Broadly neutralizing antibody treatment maintained HIV suppression in children with favorable reservoir characteristics in Botswana

Author:

Shapiro Roger L.12ORCID,Ajibola Gbolahan2ORCID,Maswabi Kenneth2ORCID,Hughes Michael3,Nelson Bryan S.3ORCID,Niesar Aischa4ORCID,Pretorius Holme Molly1,Powis Kathleen M.125ORCID,Sakoi Maureen2ORCID,Batlang Oganne2,Moyo Sikhulile12ORCID,Mohammed Terence2,Maphorisa Comfort2ORCID,Bennett Kara6ORCID,Hu Zixin7,Giguel Francoise7,Reeves Jacqueline D.8,Reeves Michael A.8,Gao Ce4ORCID,Yu Xu4ORCID,Ackerman Margaret E.9ORCID,McDermott Adrian10ORCID,Cooper Marlene11ORCID,Caskey Marina12ORCID,Gama Lucio10ORCID,Jean-Philippe Patrick13,Yin Dwight E.13ORCID,Capparelli Edmund V.14ORCID,Lockman Shahin127ORCID,Makhema Joseph12,Kuritzkes Daniel R.7,Lichterfeld Mathias47ORCID

Affiliation:

1. Department of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA.

2. Botswana Harvard Health Partnership, Gaborone, Botswana.

3. Department of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA.

4. Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA 02139, USA.

5. Departments of Internal Medicine and Pediatrics, Massachusetts General Hospital, Boston, MA 02114, USA.

6. Bennett Statistical Consulting Inc., Ballston Lake, NY 12019, USA.

7. Division of Infectious Diseases, Brigham and Women’s Hospital, Boston, MA 02115, USA.

8. Labcorp-Monogram Biosciences Inc., South San Francisco, CA 94080, USA.

9. Thayer School of Engineering, Dartmouth College, Hanover, NH 03755, USA.

10. Vaccine Research Center, Bethesda, MD 20892, USA.

11. Frontier Science & Technology Research Foundation Inc., Amherst, NY 14226, USA.

12. Rockefeller University, New York, NY 10065, USA.

13. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20892, USA.

14. Department of Pediatrics, University of California San Diego, La Jolla, CA 92037, USA.

Abstract

Broadly neutralizing antibodies (bNAbs) may provide an alternative to standard antiretroviral treatment (ART) for controlling HIV-1 replication and may have immunotherapeutic effects against HIV-1 reservoirs. We conducted a prospective clinical trial with two HIV-1 bNAbs (VRC01LS and 10-1074) in children ( n = 25) who had previously initiated small-molecule ART treatment before 7 days of age and who continued treatment for at least 96 weeks. Both bNAbs were dosed intravenously every 4 weeks, overlapping with ART for at least 8 weeks and then continued for up to 24 weeks or until detectable viremia of HIV-1 RNA rose above 400 copies per milliliter in the absence of ART. Eleven (44%) children maintained HIV-1 RNA below 400 copies per milliliter through 24 weeks of bNAb-only treatment; 14 (56%) had detectable viremia above 400 copies per milliliter at a median of 4 weeks. Archived HIV-1 provirus susceptible to 10-1074, lower birth HIV-1 DNA reservoir in peripheral blood mononuclear cells, sustained viral suppression throughout early life, and combined negative qualitative HIV-1 DNA polymerase chain reaction and negative HIV-1 serology at entry were associated with maintaining suppression on bNAbs alone. This proof-of-concept study suggests that bNAbs may represent a promising treatment modality for infants and children living with HIV-1. Future studies using newer bNAb combinations with greater breadth and potency are warranted.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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