Hemagglutinin Stalk-Specific Fc-Mediated Functions Are Associated With Protection Against Influenza Illness After Seasonal Influenza Vaccination

Author:

Motsoeneng Boitumelo M12,Dhar Nisha3,Nunes Marta C345,Krammer Florian678ORCID,Madhi Shabir A349,Moore Penny L1210,Richardson Simone I12ORCID

Affiliation:

1. South African Medical Research Council Antibody Immunity Research Unit, Faculty of Health Sciences, University of the Witwatersrand , Johannesburg , South Africa

2. HIV Virology Section, Centre for HIV and STIs, National Institute for Communicable Diseases, National Health Laboratory Services , Johannesburg , South Africa

3. South African Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, Faculty of Health Sciences, University of the Witwatersrand , Johannesburg , South Africa

4. Department of Science and Innovation/National Research Foundation, South African Research Chair Initiative in Vaccine Preventable Diseases Unit, Faculty of Health Sciences, University of the Witwatersrand , Johannesburg , South Africa

5. Center of Excellence in Respiratory Pathogens, Hospices Civils de Lyon and Centre International de Recherche en Infectiologie, Équipe Santé Publique, Épidémiologie et Écologie Évolutive des Maladies Infectieuses (PHE3ID), Inserm U1111, CNRS UMR5308, École Normale Supérieure de Lyon, Université Claude Bernard , Lyon , France

6. Department of Microbiology, Icahn School of Medicine at Mount Sinai , New York, New York , USA

7. Department of Pathology, Molecular and Cell Based Medicine, Icahn School of Medicine at Mount Sinai , New York, New York , USA

8. Center for Vaccine Research and Pandemic Preparedness, Icahn School of Medicine at Mount Sinai , New York, New York , USA

9. African Leadership in Vaccinology Expertise, Faculty of Health Sciences, University of the Witwatersrand , Johannesburg , South Africa

10. Centre for the AIDS Programme of Research in South Africa, University of KwaZulu Natal , Durban , South Africa

Abstract

Abstract Background Future vaccine candidates aim to elicit antibodies against the conserved hemagglutinin stalk domain. Understanding the protective mechanism of these antibodies, which mediate broad neutralization and Fc-mediated functions, following seasonal vaccination is critical. Methods Plasma samples were obtained from pregnant women with or without HIV-1 enrolled in a randomised trial (138 trivalent inactivated vaccine [TIV] and 145 placebo recipients). Twenty-three influenza cases were confirmed within 6 months postpartum. We measured H1 stalk-specific antibody-dependent cellular phagocytosis (ADCP), complement deposition (ADCD) and cellular cytotoxicity (ADCC) at enrolment and 1-month postvaccination. Results Lower H1 stalk-specific ADCP and ADCD activity was detected for participants with confirmed influenza compared with individuals without illness 1-month postvaccination. Pre-existing ADCP scores ≥250 reduced the odds of A/H1N1 infection (odds ratio [OR], 0.11; P = .01) with an 83% likelihood of risk reduction. Following TIV, ADCD scores of ≥25 and ≥15 significantly reduced the odds against A/H1N1 (OR, 0.10; P = .01) and non-group 1 (OR, 0.06; P = .0004) influenza virus infections, respectively. These ADCD scores were associated with >84% likelihood of risk reduction. Conclusions Overall, H1 stalk-specific Fc effector function correlates with protection against influenza illness following influenza vaccination during pregnancy. These findings provide insight into the protective mechanisms of hemagglutinin stalk antibodies. Clinical Trials Registration NCT01306669 and NCT01306682 (ClinicalTrials.gov).

Funder

University of the Witwatersrand

South African National Research Foundation

Poliomyelitis Research Foundation

Department of Science and Innovation

South Africa

National Research Foundation, South Africa

Centre for the AIDS Program of Research

Department of Science and Technology

National Research Foundation

Centers of Excellence for Influenza Research and Response

Collaborative Influenza Vaccine Innovation

Centers

Publisher

Oxford University Press (OUP)

Reference40 articles.

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