| Literature DB >> 35177857 |
Maria Auladell1, Hoang Vu Mai Phuong2, Le Thi Quynh Mai2, Yeu-Yang Tseng3,4, Louise Carolan3, Sam Wilks5, Pham Quang Thai2, David Price6,7, Nguyen Thanh Duong8, Nguyen Le Khang Hang2, Le Thi Thanh2, Nguyen Thi Hong Thuong9, Tran Thi Kieu Huong9, Nguyen Thi Ngoc Diep9, Vu Thi Ngoc Bich9, Arseniy Khvorov3,4, Luca Hensen1, Tran Nhu Duong2, Katherine Kedzierska1, Dang Duc Anh2, Heiman Wertheim9,10, Scott D Boyd11, Kim L Good-Jacobson12,13, Derek Smith5, Ian Barr3, Sheena Sullivan3,4, H Rogier van Doorn9,14, Annette Fox15,16,17.
Abstract
Studies of successive vaccination suggest that immunological memory against past influenza viruses may limit responses to vaccines containing current strains. The impact of memory induced by prior infection is rarely considered and is difficult to ascertain, because infections are often subclinical. This study investigated influenza vaccination among adults from the Ha Nam cohort (Vietnam), who were purposefully selected to include 72 with and 28 without documented influenza A(H3N2) infection during the preceding 9 years (Australian New Zealand Clinical Trials Registry 12621000110886). The primary outcome was the effect of prior influenza A(H3N2) infection on hemagglutinin-inhibiting antibody responses induced by a locally available influenza vaccine administered in November 2016. Baseline and postvaccination sera were titrated against 40 influenza A(H3N2) strains spanning 1968-2018. At each time point (baseline, day 14 and day 280), geometric mean antibody titers against 2008-2018 strains were higher among participants with recent infection (34 (29-40), 187 (154-227) and 86 (72-103)) than among participants without recent infection (19 (17-22), 91 (64-130) and 38 (30-49)). On days 14 and 280, mean titer rises against 2014-2018 strains were 6.1-fold (5.0- to 7.4-fold) and 2.6-fold (2.2- to 3.1-fold) for participants with recent infection versus 4.8-fold (3.5- to 6.7-fold) and 1.9-fold (1.5- to 2.3-fold) for those without. One of 72 vaccinees with recent infection versus 4 of 28 without developed symptomatic A(H3N2) infection in the season after vaccination (P = 0.021). The range of A(H3N2) viruses recognized by vaccine-induced antibodies was associated with the prior infection strain. These results suggest that recall of immunological memory induced by prior infection enhances antibody responses to inactivated influenza vaccine and is important to attain protective antibody titers.Entities:
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Year: 2022 PMID: 35177857 DOI: 10.1038/s41591-022-01690-w
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 87.241