世卫组织首个国际标准抗SARS-CoV-2免疫球蛋白(人类)
【编号】:NIBSC20/136 【产品名称】:世卫组织首个国际标准抗SARS-CoV-2免疫球蛋白(人类) 【规格】:个 【价格】:断货 世卫组织首个国际标准抗SARS-CoV-2免疫球蛋白(人类)
编号:NIBSC20/136
英文:First WHO International Standard Anti-SARS-CoV-2 Immunoglobulin (Human)
标准类型:国际标准
1. INTENDED USE
The First WHO International Standard for anti-SARS-CoV-2
immunoglobulin is the freeze-dried equivalent of 0.25 mL of pooled
plasma obtained from eleven individuals recovered from SARS-CoV-2
infection. The preparation has been evaluated in a WHO International
Collaborative study (1). The intended use of the International Standard is
for the calibration and harmonisation of serological assays detecting antiSARS-CoV-2
neutralising antibodies. The preparation can also be used
as an internal reference reagent for the harmonisation of binding antibody
assays. The preparation has been solvent-detergent treated to minimise
the risk of the presence of enveloped viruses (2).
2. CAUTION
This preparation is not for administration to humans or animals in
the human food chain.
The preparation contains material of human origin, and either the final
product or the source materials, from which it is derived, have been
tested and found negative for HBsAg, anti-HIV and HCV RNA. As with
all materials of biological origin, this preparation should be regarded as
potentially hazardous to health. It should be used and discarded
according to your own laboratory's safety procedures. Such safety
procedures should include the wearing of protective gloves and
avoiding the generation of aerosols. Care should be exercised in
opening ampoules or vials, to avoid cuts.
3. UNITAGE
The assigned potency of the WHO International Standard for SARS-CoV2
is 250 IU/ampoule for neutralising antibody activity. After reconstitution
in 0.25 mL of distilled water, the final concentration of the preparation is
1000 IU/mL.
For binding antibody assays, an arbitrary unitage of 1000 binding antibody
units (BAU)/mL can be used to assist the comparison of assays detecting
the same class of immunoglobulins with the same specificity (e.g. antiRBD
IgG, anti-N IgM, etc.)
4. CONTENTS
Country of origin of biological material: United Kingdom.
Each ampoule contains the freeze-dried equivalent of 0.25 mL pooled
human plasma.
5. STORAGE
The International Standard 20/136 should be stored at -20°C or below
upon receipt.
Please note: because of the inherent stability of lyophilized
material, NIBSC may ship these materials at ambient temperature.
6. DIRECTIONS FOR OPENING
DIN ampoules have an 'easy-open' coloured stress point, where the
narrow ampoule stem joins the wider ampoule body. Various types of
ampoule breaker are available commercially. To open the ampoule,
tap the ampoule gently to collect material at the bottom (labelled) end
and follow manufactures instructions provided with the ampoule
breaker.
7. USE OF MATERIAL
No attempt should be made to weigh out any portion of the freeze-dried
material prior to reconstitutionThis material should be reconstituted in 0.25 mL sterile distilled water.
Following addition of water, the ampoule may be left at ambient temperature
for approximately 30 minutes until dissolved and then mixed thoroughly,
avoiding the generation of excessive foam.
8. STABILITY
Reference materials are held at NIBSC within assured, temperaturecontrolled
storage facilities. Reference Materials should be stored on
receipt as indicated on the label.
NIBSC follows the policy of WHO with respect to its reference materials.
9. REFERENCES
(1) Mattiuzzo et al. Establishment of the WHO International Standard and
Reference Panel for anti-SARS-CoV-2 antibody. 2020, WHO Expert
Committee on Biological Standardization. WHO/BS/2020.2403
(2) Dichtelmüller et al. Robustness of solvent/detergent treatment of plasma
derivatives: a data collection from Plasma Protein Therapeutics Association
member companies. Transfusion. 2009;49:1931–43.
10. ACKNOWLEDGEMENTS
We would like to wholeheartedly thank the anonymous donors of the plasma
samples for their consent which has allowed this material to be prepared; we
would like to express our gratitude to those groups and individuals who have
coordinated the collection of the convalescent plasma: Malcom Semple
(Univeristy of Liverpool, UK), Lance Turtle (University of Liverpool, UK),
Peter Openshaw (Imperial College London, UK) and Kenneth Baillie
(University of Edinburgh) on behalf of the ISARIC4C Investigators; Heli
Harvala Simmonds and David Roberts (National Health Service Blood and
Transplant, UK). We would also like to thank NIBSC Standards Production
and Development staff for the formulation and distribution of materials. The
Internatinal Standard for SARS-CoV-2 antibody wouldn't have been possible
without the Coalition for Epidemic Preparedness Innovations (CEPI)
sponsored the sourcing and formulation of the candidate material.
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