1/292
pertaining to a chromosome that is not a sex chromosome
autosomal
gene mutation is present on a sex chromosome
sex linked
one variant of a gene on a chromosome masking or overriding the effect of a different variant
dominant
relating to two alleles of a gene that are both fully expressed
codominant
an allele that does not produce a characteristic effect when present with a dominant allele
recessive
sequence of DNA that is inherited
genotype
expression of the genotype
phenotype
at each locus there may be only one or several different forms of the gene
allele
presence of two identical alleles
homozygous
inheritance of different alleles
heterozygous
effect of a significant difference in antibody reaction depending on the quantity of the target antigen present on a target RBC
dosage
most blood group genes are inherited in an _______ manner
autosomal dominant or codominant
the segregation of the parents gene copies during the formation of reproductive cells occurs during
meiosis
when genes for separate traits are closely linked on a chromosome, they can be inherited together as a single unit
linkage
example of linkage
MNSs
a square diagram used to predict the genotypes of a particular cross or breeding event
punnett square
inheritance on the same chromosome
cis
inheritance on the opposite chromosome
trans
inheriting antigens from each parent as a unit due to linkage
haplotype
specific location of a gene on a chromosome
locus
one chromosome has a copy of the gene and the other chromosome has that gene deleted or absent
hemizygous
males are
square
females are
circle
vertical line
offspring
double line
consanguineous mating
stillbirth or abortion
small black circle
most interesting or important member of pedigree indicated by an arrow
prospositus
prevalence at the genetic level, occurrence of an allele in a population
frequency
occurrence of a permanent inherited characteristic at the phenotype level in any given population
prevalence
the rate of occurrence in a population of a condition that changes over time
incidence
can estimate allele frequencies based on observations of phenotypes in a large number of individuals in a sample population
hardy wienberg
hardy weinberg equation
(p+q)2=p2+2pq+q2=1
p²
AA
2pq
Aa
q²
aa
(p+q)(p+q)=
1
antigen frequencies vary with
race
gene and phenotype frequencies are based on
probability
A patient has an anti-E and anti-K. How many units of ABO compatible RBCs must be tested to find three compatible units?
Approx 30% of population E positive
•(70% E negative)
•Approx 10% of population K positive
•(90% K negative)
63% or 3/5
antigenic determinants or molecular sites that stimulate immunte response
epitopes
capable of eliciting immune response
immunogen
antibodies against foreign antigens
allo
antibodies against own cells
auto
antigen antibody ratio
zone of equilibrium
predominant antibody produced after first exposure
IgM
predominant antibody produced after second exposure
IgG
we make antibodies for antigens we possess true or false
false
newborn baby’s type is determined by
mother
we obtain antibodies from antigens in
environment
antibody that results from exposure to foreign red cell antigen by transfusion or pregnancy
rbc immune antibody
antibody present without evidence of exposure to foreign antigens
naturally occurring antibody
antibody that decreases the red cell survival, can destroy rbcs in vivo
clinically significant antibody
• genes code for the HLA-A, HLA-B, and HLA-C antigens
• Found on most nucleated cells in the body
class 1 MHC
ABO MHC
class 1
• Genes code for HLA-DR, HLA-DQ, and HLA-DC antigens
• Found on most antigen-presenting cells
class 2 MHC
transplant mhc class
class 2
time where antibody cannot be detected with serologic testing
lag phase
time to make antibodies after first exposure
days weeks months
time to make antibodies after 2nd exposure
hours days
1/3 rule
1/3 will make antibodies after first exposure, 1/3 will take 2-3 exposures, 1/3 will never make antibodies
make antibodies after first exposure
high responders
IgM fixes complement
often
IgM direct agglutinin
yes
IgG placental transfer
yes
IgG biologic half life
22 days
IgG heavy chain composition
gamma
IgG molecular weight
50000
IgG valency
2
IgM molecular weight
900000
IgM heavy chain composition
Mu
IgM valency
IgG warm or cold reacting
warm @ 37
IgG complement activators
poor to good
IgG is usually clinically
significant
IgM is warm or cold reacting
cold at 10 or 22C
IgM is usually clinically
unsignificant except ABO
IgM complement activators
good
immunoglobulins with most significance
IgG IgM IgA
immunoglobulins are clinically significant if they react at
body temp
Are IgG blood group antibodies of a single specificity in one specific subclass
no, all may be present or one may predominate
Rh system antibodies
IgG1 and 3
AntiK and AntiFy antibodies
IgG1
AntiJk antibodies
IgG3
Jk
Kidd
antibodies for complement fixation (classic)
Ig1 and 3
IgG subclasses that can cross placenta
all
subclasses with half life of 21 days
Ig1 2 4
biological half life of 4-7
IgG3
does IgG4 activate compliment
no
IgG1 and 3 bind strongly to
Fc receptors
if IgA deficient patients are transfused with IgA
severe anaphylaxis
IgA can increase the effect of
IgG induced RBC hemolysis
immunoglobulin important in allergic reactions
IgE
important immunoglobulins
MGAE
complex group of over 20 circulating and cell membrane protrims that have a multitude of functions within the immune response
complement system
lysis of cells, bacteria, and enveloped viruses as well as assisting with opsonization to facilitate phagocytosis
complement
complement pathways
classical, alternative, and lectin
pathway activated with binding of an antigen with an IgM IgG1 or IgG3 antibody
classical
____ molecules of IgG need to be bound to a single target to activate complement
many
do IgG Rh antibodies bind complement
usually not bc low Rh antigens on rbc surfaces