Chapter 27 Part 2 Flashcards

1
Q

2 main types of systems by which human blood can be classified are

A

ABO system

Rh system

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2
Q

ABO system

A

In this system, blood types are identified by ‘self’-antigens in the plasma membranes of RBCs. We are born with these self-antigens.

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3
Q

Antigen

A

substance that can activate various responses from the immune system, including the production of antibodies. Almost all substances that stimulate an immune system response are foreign proteins called ‘non-self’ antigens

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4
Q

Antibody

A

Substance made by the body in response to stimulation by an antigen. It will destroy or neutralize the antigen. Many react with their antigens by making them clump or stick together (agglutination).

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5
Q

4 blood types

A

A, B, AB and O

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6
Q

The letter of blood types stands for

A

The type of slef antigen in the plasma membrane of the individual RBCs

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7
Q

There are no atibodies in the blood that are

A

The same as the self antigen on the RBC

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8
Q

TYPE AB has which antibody and what antigen

A

Doesnt have A or B

Antigen a and B

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9
Q

Type B has what antibody and what antigen

A

Antibody A

B antigen

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10
Q

GRoup O ha swhat antibodies in plasma and what antigens in RBC

A

Anti A and B

No anitgens in RBC

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11
Q

Additional antigen

A

Rh antigen

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12
Q

Rh antigen make blood type

A

Positive or negative

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13
Q

Rh positive

A

Rh antigen is present in plasma membrane of RBC

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14
Q

RH negative

A

Rh antigen is not present in plasma membrane of RBC

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15
Q

Rh system

A

Follows the same principle of ABO system

Important to consider in blood transfusion

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16
Q

___% of us population is rh+

A

82%

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17
Q

No anti-Rh antibodies are

A

Naturally present in plasma

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18
Q

Anti Rh antibodies appear in the plasma of Rh negative people if

A

Rh-positive RBCs have been introduced into their bodies

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19
Q

matching appropriate blood types for blood transfusions is crucial in order to avoid

A

Agglutination

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20
Q

O- is

A

Universal donor

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21
Q

AB is

A

Universal recipient

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22
Q

Erythroblastosis fetalis commonly occurs when

A

Mother is Rh-
Father is Rh+
The baby inherits the fathers Rh+ trait
The mother carries a sceond Rh+ fetus

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23
Q

During pregnancy while erythroblastosis fetalis

A

the mixing of mother and baby’s blood doesn’t normally occur, but there are circumstances where this may happen; then, RBCs from the Rh+ unborn baby can cross into the mother’s Rh- blood through the placenta (this sould normally happen during delivery)
The mother’s immune system considers the baby’s Rh+ RBCs as a pathogen of sorts and so will make anti-Rh antibodies against them
These Anti-Rh antibodies may cross back through the placenta into the baby’s blood and destroy the baby’s circulating RBCs

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24
Q

erythroblastosis fetalis first born infants

A

First born infants (from first time pregnancies) are often not affected because it takes the mother some time to develop the Anti-Rh antibodies, but all babies she has afterwards who inherit the Rh+ trait from the father are at risk

Can be diagnosed and prevented by administration of a protein called RhoGAM which prevents the mother’s body from forming anti-Rh antibodies

25
When RBC are destroyed it can lead to
When RBCs are destroyed/broken down it can lead to severe anemia. In addition, a substance called bilirubin is released and causes a baby to ‘turn’ yellow – a condition known as jaundice
26
WBC generally function in
Defense/immunity
27
WBC categorized as
Granulocytes or agranulocytes
28
Granulocytes are
Granules in cytoplasm
29
Agranulocyts have
No granules in cytoplasm
30
Types of granular leukocytes
Neutrophils Eosinophils Basophils
31
Types of non-granular or agranular leukocytes
Lymphocytes | Monocytes
32
Neutrophiles
Most numerous type of WBC (65%) Very active phagocytosis against pathogens Attracted to damaged cells at infection site by chemotaxis
33
Eosinophils
Weak phagocytes, abundant in mucus membranes Protection against certain parasitic infections
34
Basophils
Scretes heparin | Secretes histamine
35
What is heparin
A strong anticoagulant
36
Histamine is released during
Inflammatory
37
Lymphocytes are ______ and ________WBCs
Smallest and 2nd most numerous
38
Lymphocytes make _____% of WBC
25%
39
B Lymphocytes produce
Antibodies
40
T lymphocytes directly
Attack foreign cells
41
Differential WBC count test
Gives the proportions of each type of WBC as a percentage of the total WBC count Important information as not all disorders affect each type of WBC in the same way 1 mm3 (a drop) of normal blood usually contains 5000 to 9000 leukocytes, with different percentages for each type WBC disorders than can be detected include: Leukopenia Leukocytosis leuko = white Leukemia
42
Leukopenis
Low WBC count <5000/mm3
43
Leukocytosis
Abnormally high WBC count >10000/mm3 More common than leukopenia Usually do to bacterial infection
44
Leukemia
WBC >100000/mm3 WBCs dont function properly Blood cancer
45
Monocytes
Largest WBC Mobile and highly phagocytic: Aggressive phagocytes (due to size, can engulf larger pathogens and cancerous cells) Macrophages (‘large eaters’) are specialized monocytes that grow to several times their original size after they migrate out of the blood
46
RBC and WBC are produced by what two types of tissue
Myeloid (red bone marrow) | Lymphatic tissue
47
Myloid tissue
Found mainly in adult sternum ribs and hip bones Formas all types of blood cells, most lymphocytes and monocytes develop in lymphatic tissue
48
Lymphatic tissue
Found in lymph nodes,thymus and spleen Forms lymphocytes and monocytes
49
Platelets are the same thing as
Thrombocytes
50
Average adult count of placelets
250000/mm3
51
Platelets have 3 important properties
Agglutination Adhesiveness Aggregration
52
Platelets play an essential role in blood clotting, which occurs throug hthe following steps
Injury to a blood vessel rough/damaged lining Clotting factors released at the injury site produce prothrombin activator Platelets become ‘sticky’ and accumulate at injury site  soft, temporary ‘platelet plug’ Prothrombin activator and calcium convert prothrombin (a protein normally present in the blood) in to thrombin (a protein important to blood clotting) Thrombin reacts with fibrinogen (a soluble blood protein), changing it into fibrin (looks like a tangle of threads) Fibrin, traps RBC to form a clot
53
Vitakin K is responsible for
Coagulation
54
Process of. Vitamin k use
``` Stimulates liver cells to increase synthesis of prothrombin -> Faster production of thrombin -> Faster clot formation ```
55
Thrombus
Stationary blood clot - stays where formed
56
Thrombosis
Condition of having a thrombus
57
Embolus
Term used for a part of thrombus which dislodges and circulates through the bloodstream; may block a blood vessel
58
Embolism
Condition of having an embolus
59
Hemophilia
Characterized by an inability to form blood clots X-linked inherited disorder (X recessive) Affects 1/10,000 males Failure to produce one or more of the plasma proteins involved in blood clotting Can be life-threatening Must be treated