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Breaking the Glyco-Code of HIV Persistence and Immunopathogenesis (CROSBI ID 265119)

Prilog u časopisu | pregledni rad (znanstveni) | međunarodna recenzija

Colomb, Florent ; Giron, Leila B. ; Trbojević-Akmačić, Irena ; Lauc, Gordan ; Abdel-Mohsen, Mohamed Breaking the Glyco-Code of HIV Persistence and Immunopathogenesis // Current HIV/AIDS Reports, 16 (2019), 2; 151-168. doi: 10.1007/s11904-019-00433-w

Podaci o odgovornosti

Colomb, Florent ; Giron, Leila B. ; Trbojević-Akmačić, Irena ; Lauc, Gordan ; Abdel-Mohsen, Mohamed

engleski

Breaking the Glyco-Code of HIV Persistence and Immunopathogenesis

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. 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.

fucosylation ; galactosylation ; galectins ; glycosylation ; HIV persistence ; sialylation

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Podaci o izdanju

16 (2)

2019.

151-168

objavljeno

1548-3568

1548-3576

10.1007/s11904-019-00433-w

Povezanost rada

Biologija, Interdisciplinarne prirodne znanosti, Kliničke medicinske znanosti

Poveznice