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(ImmunoSero) Lesson 9 Principles of Serological Testing

- The document discusses principles of serological testing including blood specimen preparation, dilution techniques, and testing parameters. It describes how to centrifuge blood to separate serum, use pipettes to measure small volumes of serum, and perform simple and serial dilutions. Serial dilution is used to determine the titer or strength of an antibody by making successive dilutions until the last tube no longer shows a positive reaction. Sensitivity and specificity are testing parameters that indicate how well a test identifies true positives and negatives.

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0% found this document useful (0 votes)
363 views3 pages

(ImmunoSero) Lesson 9 Principles of Serological Testing

- The document discusses principles of serological testing including blood specimen preparation, dilution techniques, and testing parameters. It describes how to centrifuge blood to separate serum, use pipettes to measure small volumes of serum, and perform simple and serial dilutions. Serial dilution is used to determine the titer or strength of an antibody by making successive dilutions until the last tube no longer shows a positive reaction. Sensitivity and specificity are testing parameters that indicate how well a test identifies true positives and negatives.

Uploaded by

Angelica Aguilar
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd
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Immunology and Serology Lec

[MIDTERMS] LESSON 9
Transcribed by: ANGELICA AGUILAR
DO NOT REDISTRIBUTE WITHOUT PERMISSION!
PRINCIPLES OF SEROLOGICAL TESTING B. GRADUATED
- marked to allow for varying amounts
TABLE OF CONTENTS  Serological
1 Blood Specimen Preparation and Measuring  Blowout
2 Dilution
3 Simple dilutions C. MICROPIPETTES
4 Compound dilutions - deliver small volumes
5 Testing parameters  Maximum capacity of 1mL or 1000uL

BLOOD SPECIMEN PREPARATIONG AND


MEASURING
SEROLOGY
-study of fluid components in the blood, especially
ANTIBODIES
 Immunology = reaction of blood in vivo (inside)
 Serology = reaction of
SERUM
-liquid portion of blood minus coagulation factors
 Coagulated blood
o Fibrinogen  fibrin  clot formation
 serum
 Appearance: Clear yellow
o Due to loss of fibrinogen

-most frequently encountered specimen in immunologic


testing

-separated from other components of a blood specimen


via CENTRIFUGE Use mechanical suction
 Due to difference in SPECIFIC GRAVITY  Before dipping pipette, always press bulb
o Top (lighter) = serum  Place on top of serological pipette
o Bottom (heavier) o Snuggly fit
1
 WBCs,  Dip the pipette inside the tube
 RBCs  Release the bulb to aspirate desired
 Platelet volume
 Place gloved finger on top
-ideally, use fresh serum that has not been heated Wipe off outside of pipette with gauze
 Heating 2  Do not wipe the tip
o inactivates factors o Gauze/ tissue may absorb the fluid
o denatures proteins 3 Adjust the meniscus
 Ex. Antibody Drain into receiving vessel
4
 After setting the volume to “0”
-for certain tests, complement may need to be
inactivated
 COMPLEMENT = proteins that help fight off
antigen
o Goal: cell lysis
 Complement may interfere with tests results.
 Heat sample to 56 C for 30 minutes
o 30 mins start when the temp of water
bath reaches 56 C
 When temp is reached, put the
sample inside
o Alternative: 65 C for 10 mins
STORAGE
-if testing is delayed
 Bet. 2C – 8C for up to 72 hours
 Frozen at -20C or below
o For >3 days
PIPETTE - Look at the pipette at eye level when setting the pipette
A. VOLUMETERIC to “0”
- deliver only 1 volume  Clear sample = lower meniscus
 Colored = upper meniscus
Page 1 of 3
Immunology and Serology Lec
[MIDTERMS] LESSON 9
Transcribed by: ANGELICA AGUILAR
DO NOT REDISTRIBUTE WITHOUT PERMISSION!

DILUTION
- Demonstration of visible end point (
 If the relative proportions of antigen and antibody
present are not similar, the reaction cannot be
detected
o Too much Antibody = end point may
not be reached
 Serum w/ antibody must be
diluted

- SOLUTE = material being diluted -Ex. SERIAL DILUTON


 Serum = most common  same amount of diluent in each tube, w/ dye
 antibiotic  every dilution made, amount of dye is cut in
 RBC & WBC half in each successive tubes
 final volume of each tube should be the same
- DILUENT = medium making up the rest of the solution  color becomes lighter
 Normal Saline Solution (NSS) = most
common - STEPS
 1st tube = 1mL solute and 1mL solvent = ½
- indication of relative concentration (expression of  2nd tube = 1mL of 1st tube and 1mL solvent = ½ x
concentration) 2=¼
 3rd tube = 1mL of 2nd tube and 1 mL solvent = ¼
- relationship between the two is express as fraction or x 2 = 1/8
ratio STEPS
 Ex. 1:2 = 1 part serum: 2 part of NSS Plan the number and size of simple dilution
1
necessary to reach the desired end point
-Equations are used to determine Calculate each simple dilution, keeping the dilution
2
 Total volume of solution factor the same at each step
 Amount of solute needed 3 Set up the series of tube
 Amount of diluent needed Obtain the final dilution
 Count the number of tube used
4  Set up a multiplication series in w/c the
-3 WAYS original dilution factor is raised to a
power equal to the number of tubes
 Serial dilution
*TITER
 Compound Dilution
-the last tube in w/c a positive reaction is visible
 Simple dilution

SIMPLE DILUTIONS -an indicator of an antibody’s strength


-  ↑ titer = ↑ analyte of interest
o Ex. Titer 32 vs 1028
1 amount of solute  1028 = higher (more
= antibodies)
dilution total volume
FORMULA -Ex.

or
1 1 1 1 1
1 amount of solute Dilution:
= 2 4 8 16 32
dilution−1 amount of diluent 1
64
Rxn: (+) (+) (+) (+) (+) (-)
COMPOUND DILUTIONS Titer: 32
-made when large dilutions are needed
 Ex. 1:500, 1:600 TEST PARAMETERS
A. SENSITIVITY
-requires several steps of making several smaller - proportion of people who have a disease or condition
dilutions (SERIAL DILUTION) and who have a positive test

Page 2 of 3
Immunology and Serology Lec
[MIDTERMS] LESSON 9
Transcribed by: ANGELICA AGUILAR
DO NOT REDISTRIBUTE WITHOUT PERMISSION!

-indicates how small an amount can be and still -SERIAL DILUTION involves making a several dilutions in
produce a positive test result which the dilution factor is the same

true positives - Serial dilutions are used to determine the TITER, or


%= × 100 strength, of an antibody.
t rue positives+ false negatives
B. SPECIFICITY  The last tube in which a visible reaction is
seen is considered the END POINT.
- proportion of people who have DO NOT HAVE a
disease or condition and who have a negative test
- SENSITIVITY is defined as the proportion of people who
have a specific disease or condition and have a positive
- measure the substance that is designed to measure,
test for that disease or condition.
not interfering substances

true negatives - SPECIFICITY refers to the proportion of people who do


%= × 100 not have the disease or condition and who have a
t rue negatives+ false positives negative test for that disease or condition
C. POSITIVE PREDICTIVE VALUE
- The probability that a person with a positive screening - If a test is HIGHLY SENSITIVE and HIGHLY SPECIFIC,
test actually has the disease it is a good indicator that a patient has the disease or
condition if positive results are obtained.
true positives
%= ×100
t rue positives+ false postives - The POSITIVE PREDICTIVE VALUE is the likelihood
D. NEGATIVE PREDICTIVE VALUE that a person with a positive screening test actually
- The probability that a person with a negative screening has the disease
test does not have the disease
- The NEGATIVE PREDICTIVE VALUE is the probability
true negative that a person with a negative screening test does not
%= ×100 have the disease
t rue negative+ false negative
- POSITIVE and NEGATIVE PREDICTIVE VALUES help
SUMMARY the clinician to determine whether a positive or a
- SERUM for serological testing is obtained by allowing a negative test is likely to be a true result based on a
sterile tube to clot at either room temperature or 4°C specific test population.
and then carefully removing the serum from the clot
after centrifugation
 Minimum time for clotting = 30 mins
o Thrombin tube = 5 minutes
 Minimum centrifuge time = 15 minutes

-TYPE OF PIPETTES
 Volumetric
o hold a specified amount of liquid
o To deliver
 Graduated
 Serological
o Calibrated all the way to the bottom
o Blownout
 Micropipettes

- A DILUTION is the addition of a liquid to make a


weaker solution of either a reagent or a patient
specimen.
 Done to see a visible end point in an antigen-
antibody reaction

- Patient serum, the SOLUTE, is made weaker by


adding diluent so that the antibody present is not as
concentrated.

- The relationship between the serum and the total


volume can be expressed as a:
 Ratio = Ex. 1:20,
 Fraction = Ex. 1/ 20.
Page 3 of 3

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