Gils Tinne, Hella Jerry, Jacobs Bart K M, Sossen Bianca, Mukoka Madalo, Muyoyeta Monde, Nakabugo Elizabeth, Van Nguyen Hung, Ubolyam Sasiwimol, Macé Aurélien, Vermeulen Marcia, Nyangu Sarah, Sanjase Nsala, Sasamalo Mohamed, Dinh Huong Thi, Ngo The Anh, Manosuthi Weerawat, Jirajariyavej Supunnee, Denkinger Claudia M, Nguyen Nhung Viet, Avihingsanon Anchalee, Nakiyingi Lydia, Székely Rita, Kerkhoff Andrew D, MacPherson Peter, Meintjes Graeme, Reither Klaus, Ruhwald Morten
Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Global Health Institute, University of Antwerp, Wilrijk, Belgium.
J Infect Dis. 2025 Feb 4;231(1):e82-e90. doi: 10.1093/infdis/jiae374.
CD4 measurement is pivotal in the management of advanced human immunodeficiency virus (HIV) disease. VISITECT CD4 Advanced Disease (VISITECT; AccuBio, Ltd) is an instrument-free, point-of-care, semiquantitative test allowing visual identification of CD4 ≤ 200 cells/µL or >200 cells/ µL from finger-prick or venous blood.
As part of a diagnostic accuracy study of FUJIFILM SILVAMP TB LAM, people with HIV ≥18 years old were prospectively recruited in 7 countries from outpatient departments if a tuberculosis symptom was present, and from inpatient departments. Participants provided venous blood for CD4 measurement using flow cytometry (reference standard) and finger-prick blood for VISITECT (index text), performed at point-of-care. Sensitivity, specificity, and positive and negative predictive values of VISITECT to determine CD4 ≤ 200 cells/ µL were evaluated.
Among 1604 participants, the median flow cytometry CD4 was 367 cells/µL (interquartile range, 128-626 cells/µL) and 521 (32.5%) had CD4 ≤ 200 cells/µL. VISITECT sensitivity was 92.7% (483/521; 95% confidence interval [CI], 90.1%-94.7%) and specificity was 61.4% (665/1083; 95% CI, 58.4%-64.3%). For participants with CD4 0-100, 101-200, 201-300, 301-500, and >500 cells/µL, VISITECT misclassified 4.5% (95% CI, 2.5%-7.2%), 12.5 (95% CI, 8.0%-18.2%), 74.1% (95% CI, 67.0%-80.5%), 48.0% (95% CI, 42.5%-53.6%), and 22.6% (95% CI, 19.3%-26.3%), respectively.
VISITECT's sensitivity, but not specificity, met the World Health Organization's minimal sensitivity and specificity threshold of 80% for point-of-care CD4 tests. VISITECT's quality needs to be assessed and its accuracy optimized. VISITECT's utility as CD4 triage test should be investigated. Clinical Trials Registration. NCT04089423.
CD4检测在晚期人类免疫缺陷病毒(HIV)疾病的管理中至关重要。VISITECT CD4晚期疾病检测(VISITECT;AccuBio有限公司)是一种无需仪器的即时检测半定量检测方法,可通过手指刺血或静脉血直观识别CD4≤200个细胞/µL或>200个细胞/µL。
作为富士胶片SILVAMP结核杆菌脂阿拉伯甘露聚糖诊断准确性研究的一部分,如果出现结核病症状,在7个国家的门诊部门前瞻性招募≥18岁的HIV感染者,也从住院部招募。参与者提供静脉血用于流式细胞术检测CD4(参考标准),并提供手指刺血用于VISITECT检测(指标检测),在即时检测点进行。评估VISITECT检测CD4≤200个细胞/µL的敏感性、特异性以及阳性和阴性预测值。
在1604名参与者中,流式细胞术检测的CD4中位数为367个细胞/µL(四分位间距,128 - 626个细胞/µL),521人(32.5%)的CD4≤200个细胞/µL。VISITECT的敏感性为92.7%(483/521;95%置信区间[CI],90.1% - 94.7%),特异性为61.4%(665/1083;95% CI,58.4% - 64.3%)。对于CD4为0 - 100、101 - 200、201 - 300、301 - 500和>500个细胞/µL的参与者,VISITECT的错误分类率分别为4.5%(95% CI,2.5% - 7.2%), 12.5%(95% CI,8.0% - 18.2%), 74.1%(95% CI,67.0% - 80.5%), 48.0%(95% CI,42.5% - 53.6%)和22.6%(95% CI,19.3% - 26.3%)。
VISITECT的敏感性达到了世界卫生组织即时检测CD4检测80%的最低敏感性阈值,但特异性未达到。需要评估VISITECT的质量并优化其准确性。应研究VISITECT作为CD4分流检测的效用。临床试验注册。NCT04089423。