Authors:
Farina Karim1,2, Catherine Riou3,4, Mallory Bernstein1, Zesuliwe Jule1, Gila Lustig5, Strauss van Graan6,7, Roanne S. Keeton3, Janine-Lee Upton1, Yashica Ganga1, Khadija Khan1,2, Kajal Reedoy1, Matilda Mazibuko1, Katya Govender1, Kershnee Thambu1, Nokuthula Ngcobo1, Elizabeth Venter6,7, Zanele Makhado6,7, Willem Hanekom1,8 , Anne von Gottberg9,10, Monjurul Hoque11, Quarraisha Abdool Karim5,12, Salim S. Abdool Karim5,12, Nithendra Manickchund13, Nombulelo Magula14, Bernadett I. Gosnell13, Richard J. Lessells5,15, Penny L. Moore6,7, Wendy A. Burgers3,4, Tulio de Oliveira5,15,16,17, Mahomed-Yunus S. Moosa13, Alex Sigal1,2,5
Abstract
The emergence of new variants through SARS-CoV-2 evolution compromises the effectiveness of current vaccines. Persistent SARS-CoV-2 infection because of immunosuppression may drive accelerated SARS-CoV-2 evolution and it is therefore critical to understand how such persistent infections can be cleared. While adaptive immunity is known to be required for SARS-CoV-2 clearance, the relative contribution of neutralizing antibodies and T cells to clearance in immunosuppression is not well understood. Here we examined whether neutralizing antibody and T-cell responses are associated with the clearance of persistent SARS-CoV-2 infection in people recovering from advanced HIV-mediated immunosuppression through adherence to HIV antiretroviral therapy.
This study demonstrated that neutralizing antibodies may be required for SARS-CoV-2 clearance in recovery from HIV-mediated immunosuppression. Successful management of HIV is necessary to curtail the evolution of co-infecting pathogens.
Affiliations
1Africa Health Research Institute, Durban, South Africa.
2School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa.
3Institute of Infectious Disease and Molecular Medicine, Division of Medical Virology, Department of Pathology, University of Cape Town, Observatory, South Africa.
4Wellcome Centre for Infectious Diseases Research in Africa, University of Cape Town, Observatory, South Africa.
5Centre for the AIDS Programme of Research in South Africa, Durban, South Africa.
6SAMRC Antibody Immunity Research Unit, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
7National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.
8Division of Infection and Immunity, University College London, London, UK.
9Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a division of the National Health Laboratory Service, Johannesburg, South Africa.
10School of Pathology, University of the Witwatersrand, Johannesburg, South Africa.
11KwaDabeka Community Health Centre, KwaDabeka, South Africa.
12Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, United States.
13Department of Infectious Diseases, Nelson R. Mandela School of Clinical Medicine, University of KwaZulu-Natal, Durban, South Africa.
14Department of Internal Medicine, Nelson R. Mandela School of Medicine, University of Kwa-Zulu Natal, Durban, South Africa.
15KwaZulu-Natal Research Innovation and Sequencing Platform, Durban, South Africa.
16Centre for Epidemic Response and Innovation, School of Data Science and Computational Thinking, Stellenbosch University, Stellenbosch, South Africa.
17Department of Global Health, University of Washington, Seattle, USA.