Journal of Internal Medicine Concepts & Practice >
Analysis on etiological characteristics of 322 patients with human immunodeficiency virus infection / acquired immunodeficiency syndrome complicated with pulmonary infection in Henan province
Received date: 2026-01-16
Revised date: 2026-01-31
Accepted date: 2026-02-12
Online published: 2026-04-08
Copyright
Objective To discuss the etiological characteristics of patients with human immunodeficiency virus (HIV) / acquired immunodeficiency syndrome (AIDS) [collectively referred to as people living with HIV (PLWH)] complicated with pulmonary infection, and to evaluate the diagnostic value of metagenomic next-generation sequencing (mNGS) technology. Methods A retrospective study was conducted on 322 PLWH with pulmonary infection, whose clinical data and bronchoalveolar lavage fluid samples were collected. All samples underwent both conventional etiological tests [smear, culture, polymerase chain reaction (PCR)] and mNGS. The pathogen detection rates, reporting times, and detected etiological characteristics were compared between the two methods. Etiological variations under different CD4+ T lymphocyte levels were also analyzed. Results Among the 322 patients, 80.1% (258/322) were male, with a median age of 35 years. The median CD4+ T lymphocyte count was 61 (22, 205) cells/µL, and the median HIV RNA load was 1 343 (0, 159 423) copies/mL. mNGS was successfully performed on 294 patients, detecting a total of 93 pathogen species across 786 instances. Viruses were the predominant pathogens (34.4%, 32 species), with the most common being cytomegalovirus (CMV, 44.7%), Pneumocystis jirovecii (40.4%), Epstein-Barr virus (14.6%), Mycobacterium tuberculosis complex (11.2%), coronavirus disease 2019(COVID-19)(9.0%), and Aspergillus flavus/A. oryzae(8.7%). The overall sensitivity of conventional methods was 64%, with a statistically significant difference (P<0.001) compared to 91.0% for mNGS. The reporting time of mNGS was significantly shorter than of conventional methods. Patients at the AIDS stage, whose CD4+ T lymphocytes<200 cells/µL, had the highest total number of detected pathogens (648 instances). Conclusions Pulmonary infections in PLWH are primarily caused by CMV, P. jirovecii, M. tuberculosis complex, COVID-19, and Aspergillus species, with the etiological spectrum varying according to immune status. Patients with low CD4 counts are susceptible to opportunistic pathogens such as Pneumocystis jirovecii and CMV. As the CD4 count increases, viruses and fungi remain the predominant types of pathogens, but the proportion of bacterial detection relatively increases. mNGS can significantly improve the pathogen detection rate in PLWH with pulmonary infection.
WANG Yanli , HOU Mingjie , YUAN Haizhen , XIN Ningbo , ZHANG Yuwei , HAN Lei , ZHANG Yifan , MA Yuqing , ZHAO Qingxia . Analysis on etiological characteristics of 322 patients with human immunodeficiency virus infection / acquired immunodeficiency syndrome complicated with pulmonary infection in Henan province[J]. Journal of Internal Medicine Concepts & Practice, 2026 , 21(01) : 21 -27 . DOI: 10.16138/j.1673-6087.2026.01.03
| [1] | GBD 2019 HIV Collaborators. Global, regional, and national sex-specific burden and control of the HIV epidemic, 1990-2019, for 204 countries and territories[J]. Lancet HIV, 2021, 8(10):e633-e651. |
| [2] | Li X, Liang S, Zhang D, et al. The clinical application of metagenomic next-generation sequencing in sepsis of immunocompromised patients[J]. Front Cell Infect Microbiol, 2023, 13:1170687. |
| [3] | Guo C, Chen Q, Fan G, et al. gcPathogen: a comprehensive genomic resource of human pathogens for public health[J]. Nucleic Acids Res, 2024, 52(D1):D714-D723. |
| [4] | 刘颖, 赵红心. 中国艾滋病相关机会性感染研究进展[J]. 中国艾滋病性病, 2022, 28(5):512-518. |
| Liu Y, Zhao HX. Research progress in AIDS-related opportunistic infections in China[J]. Chin J AIDS STD, 2022, 28(5):512-518. | |
| [5] | 莫平征, 张忠威, 陈小平, 等. 宏基因组学二代测序在艾滋病合并肺部感染患者中的临床应用[J]. 中华传染病杂志, 2023, 41(8):507-513. |
| Mo PZ, Zhang ZW, Chen XP, et al. Clinical application of metagenomic next-generation sequencing in acquired immunodeficiency syndrome patients with pulmonary infections[J]. Chin J Infect Dis, 2023, 41(8):507-513. | |
| [6] | World Health Organization. Global tuberculosis report 2025 [EB/OL]. 2025. https://www.who.int/teams/global-programme-on-tuberculosis-and-lung-health/tb-reports/global-tuberculosis-report-2025. |
| [7] | 曾妍茗, 李瑶, 刘敏, 等. 巨细胞病毒血症对艾滋病合并中重度肺孢子菌肺炎患者临床预后影响的回顾性研究[J]. 中国感染与化疗杂志, 2023, 23(2):137-142. |
| Zeng YM, Li Y, Liu M, et al. Retrospective analysis of the effect of cytomegalovirus viremia on clinical prognosis of AIDS patients complicated with moderate to severe Pneumocystis pneumonia[J]. Chin J Infect Chemother, 2023, 23(2):137-142. | |
| [8] | 郭晶晶, 王雅杰, 方伟, 等. 艾滋病合并巨细胞病毒感染的病毒学和血清学特点探讨[J]. 标记免疫分析与临床, 2022, 29(12):1986-1989. |
| Guo JJ, Wang YJ, Fang W, et al. The virology and serologic characteristics of HIV infection with cytomegalovirus[J]. Labeled Immunoassays & Clin Med, 2022, 29(12):1986-1989. | |
| [9] | Zhao M, Zhuo C, Li Q, et al. Cytomegalovirus (CMV) infection in HIV/AIDS patients and diagnostic values of CMV-DNA detection across different sample types[J]. Ann Palliat Med, 2020, 9(5):2710-2715. |
| [10] | Kovacs JA, Gill VJ, Meshnick S, et al. New insights into transmission, diagnosis, and drug treatment of Pneumocystis carinii pneumonia[J]. JAMA, 2001, 286(19):2450-2460. |
| [11] | Gérard L, Leport C, Flandre P, et al. Cytomegalovirus (CMV) viremia and the CD4+ lymphocyte count as predictors of CMV disease in patients infected with human immunodeficiency virus[J]. Clin Infect Dis, 1997, 24(5):836-840. |
| [12] | 中华医学会感染病学分会艾滋病丙型肝炎学组. 艾滋病合并巨细胞病毒病诊疗专家共识(2024年版)[J]. 中华传染病杂志, 2024, 42(3):129-140. |
| AIDS and Hepatitis C Professional Group of Society of Infectious Diseases of Chinese Medical Association. Expert consensus on diagnosis and treatment of cytomegalovirus disease in acquired immunodeficiency syndrome patients in China (2024 edition)[J]. Chin J Infect Dis, 2024, 42(3):129-140. | |
| [13] | 陈娜, 邓美菊, 刘颖, 等. 152例艾滋病合并肺部感染疾病谱分析[J]. 国际病毒学杂志, 2024, 31(3):211-214. |
| Chen N, Deng MJ, Liu Y, et al. Spectrum of complicated pulmonary infections in 152 AIDS patients[J]. International Journal of Virology, 2024, 31(3):211-214. | |
| [14] | Patel EU, Gianella S, Newell K, et al. Elevated cytomegalovirus IgG antibody levels are associated with HIV-1 disease progression and immune activation[J]. AIDS, 2017, 31(6):807-813. |
| [15] | Perello R, Vergara A, Monclus E, et al. Cytomegalovirus infection in HIV-infected patients in the era of combination antiretroviral therapy[J]. BMC Infect Dis, 2019, 19(1):1030. |
| [16] | 任立敏, 李妍, 张春芳, 等. 系统性风湿病合并巨细胞病毒感染的临床特点及其相关危险因素分析[J]. 中华医学杂志, 2016, 96(35):2772-2776. |
| Ren LM, Li Y, Zhang CF, et al. Clinical characteristics and associated risk factors of cytomegalovirus infection in patients with underlying systemic rheumatic diseases[J]. Natl Med J China, 2016, 96(35):2772-2776. | |
| [17] | 宋聪, 余小舒, 周昌静, 等. 艾滋病合并耶氏肺孢子菌肺炎患者巨细胞病毒活动情况的影响因素[J]. 名医, 2025(9):51-53. |
| Song C, Yu XS, Zhou CJ, et al. Factors influencing cytomegalovirus activity in AIDS patients with Pneumocystis jirovecii pneumonia[J]. Renowned Doctor, 2025(9):51-53. | |
| [18] | Grabar S, Le Moing V, Goujard C, et al. Clinical outcome of patients with HIV-1 infection according to immunologic and virologic response after 6 months of highly active antiretroviral therapy[J]. Ann Intern Med, 2000, 133(6):401-410. |
| [19] | Affandi JS, Montgomery J, Brunt SJ, et al. The immunological footprint of CMV in HIV-1 patients stable on long-term ART[J]. Immun Ageing, 2015, 12:14. |
| [20] | Tan Y, Chen Z, Zeng Z, et al. Microbiomes detected by bronchoalveolar lavage fluid metagenomic next-generation sequencing among HIV-infected and uninfected patients with pulmonary infection[J]. Microbiol Spectr, 2023, 11(4):e0000523. |
| [21] | Fan Q, Tang G, Jiang M, et al. Clinical prognostic value of TTV and HCMV but not EBV for outcomes in hospitalized HIV-positive patients[J]. Biosaf Health, 2025, 7(3):173-182. |
| [22] | 中华医学会热带病与寄生虫学分会艾滋病学组. 人类免疫缺陷病毒/艾滋病患者合并非结核分枝杆菌感染诊治专家共识[J]. 中华传染病杂志, 2019, 37(3):129-138. |
| AIDS Professional Group of Society of Tropical Disease and Parasitology of Chinese Medical Association. Expert consensus on diagnosis and treatment of HIV/AIDS complicated with non-tuberculous mycobacteria infection[J]. Chin J Infect Dis, 2019, 37(3):129-138. | |
| [23] | 张沛, 赵阿会, 高敏, 等. 2016-2021年河南省MTB/HIV双重感染流行特征分析[J]. 中国防痨杂志, 2023, 45(4): 377-382. |
| Zhang P, Zhao AH, Gao M, et al. Epidemiological characteristics of MTB/HIV co-infection in Henan from 2016 to 2021[J]. Chin J Antitubercul, 2023, 45(4):377-382. | |
| [24] | Geldmacher C, Ngwenyama N, Schuetz A, et al. Preferential infection and depletion of Mycobacterium tuberculosis-specific CD4+ T cells after HIV-1 infection[J]. J Exp Med, 2010, 207(13):2869-2881. |
| [25] | Bertagnolio S, Thwin SS, Silva R, et al. Clinical features of, and risk factors for, severe or fatal COVID-19 among people living with HIV admitted to hospital: analysis of data from the WHO Global Clinical Platform of COVID-19[J]. Lancet HIV, 2022, 9(7):e486-e495. |
| [26] | Parize P, Muth E, Richaud C, et al. Untargeted next-generation sequencing-based first-line diagnosis of infection in immunocompromised adults: a multicentre, blinded, prospective study[J]. Clin Microbiol Infect, 2017, 23(8):574.. |
/
| 〈 |
|
〉 |