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7/14/2015 1 Serologic Weak D Phenotype to RHD Genotyping: How will I know? Part 1 Sue Johnson, MSTM, MT(ASCP)SBB Director, Clinical Education BloodCenter of Wisconsin Commentary It’s time to phase-in RHD genotyping for patients with a serologic weak D phenotype Sandler SG, Flegel WA, Westhoff CM, Denomme GA, Delaney M, Keller MA, Johnson ST, Louis Katz, Queenan JT, Vassallo RR, Simon CD Transfusion 2015 Mar;55(3):680-9 How will I know? Objectives Identify causes for variability of expression of RhD antigen Describe specificity, sensitivity & intended use of current commercial RhD typing reagents used in test tube & automated methods. List challenges of typing for RhD by serologic methods. Define management & transfusion options for patients with weak or variable RhD typing.

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Page 1: Serologic Weak D Phenotype to RHD Genotyping: How will I … Program Handouts... · 2015-07-14 · 7/14/2015 1 Serologic Weak D Phenotype to RHD Genotyping: How will I know? Part

7/14/2015

1

Serologic Weak D Phenotype

to RHD Genotyping:

How will I know?

Part 1

Sue Johnson, MSTM, MT(ASCP)SBB

Director, Clinical Education

BloodCenter of Wisconsin

Commentary

It’s time to phase-in RHD genotyping

for patients with a serologic

weak D phenotype

Sandler SG, Flegel WA, Westhoff CM, Denomme GA,

Delaney M, Keller MA, Johnson ST, Louis Katz,

Queenan JT, Vassallo RR, Simon CD

Transfusion 2015 Mar;55(3):680-9

How will I know?

Objectives

• Identify causes for variability of expression of

RhD antigen

• Describe specificity, sensitivity & intended use

of current commercial RhD typing reagents

used in test tube & automated methods.

• List challenges of typing for RhD by

serologic methods.

• Define management & transfusion options for

patients with weak or variable RhD typing.

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CONTRIBUTORS

OF VARIABILITY

VARIABLES

RHD Gene Weak D C in Trans

to RHD

Partial D Del

D epitopes on

RhCE Protein

ceCF ceHAR

Anti-D Reagents Polyspecific

Slide and

Modified Tube

Human IgG

Monoclonal

IgG

Monoclonal

IgM

Monoclonal

IgM

Human IgG

Monoclonal

Blends

Testing Platform Test Tubes

IS & IAT

Column

Agglutination

Solid Phase Liquid

Microtiter

Individual being

Rh Typed

Transfusion

Recipient

Obstetrical

Patient

Cord Blood Donor Blood

Variables Impacting Rh Typing

Transfusion Technology Report Vol. #013 Immucor, Inc.

2 3 4 9 1 2 3 4 5 6 7 8 9 10 1 2 3 4 5 6 7 8 10

Locus 1 Locus 2

RH Genes – Rh Positive

RHD

RHCE

Chromosome 1

Locus 1 - presence of RHD

codes for the presence of D or

no D.

Locus 2 - presence of RHCE

codes for Ce, CE, cE, ce.

RhD Protein

COOH

417 NH2

53 107 167 230

321

358

391

Vestibule

282

•Crosses RBC membrane 12 times

•No sugars attached

http://www.jic.ac.uk/corporate/about/publications/advances/images_10/protein.jpg

231 347

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11 72

32 53 94 107 158 167 230 231 282 290 347 358

75 131 135 186 201 263 266 321 324 391

417

RhD differs from RhCE by 34 to 37 amino acids =

E= C=

RhD Negative

• Deletion of RHD

• Inactivating mutations of RHD

• RHD in African Americans

• Hybrid RHD-CE-D in African backgrounds

1 3 4 5 6 7 8 9 1 2 3 4 5 6 7 8 10

Locus 1 Locus 2

Exons

RH Genes in Rh Negative Caucasians

No D antigens ce antigens

RHCE

Locus 1 deletion of RHD therefore, no D antigen.

Chromosome 1

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2 3 4 9 1 2 3 4 5 6 7 8 9 10 1 2 3 4 5 6 7 8 10

Locus 1 Locus 2

Exons Exons

RH Genes in Rh Negative - African Background

No D antigen C/c and E/e antigens

RHD

RHCE

Locus 1 – 37 bp insertion & several mutations in

RHD results in no product

Chromosome 1

RHD Allele frequency of ~.030 African Americans* *Reid ME, et al Blood Cells, Molecules & Diseases 2013

Chou S, et al. Blood 2013

2 3 4 9 1 2 3 4 5 6 7 8 9 10 1 2 3 4 5 6 7 8 10

Locus 1 Locus 2

Rh (D) Negative – African Background

RHD

RHCE

Chromosome 1

C/c and E/e antigens No D antigen

Locus 1 – RHCE inserted in RHD results in no

D antigen and weak C.

Allele frequency of hybrid RHD-CE-D is ~ .029-.09*

*Reid ME, et al Blood Cells, Molecules & Diseases 2013

Chou S, et al. Blood 2013

What About

Weak Expression of D?

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Traditional Weak D

Reactivity with Anti-D

• Agglutinated with some anti-D on

direct agglutination (IS)

• Negative on direct agglutination (IS)

• D antigen detected by IAT only

Commentary

It’s time to phase-in RHD genotyping

for patients with a serologic

weak D phenotype

Sandler SG, Flegel WA, Westhoff CM, Denomme GA,

Delaney M, Keller MA, Johnson ST, Louis Katz,

Queenan JT, Vassallo RR, Simon CD

Transfusion 2015 Mar;55(3):680-9

Serologic Weak D Phenotype

Definition

• Anti-D reagent agglutinates RBCs

weakly (≤ 2+) or not at all by test

tube method at IS, but agglutinating

moderately or strongly with

antihuman globulin

Identified by weak reactivity or

by discordant typing results

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Frequency of Serologic Weak D

• RhD-negative individuals

• Estimated to be 2.9% among

a mixed population

Weakened Expression of D

2 Categories

• Not at risk of making anti-D

• At risk of making anti-D

WEAK D

Not at Risk of Making Anti-D

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Weak Expression of D Not at Risk of Making Anti-D

• C in trans with RHD

(Ceppellini effect)

• r’ haplotype (R1r’ – DCe/Ce)

• Weak D “Types”: amino acid change(s),

usually a single change

• Types 1, 2, 3

Weak D Types

Most Not At Risk of Making Anti-D

• Changes in regions of RHD predicted to be

in the RBC membrane or inside RBC

• Less Rh protein in RBC membrane

• Can type as Rh-positive or Rh-negative by

direct agglutination with monoclonal (IgM)

anti-D reagents

IS D IAT Ct. IAT

Anti-D 0 3 0

IS

Anti-D w+ - 2+ or

11 72

32 53 94 107 158 167 230 231 282 290 347 358

75 131 135 186 201 263 266 321 324 391

417

Type 2

Gly(385)Ala

Type 1 Val(270)Gly

Account for 80-90% of Weak D

Not at risk of making Anti-D

Type 3 Ser(3)Cys

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Normal RhD Positive

Normal Rh Protein

Normal RhD antigen

~ Antigens/RBC*

DCe/ce 9900-14,600

DcE/ce 12,000-19,700

DCe/DCe 14,500–22,800

*Daniels G. Human Blood Groups

Weak D Type 1- 81

Fewer Copies of Rh Protein

Normal RhD antigen

~ Antigens/RBC*

Type 1 759

Type 2 491

Type 3 1948

*Blood 2000;95:2699-2708

WEAK EXPRESSION OF D

At Risk of Making Anti-D

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Weak Expression of D

At Risk of Making Anti-D

• Partial Ds: hybrid RHD alleles

• DVI

• Others…

• Del: detected by adsorption/elution

• D epitopes on RHCE gene

Partial D

• Lack exofacial epitopes or have

altered exofacial epitopes

• Hybrid proteins

• Missense mutations affecting

exofacial protein

Partial D

Missing RhD Epitopes

Normal RhD antigen

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Partial D

Altered RhD Epitopes

Normal RhD antigen

Partial D – European Ancestry

• DNB, DVI and DVII most common in

European ancestry

• DVI

• 2 reports of fatal hydrops fetalis • Transfusion.1983 Mar-Apr;23(2):91-4

• Obstet Gynecol. 2003 Nov;102(5 Pt 2):1143-5 2003

• Anti-D reagents designed to be neg

at IS/pos at IAT

IS D IAT Ct. IAT

Anti-D 0 3 0

Partial D – African American

• DIIIa & DIVa most common

• Type as RhD positive at IS

IS

Anti-D 3+

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Deletion of exon 9 in Asians occurs in 10-30%

Del

•Type as D-negative (IS & IAT), only adsorb & elute anti-D

•Severely reduced protein

D Epitope on RHCE Genes

• ceHAR - formally known as R0Har or DHAR

• ceCF (ceRT, ceSL) - Crawford phenotype

1 3 4 5 6 7 8 9 1 2 3 4 5 6 7 8 10

Locus 1 Locus 2

Exons

No D antigens ce antigens

RHCE

ceHAR results from one RHD exon inserted into the RHCE gene.

D Epitope on RHCE Gene - ceHAR

IS

Anti-D 3+

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ceHAR Phenotype: Reactivity with Reagent Anti-D

Anti-D RBCs

Reagent IgM IgG ceHAR

Gamma-Clone GAMA401 F8D8 Pos*

Immucor-4 MS201 MS26 Pos*

Immucor-5 TH28 MS26 Pos*

Ortho Bioclone MAD2 Human

polyclonal

Neg

Ortho (ID-MTS) MS201 Pos

Biotest (Bio-Rad) BS232 BS221

H41 11B7

Pos

Quotient - Alpha LDM1 Pos

Quotient - Delta LDM1 ESD1M Pos

*Positive reactions often weaker at IAT

AABB Tech Manual, 18th ed. 2014

1 3 4 5 6 7 8 9 1 2 3 4 5 6 7 8 10

Locus 1 Locus 2

Exons

No D antigens ce antigens

RHCE

ceCF results from 3 nucleotide changes,

48G>C, 697C>G, 733C>G in RHce

gene.

D Epitope on RHce Gene - ceCF

GammaClone

IS

Anti-D 3+

Anti-D Reagents: Reactions with Crawford Phenotype RBCs

Anti-D RBCs

Reagent IgM IgG Crawford

IS/IAT

GammaClone GAMA401 F8D8 Pos/Neg

Immucor-4 MS201 MS26 Neg/Neg

Immucor-5 TH28 MS26 Neg/Neg

Ortho Bioclone MAD2 Human

polyclonal

Neg/Neg

Ortho (ID-MTS) MS201 Neg/Neg

Biotest (Bio-Rad) BS232 BS221

H41 11B7

Neg/Neg

Quotient - Alpha LDM1 Neg/Neg

Quotient - Delta LDM1 ESD1M Neg/Neg

AABB Tech Manual, 18th ed. 2014

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Anti-D

Reagents & Methods

Monoclonal Reagent Types

• Blend of monoclonal & polyclonal antibodies

• Blend of two or more monoclonal antibodies,

each secreted by a different cell line

• IgG or IgM, or combination of IgG + IgM

• Why?

• D antigen has >30 different epitopes

• Variant D antigens

FDA Approved Reagent Anti-D - Tubes

Anti-D

Reagent IgM IgG

Gamma-Clone GAMA401 F8D8

Immucor-4 MS201 MS26

Immucor-5 TH28 MS26

Ortho Bioclone Tube MAD2 Human polyclonal

Bio-Rad Seraclone - Blend BS232 BS221

H41 11B7

Bio-Rad Seraclone - 226 BS226

Quotient (Alba) – Alpha LDM1

Quotient (Alba) – Beta LDM3

Quotient (Alba) – Delta* LDM1

ESD1-M

Quotient (Alba) – Blend LDM3 EDS1

*Not for patient testing, detects DVI at IS

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FDA Approved Reagent Anti-D - Other Methods

Anti-D

Anti-D Method IgM IgG

Immucor – Series 4 Galileo Echo®/Neo® MS201 MS26

Immucor– Series 5 Galileo Echo®/Neo® TH28 MS26

Ortho Gel/Provue® MS201

PK1 PK7200®/PK7300® P3X61

PK2 PK7200®/PK7300® HM10

Blend PK7200®/PK7300® P3X61

P3X21223B10

P3X290

P3X35

Bio-Rad 226 Tango® BS226

Bio-Rad 232 Tango® BS232

Solidscreen II Blend

(weak D testing)

Tango® H411B7

BS221

Grifols DG Gel/Erytra® P3x61

Specificity of Anti-D CFR 660.26

• Panel of antigen positive RBCs must be

tested and include at least 3 donors of

each phenotype:

• DCe/ce, Dce/ce

• dCe/ce, dce/cE

• Group A, B and O dce/dce

• Most include testing with DVI

Sensitivity of Anti-D

• Reagent Anti-D compared to Reference

Blood Grouping Sera (FDA) for potency

• Monoclonal Anti-D WILL NOT detect all

weak D and partial D

• Weak D Test (IAT/AHG) enhances

reactivity with most examples of weak

D and partial D

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Human IgG Anti-D

Monoclonal IgM/IgG ANTI-D

Monoclonal IgM/IgG ANTI-D #1

Direct Agglutination - IS

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Monoclonal IgM/IgG ANTI-D #1

Weak D Test - IAT

Monoclonal IgM/IgG ANTI-D #2

Method Variability

• Test Tube Methods

• Reagents used

• Technologist-dependent

• Weak D IAT/AHG or not…

• Other Methods

• Liquid microtiter

• Column Agglutination

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Direct Agglutination in Test Tubes

Reading Direct Agglutination

ABO vs. RhD Reagents

Anti-A / Anti-B Anti-D

Antibody Class IgM IgM or

IgM & IgG

Antigen Structure

Carbohydrate

Integral Membrane

Protein

Antigen Sites/RBC ~2 – 10 x 105

~ 9,900 – 33,000

Reading Direct Agglutination

Shake, Rock, Roll, Swirl, Tilt, or some combination… Grade as soon as

RBC button is

resuspended

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Microplate ABO/Rh Typing

Fluid Phase – Hemagglutination by Settling

www.beckmancoulter.eu/diagnostics/3108_PK7300.htm

PK7300

Settling Method

Neg Pos

Microplate ABO/Rh Typing Fluid Phase – Hemagglutination

Galileo Echo® & NEO ®

Microtiter Plate ABO/Rh Typing

Hemagglutination Method

Monoclonal Control

Anti-A

Anti-B

Anti-D Series 4

Anti-D Series 5

A1 Cells

B Cells

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Microplate ABO/Rh Typing Hemagglutination by Aggitation

Column Agglutination Hemagglutination Methods

http://www.grifols.com

www.ortho-wire.com/en/blood-group-serology/learning-library/AgAb/page5.cfm

Questionable RhD Typing Results

Using Automation

Microplate

Anti-D ? Or NTD

Discordant with historical typing

Gel

Anti-D ? or <2+

or

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RhD Typing Results

Test Tube Method

Tube IS IAT

Anti-D 0-2+ 2-4+

Consider RHD genotyping

Tube IS

Anti-D 3-4+

or

Serologic Weak D Phenotype

Reasons to Resolve Weak Expression

Pregnancy

• Avoid giving RhIG to women who do not

need it (Rh status is confirmed for

historical discrepancies)

• Resolve early in pregnancy to eliminate

false-positive rosette tests

Rosette Test Results

Negative Control Positive Control

Weak D+ Mom Courtesy of MR Combs

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Reasons to Resolve Weak Expression

Transfusion

• Conserve Rh-negative blood for D-

negative recipients (high risk of

making anti-D)

Sandler SG, et al. Commentary – Transfusion March 2015)

Objectives

• Identify causes for variability of expression of

RhD antigen

• Describe specificity, sensitivity & intended use

of current commercial RhD typing reagents

used in test tube & automated methods.

• List challenges of typing for RhD by

serologic methods.

• Define management & transfusion options for

patients with weak or variable RhD typing.

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References • Wagner FF, Gassner C, Mu¨ller TH, et al. Molecular basis of weak D

phenotypes. Blood 1999; 93:385–393.

• Wagner FF, Frohmajer A, Ladewig B, Eicher NI, Lonicer CB, Mu¨ller TH,

Siegel MH, Flegel WA. Blood 2000;95:2699-2708.

• Denomme GA, Wagner FF, Fernandes BJ, et al. Partial D, weak D types,

and novel RHD alleles among 33 864 multiethnic patients: implications for

anti-D alloimmunization and prevention. Transfusion 2005; 45:1554–1560.

• Flegel WA, Denomme GA, Yazer MH. On the complexity of D antigen

typing: a handy decision tree in the age of molecular blood group

diagnostics. J Obstet Gynaecol Can. 2007;29:746-52.

• Flegel WA. How I manage donors and patients with a weak D phenotype.

Curr Opin Hematol 2006;13:476–483.

• Denomme GA, Dake LR, Vilensky D, Ramyar L, Judd WJ. Rh

discrepancies caused by variable reactivity of partial and weak D types with

different serologic techniques.Transfusion 2008;48:473-476.

• Roback JD, Grossman BJ, Harris T, Hillyer CD. Technical Manual, 18 th ed.

2014.

• Sandler SG, Flegel WA, Westhoff CM, Denomme GA, Delaney M, Keller

MA, Johnson ST, Louis Katz, Queenan JT, Vassallo RR, Simon CD,

Transfusion. 2015 Mar;55(3):680-9.

References • Flegel WA. Molecular genetics and clinical applications for RH.

Transfusion and Apheresis Science 2011;44:81-91.

• Sandler SG, Li W, Langeberg AL, Landy HJ. New Laboratory

Procedures and Rh Blood Type Changes in a Pregnant Woman. Obstet

Gynecol 2012;119:426–8.

• Wang D, Lane C, Quillen K. Prevalence of RhD variants, confirmed by

molecular genotyping, in a multiethnic prenatal population. Am J Clin

Pathol 2010;134:438-442

• Credidio DC, Pellegrino J, Castilho L, Serologic and molecular

characterization of D variants in Brazilians: impact for typing and

transfusion strategy. Immunohematology 2011;27:6-11.

• Abelrazik AM, Elshafie SM, Ahmed GME, Abdelaziz HM. Combining

serology and molecular typing of weak D role in improving D typing

strategy in Egypt. Transfusion. 2013 Nov;53(11 Suppl 2):2940-4

• Chou ST, Jackson T, Vege S, Smith-Whitley K, Friedman DF, Westhoff

CM. High prevalence of red blood cell alloimmunization in sickle cell

disease despite transfusion from Rh-matched minority donors. Blood.

2013 Aug 8;122(6):1062-71.

References

• Reid ME, Hipsky CH, Hue-Roye, K, Hoppe C. Genomic analysis of RH

alleles to improve transfusion therapy in patients with sickle cell

disease. Blood Cells Mol Dis. 2014 Apr;52(4):195-202

• Garratty G, Glynn SA, McEntire for the Retrovirology Epidemiology

Donor Study. ABO and Rh(D) phenotype frequencies of different

racial/ethnic groups in the United States. Transfusion 2004;44:703-6.

• Haspel RH, Westhoff CM. How do I manage Rh typing in obstetrical

patients. Transfusion 2015;55;470–474.

• Cannon M, Pierce R, Taber EB, Schucker J. Fatal hydrops fetalis

caused by anti-D in a mother with partial D. Obstet Gynecol. 2003

Nov;102(5 Pt 2):1143-5.

• Lacey PA, Caskey CR, Werner DJ, Moulds JJ. Fatal hemolytic disease

of a newborn due to anti-D in an Rh-positive Du variant mother.

Transfusion. 1983 Mar-Apr;23(2):91-4.

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Thank You

[email protected]