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Northern Hemisphere 2013/20141
Candidate influenza vaccine viruses
NIBSC code
H1N1
A/California/7/2009 wild type virus
12/174
NYMC X-179A reassortant derived from A/California/7/2009
11/112
NYMC X-181 reassortant derived from A/California/7/2009
11/128
NIBRG-121xp reassortant derived from A/California/7/2009
09/268
NIBRG-122 reassortant derived from A/England/195/2009 (A/California/7/2009 – like)
09/130
H3N2
A/Texas/50/2012 wild type virus
12/298
NYMC X-223A reassortant derived from A/Texas/50/2012
12/286
NYMC X-223 reassortant derived from A/Texas/50/2012
12/292
B (Yamagata lineage)
B/Massachusetts/2/2012 wild type virus
12/288
NYMC BX-51B reassortant derived from B/Massachusetts/2/2012
12/296
NYMC BX-51C reassortant derived from B/Massachusetts/2/2012
12/294
B (Victoria lineage)
B/Brisbane/60/2008
12/200
08/280
10/276
09/318
1 Recommended composition of influenza virus vaccines for use in the 2013-14 northern hemisphere influenza season
Reagents for influenza vaccine standardisation
A/California/7/2009 (NYMC X-179A) egg derived antigen
N/A
A/California/7/2009 (NYMC X-179A) cell derived antigen
09/174
A/California/7/2009 (NIBRG-121xp) egg derived antigen
09/196
A/California/7/2009 (NYMC X-181)
12/168
A/Brisbane/10/2010 cell derived antigen
11/134
A/California/7/2009 antiserum
12/108
A/Texas/50/2012 (NYMC-X223) egg derived antigen
13/112
A/Texas/50/2012 (NYMC-X223A) egg derived antigen
tbc
B/Massachusetts/02/2012 egg derived antigen
B/Massachusetts/02/2012 cell derived antigen
B/Massachusetts/02/2012 (NYMCBX-51B) egg derived antigen
13/106
B/Massachusetts/02/2012-Like antiserum
Neuraminidase reagents
N1
antiserum prepared from A/New Caledonia/20/99
04/230
N2
antiserum prepared from A/Wyoming/3/2003
04/258
B
NA antiserum prepared from B/Jiangsu/10/2003
04/228
NA antiserum prepared from B/Malaysia/2506/2004
05/252
NA antiserum prepared for B/Florida/4/2006
09/316
Southern Hemisphere 20132
A/Victoria/361/2011 wild type virus
11/226
B/Wisconsin/1/2010 wild type virus
11/224
B/Texas/6/2011 wild type virus (B/Wisconsin/1/2010 – like)
11/232
NYMC BX-39 reassortant derived from B/Hubei Wujiagang/158/2009
(B/Wisconsin/1/2010 – like)
12/202
NYMC BX-49 reassortant derived from B/Texas/6/2011
2 Recommended composition of influenza virus vaccines for use in the 2013 southern hemisphere influenza season
A/Victoria/361/2011 (IVR-165) egg derived antigen
12/114
A/Victoria/361/2011 antiserum
B/Hubei Wujiagang/158/2009 (NYMC BX-39) egg derived antigen
12/106
B/Wisconsin/1/2010 cell derived antigen
12/110
B/Wisconsin/1/2010-like antiserum
12/118
Antiserum prepared from A/New Caledonia/20/99
Antiserum prepared from A/Wyoming/3/2003
N/A- Not available
Tbc- to be confirmed
Pricing information
Viruses are free of charge (normally a maximum of two vials per recipient), but customers are expected to pay shipping and packing costs. Reagents for Single Radial Diffusion assay are subject to the usual NIBSC handling charge of £70 per vial, plus shipping and packing costs. Approved National Control Laboratories for human health are exempt from the £70 handling fee.
Calibration of Reagents for Influenza vaccine standardisation
Reference antigens and antiserum reagents for the standardization of vaccines are produced by the following WHO laboratories:
Essential Regulatory Laboratories (ERL)
National Institute for Biological Standards and Control (NIBSC), UK
Center for Biologics Evaluation and Research (CBER), USA
National Institute for Infectious Disease (NIID), Japan
Therapeutic Goods Administration (TGA), Australia
Here is the link to the document providing a generic protocol for the calibration of influenza antigen working reagents by the four WHO Essential Regulatory Laboratories (ERLs):
Generic protocol for the calibration of seasonal/pandemic influenza antigen working reagents by WHO Essential Regulatory Laboratories (PDF, 191kb)
It represents the consensus of the ERLs on the process of assigning a potency value to a newly established influenza antigen reagent for use in potency testing of inactivated influenza vaccines. An influenza antigen working (or reference) reagent is a preparation of inactivated whole virus that has been freeze-dried and calibrated as outlined in this document.
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