Montaño Michalina, Shapiro Adrienne E, Whitney Bridget M, Bamford Laura, Burkholder Greer, Cachay Edward R, Christopoulos Katerina A, Crane Heidi M, Delaney Joseph A C, Eron Joseph J, Fredericksen Rob J, Hunt Peter W, Jacobson Jeffrey M, Keruly Jeanne C, Kim H Nina, Mayer Kenneth H, Moore Richard D, Napravnik Sonia, Pettit April, Saag Michael S, Yendewa George A, Kitahata Mari M, Bender Ignacio Rachel A
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Division of Allergy and Infectious Diseases, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, USA.
Clin Infect Dis. 2024 Oct 8. doi: 10.1093/cid/ciae464.
Since its global reemergence in 2022, monkeypox (mpox) has demonstrated increased incidence and severity among people with human immunodeficiency virus (HIV [PWH]). Predictors of mpox diagnosis, vaccination, and outcomes among PWH are limited.
We included PWH with primary care visits after 1 January 2022 at 9 US sites participating in the Centers for AIDS Research Network of Integrated Clinic Systems Network. We identified mpox diagnosed between 1 June 2022 and 31 May 2023, through a combination of polymerase chain reaction result, diagnosis code, and/or tecovirimat receipt. We examined validated clinical diagnoses, laboratory results, vaccine data, and patient reported outcomes. We evaluated relative risks (RR) of mpox diagnosis, hospitalization, tecovirimat treatment, and vaccine receipt.
Among 19 777 PWH in care, 413 mpox cases (all male sex at birth) occurred (2.2 cases/100 person-years). Age <40 years, geographic region, Hispanic/Latine ethnicity, lack of antiretroviral therapy, detectable HIV viral load, and recent bacterial sexually transmitted infection predicted mpox diagnosis. PWH with CD4 200-349 cells/mm3 were most likely to be hospitalized (adjusted RR, 3.20; 95% confidence interval: 1.44-7.09) compared to CD4 ≥500, but half as likely as those with CD4 <200 to receive tecovirimat. Overall, smallpox/mpox vaccine effectiveness of ≥1 vaccine was 71% (adjusted RR, 0.29; 95% confidence interval: .14-.47) at preventing mpox, and 86% or better with CD4 ≥350 or HIV viral suppression. Non-Hispanic Black PWH were less likely to be vaccinated than other racial/ethnic identities.
PWH not on antiretroviral therapy or with unsuppressed HIV were more likely to be diagnosed with, and hospitalized for, mpox. Mpox/smallpox vaccine effectiveness was high, inclusive of those with low CD4 count and HIV viremia.
自2022年在全球再度出现以来,猴痘在人类免疫缺陷病毒(HIV)感染者(PWH)中的发病率和严重程度有所增加。关于PWH中猴痘诊断、疫苗接种及预后的预测因素有限。
我们纳入了2022年1月1日后在美国9个参与综合临床系统艾滋病研究网络的地点接受初级保健就诊的PWH。我们通过聚合酶链反应结果、诊断代码和/或接受特考韦瑞的综合信息,确定了2022年6月1日至2023年5月31日期间诊断的猴痘病例。我们检查了经过验证的临床诊断、实验室结果、疫苗数据以及患者报告的结局。我们评估了猴痘诊断、住院、特考韦瑞治疗和疫苗接种的相对风险(RR)。
在接受治疗的19777名PWH中,发生了413例猴痘病例(均为出生时男性)(2.2例/100人年)。年龄<40岁、地理区域、西班牙裔/拉丁裔种族、未接受抗逆转录病毒治疗、可检测到的HIV病毒载量以及近期细菌性性传播感染可预测猴痘诊断。与CD4≥500的PWH相比,CD4为200 - 349个细胞/mm³的PWH最有可能住院(调整后的RR,3.20;95%置信区间:1.44 - 7.09),但接受特考韦瑞的可能性仅为CD4<200的PWH的一半。总体而言,接种≥1剂天花/猴痘疫苗预防猴痘的有效性为71%(调整后的RR,0.29;95%置信区间:0.14 - 0.47),CD4≥350或HIV病毒得到抑制时有效性为86%或更高。非西班牙裔黑人PWH接种疫苗的可能性低于其他种族/族裔身份的PWH。
未接受抗逆转录病毒治疗或HIV未得到抑制的PWH更有可能被诊断为猴痘并因猴痘住院。猴痘/天花疫苗有效性较高,包括CD4计数低和HIV病毒血症患者。