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Author(s) -
Sharon E. Frey,
Ron Dagan,
Yaffa Ashur,
Xiao Q. Chen,
J. Ibarra,
Herwig Kollaritsch,
Mark H. Mazur,
Gregory A. Poland,
Keith S. Reisinger,
Emmanuel B. Walter,
Pierre Van Damme,
Jean Henrik Braconier,
Ingrid Uhnoo,
Martin Wahl,
Mark M. Blatter,
Dennis A. Clements,
David Greenberg,
Robert M. Jacobson,
S. Ragnar Norrby,
Mina Rowe,
Daniel Shouval,
Stefanie Simmons,
Jan van Hattum,
Solveig Wennerholm,
Jacqueline Gress,
Ivan S. F. Chan,
Barbara J. Kuter
Publication year - 2000
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/315793
Subject(s) - medicine
To the Editor—It was with interest that we read the study by Frey et al. [1], which describes a randomized trial in which 3 manufacturing consistency lots of a combined hepatitis A and B vaccine were compared with the corresponding monovalent vaccines. The authors observed a nonsatisfactory response to the hepatitis B component in the combined vaccine. We are concerned that this report may be misleading, because SmithKline Beecham is mentioned on 2 occasions in the report in either misleading or inaccurate statements. The first instance is in the last paragraph of the introduction [1, page 2019]. As it is written, the reader may incorrectly infer that the vaccine used in this trial was Twinrix (hepatitis A inactivated and hepatitis B [recombinant], SmithKline Beecham Biologicals, Rixensart, Belgium). In fact, the product under discussion in the article was an unnamed combination hepatitis A and B vaccine, developed by Merck & Co. and tested in a 2-dose schedule. In the Materials and Methods section, it is incorrectly stated that RECOMBIVAX HB/H-B-VAXII is manufactured by SmithKline Beecham [1, page 2019], whereas, in fact, it is manufactured and distributed by Merck & Co.; SmithKline Beecham Biologicals manufactures Engerix-B (hepatitis B vaccine [recombinant]). The above statements might lead to the misconception that interference with the hepatitis B response may occur after administration of any combined hepatitis A and B vaccine. However, there are sufficient published data to demonstrate that SmithKline Beecham Biologicals’ combined hepatitis A and B vaccine, Twinrix, administered on a 0-, 1-, 6-month schedule, induces a strong immune response to both vaccine components. Pooled data from 6 pivotal clinical trials [2] carried out in young adults demonstrated high seroprotection rates and geometric mean titers (GMTs) against hepatitis B after vaccination with Twinrix (on a 0-, 1-, and 6-month schedule), as is shown in table 1. Additionally, in a US study conducted in adults (more than half were 140 years old), the immunogenicity of Twinrix (administered as a 3-dose series) was compared with separate injections of the corresponding monovalent products. A better immune response to the hepatitis B component was demonstrated in the combined vaccine than in the monovalent vaccine [3]. After the third dose, 95.1% of subjects receiving Twinrix and 92.2% of subjects receiving Engerix-B had protective titers. GMTs were 2099 mIU/mL and 1871 mIU/mL for Twinrix and Engerix-B, respectively. In conclusion, although Frey et al. [1] did show interference with the hepatitis B response after administration of the combination hepatitis A and B vaccine developed by Merck & Co., SmithKline Beecham Biologicals’ combination hepatitis A and B vaccine, Twinrix, shows no evidence of interference with either component.

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