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Clearance of persistent SARS-CoV-2 associates with increased neutralizing antibodies in advanced HIV disease post-ART initiation
SARS-CoV-2 clearance requires adaptive immunity but the contribution of neutralizing antibodies and T cells in different immune states is unclear. Here we ask which adaptive immune responses associate with clearance of long-term SARS-CoV-2 infection in HIV-mediated immunosuppression after suppressiv...
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Published in: | Nature communications 2024-03, Vol.15 (1), p.2360-2360, Article 2360 |
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creator | Karim, Farina Riou, Catherine Bernstein, Mallory Jule, Zesuliwe Lustig, Gila van Graan, Strauss Keeton, Roanne S. Upton, Janine-Lee Ganga, Yashica Khan, Khadija Reedoy, Kajal Mazibuko, Matilda Govender, Katya Thambu, Kershnee Ngcobo, Nokuthula Venter, Elizabeth Makhado, Zanele Hanekom, Willem von Gottberg, Anne Hoque, Monjurul Karim, Quarraisha Abdool Abdool Karim, Salim S. Manickchund, Nithendra Magula, Nombulelo Gosnell, Bernadett I. Lessells, Richard J. Moore, Penny L. Burgers, Wendy A. de Oliveira, Tulio Moosa, Mahomed-Yunus S. Sigal, Alex |
description | SARS-CoV-2 clearance requires adaptive immunity but the contribution of neutralizing antibodies and T cells in different immune states is unclear. Here we ask which adaptive immune responses associate with clearance of long-term SARS-CoV-2 infection in HIV-mediated immunosuppression after suppressive antiretroviral therapy (ART) initiation. We assembled a cohort of SARS-CoV-2 infected people in South Africa (
n
= 994) including participants with advanced HIV disease characterized by immunosuppression due to T cell depletion. Fifty-four percent of participants with advanced HIV disease had prolonged SARS-CoV-2 infection (>1 month). In the five vaccinated participants with advanced HIV disease tested, SARS-CoV-2 clearance associates with emergence of neutralizing antibodies but not SARS-CoV-2 specific CD8 T cells, while CD4 T cell responses were not determined due to low cell numbers. Further, complete HIV suppression is not required for clearance, although it is necessary for an effective vaccine response. Persistent SARS-CoV-2 infection led to SARS-CoV-2 evolution, including virus with extensive neutralization escape in a Delta variant infected participant. The results provide evidence that neutralizing antibodies are required for SARS-CoV-2 clearance in HIV-mediated immunosuppression recovery, and that suppressive ART is necessary to curtail evolution of co-infecting pathogens to reduce individual health consequences as well as public health risk linked with generation of escape mutants.
There is limited data on immune factors contributing to SARS-CoV-2 viral clearance in people living with HIV. Here, the authors show that re-emergence of the neutralizing antibody response may be key to clearing persistent SARS-CoV-2 infection in ART-mediated recovery from immunosuppression in advanced HIV disease. |
doi_str_mv | 10.1038/s41467-024-46673-2 |
format | article |
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n
= 994) including participants with advanced HIV disease characterized by immunosuppression due to T cell depletion. Fifty-four percent of participants with advanced HIV disease had prolonged SARS-CoV-2 infection (>1 month). In the five vaccinated participants with advanced HIV disease tested, SARS-CoV-2 clearance associates with emergence of neutralizing antibodies but not SARS-CoV-2 specific CD8 T cells, while CD4 T cell responses were not determined due to low cell numbers. Further, complete HIV suppression is not required for clearance, although it is necessary for an effective vaccine response. Persistent SARS-CoV-2 infection led to SARS-CoV-2 evolution, including virus with extensive neutralization escape in a Delta variant infected participant. The results provide evidence that neutralizing antibodies are required for SARS-CoV-2 clearance in HIV-mediated immunosuppression recovery, and that suppressive ART is necessary to curtail evolution of co-infecting pathogens to reduce individual health consequences as well as public health risk linked with generation of escape mutants.
There is limited data on immune factors contributing to SARS-CoV-2 viral clearance in people living with HIV. 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The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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Here we ask which adaptive immune responses associate with clearance of long-term SARS-CoV-2 infection in HIV-mediated immunosuppression after suppressive antiretroviral therapy (ART) initiation. We assembled a cohort of SARS-CoV-2 infected people in South Africa (
n
= 994) including participants with advanced HIV disease characterized by immunosuppression due to T cell depletion. Fifty-four percent of participants with advanced HIV disease had prolonged SARS-CoV-2 infection (>1 month). In the five vaccinated participants with advanced HIV disease tested, SARS-CoV-2 clearance associates with emergence of neutralizing antibodies but not SARS-CoV-2 specific CD8 T cells, while CD4 T cell responses were not determined due to low cell numbers. Further, complete HIV suppression is not required for clearance, although it is necessary for an effective vaccine response. Persistent SARS-CoV-2 infection led to SARS-CoV-2 evolution, including virus with extensive neutralization escape in a Delta variant infected participant. The results provide evidence that neutralizing antibodies are required for SARS-CoV-2 clearance in HIV-mediated immunosuppression recovery, and that suppressive ART is necessary to curtail evolution of co-infecting pathogens to reduce individual health consequences as well as public health risk linked with generation of escape mutants.
There is limited data on immune factors contributing to SARS-CoV-2 viral clearance in people living with HIV. 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Tulio</creatorcontrib><creatorcontrib>Moosa, Mahomed-Yunus S.</creatorcontrib><creatorcontrib>Sigal, Alex</creatorcontrib><collection>Springer Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical 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Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Nature communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karim, Farina</au><au>Riou, Catherine</au><au>Bernstein, Mallory</au><au>Jule, Zesuliwe</au><au>Lustig, Gila</au><au>van Graan, Strauss</au><au>Keeton, Roanne S.</au><au>Upton, Janine-Lee</au><au>Ganga, Yashica</au><au>Khan, Khadija</au><au>Reedoy, Kajal</au><au>Mazibuko, Matilda</au><au>Govender, Katya</au><au>Thambu, Kershnee</au><au>Ngcobo, Nokuthula</au><au>Venter, Elizabeth</au><au>Makhado, Zanele</au><au>Hanekom, Willem</au><au>von Gottberg, Anne</au><au>Hoque, Monjurul</au><au>Karim, Quarraisha Abdool</au><au>Abdool Karim, Salim S.</au><au>Manickchund, Nithendra</au><au>Magula, Nombulelo</au><au>Gosnell, Bernadett I.</au><au>Lessells, Richard J.</au><au>Moore, Penny L.</au><au>Burgers, Wendy A.</au><au>de Oliveira, Tulio</au><au>Moosa, Mahomed-Yunus S.</au><au>Sigal, Alex</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clearance of persistent SARS-CoV-2 associates with increased neutralizing antibodies in advanced HIV disease post-ART initiation</atitle><jtitle>Nature communications</jtitle><stitle>Nat Commun</stitle><addtitle>Nat Commun</addtitle><date>2024-03-15</date><risdate>2024</risdate><volume>15</volume><issue>1</issue><spage>2360</spage><epage>2360</epage><pages>2360-2360</pages><artnum>2360</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>SARS-CoV-2 clearance requires adaptive immunity but the contribution of neutralizing antibodies and T cells in different immune states is unclear. Here we ask which adaptive immune responses associate with clearance of long-term SARS-CoV-2 infection in HIV-mediated immunosuppression after suppressive antiretroviral therapy (ART) initiation. We assembled a cohort of SARS-CoV-2 infected people in South Africa (
n
= 994) including participants with advanced HIV disease characterized by immunosuppression due to T cell depletion. Fifty-four percent of participants with advanced HIV disease had prolonged SARS-CoV-2 infection (>1 month). In the five vaccinated participants with advanced HIV disease tested, SARS-CoV-2 clearance associates with emergence of neutralizing antibodies but not SARS-CoV-2 specific CD8 T cells, while CD4 T cell responses were not determined due to low cell numbers. Further, complete HIV suppression is not required for clearance, although it is necessary for an effective vaccine response. Persistent SARS-CoV-2 infection led to SARS-CoV-2 evolution, including virus with extensive neutralization escape in a Delta variant infected participant. The results provide evidence that neutralizing antibodies are required for SARS-CoV-2 clearance in HIV-mediated immunosuppression recovery, and that suppressive ART is necessary to curtail evolution of co-infecting pathogens to reduce individual health consequences as well as public health risk linked with generation of escape mutants.
There is limited data on immune factors contributing to SARS-CoV-2 viral clearance in people living with HIV. Here, the authors show that re-emergence of the neutralizing antibody response may be key to clearing persistent SARS-CoV-2 infection in ART-mediated recovery from immunosuppression in advanced HIV disease.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>38491050</pmid><doi>10.1038/s41467-024-46673-2</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-3027-5254</orcidid><orcidid>https://orcid.org/0000-0001-7565-7400</orcidid><orcidid>https://orcid.org/0000-0001-5753-0107</orcidid><orcidid>https://orcid.org/0000-0001-6191-4023</orcidid><orcidid>https://orcid.org/0000-0003-3396-9398</orcidid><orcidid>https://orcid.org/0000-0003-3070-6154</orcidid><orcidid>https://orcid.org/0000-0002-6336-7489</orcidid><orcidid>https://orcid.org/0000-0002-0985-477X</orcidid><orcidid>https://orcid.org/0000-0003-0926-710X</orcidid><orcidid>https://orcid.org/0000-0001-9679-0745</orcidid><orcidid>https://orcid.org/0000-0001-7498-2391</orcidid><orcidid>https://orcid.org/0000-0002-0243-7455</orcidid><orcidid>https://orcid.org/0000-0002-4986-2133</orcidid><orcidid>https://orcid.org/0000-0001-8719-4028</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2041-1723 |
ispartof | Nature communications, 2024-03, Vol.15 (1), p.2360-2360, Article 2360 |
issn | 2041-1723 2041-1723 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_cf97d17abeb74e59ba27f92ef737342a |
source | Nature; Publicly Available Content (ProQuest); PubMed Central; Springer Nature - nature.com Journals - Fully Open Access |
subjects | 13 13/106 13/109 13/31 631/181/2474 631/250/2152/2153/1291 631/250/254 631/250/255/1901 631/326/596/4130 Adaptive immunity Antibodies Antibody response Antiretroviral agents Antiretroviral therapy CD4 antigen CD8 antigen Clearances COVID-19 Evolution Health risks HIV Human immunodeficiency virus Humanities and Social Sciences Immune clearance Immunosuppression Infections Lymphocytes Lymphocytes T multidisciplinary Neutralization Neutralizing Persistent infection Public health Recovery Science Science (multidisciplinary) Severe acute respiratory syndrome coronavirus 2 Viral diseases |
title | Clearance of persistent SARS-CoV-2 associates with increased neutralizing antibodies in advanced HIV disease post-ART initiation |
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