Marburg virus survivor immune responses are Th1 skewed with limited neutralizing antibody responses

Author:

Stonier Spencer W.1ORCID,Herbert Andrew S.1,Kuehne Ana I.1,Sobarzo Ariel2,Habibulin Polina2,Dahan Chen V. Abramovitch2,James Rebekah M.1ORCID,Egesa Moses34ORCID,Cose Stephen345ORCID,Lutwama Julius Julian6,Lobel Leslie26,Dye John M.1ORCID

Affiliation:

1. Virology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD

2. Department of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel

3. Uganda Research Unit on AIDS, Medical Research Council/Uganda Virus Research Institute, Entebbe, Uganda

4. Department of Medical Microbiology, School of Biomedical Sciences, Makerere University College of Health Sciences, Kampala, Uganda

5. London School of Hygiene & Tropical Medicine, London, England, UK

6. Department of Arbovirology, Emerging, and Re-emerging Infection, Uganda Virus Research Institute, Entebbe, Uganda

Abstract

Until recently, immune responses in filovirus survivors remained poorly understood. Early studies revealed IgM and IgG responses to infection with various filoviruses, but recent outbreaks have greatly expanded our understanding of filovirus immune responses. Immune responses in survivors of Ebola virus (EBOV) and Sudan virus (SUDV) infections have provided the most insight, with T cell responses as well as detailed antibody responses having been characterized. Immune responses to Marburg virus (MARV), however, remain almost entirely uncharacterized. We report that immune responses in MARV survivors share characteristics with EBOV and SUDV infections but have some distinct differences. MARV survivors developed multivariate CD4+ T cell responses but limited CD8+ T cell responses, more in keeping with SUDV survivors than EBOV survivors. In stark contrast to SUDV survivors, rare neutralizing antibody responses in MARV survivors diminished rapidly after the outbreak. These results warrant serious consideration for any vaccine or therapeutic that seeks to be broadly protective, as different filoviruses may require different immune responses to achieve immunity.

Funder

Defense Threat Reduction Agency

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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