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Research Paper

Long-Term Thermal Stability of Group C Meningococcal Polysaccharide-Tetanus Toxoid Conjugate Vaccine

Shwu-Maan Lee, Robert Petermann, Quallyna Porte, Greg Berezuk, Brian Crowe and John Shirtz

volume 3 | issue 1

january/february 2007
Pages: 27 - 32

This is an open-access article

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The stability of vaccines during storage and handling is a prerequisite for optimal potency at the time of immunization. Meningococcal group C conjugate vaccines have been successfully incorporated in mass immunization programs, however, thus far no long-term real-time stability studies of these vaccines have been reported. Stability of de-O-acetylated group C meningococcal polysaccharide coupled to tetanus toxoid (GCMP-TT) was evaluated in real time on the basis of immunogenicity and physiochemical properties. The vaccine is formulated as a 0.5 mL suspension containing 10 microgram GCMP conjugated to 10-20 microgram of TT adsorbed on 0.5 mg aluminum in saline. The single dose syringes were stored under refrigeration (5 ± 3 {degree sign}C) and at room temperature (25 ± 2 {degree sign}C) for up to 42 months and at elevated temperature (40 ± 2 {degree sign}C) for up to 6 months. At both refrigerated and room temperatures, no time-dependent change in animal potency was detectable through 42 months. After the 9 months maximum recommended storage period at room temperature, 96% of the baseline serum bactericidal antibody (SBA) titer was maintained. Time-dependent decreases in SBA level and anti-GCMP-TT IgG level were observed at 40 ± 2 {degree sign}C. No changes in GCMP-TT adsorption and pH occurred in all the studies. Loss of integrity increased over 6 months at 40 ± 2 {degree sign}C (p = 0.004). Free sugar content did not change over 36 months under refrigeration. GCMP-TT retained immunogenicity and physicochemical properties under refrigeration and at room temperature (25 ± 2 {degree sign}C) for up to 42 months.

Authors

Shwu-Maan Lee

Baxter BioScience; Vienna, Austria

Robert Petermann

Baxter BioScience; Vienna, Austria

Quallyna Porte

Baxter BioScience; Vienna, Austria

Greg Berezuk

Baxter BioScience; Vienna, Austria

Brian Crowe

Baxter BioScience; Vienna, Austria

John Shirtz

Baxter BioScience; Vienna, Austria


This is an open-access article

 Download PDF

If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.