Breaking the Glyco-Code of HIV Persistence and Immunopathogenesis

Florent Colomb, Leila B. Giron, Irena Trbojevic-Akmacic, Gordan Lauc, Mohamed Abdel-Mohsen*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

26 Scopus citations

Abstract

Purpose of review: Glycoimmunology is an emerging field focused on understanding how immune responses are mediated by glycans (carbohydrates) and their interaction with glycan-binding proteins called lectins. How glycans influence immunological functions is increasingly well understood. In a parallel way, in the HIV field, it is increasingly understood how the host immune system controls HIV persistence and immunopathogenesis. However, what has mostly been overlooked, despite its potential for therapeutic applications, is the role that the host glycosylation machinery plays in modulating the persistence and immunopathogenesis of HIV. Here, we will survey four areas in which the links between glycan-lectin interactions and immunology and between immunology and HIV are well described. For each area, we will describe these links and then delineate the opportunities for the HIV field in investigating potential interactions between glycoimmunology and HIV persistence/immunopathogenesis. Recent findings: Recent studies show that the human glycome (the repertoire of human glycan structures) plays critical roles in driving or modulating several cellular processes and immunological functions that are central to maintaining HIV infection. Summary: Understanding the links between glycoimmunology and HIV infection may create a new paradigm for discovering novel glycan-based therapies that can lead to eradication, functional cure, or improved tolerance of lifelong infection.

Original languageEnglish (US)
Pages (from-to)151-168
Number of pages18
JournalCurrent HIV/AIDS Reports
Volume16
Issue number2
DOIs
StatePublished - Apr 15 2019

Funding

Funding Information MA-M is funded by the following grants: NIH (R21 AI129636, R21 NS106970, and P30CA010815-49S2), W.W. Smith Charitable Trust (grant # A1701), Campbell Foundation award, Penn Center for AIDS Research (P30 AI 045008), and The Foundation for AIDS Research (amfAR) Impact grant # 109840-65-RGRL. MA-M is a member of the investigation team of the NIH-funded BEAT-HIV Martin Delaney Collaboratory to cure HIV-1 infection (1UM1Al126620). Additionally, GL is supported by funding from the European Structural and Investments funds for projects “New generation of high throughput glycoanalytical services” (contract # KK.01.2.1.01.0003) and “Croatian National Centre of Research Excellence in Personalized Healthcare” (contract # KK.01.1.1.01.0010). The authors would like to thank Marli Markovitz for providing the artwork and graphic design (https://marlimark13.wixsite.com/marlim) and to Rachel E. Locke, Ph.D, who provided critical comments and editing.

Keywords

  • Fucosylation
  • Galactosylation
  • Galectins
  • Glycosylation
  • HIV persistence
  • Sialylation

ASJC Scopus subject areas

  • Virology
  • Infectious Diseases

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