Evidence map›Paper›PMID 39828283›Full record

ArticleKorean journal of ophthalmology : KJO2025

Ocular Manifestations of Immune Reconstitution Inflammatory Syndrome in HIV after Highly Active Antiretroviral Therapy: Clinical Use of CD8+ T cell.

Jae Hyun Kim, Myung Ho Cho, Ji Hoon Ban, Sun Hee Lee, Jong Soo Lee

Abstract read
In one paragraph

Article in Korean journal of ophthalmology : KJO, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jae Hyun KimDepartment of Ophthalmology, Pusan National University School of Medicine, Busan, Korea.
Myung Ho ChoDepartment of Ophthalmology, Pusan National University School of Medicine, Busan, Korea.
Ji Hoon BanDepartment of Ophthalmology, Pusan National University School of Medicine, Busan, Korea.
Sun Hee LeeDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Korea.
Jong Soo LeeDepartment of Ophthalmology, Pusan National University School of Medicine, Busan, Korea.

Funding

Pusan National University
6 · The paper itself

Abstract

purposeTo investigate ocular manifestation of immune reconstitution inflammatory syndrome (IRIS) in HIV patients after starting highly active antiretroviral therapy (HAART) and its relationship to T cell immunity.

methodsHIV patients with ocular IRIS after HAART were retrospectively reviewed. Clinical presentations with previous opportunistic infection, duration from initiation of HAART to IRIS, blood CD4+, CD8+ T cell count, and HIV RNA copies before HAART and at IRIS were analyzed.

resultsAmong 19 patients (27 eyes) included, the most common previous opportunistic infection was cytomegalovirus (17 patients, 89.5%) followed by tuberculosis choroiditis (2 patients, 10.5%). The clinical manifestations included vitritis (20 eyes, 74.0%), retinitis (14 eyes, 51.9%), and anterior uveitis (5 eyes, 18.5%). The median duration from initiation of HAART to IRIS was 70 days. CD4+ T cell count before HAART increased at IRIS (p < 0.001). CD8+ T cell count before HAART was negatively correlated with duration from HAART to IRIS (p < 0.001). The cutoff value of CD8+ T cell count for discerning early or late onset of ocular IRIS was 258/mm3 (p = 0.001). When divided into two groups by CD8+ T cell count of 258/mm3, 90% patients with CD8+ T cell count higher than 258/mm3 before HAART developed ocular IRIS within 70 days.

conclusionsThere was a negative relationship between CD8+ T cell count before HAART and duration from HAART to ocular IRIS. Ocular IRIS with higher CD8+ T cell count before HAART developed earlier after HAART initiation compared to those with lower CD8+ T cell count.

Indexed as

Antiretroviral Therapy, Highly ActiveCD8-Positive T-LymphocytesHIV InfectionsImmune Reconstitution Inflammatory SyndromeAdultCD4 Lymphocyte CountFemaleFollow-Up StudiesHumansMaleMiddle AgedRetrospective StudiesCD8+ T cellCytomegalovirus retinitisHIVImmune reconstitution inflammatory syndrome

Identifiers

PMID39828283
PMCPMC11856080

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.