Influenza A(H1N1)pdm09 But Not A(H3N2) Virus Infection Induces Durable Seroprotection: Results From the Ha Nam Cohort

Author:

Hoa Le Nguyen Minh1,Sullivan Sheena G234,Mai Le Quynh5,Khvorov Arseniy3,Phuong Hoang Vu Mai5,Hang Nguyen Le Khanh5,Thai Pham Quang5,Thanh Le Thi5,Carolan Louise2,Anh Dang Duc5,Duong Tran Nhu5,Bryant Juliet E16,van Doorn H Rogier16,Wertheim Heiman F L17,Horby Peter16,Fox Annette128ORCID

Affiliation:

1. Oxford University Clinical Research Unit and Wellcome Trust Major Overseas Programme, Hanoi, Viet Nam

2. WHO Collaborating Centre for Reference and Research on Influenza, Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia

3. Doherty Department, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia

4. Fielding School of Public Health, University of California, Los Angeles, California, USA

5. National Institute of Hygiene and Epidemiology, Hanoi, Viet Nam

6. Center for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK

7. Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands

8. Department of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia

Abstract

Abstract Background The extent to which influenza recurrence depends upon waning immunity from prior infection is undefined. We used antibody titers of Ha-Nam cohort participants to estimate protection curves and decay trajectories. Methods Households (270) participated in influenza-like–illness (ILI) surveillance and provided blood at intervals spanning laboratory–confirmed virus transmission. Sera were tested in hemagglutination inhibition assay. Infection was defined as influenza virus-positive ILI and/or seroconversion. Median protective titers were estimated using scaled-logistic regression to model pretransmission titer against infection status in that season, limiting analysis to households with infection(s). Titers were modelled against month since infection using mixed-effects linear regression to estimate decay and when titers fell below protection thresholds. Results From December 2008–2012, 295 and 314 participants were infected with H1N1pdm09-like and A/Perth/16/09-like (H3N2Pe09) viruses, respectively. The proportion protected rose more steeply with titer for H1N1pdm09 than for H3N2Pe09, and estimated 50% protection titers were 19.6 and 37.3, respectively. Postinfection titers started higher against H3N2Pe09 but decayed more steeply than against H1N1pdm09. Seroprotection was estimated to be sustained against H1N1pdm09 but to wane by 8-months for H3N2Pe09. Conclusions Estimates indicate that infection induces durable seroprotection against H1N1pdm09 but not H3N2Pe09, which could in part account for the younger age of A(H1N1) versus A(H3N2) cases.

Funder

Wellcome Trust

Department of Health, Australian Government

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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