{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,23]],"date-time":"2026-10-23T23:53:12Z","timestamp":1792799592621,"version":"4.5.0"},"reference-count":50,"publisher":"American Society for Clinical Investigation","issue":"12","funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"crossref","award":["Intramural program"],"award-info":[{"award-number":["Intramural program"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100015624","name":"Leidos","doi-asserted-by":"crossref","award":["l3XS110"],"award-info":[{"award-number":["l3XS110"]}],"id":[{"id":"10.13039\/100015624","id-type":"DOI","asserted-by":"crossref"}]},{"name":"NCI, NIH","award":["HHSN261200800001E"],"award-info":[{"award-number":["HHSN261200800001E"]}]},{"name":"NIH","award":["UM1AI100645"],"award-info":[{"award-number":["UM1AI100645"]}]},{"name":"Center for Aids Research","award":["grant P30 AI50410"],"award-info":[{"award-number":["grant P30 AI50410"]}],"id":[{"id":"https:\/\/ror.org\/05n52x113","id-type":"ROR","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2019,6,20]]},"abstract":"<jats:p>\n                    In HIV-infected individuals on long-term antiretroviral therapy (ART), more than 40% of the infected cells are in clones. Although most HIV proviruses present in individuals on long-term ART are defective, including those in clonally expanded cells, there is increasing evidence that clones carrying replication-competent proviruses are common in patients on long-term ART and form part of the HIV reservoir that makes it impossible to cure HIV infection with current ART alone. Given the importance of clonal expansion in HIV persistence, we determined how soon after HIV acquisition infected clones can grow large enough to be detected (clones larger than ca. 1 \u00d7 10\n                    <jats:sup>5<\/jats:sup>\n                    cells). We studied 12 individuals sampled in early HIV infection (Fiebig stage III\u2013V\/VI) and 5 who were chronically infected. The recently infected individuals were started on ART at or near the time of diagnosis. We isolated more than 6,500 independent integration sites from peripheral blood mononuclear cells before ART was initiated and after 0.5\u201318 years of suppressive ART. Some infected clones could be detected approximately 4 weeks after HIV infection and some of these clones persisted for years. The results help to explain how the reservoir is established early and persists for years.\n                  <\/jats:p>","DOI":"10.1172\/jci.insight.128432","type":"journal-article","created":{"date-parts":[[2019,6,19]],"date-time":"2019-06-19T11:01:08Z","timestamp":1560942068000},"source":"Crossref","is-referenced-by-count":86,"title":["Clones of infected cells arise early in HIV-infected individuals"],"prefix":"10.1172","volume":"4","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3856-762X","authenticated-orcid":true,"given":"John M.","family":"Coffin","sequence":"first","affiliation":[{"name":"Department of Molecular Biology and Microbiology, Tufts University, Boston, Massachusetts, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David W.","family":"Wells","sequence":"additional","affiliation":[{"name":"Cancer Research Technology Program, and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jennifer 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