps pathogens in GUT.

A

Mucous Membranes

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4
Q

Secreted by the stomach; aids digestion & destroys pathogens; normal flora also helps eliminate ingested pathogens.

A

Gastric Acid

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5
Q

Identifies self-cells vs. foreign cells through proteins (HLAs); targets foreign cells for destruction.

A

Major Histocompatibility Complex (MCH)

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6
Q

involves the mononuclear phagocyte system (MPS), including leukocytes, lymphocytes, lymphoid tissues, and chemical mediators to combat pathogens.

A

Cellular Defense

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7
Q

Key components of the immune system, including T cells, B cells, and natural killer cells.

A

Lymphocytes

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8
Q

Develop into various cell types essential for inflammatory and immune responses, such as neutrophils, basophils, eosinophils, and monocytes/macrophages

A

Myelocytes

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9
Q
  • Polymorphonuclear leukocytes capable of moving outside the bloodstream.
  • Perform phagocytosis (engulfing and digesting foreign material).
  • Rapidly produced during injury or infection, move to the site via chemotaxis.
A

Neutrophils

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10
Q
  • Myelocytic leukocytescontaining chemicals like histamine and heparin.
  • Initiate and maintain immune and inflammatory responses.
A

Basophils

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11
Q

These are known as mast cells, found in the respiratory and GI tracts and skin.

A

Fixed Basophils

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12
Q
  • Circulating leukocytes involved in allergic reactions.
  • May remove proteins and active components from allergic response sites.
A

Eosinophils

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13
Q
  • Mature leukocytes capable of phagocytizing antigens.
  • Remove pathogens, dead cells, & necrotic tissue.
  • Can be fixed in specific tissues or circulate in the bloodstream.
  • Release chemicals for a strong inflammatory reaction.
A

Monocytes/Macrophages

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14
Q
  • Include lymph nodes, spleen, thymus gland, bone marrow, & lymphoid tissue in the respiratory & GI tracts.
  • Bone marrow and thymus are crucial for creating and differentiating cellular components of MPS.
A

Lymphoid Tissues

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15
Q

body’s local reaction to injury or invasion.

A

Inflammatory Response

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16
Q

activated by cell injury

A

Hageman Fcator

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17
Q

Hageman Factors triggers what?

A

Kinin system
Clotting Cascade
Plasminogen System

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18
Q

converts kininogen to bradykinin, leading to vasodilation, increased capillary permeability, and pain.

A

Kinin system

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19
Q

initiates blood clotting

A

Clotting casacade

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20
Q

initiates dissolution of blood clots

A

Plasminogen System

21
Q

It releases arachidonic acid, leading to the production of autocoids (prostaglandins, cyclooxygenase, thromboxanes) that regulate inflammation.

A

Bradykinin

22
Q

It is locally released during injury, causing vasodilation, increased capillary permeability, and pain.

23
Q

It is activated by arachidonic acid, attract neutrophils through chemotaxis, leading to cell injury and potentially a cycle of inflammation and cell death.

A

Leukotrienes

24
Q

when activated during the inflammatory response, release pyrogens that cause fever.

A

Neutrophils

25
What are the Clinical Signs of Inflammation
Heat (Calor) Swelling (Tumor) Redness (Rubor) Pain (Dolor) Note: These signs occur universally with cell injury and are also seen in conditions like pneumonia, where the lungs exhibit inflammation signs.
26
targets specific invasions thru **lymphocytes**, which are produced by stem cells in the ***bone marrow***.
Immune Response
27
Develop in the thymus and provide cell- mediated immunity.
T cells
28
destroy nonself cells.
Effector T cells (cytotoxic)
29
stimulate other lymphocytes.
Helper T cells (CD4)
30
It regulate and slow down immune responses.
Suppressor T cells (CD8)
31
- Provide humoral immunity and produce antibodies (immunoglobulins) when activated by specific antigens. - contains Five types of immunoglobulins - It form memory cells for quicker future responses to the same antigen
B cells
32
Five types of immunoglobulins
IgM, IgG, IgA, IgE, and IgD
33
React in a cascade to destroy antigens and enhance the inflammatory response.
Complement Proteins
34
prevent viral replication and suppress tumor growth.
Interferons
35
stimulate immune responses and cause fever, myalgia, and slow-wave sleep.
Interleukins
36
aids in T cell maturation.
Thymosin
37
inhibits tumor growth and enhances immune responses.
Tumor Necrosis Factor (TNF)
38
These responses work together to protect the body, w/ helper & suppressor T cells coordinating activity & maintaining balance.
Immune and inflammatory responses
39
Occur when mutant cells evade immune system detection and begin growing.
Neoplasms
40
Factors contributing to neoplasm development:
- Aging decreases immune efficiency. - Location of mutant cells can hinder immune response (e.g., breast tissue). - Tumors can produce blocking antibodies to avoid detection. - Weakly antigenic tumors elicit mild immune responses.
41
It invades host cells for replication, altering the cell membrane and antigenic presentation.
Viruses
42
- This can either trigger a cellular immune response or go undetected by the immune system. - Subtle immune responses to viral invasion may lead to autoimmune diseases.
Viral Invasion of Cells
43
Body produces antibodies or immune responses against its own cells.
Autoimmune Disease
44
Immune response to a what cell leads to antibodies against similar cells.
Virus altered
45
Autoantibody production may normally occur but isn't suppressed due to?
Immunosuppression
46
Genetic predisposition to what development.
autoantibody
47
What cells introduced via organ transplants often trigger an immune reaction.
Foreign
48
This typically does not elicit an immune response.
Self-transplantation (autotransplantation)
49
Matching donor HLA markers with recipient's as closely as possible (reduces/increases) transplant rejection risk.
Reduces