Full Reagent Update

Current availability from NIBSC of candidate influenza vaccine viruses, SRD reagents and neuraminidase reagents for use in the 2013/2014 northern hemisphere and the 2013 southern hemisphere season. (See below for  pricing information)

 

Update 41, 06 May 2013

 

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

 NIB-74xp reassortant derived from A/Christchurch/16/2010 (A/California/7/2009 – like)  11/186

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

 B/Brisbane/33/2008

08/280

 NYMC BX-31 reassortant derived from B/Brisbane/60/2008

10/276

 NYMC BX-35 reassortant derived from B/Brisbane/60/2008

09/318

 

1 Recommended composition of influenza virus vaccines for use in the 2013-14 northern hemisphere influenza season

 

Reagents for influenza vaccine standardisation

NIBSC code

H1N1

 

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/Christchurch/16/2010 (NIB-74)  10/258

A/Brisbane/10/2010 cell derived antigen

11/134

A/California/7/2009 antiserum

12/108

H3N2

 

A/Texas/50/2012 (NYMC-X223) egg derived antigen

13/112

A/Texas/50/2012 (NYMC-X223A) egg derived antigen

tbc

 A/Texas/50/2012-Like antiserum  13/110

B (Yamagata lineage)

 

B/Massachusetts/02/2012 egg derived antigen

tbc

B/Massachusetts/02/2012 cell derived antigen

tbc

B/Massachusetts/02/2012 (NYMCBX-51B) egg derived antigen

13/106

B/Massachusetts/02/2012-Like antiserum

 13/114
 B (Victoria lineage)  
 B/Brisbane/60/2008 antigen  08/352
 B/Brisbane/60/2008 like antigen (NYMC BX-35)  10/106
 B/Brisbane/60/2008 like antiserum  11/136

 

Neuraminidase reagents

NIBSC code

N1

 

Antiserum prepared from A/California/7/2009  10/218

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 2013 

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  09/130
 NIB-74xp reassortant derived from A/Christchurch/16/2010(A/California/7/2009 – like)  11/186

H3N2

 

A/Victoria/361/2011 wild type virus

11/226

 IVR-165 reassortant derived from A/Victoria/361/2011  11/220
 NIB-79 reassortant derived from A/Victoria/361/2011  11/222
 NYMC X-217 reassortant derived from A/Victoria/361/2011  12/100

B

 

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

 (B/Wisconsin/1/2010 – like)
 11/244
 NYMC BX-41A reassortant derived from B/Wisconsin/1/2010  11/240

2 Recommended composition of influenza virus vaccines for use in the 2013 southern hemisphere influenza season

 

Reagents for influenza vaccine standardisation

NIBSC code

H1N1

 

 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/Christchurch/16/2010 (NIB-74)  10/258
A/Brisbane/10/2010 cell derived antigen   11/134
A/California/7/2009 antiserum   12/108

H3N2

 

A/Victoria/361/2011 (IVR-165) egg derived antigen

12/114 

A/Victoria/361/2011 antiserum

 12/116

B

 

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

 

 

Neuraminidase reagents

NIBSC code

N1

 

 Antiserum prepared from A/California/7/2009  10/218

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

 

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.