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1.
Vaccine ; 37(43): 6415-6425, 2019 10 08.
Article in English | MEDLINE | ID: mdl-31519445

ABSTRACT

Hepatitis B virus causes acute and chronic infections in millions of people worldwide and, since 1982, a vaccine with 95% effectiveness has been available for immunization. The main component of the recombinant hepatitis B vaccine is the surface antigen protein (HBsAg). In this work, the effect of pH, ionic strength and temperature on the native state of the HBsAg antigen were studied by a combination of biophysical methods that included small angle X-ray scattering, synchrotron radiation circular dichroism, fluorescence and surface plasmon resonance spectroscopies, as well as in vivo and in vitro potency assays. The native conformation, morphology, radius of gyration, and antigenic properties of the HBsAg antigen demonstrate high stability to pH treatment, especially in the pH range employed in all stages of HBsAg vaccine production and storage. The HBsAg protein presents thermal melting point close to 56 °C, reaching a more unfolded state after crossing this point, but it only experiences loss of vaccine potency and antigenic properties at 100 °C. Interestingly, a 6-month storage period does not affect vaccine stability, and the results are similar when the protein is kept under refrigerated conditions or at room temperature (20 °C). At frozen temperatures, large aggregates (>200 nm) are formed and possibly cause loss of HBsAg content, but that does not affect the in vivo assay. Furthermore, HBsAg has a well-ordered secondary structure content that is not affected when the protein is formulated with silica SBA-15, targeting the oral delivery of the vaccine. The combined results from all the characterization techniques employed in this study showed the high stability of the antigen at different storage temperature and extreme values of pH. These findings are important for considering the delivery of HBsAg to the immune system via an oral vaccine.


Subject(s)
Hepatitis B Surface Antigens/chemistry , Hepatitis B Surface Antigens/immunology , Protein Stability , Temperature , Animals , Circular Dichroism , Female , Fluorescence , Hepatitis B Vaccines/chemistry , Hepatitis B Vaccines/immunology , Hepatitis B virus/chemistry , Hydrogen-Ion Concentration , Immunogenicity, Vaccine , Mice , Mice, Inbred BALB C , Protein Denaturation , Silicon Dioxide/chemistry , Surface Plasmon Resonance , Vaccine Potency
2.
Rev Saude Publica ; 24(1): 51-9, 1990 Feb.
Article in Portuguese | MEDLINE | ID: mdl-2218376

ABSTRACT

Three different lots of measles vaccines produced with the Biken CAM-70 virus strain were requested from the central cold store of the Public Health Department of the State of S. Paulo, Brazil, and assays on photosensitivity at 2-8 degrees C, and on stability at 28, 36.5 and 45 degrees C were carried out to find out for how long these vaccines would maintain their minimum potency, established as being 3.70 log10 or 5000 TCID50 (50% tissue culture infective dose) per human dose. The analysis of the adjusted straight regression lines indicated that, with the passage of time, the potency of lyophilized or reconstituted vaccines, as well as of vaccines exposed to or protected from light decreased. Light-exposed vaccines, however, became less potent than vaccines protected from the light. None of the vaccine lots studied, reconstituted and stored at 2-8 degrees C, exhibited homogeneity as to sensitivity to light. When freeze-dried vaccines had their photosensitivity studied at 2-8 degrees C, lots 1 and 2 presented greater thermal degradation when exposed to light than when protected from it. However, in both instances, it was found that potency fell below that taken as minimum for the Biken CAM-70 virus strain. At all other temperatures considered, even when protected from light, lots 1 and 2 did not retain the minimum potency. Lot 3 kept the expected stability for 60 days at 2-8 degrees C when protected from light and for 40 days when unprotected, but its thermal degradation at other temperatures was more intense (28 degrees C: 5 days; 36.5 degrees C: 2 days; 45 degrees C: 0.5 day).(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Measles Vaccine/standards , Drug Stability , Drug Storage , Evaluation Studies as Topic , Freeze Drying , Hot Temperature/adverse effects , Light/adverse effects , Vaccines, Attenuated/standards
3.
Rev Saude Publica ; 23(2): 162-9, 1989 Apr.
Article in Portuguese | MEDLINE | ID: mdl-2617108

ABSTRACT

Eight lots of the calf sera employed to supplement culture media for the cultivation of animal cells, of widespread use in virology obtained from calves above and below six months of age were rated as good or as poor cell growth promoters according to their growth promoting capacity (GPC). Parameters related to macronutrients contained in these serum lots were then evaluated with the purpose of establishing their biochemical profiles. The results obtained can be considered as normal values for apparently healthy animal donors. Fluctuations found between the data of this investigation and those mentioned in the literature for certain biochemical parameters are probably due to the methodology employed, the breed and age of the animals, or even to regional diet. Student's "t" test was applied for the statistical analysis of the results and demonstrated that, as far as serum fractions were concerned, no significant differences occurred between sera rated as good and poor cell growth promoters, taking tc = 2.45. For calf sera from animals above and below six months of age, two tests relating to alfa and beta fractions were significant (t = 2.68 and 2.61 respectively). It was demonstrated that the evaluation of the biochemical parameters mentioned "per se" neither leads to the identification of calf sera presenting good or poor GPC, nor of sera harvested from calves younger or older than six months.


Subject(s)
Blood/metabolism , Growth Substances/pharmacology , Virology/methods , Animals , Blood Chemical Analysis , Blood Proteins/metabolism , Cattle , Cell Division/drug effects , Cells, Cultured/drug effects , Electrophoresis
4.
Bull Pan Am Health Organ ; 23(3): 299-305, 1989.
Article in English | MEDLINE | ID: mdl-2571379

ABSTRACT

The work reported here sought to assess the protection afforded by two stabilizing solutions (sorbitol-gelatin and glutamic acid-lactose) in preserving the potency of freeze-dried Schwarz strain measles virus during storage with a view to the production of reference preparations and working lots of virus suspensions. Stabilized virus suspensions and control suspensions were stored at -70 degrees C or were freeze-dried and stored at -20 degrees C, and their potency was determined over a storage period of 21 months. It was found that the sorbitol-gelatin imparted more satisfactory stability (r = +0.18) to the freeze-dried virus suspensions than did the glutamic acid-lactose. The results also indicate that sorbitol-gelatin, used under the conditions of this study, is an effective stabilizer in the preparation of freeze-dried suspensions of Schwarz strain measles virus employed as reference preparation working lots.


Subject(s)
Measles Vaccine/standards , Measles virus/physiology , Virus Cultivation/methods , Culture Media , Freeze Drying , Gelatin , Glutamates , Glutamic Acid , Humans , Lactose , Reference Standards , Sorbitol , Vaccines, Attenuated/standards
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