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Publication Name World Journal of Virology
Manuscript ID 117643
Country Morocco
Category Immunology
Manuscript Type Minireviews
Article Title Major histocompatibility complex class I chain-related A and B molecules and their potential role in virus-associated cancers
Manuscript Source Invited Manuscript
All Author List Abdellatif Bouayad
Funding Agency and Grant Number
Corresponding Author Abdellatif Bouayad, Associate Professor, MD, Department of Immunology, Faculty of Medicine and Pharmacy of Oujda, Mohammed First University, Mohammed V Avenue, Oujda-Angad 4867, Oriental, Morocco. abdellatifbouayad@hotmail.fr
Key Words Major histocompatibility complex class I chain-related genes A; Major histocompatibility complex class I chain-related genes B; Virus-associated cancers; Polymorphism; Natural killer group 2-member D; Natural killer-cell cytotoxicity
Core Tip Several oncogenic viruses have evolved multi-layered strategies to subvert the natural killer group 2-member D (NKG2D)-major histocompatibility complex class I chain-related genes A (MICA)/B axis and promote cancer progression. Human papillomavirus drives immune evasion through exosomal release of the truncated MICA*008 variant, which potently downregulates NKG2D and impairs natural killer (NK) cell cytotoxicity. Chronic hepatitis B virus and hepatitis C virus infections create a hypoxic/inflammatory tumor milieu that induces metalloproteases, generating soluble MICA/B that suppresses NKG2D on NK and CD8+ T cells. EBV evades NKG2D-mediated immunity through miR-bamHI-A rightward transcript 7-mediated repression of the transforming growth factor beta 1/cellular myelocytomatosis oncogene/MICA axis and latent membrane protein 2A-driven disruption of stress-induced ligand expression, reinforced by UPR-protein disulfide isomerase inhibition of proper MICA/MICB folding and trafficking. Kaposi’s sarcoma-associated herpesvirus exploits its E3 ubiquitin ligases K3 and K5 to ubiquitinate MICA and other NK-activating ligands such as activation-induced C-type lectin, triggering their endocytic removal and intracellular sequestration to disable multiple NK cell recognition pathways. Therapeutic strategies targeting this axis show considerable promise.
Citation Bouayad A. Major histocompatibility complex class I chain-related A and B molecules and their potential role in virus-associated cancers. World J Virol 2026; In press
Received
2025-12-12 00:01
Peer-Review Started
2025-12-12 00:01
First Decision by Editorial Office Director
2026-01-07 08:42
Return for Revision
2026-01-07 08:42
Revised
2026-01-15 13:55
Publication Fee Transferred
Second Decision by Editor
2026-02-09 02:42
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director
2026-02-09 10:02
Articles in Press
2026-02-09 10:02
Edit the Manuscript by Language Editor
Typeset the Manuscript
ISSN 2220-3249 (online)
Open Access This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
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