Reagent manufacture and reference preparations - Platelet immunology - Chapter 18

18.1.1: HPA typing reagents

There are several human platelet antigen (HPA) genotyping and phenotyping techniques. The latter are generally based on the use of polyclonal HPA alloantibodies obtained from immunised donors or patients, or monoclonal antibodies. HPA typing techniques that do not require polyclonal antibodies derived from donors or patients are the techniques of choice.

HPA typing reagents prepared from human source material should comply with the guidelines in section 11.1.4.10. An ‘Instructions for use’ sheet (package insert) should be prepared and supplied with antibody typing reagents. Information in the ‘Instructions for use’ should further indicate the immunoglobulin class of the antibodies and the presence of any other contaminating antibodies reactive by the recommended methods.

HPA typing reagents used in genomic DNA and polymerase chain reaction (PCR)-based techniques should comply with the guidelines in Chapter 14.

18.1.2: Composition of platelet cell panel for HPA antibody detection

It is recommended that laboratories make all reasonable efforts to include cells in their panel that will aid the detection and identification of clinically significant HPA antibodies. The panel should consist of platelets typed at a minimum for HPA-1, -2, -3, -5 and -15 by validated HPA typing techniques. Ideally, the panel should contain platelets that are homozygous for HPA-1a, -1b, -2a, -2b, -3a, -3b, -5a, -5b, -15a and -15b and be from Group O donors.

HPA typing of a platelet panel donor should be based on two concordant typing results using samples obtained on different occasions.

18.1.3: Selection of normal control sera

Normal control sera should be taken from non-transfused group AB male or ABO compatible blood donors. The sera should be screened and found negative for platelet-reactive-antibodies (e.g. clinically non-significant autoantibodies or EDTA-dependent antibodies are occasionally detected in apheresis donors).

An appropriate number of normal sera should be used so that a statistically relevant normal range in a given assay can be determined.

18.1.4: Selection of positive control sera

At least one positive control should be included in each assay. The selection and number of positive control sera will depend on the technique and the HPA type of the platelets being used.

In glycoprotein-specific assays a positive control for each glycoprotein used should be included as a minimum.

18.1.5: Reference preparations

Sensitivity of techniques should be monitored on the basis of the inclusion of a ‘weak positive’ control. For anti-HPA-1a, -3a and -5b, the internal sensitivity control should be calibrated against the WHO International Reference Reagents for anti-HPA-1a (NIBSC code 05/106), anti-HPA-3a (NIBSC code 03/190), anti-HPA-5b (NIBSC code 99/666) ans anti-HPA-15b (NIBSC code 18/220) when diluted as instructed by the manufacturer.

In-house sensitivity standards, with similar reaction strengths to the above reagents, should be prepared for anti-HPA-1, -3 and -5, and, if possible, for anti-HPA-2 and -15 antibodies.

18.1.6: Quality control schemes

Laboratories should take part in regular external quality control exercises such as the UK NEQAS for Histocompatibility and Immunogenetics schemes for HPA genotyping and HPA antibody detection/specification. Effective mechanisms should be in place to correct poor performance in the quality scheme.

18.1.7: Nomenclature

The current HPA nomenclature must be used for recording platelet-specific alloantigen and alloantibody specificities [Metcalfe, 2003]. See Tables 18.1.1 to 18.1.6 for details of each HPA system. Any subsequent additions can be found in the Human Platelet Antigen Database (www.versiti.org/products-services/human-platelet-antigen-hpa-database).

Table 18.1.1: Current HPA nomenclature – HPA-1 system
Antigen	Original names	Glycoprotein	CD
HPA-1a	Zwa, PlA1	GPIIIa	CD61
HPA-1b	Zwb, PlA2	n/a	n/a

Table 11.8.2: Current HPA nomenclature – HPA-2 system
Antigen	Original names	Glycoprotein	CD
HPA-2a	Kob	GPIb alpha	CD42b
HPA-2b	Koa, Siba	n/a	n/a

Table 11.8.3: Current HPA nomenclature – HPA-3 system
Antigen	Original names	Glycoprotein	CD
HPA-3a	Baka, Leka	GPIIb	CD41
HPA-3b	Bakb	n/a	n/a

Table 11.8.4: Current HPA nomenclature – HPA-4 system
Antigen	Original names	Glycoprotein	CD
HPA-4a	Yukb, Pena	GPIIIa	CD61
HPA-4b	Yuka, Penb	n/a	n/a

Table 11.8.5: Current HPA nomenclature – HPA-5 system
Antigen	Original names	Glycoprotein	CD
HPA-5a	Brb, Zavb	GPIa	CD49b
HPA-5b	Bra, Zava, Hca	n/a	n/a
HPA-6bw	Caa, Tua	GPIIIa	CD61
HPA-7bw	Moa	GPIIIa	CD61
HPA-8bw	Sra	GPIIIa	CD61
HPA-9bw	Maxa	GPIIb	CD41
HPA-10bw	Laa	GPIIIa	CD61
HPA-11bw	Groa	GPIIIa	CD61
HPA-12bw	Iya	GPIb beta	CD42c
HPA-13bw	Sita	GPIa	CD49b
HPA-14bw	Oea	GPIIIa	CD61

Table 11.8.6: Current HPA nomenclature – HPA-15 system
Antigen	Original names	Glycoprotein	CD
HPA-15a	Govb	n/a	CD109
HPA-15b	Gova	n/a	n/a
HPA-16b	Duva	GPIIIa	CD61
HPA-17b	Vaa	GPIIIa	CD61
HPA-18b	Caba	GPIa	CD61
HPA-19b	Sta	GPIIIa	CD61
HPA-20b	Kno	GPIIb	CD41
HPA-21b	Nos	GPIIIa	CD61
HPA-22b	Sey	GPIIb	CD41
HPA-23b	Hug	GPIIIa	CD61
HPA-24b	Cab2a+	GPIIb	CD41
HPA-25b	Swia	GPIa	CD49b
HPA-26b	Seca	GPIIIa	CD61
HPA-27b	Cab3a+	GPIIb	CD41
HPA-28b	War	GPIIb	CD41
HPA-29b	Khab	GPIIIa	CD61
HPA-30b	Laba	GPIIb	CD41
HPA-31b	Cab4b	GPIX	CD42a
HPA-32b	Domb	GPIIIa	CD61
HPA-33b	BIa	GPIIIa	CD61
HPA-34b	Bzha	GPIIIa	CD61
HPA-35b	Efsa	GPIIIa	CD61

References

Metcalfe P, Watkins NA, Ouwehand WH, Kaplan C, Newman P, Kekomaki R, De Haas M, Aster R, Shibata Y, Smith J, Kiefel V, Santoso S. (2003). Nomenclature of Human Platelet Antigens. Vox Sanguinis, 85, 240–245.