An Overiew: PEG - Auto-abs Adsorption & Allo
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Transcript An Overiew: PEG - Auto-abs Adsorption & Allo
An Overview: Polyethylene glycol
(PEG) - Adsorption of Auto-abs &
Detection of Allo-abs in WAIHA
Cheng Chun Kwok
What is Polyethylene glycol (PEG)?
Linear, neutral, water-soluble, non-toxic,
ethylene glycol polymer.
Consistency (liquid to solid) depends on Mol. Wt.
Surfactant in industry (food, cosmetics,
pharmaceutics)
Biomedicine (dispersing agents, solvents,
ointment, suppository bases, vehicles, tablet
excipients).
How Does PEG Work?
Macro-molecules remove water
concentrate abs abs uptake.
Test mixture cannot be centrifuged.
Ab detection depends on IAT phase.
Anti-IgG AHG is recommended.
PEG in Blood Banking
First described by Nance & Garratty in 1987.
Mol. Wt. around 3,500 - 4,000.
Two types of PEG solutions.
20% PEG (20 g PEG / 100 mL NISS)
(4 drops 20% PEG + 2 drops serum)
PEG in LISS - commercial available
(2 drops PEG + 2 drops serum)
Liew & Duncan proposed to use in auto-abs
adsorption & allo-abs detection in 1995.
Auto-immune Hemolytic Anemia (1)
3 broad categories IHA: alloimmune, autoimmune,
& drug-induced.
AI: auto-abs on patient rbc in patient’s serum.
Patient anemia ( Hb / Hct) / compensated?
Anemia not present: DAT+ with free auto-abs.
Anemia compensated: compensated WAIHA.
Hemolytic anemia present: WAIHA.
Difficult to distinguish bet them in BB.
Auto-immune Hemolytic Anemia (2)
Blood smear: spherocytes, reticulocytosis.
Biochem: unconjugated bilirubin , LDH , Hp.
Hemoglobinemia & hemoglobinuria.
Serological tests: DAT, AS / abs id on serum
&/or eluate.
HA may due to structural membrane defect,
erythrocytic enzyme deficient, abn Hb molecules.
All Positive DAT
Free Auto-abs present HA?
No, affected not clearly understood.
Positive DAT + free auto-abs - HA (not
WAIHA).
Positive DAT + free auto-abs + HA
(WAIHA).
Complicated.
Lots of factors may involved.
Possible Factors Influence an Antibody
to cause Hemolytic Anemia (1)
Thermal amplitude of abs reactivity.
Titer in serum.
Avidity for red cells antigen.
amount of abs bound to red cells.
Ability of abs to fix complement in vivo.
Activity of individual’s macrophages.
Possible Factors Influence an Antibody
to cause Hemolytic Anemia (2)
IgG subclass (IgG3 > IgG1 > IgG2 > IgG4)
Rh abs mostly IgG1 & IgG3.
Anti-K & anti-Fy usually IgG1.
Anti-Jk mainly IgG3.
Severe HDN mostly often associated with IgG1.
Why Interested in WAIHA?
Create problems in BB mask concomitant
presence of clinically significant allo-abs.
Identify clinically significant allo-abs to avoid
HTR.
Warm auto-abs adsorption procedures are
tedious & time-consuming.
Auto-abs react with all donor red cells
compatible blood almost always impossible.
Question: If we give phenotype matched blood, should we
border the tedious auto-abs adsorption & allo-abs detection?
What is Clinically Significant Ab?
Known to cause HDN.
Known to cause HTR.
Unacceptably shorten survival of
transfused red cells.
Examples: ABO, Rh, Duffy, Kidd, Kell, SsU,
& MUR.
All of them are reactive at 37oC &/or IAT.
All abs Reactive at 37oC &/or
IAT are Clinically Significant?
No.
All clinically significant abs are reactive at 37oC
&/or IAT.
Abs reactive at 37oC &/or IAT may not be
clinically significant.
Can be distinguished in Blood Bank? not easy.
When an allo-ab reactive at 37oC &/or IAT is
identified antigen negative cells are selected
for transfusion.
Detection of allo-abs
in patients with auto-abs (1)
1-in-5 dilute auto-abs to detect allo-abs is
unreliable & should be strongly discouraged.
“least incompatible” blood without allo-abs
detection in urgent transfusion is unacceptable.
Auto-adsorption is ideal but procedures are
tedious, labor intensive & time-consuming.
Urgent transfusion may be delay.
Limitation: patient severely anemia or recently
transfused.
Detection of allo-abs
in patients with auto-abs (2)
Allogeneic adsorption is an alternative.
Differential warm allogeneic adsorption.
One-cell sample allogeneic adsorption.
Differential warm allogeneic adsorption.
Patient phenotypes not known / uncertain.
Patient recently transfused.
Tedious, time-consuming & labor intensive.
Abs to high-incidence antigen may be removed.
Repeat the procedures in transfused patients.
Detection of allo-abs
in patients with auto-abs (3)
One-cell sample allogeneic adsorption.
Patient not recently transfused.
Patient phenotypes known.
Abs adsorption with phenotype-matched red cells.
Serum insufficient.
Recently transfused patient: phenotype with
reticulocyte-riched region red cells gel(LISS-IAT).
Young red cells: MCHC ; acetylcholinesterase activity .
Evaluations of PEG in WAIHA
Abs Adsorption & Detection
Barron & Brown
Immunohematoloty 1997;13:119-22.
Cheng et al
Transfusion 2001;41:13-7.
Judd & Dake
Immunohematology 2001;17:82-5.
Barron & Brown
Immunohematoloty 1997;13:119-22.
19 patients with warm auto-abs were tested.
14/19 contained allo-abs / + auto-abs specificities.
Adsorption: equal part papain-treated rbc & serum
Vs equal part untreated rbc, serum, & 20% PEG in
PBS.
Detection: LISS (2 drops serum + 2 drops LISS + 1 drop 5%
reagent cells). Vs PEG-IAT (6 drops serum/PEG mixture + 1
drop 5% reagent cells).
?? Optimal reactivity of 20% PEG; serum:PEG:rbc = 2:4:1 (Nance &
Garratty, Am J Clin Pathol 1987).
Barron & Brown
Immunohematoloty 1997;13:119-22.
Ref
PEG
serum
serum
20% PEG
papain-treated
red cells
red cells
?? Optimal reactivity of 20% PEG; serum:PEG:rbc = 2:4:1 (Nance & Garratty,
Am J Clin Pathol 1987).
Barron & Brown (Result 1)
Immunohematoloty 1997;13:119-22.
Total adsorption time
Total number of adsorption
Ref
PEG
59.5 hrs
10 hrs
42x
30x
Average time
161.5 mins
30 mins
Abs reactivity
4 stronger
5 stronger
Remarks
ND - Not Detected.
anti-K, -Fya, 2 -E
1 auto- ND
anti-E, -Jkb, 3 -C
1 auto- & 2 allo- ND
Ref: 10 mins enzyme + 10 mins wash + 60 mins incubation + 5 mins harvest.
PEG: 15 mins inucbation + 5 mins harvest.
Barron & Brown (Result 2)
Immunohematoloty 1997;13:119-22.
2 allo-abs not detected with PEG.
Anti-K weak reactive with ref but non-reactive with PEG.
Anti-Jkb microscopic positive but non-reactive with PEG.
?? Optimal reactivity of 20% PEG; serum:PEG:rbc = 2:4:1 (Nance &
Garratty, Am J Clin Pathol 1987).
?? Macroscopic but not microscopic reading at all stages of LISS, +
IAT reading, is recommended (Issit & Anstee, Applied blood
group Serology).
Barron & Brown (Result 3)
Immunohematoloty 1997;13:119-22.
Decreases in adsorption time.
Efficient & cost-effective.
Very weak allo-abs may not be detected.
Option to reduce time & cost in adsorptions.
When non-detection is suspected, use
standard procedures.
Cheng et al
Transfusion 2001;41:13-7.
16 patients with warm auto-abs were tested.
8/16 contained allo-abs / + auto-abs specificities.
Adsorption: equal part untreated rbc & serum Vs
equal part untreated rbc, serum, & PEG (PeG).
Detection: gel (LISS-IAT) Vs PEG-IAT (4 drops
serum/PEG mixture + 1 drop 5% reagent cells).
Cheng et al
Transfusion 2001;41:13-7.
Conventional
PEG
serum
serum
PeG
untreated
red cells
red cells
Cheng et al (Result 1)
Transfusion 2001;41:13-7.
Conventional
PEG
Total adsorption time
2,400 hrs
360 hrs
Mean time
150 mins
22.5 mins
Mean fold
2.5x
1.5x
2 Not adsorbed
All adsorbed
Auto-abs adsorption (3x)
Allo-abs detection
Con: 60 mins incubation.
PEG: 15 mins incubation.
All are demonstrated
Cheng et al (Result 2)
Transfusion 2001;41:13-7.
3 allo-anti-E, 1 allo-anti-e, & 3 allo-anti-Mur
were able to be demonstrated by both
methods.
Reactivity strength not mentioned &
compared between the two methods.
40% efficiency in number of adsorptions.
85% decreases in adsorption time.
Effective in allogeneic adsorption.
Cheng et al (Result 3)
Transfusion 2001;41:13-7.
Method awaits standardization.
Fully replace conventional method not
recommended.
Further studies on weak allo-abs loss during
adsorption or IAT.
Other techniques incorporated to enhance abs
detection - gel (LISS-IAT).
Safe to male has no recent transfusion history
/ female has not been pregnant or no recent
transfusion history.
Judd & Dake
Immunohematology 2001;17:82-5.
11 warm reactive auto-abs selected to compare
ZZAP & PEG adsorption.
12 allo-abs were selected to compare abs detection
after ZZAP- & PEG-adsorption.
Adsorption: ZZAP adsorption (ficin) Vs equal part
untreated rbc, serum, & PEG (PeG).
Detection: NISS-IAT (3 drops serum + 1 drop 3-4 %
reagent cells, 60 mins 37oC, PS-AHG) Vs PEG-IAT (4 drops
serum/PEG mixture + 1 drop 5% reagent cells).
?? NISS-IAT: serum to cell = 2 to 1 (Technical Manual).
Judd & Dake
Immunohematology 2001;17:82-5.
ZZAP
PEG
serum
serum
PeG
ZZAP (ficin)treated red cells
red cells
Judd & Dake (Result 1)
Immunohematology 2001;17:82-5.
ZZAP
Auto-abs removal power
Comparable
Allo-abs studies
anti-Fya
anti-c
anti-Jka
ND - Not Detected.
PEG
1 rxn grade or more weaker
1+S
1+S
1+ - 2+S
ND
weak
w - 1+w
Judd & Dake (Test & Result 1)
Immunohematology 2001;17:82-5.
Two fold adsorption of 7 allo-abs (2 anti-D, 1 anti-E, 1
anti-K, 1 anti-Jka, & 1 anti-Jkb) with antigen negative red
cells.
PEG-serum parallel run with saline-serum.
Titration studies on adsorbed sera with saline: 60 mins at
37oC with anti-IgG.
5/7 were 2 folds lower with PEG.
2/7 were 1 fold lower with PEG.
Titers of PEG-serum Vs saline-serum : 2-8 Vs 4-32.
?? Serially dilute PEG-serum mixture with saline.
Judd & Dake (Test & Result 2)
Immunohematology 2001;17:82-5.
To demonstrate abs activity loss in PEG-adsorption
procedure but not on post-adsorption storage.
Incubate PEG-serum & saline-serum at 37oC, 15 mins,
centrifuge & harvest the supernatants.
Measure the IgG levels with nephelometer.
PEG-serum mixture: 128-243 mg/dL.
Saline-serum mixture: 265-505 mg/dL.
IgG level of PEG-serum mixture was 50% lower.
?? Compare IgG levels of ZZAP & PEG adsorbed serum.
Judd & Dake (Result 2)
Immunohematology 2001;17:82-5.
PEG adsorption effective in removing
auto-abs.
Fail to detect allo-abs due to Ig
precipitation.
PEG Does precipitate Immunoglobulin
??
Leger RM, Ciesielski DC, & Garratty G (1)
Transfusion 1999;39:1272-3.
Investigate possible loss of ab reactivity of
PEG-adsorbed sera upon storage.
7 sera contain single ab specificities
Anti-E, -K, -Fya, & -Jka.
2 sham PEG-adsorptions with ag neg red cells.
Fresh PEG-adsorbed serum reactivity: 1+ - 3+.
PEG-sera mixture left at 4oC for 1 - 4 days.
Leger RM, Ciesielski DC, & Garratty G (2)
Transfusion 1999;39:1272-3.
Stored sera mixture divided into 2 aliquots.
‘Mixed’ & ‘Settled’
‘Mixed’ was mixed before sampling.
‘Settled’ was allowed ppt to form, settle, &
sample the clear supernatant.
PEG-adsorbed sera mixture were tested and
compared to the adsorbed sera at the time
of adsorption.
Leger RM, Ciesielski DC, & Garratty G (2)
Transfusion 1999;39:1272-3.
PEG-adsorbed Sera
4oC Storage
PEG-unadsorbed
Sera
1 x anti-E
Mix Before
Sampling
Centrifuge &
Sample Supernatant
1+S
1+
1/2 +
1 x anti-Fya
2+
2+
1+
5 x abs (day 0)
-
5 x abs (day 4 )
-
Same Degree
Same Degree
4 abs Same degree
1 anti-Fya weaken
Leger RM, Ciesielski DC, & Garratty G (3)
Transfusion 1999;39:1272-3.
Precipitate formed in stored PEG-serum
mixture.
Once precipitate formed, DO NOT
centrifuge.
Remix the mixture before sampling.
Test PEG-adsorbed serum on the day of
preparation.
What Make the Differences?
Method to separate serum-PEG
mixture after adsorption.
?? Centrifugation force ??
?? Duration ??
?? Temperature ??
How to Perform PEG-incorporated
One-cell Sample Allogeneic Adsorption
Mix equal parts of
patient serum + PEG + phenotyped packed red cells
incubate at 37oC, 15-30 minutes
centrifuge & harvest adsorbed serum/PEG mixture
perform PEG-IAT with SC / PC
4 drops serum/PEG mixture to 1 drop 5% red cells
37oC, 15-30 minutes, IAT(anti-IgG)
Advantages of PEG
Enhance auto-abs adsorption.
Prior red cells treatment not necessary.
Direct benefit: time saving, & minimize the
delay of urgent transfusion in WAIHA
patients.
Indirect benefit: labor & cost
effectiveness.
Disadvantages of PEG
Precipitates Ig.
Weak allo-abs may not be detected
after PEG adsorption.
Remedy??
Avoid overnight storage PEG-serum mixture at
4oC - precipitate formed.
Adsorbed PEG-serum mixture should be tested
as soon as possible.
precipitate formed, mix thoroughly before
sampling & DO NOT centrifuge.
Other techniques may be incorporated to
enhance abs detection after PEG adsorption
gel (LISS-IAT)??
Cells to PEG/serum mixture ratio.
AHG in gel: MS/PS.
Conclusion
Potential technique in WAIHA auto-abs
adsorption & allo-abs detection.
Safe to male has no recent transfusion
history / female has not been pregnant or no
recent transfusion history.
?Method to separate serum-PEG mixture
after adsorption.
End
Questions & Comments are welcome