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First-in-human immunoPET imaging of HIV-1 infection using 89Zr-labeled VRC01 broadly neutralizing antibody.
Beckford-Vera, Denis R; Flavell, Robert R; Seo, Youngho; Martinez-Ortiz, Enrique; Aslam, Maya; Thanh, Cassandra; Fehrman, Emily; Pardons, Marion; Kumar, Shreya; Deitchman, Amelia N; Ravanfar, Vahid; Schulte, Brailee; Wu, I-Wei Katherine; Pan, Tony; Reeves, Jacqueline D; Nixon, Christopher C; Iyer, Nikita S; Torres, Leonel; Munter, Sadie E; Hyunh, Tony; Petropoulos, Christos J; Hoh, Rebecca; Franc, Benjamin L; Gama, Lucio; Koup, Richard A; Mascola, John R; Chomont, Nicolas; Deeks, Steven G; VanBrocklin, Henry F; Henrich, Timothy J.
Afiliação
  • Beckford-Vera DR; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.
  • Flavell RR; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.
  • Seo Y; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.
  • Martinez-Ortiz E; Division of HIV, Infectious Diseases and Global Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Aslam M; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.
  • Thanh C; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Fehrman E; Division of HIV, Infectious Diseases and Global Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Pardons M; Department of Microbiology, Infectiology and Immunology, Centre de Recherche du CHUM, Université de Montréal, Montreal, QC, Canada.
  • Kumar S; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Deitchman AN; Department of Clinical Pharmacy, University of California, San Francisco, USA.
  • Ravanfar V; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.
  • Schulte B; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.
  • Wu IK; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.
  • Pan T; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Reeves JD; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Nixon CC; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Iyer NS; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Torres L; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Munter SE; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Hyunh T; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.
  • Petropoulos CJ; Monogram Biosciences, Inc., Laboratory Corporation of America, South San Francisco, San Francisco, USA.
  • Hoh R; Division of HIV, Infectious Diseases and Global Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Franc BL; Department of Radiology, Stanford University, Palo Alto, CA, USA.
  • Gama L; Vaccine Research Center, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Koup RA; Vaccine Research Center, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Mascola JR; Vaccine Research Center, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Chomont N; Department of Microbiology, Infectiology and Immunology, Centre de Recherche du CHUM, Université de Montréal, Montreal, QC, Canada.
  • Deeks SG; Division of HIV, Infectious Diseases and Global Medicine, University of California San Francisco, San Francisco, CA, USA.
  • VanBrocklin HF; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA. Henry.Vanbrocklin@ucsf.edu.
  • Henrich TJ; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA. Timothy.Henrich@ucsf.edu.
Nat Commun ; 13(1): 1219, 2022 03 09.
Article em En | MEDLINE | ID: mdl-35264559
ABSTRACT
A major obstacle to achieving long-term antiretroviral (ART) free remission or functional cure of HIV infection is the presence of persistently infected cells that establish a long-lived viral reservoir. HIV largely resides in anatomical regions that are inaccessible to routine sampling, however, and non-invasive methods to understand the longitudinal tissue-wide burden of HIV persistence are urgently needed. Positron emission tomography (PET) imaging is a promising strategy to identify and characterize the tissue-wide burden of HIV. Here, we assess the efficacy of using immunoPET imaging to characterize HIV reservoirs and identify anatomical foci of persistent viral transcriptional activity using a radiolabeled HIV Env-specific broadly neutralizing antibody, 89Zr-VRC01, in HIV-infected individuals with detectable viremia and on suppressive ART compared to uninfected controls (NCT03729752). We also assess the relationship between PET tracer uptake in tissues and timing of ART initiation and direct HIV protein expression in CD4 T cells obtained from lymph node biopsies. We observe significant increases in 89Zr-VRC01 uptake in various tissues (including lymph nodes and gut) in HIV-infected individuals with detectable viremia (N = 5) and on suppressive ART (N = 5) compared to uninfected controls (N = 5). Importantly, PET tracer uptake in inguinal lymph nodes in viremic and ART-suppressed participants significantly and positively correlates with HIV protein expression measured directly in tissue. Our strategy may allow non-invasive longitudinal characterization of residual HIV infection and lays the framework for the development of immunoPET imaging in a variety of other infectious diseases.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos