Stability of diluted smallpox vaccine under simulated clinical conditions

Context: During a mass smallpox immunization campaign, vaccine may be exposed to ambient temperatures for extended periods of time. Objective: To determine the viability of undiluted and 5 x diluted DryVax smallpox vaccine after cycling vaccine in and out of refrigeration for 2 weeks, as might occur during an immunization campaign. Design: Two vials of Dryvax vaccine were reconstituted as per manufacturer's instructions (1 x) and two vials were reconstituted using 5 x the recommended diluent (5 x). Every 12 h over 2 weeks, vials were cycled between refrigeration and room temperature (1 x -RT, 5 x -RT) or ice bath (1 x -cold, 5 x -cold). Each vial was sampled in triplicate at time of reconstitution and thereafter at 24 or 48 h intervals. Main outcome measures: Viability measured by viral plaque forming Units per ml (pfu/ml). Results: All four vaccine vials showed a decline in virus titer over the 2-week period but remained well above 10(7) pfu/ml. Compared with titers on the day of reconstitution (day 0), titers at the end of the study (day 14) had declined by 0.4-0.6 log in all vials (Table 1). Linear regression analysis suggested that decay in viral titer occurred more rapidly in vials exposed to room temperature compared with vials kept on ice and in vaccine diluted 1 x compared with vaccine diluted 5 x. Conclusions: After 2 weeks, viability was greater than 10(7) pfu/ml, the titer suggested by Frey et al. as necessary to ensure successful vaccination in more than 97% of vaccinees. When removed from refrigeration, keeping the vaccine on ice lowers the decline in titer. (c) 2005 Elsevier Ltd. All rights reserved.