Immune Correlate + Guided Design of Monoclonal Therapeutics for HIV Remission

Abstract

Current HIV-specific broadly neutralizing antibodies (bNAbs), selected for their ability to recognize the virus itself, fail to sufficiently kill infected cells and have only had a very modest impact on the HIV reservoir size in humans. Spontaneous control of viral rebound does infrequently occur during natural infection (post-treatment controllers) and seems to require specific functional antibody profiles with unique antigen specificities. These antibodies shall be identified and extracted from individuals who are undergoing antiretroviral treatment interruption and be functionally optimized to enhance the rapid and highly effective deletion of virally infected cells with the goal to develop "anti-reservoir" monoclonals that may be used as stand-alone therapeutics. In three aims, this project will define the correlates of humoral immunity that track with viral remission following treatment interruption followed by development of a library of and functionally enhanced novel monoclonal antibodies poised to recognize and kill reactivated latently HIV infected cells as novel therapeutics for HIV cure strategies. From existing sample banks (The Thai Red Cross AIDS Research Centre and United States Military HIV Research Program, Walter Reed Army Institute of Research) we selected individuals who controlled or did not control viral rebound after antiretroviral treatment interruption. To define the antigen-specific titer characteristics, an array of different HIV antigens was used to measure the antigen-specific antibody isotype and IgG subclass titer in all available patients and the most relevant and targeted antigens for the functional assays were identified. While patients that initiated treatment during the chronic phase of infection developed a robust humoral immune response against the virus, early antiretroviral treatment during the acute phase of infection abolished or at least dampened such a response.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2020
Accession Number
AD1148036

Entities

People

  • Boris Juelg
  • Galit Alter

Organizations

  • Massachusetts General Hospital

Tags

DTIC Thesaurus Topics

  • Antibodies
  • Biomedical Research
  • Blood
  • Cells
  • Covid-19
  • Demographic Cohorts
  • Engineering
  • Governments
  • Health Services
  • Hospitals
  • Humoral Immunity
  • Immune System
  • Immunogenicity
  • Infection
  • Institutional Review Board
  • Lymphocytes
  • Massachusetts
  • Medical Personnel
  • Point-Of-Care Diagnostic Testing
  • Professional Development
  • Therapy
  • United States
  • Vaccines
  • Virus Diseases
  • Viruses

Fields of Study

  • Biology
  • Medicine

Readers

  • Immunology
  • Virology (or Medical Virology).