Abstract

To prevent sexually-acquired HIV-1 infection by immunoprophylaxis, effective concentrations of broadly neutralizing antibodies are likely needed at mucosal sites of exposure. Here, we examine the biodistribution of monoclonal antibody VRC01 and its extended half-life variant, VRC01LS, in colorectal and genitourinary tracts of healthy adults 1-52 weeks after intravenous infusion. At 1-2 weeks, VRC01LS levels are ~3-4 times higher than VRC01 in serum (p = 0.048), rectal (p = 0.067), vaginal (p = 0.003) and cervical tissues (p = 0.003); these differences increase over time. Both antibodies primarily localize within rectal lamina propria and cervicovaginal stroma, with limited and variable epithelial distribution. Although 8-28% of serum mAb levels reach mucosal tissues, <3% are in seminal and rectal secretions. Elimination half-lives in mucosal tissues are 20-28 days for VRC01 and 51-68 days for VRC01LS. Thus, VRC01LS infusion achieves higher, sustained concentrations in human mucosal tissues than VRC01, supporting the future investigation of potent, long-acting LS-modified antibodies to prevent HIV-1.

Antibody immunoprophylaxis for HIV-1 will require effective concentration of biologics at mucosal sites of exposure for effectivity. Here the authors show that infused Fc-modified VRC01LS antibody has increased levels in blood, in the female genital tract and male rectal tissue, compared to native antibody VRC01. VRC01LS is detectable for more than year at the sites of sexual HIV transmission.

Details

Title
Enhanced and sustained biodistribution of HIV-1 neutralizing antibody VRC01LS in human genital and rectal mucosa
Author
Lemos, Maria P. 1   VIAFID ORCID Logo  ; Astronomo, Rena D. 1 ; Huang, Yunda 1   VIAFID ORCID Logo  ; Narpala, Sandeep 2 ; Prabhakaran, Madhu 2 ; Mann, Philipp 1   VIAFID ORCID Logo  ; Paez, Carmen A. 1   VIAFID ORCID Logo  ; Lu, Yiwen 1 ; Mize, Gregory J. 1 ; Glantz, Hayley 1 ; Westerberg, Katharine 1 ; Colegrove, Hunter 1   VIAFID ORCID Logo  ; Smythe, Kimberly S. 3   VIAFID ORCID Logo  ; Lin, Minggang 4 ; Pierce, Robert H. 3 ; Hutter, Julia 5 ; Frank, Ian 6 ; Mascola, John R. 7 ; McDermott, Adrian B. 2 ; Bekker, Linda-Gail 8   VIAFID ORCID Logo  ; McElrath, M. Juliana 9   VIAFID ORCID Logo 

 Fred Hutchinson Cancer Center, Vaccine and Infectious Disease Division, Seattle, USA (GRID:grid.270240.3) (ISNI:0000 0001 2180 1622) 
 National Institutes of Health, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, USA (GRID:grid.94365.3d) (ISNI:0000 0001 2297 5165) 
 Fred Hutchinson Cancer Center, Clinical Research Division, Seattle, USA (GRID:grid.270240.3) (ISNI:0000 0001 2180 1622) 
 Fred Hutchinson Cancer Center, Human Biology Division, Seattle, USA (GRID:grid.270240.3) (ISNI:0000 0001 2180 1622) 
 National Institutes of Health, Division of AIDS, National Institute of Allergy and Infectious Diseases, Bethesda, USA (GRID:grid.94365.3d) (ISNI:0000 0001 2297 5165) 
 University of Pennsylvania, Perelman School of Medicine, Philadelphia, USA (GRID:grid.25879.31) (ISNI:0000 0004 1936 8972) 
 ModeX Therapeutics, Weston, USA (GRID:grid.25879.31) 
 University of Cape Town, Desmond Tutu HIV Centre, Cape Town, South Africa (GRID:grid.7836.a) (ISNI:0000 0004 1937 1151) 
 Fred Hutchinson Cancer Center, Vaccine and Infectious Disease Division, Seattle, USA (GRID:grid.270240.3) (ISNI:0000 0001 2180 1622); University of Washington, Department of Medicine, Seattle, USA (GRID:grid.34477.33) (ISNI:0000 0001 2298 6657) 
Pages
10332
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3133866829
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.