{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T02:39:16Z","timestamp":1792463956723,"version":"4.5.0"},"reference-count":180,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2026,7,9]],"date-time":"2026-07-09T00:00:00Z","timestamp":1783555200000},"content-version":"vor","delay-in-days":8,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Journal of Medical Virology"],"published-print":{"date-parts":[[2026,7]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>Achieving a functional cure for HIV\u20101 requires dismantling the molecular circuits that enable viral latency and immune evasion. Beyond transcriptional silencing and epigenetic repression, post\u2010translational modifications (PTMs) of host and viral proteins operate as dynamic molecular switches that regulate all phases of the viral life cycle, from integration and transcription to immune recognition and reservoir maintenance. This review synthesizes recent discoveries across major PTM types, including phosphorylation, ubiquitination, SUMOylation, acetylation, methylation, glycosylation, and ISGylation, and highlights how these modifications modulate intrinsic and adaptive immunity, chromatin state, protein turnover, and viral RNA metabolism. We further explore how targeting PTM networks offers a promising therapeutic avenue to reverse latency, destabilize reservoirs, or enhance immune clearance with minimal off\u2010target activation. 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