One- and Two-Dose Vaccinations With Modified Vaccinia Ankara-Bavarian Nordic Induce Durable B-Cell Memory Responses Comparable to Replicating Smallpox Vaccines

Author:

Ilchmann Heiko1,Samy Nathaly2,Reichhardt Daniela2,Schmidt Darja2,Powell Jacqueline D3,Meyer Thomas P H4,Silbernagl Günter2,Nichols Rick5,Weidenthaler Heinz2,De Moerlooze Laurence6,Chen Liddy3ORCID,Chaplin Paul7

Affiliation:

1. Harrison Clinical Research Deutschland, GmbH , Munich , Germany

2. Bavarian Nordic, GmbH , Martinsried , Germany

3. Bavarian Nordic, Inc , Durham, North Carolina , USA

4. Division of Infectious Diseases and Tropical Medicine, LMU University Hospital , Munich , Germany

5. Public Health Vaccines, LLC , Cambridge, Massachusetts , USA

6. Bavarian Nordic, AG , Zug , Switzerland

7. Bavarian Nordic, A/S , Kvistgård , Denmark

Abstract

Abstract Background Although modified vaccinia Ankara-Bavarian Nordic (MVA-BN) vaccination is approved for smallpox and monkeypox prevention, immunological persistence and booster effects remain undescribed. Methods Participants naive to smallpox vaccination were randomized to 1 dose MVA-BN (1×MVA, n = 181), 2 doses MVA-BN (2×MVA, n = 183), or placebo (n = 181). Participants with previous smallpox vaccination received 1 MVA-BN booster (HSPX, n = 200). Subsets of the formerly naive groups (approximately 75 each) received an MVA-BN booster 2 years later. Results Neutralizing antibody (nAb) geometric mean titers (GMTs) increased from 1.1 (baseline, both naive groups) to 7.2 and 7.5 (week 4, 1×MVA and 2×MVA, respectively), and further to 45.6 (week 6, 2×MVA after second vaccination). In HSPX, nAb GMT rapidly increased from 21.6 (baseline) to 175.1 (week 2). At 2 years, GMTs for 1×MVA, 2×MVA, and HSPX were 1.1, 1.3, and 10.3, respectively. After boosting in the previously naive groups, nAb GMTs increased rapidly in 2 weeks to 80.7 (1×MVA) and 125.3 (2×MVA), higher than after primary vaccination and comparable to boosted HSPX subjects. Six months after boosting, GMTs were 25.6 (1×MVA) and 49.3 (2×MVA). No safety concerns were identified. Conclusions Anamnestic responses to boosting without sustained high nAb titers support presence of durable immunological memory following primary MVA-BN immunization. Clinical Trials Registration NCT00316524 and NCT00686582.

Funder

National Institute of Allergy and Infectious Diseases

Bavarian Nordic

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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