1/59
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No analytics yet
Send a link to your students to track their progress
3 types of blood
a
B
O
Which is the less common blood group
AB
What is blood group/type
The classification of blood based on presence or absence of inherited antigenic substances on the surface of rbcs
Antigen
A material not found in the host and considered frorgein that provokes an immune response
Red blood cell surface antigen
Complex mixture of protines, glycoproteins and glycolipids found on the surface of all red blood cells and a range of other cells in the body
How many blood gourd systems are known
43
How many blood group antigens have been described
>600
Complete blood group
The full set of surface antigens on a persons rbc
What contributes to blood group (5)
inheritance
Infection
Malignancy
Autoimmune disease
After bone marrow transplant
How does myeloid leukaemia affect blood group
Can lead to changes that weake the antigen making people present as o blood group rather than a or b
What are the 5 sugars involved in the ABO system. Name the most important 3 first
fuctose
Galactose
N-acetylgalactosamine
N-acteylglucosamine
Salic acid
What are the 3 enzymes involved in ABO system ad what class of enzymes are they
fucosyl transferase (FUT1)
N-acetyl galactosamine (A Transferase)
Galactose transferase (B transferase)
Are glycosyl transferases
What are the 2 genes involved int he ABO system
ABO
H
What is the ABO blood group determined by
the terminal sugar structure of substances found on surface of rbcs
What do the ABO and H genes encode for and what does this do
Glycosyltrasnferases→ transfer monosaccharides to polysaccharide chains
What are the 3 possible allles of teh ABO gene and what are their relative dominance’s
A,B and O
A and B are dominant to O
What does the o allele encode for
A truncated non
What allele does the H gene have
H and h
What does H code for
Fucosyl transferase (FUT1)
What does FUT1 do
Adds a fucose to the pre cursor glycoprotein on the surface of RBCs to form a H antigen/substance
Which chromomes is H/h found on
19
Which allele combination makes H substance
HH and Hh individuals → hh do NOT
Which allele combination is called the Bombay phenotype
hh
Features of Bombay phenotype (2)
very rare (1 in 1,000,000) except ni parts of india where it is i in 8000
Has no symptoms or related disease but hh individuals can only receive transfusions from others with the same blood group
Where is the ABO gene found
The seven exon on chromomse. 9
What made the o allele
A deletion in exon 6 due to framshift mutation making an inactive protein
What is the difference between teh A and B alleles
They differ by 7 nucleotide substitutions → 4 translate into amino acid differences in the gene product
What determines a or b specificity of glycosyltrasnferase that they encode
Residuces at positions 266 and 268
Which trasnferase makes a substance
A trasnferase (N-acetyl galactosamne trasnferase)
Which trasnferase makes b substance
B- galactose transferase
Why cant hh individuals make ABO antigens
Dont have functional FUT1 genes so cant make substance H so cant make ABO antigens
What are the six genotype ABO allel Indian ale can be
AA
AO
BB
BO
AB
OO
What substance does AA make
A substance only
What substance does AO make
AO
What substance does BO make
Makes b substance only
What substance does BB substance
B substance only
What substance does AB make
A and B
What substance does OO make
H substance
What diseases are inked to ABO phenotype
gastric cancer in a group individuals
Increase occur endo fo gastric and duodenal ulcers in group o individuals
What does ABO correlate with
Levels of factor VIII and con Willebrand factor
Why do A, B and H provoke an immune response
They are glycoproteins and therefore antigenic
What are blood group antigens also known as
Agglutinogens
What are the antibodies raised against blood group antigens also known as
Agglutinins
What will happen if two different blood groups are mixed
The opposing antibodies will causes clumping (agglutination) of the donated RBCs
What does agglutination result in
RBClysis
What does ABo blood group incompatibility lead to (6)
donated RBCs lyse in the blood vessles
Complement system is activated
Leads to kidney failure
Uncontrolled clotting
Circulatory shock
Can be fatal
What kind of moelcuels are rhesus proteins
Protines
How many rhesus antigens can be present on the rbc
Over 49
Which is the most common And important rhesus antigen
The D antigen
Which individuals are Rh+
Those who are homozygous dominant (DD) or heterozygous (Dd)
Which individuals are Rh negative
Homozygous recessive (dd)
What s the rarest blood type
Golden blood→ less than 50 incidences worldwide
What antibody do golden rice individual not have
No Rh antibody
Who can golden rice individuals not recieve donation from / give donations to
Can only receive donations from other Rh null individuals but can donate to any ABO
What condition is associated with golden rice blood and why
Haemolytic anaemia→ RBCs have a shortened life
Distributions of rhesus group d antigen by race
Asian-99%
Black-92%
Caucasian-82%
What is the orle of the RhD antigen (2)
Membrane stability and ammonia transport
What are anti-Rh(D) antibodies produced by
Not normally produced by sensitisation to Environemtnal antigens→ exposure is needed
What do Anti-Rh(D) antibodies desotyred and how
Destoryed any Rh(D)+ RBCs they come into contact with
the rbc is bound by IgG, engulfed by macrophages, transported to the liver and spleen for removal
Less serious than intramuscular haemolytic
Stages of haemolytic disease of the newborn (4)
Rh+ father and Rh- carrying mother have a child
The Rh antigens form the developing foetus can enter the mothers blood and are recognised as foreign so makes antibodies against it
They have a second child and her mother is exposed again
The anti rh antibodies from the mother cross the placenta and damge the foetal rbcs causing anaemia, jaundice and sometimes death