New signatures of poor CD4 cell recovery after suppressive antiretroviral therapy in HIV-1-infected individuals: involvement of miR-192, IL-6, sCD14 and miR-144

被引:25
作者
Hernandez-Walias, Francisco [1 ]
Ruiz-de-Leon, Maria J. [1 ]
Rosado-Sanchez, Isaac [2 ]
Vazquez, Esther [1 ]
Leal, Manuel [2 ,3 ]
Moreno, Santiago [1 ]
Vidal, Francesc [4 ]
Blanco, Julia [5 ,6 ]
Pacheco, Yolanda M. [2 ]
Vallejo, Alejandro [1 ]
机构
[1] Univ Hosp Ramon y Cajal, Hlth Res Inst Ramon y Cajal IRyCIS, Lab Immunovirol, Dept Infect Dis, Madrid, Spain
[2] Univ Hosp Virgen del Rocio, Biomed Inst Seville IBiS, Seville, Spain
[3] Hosp Viamed, Dept Internal Med & Infect Dis, Seville, Spain
[4] Univ Rovira & Virgili, Univ Hosp Joan XXIII, Dept Internal Med, Infect Dis Unit & HIV AIDS,IISPV, Tarragona, Catalonia, Spain
[5] Res Inst Hlth Sci Germans Trias & Pujol, AIDS Res Inst IrsiCaixa HIVACAT, Badalona, Catalonia, Spain
[6] Univ Vic Univ Cent Catalonia UVIC UCC, Vic, Catalonia, Spain
关键词
HIV-INFECTED PATIENTS; LONG-TERM MORTALITY; MICRORNAS; PROLIFERATION; RECONSTITUTION; INFLAMMATION; EXPRESSION; APOPTOSIS; COHORT; CORIS;
D O I
10.1038/s41598-020-60073-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Up to 40% of newly diagnosed cases of HIV-1 infection are late diagnoses, with a profound decrease in CD4 cell counts in many cases. One-third of these individuals do not achieve optimal CD4 cell recovery (OR) after suppressive antiretroviral treatment (ART). This retrospective/longitudinal study of poor recovery (PR) included 79 HIV-1-infected individuals with CD4 count <200 cells/mm(3) (25 PR and 54 OR) before ART. After suppressive ART, 21 PR and 24 OR individuals were further analysed, including paired samples. Selected miRs and plasma inflammatory markers were determined to investigate their potential predictive/diagnostic value for poor recovery. miR-192, IL-6 and sCD14 were independently associated with CD4 recovery before ART (p=0.031, p=0.007, and p=0.008, respectively). The combination of these three factors returned a good discrimination (predictive value for PR) value of 0.841 (AUC, p<0.001). After suppressive ART, miR-144 was independently associated with CD4 recovery (p=0.017), showing a moderate discrimination value of 0.730 (AUC, p=0.008) for PR. Our study provides new evidence on the relationship between miRs and HIV-1 infection that could help improve the management of individuals at HIV-1 diagnosis. These miRs and cytokines signature sets provide novel tools to predict CD4 cell recovery and its progression after ART.
引用
收藏
页数:11
相关论文
共 48 条
[1]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[2]   MicroRNAs: Novel Regulators During the Immune Response [J].
Bi, Yujing ;
Liu, Guangwei ;
Yang, Ruifu .
JOURNAL OF CELLULAR PHYSIOLOGY, 2009, 218 (03) :467-472
[3]   Induced Packaging of Cellular MicroRNAs into HIV-1 Virions Can Inhibit Infectivity [J].
Bogerd, Hal P. ;
Kennedy, Edward M. ;
Whisnant, Adam W. ;
Cullen, Bryan R. .
MBIO, 2017, 8 (01)
[4]   Spanish cohort of naive HIV-infected patients (CoRIS):: Rationale, organization and initial results [J].
Caro-Murillo, Ana Maria ;
Castilla, Jesus ;
Perez-Hoyos, Santiago ;
Miro, Jose M. ;
Podzamczer, Daniel ;
Rubio, Rafael ;
Riera, Melchor ;
Viciana, Pompeyo ;
Lopez Aldeguer, Jose ;
Iribarren, Jose Antonio ;
de los Santos-Gil, Ignacio ;
Gomez-Sirvent, Juan Luis ;
Berenguer, Juan ;
Gutierrez, Felix ;
Saumoy, Maria ;
Segura, Ferran ;
Soriano, Vicente ;
Pena, Alejandro ;
Pulido, Federico ;
Oteo, Jose Antonio ;
Leal, Manuel ;
Casabona, Jordi ;
del Amo, Julia ;
Moreno, Santiago .
ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA, 2007, 25 (01) :23-31
[5]   Next-Generation Sequencing of Small RNAs from HIV-Infected Cells Identifies Phased microRNA Expression Patterns and Candidate Novel microRNAs Differentially Expressed upon Infection [J].
Chang, Stewart T. ;
Thomas, Matthew J. ;
Sova, Pavel ;
Green, Richard R. ;
Palermo, Robert E. ;
Katze, Michael G. .
MBIO, 2013, 4 (01)
[6]   Baseline viral load and immune activation determine the extent of reconstitution of innate immune effectors in HIV-1-infected subjects undergoing Antiretroviral treatment [J].
Chehimi, Jihed ;
Azzoni, Livio ;
Farabaugh, Matthew ;
Creer, Shenoa A. ;
Tomescu, Costin ;
Hancock, Aidan ;
Mackiewicz, Agnes ;
D'Alessandro, Lara ;
Gbanekar, Smita ;
Foulkes, Andrea S. ;
Mounzer, Karam ;
Kostman, Jay ;
Montaner, Luis J. .
JOURNAL OF IMMUNOLOGY, 2007, 179 (04) :2642-2650
[7]   Constructing an integrated genetic and epigenetic cellular network for whole cellular mechanism using high-throughput next-generation sequencing data [J].
Chen, Bor-Sen ;
Li, Cheng-Wei .
BMC SYSTEMS BIOLOGY, 2016, 10
[8]   Virologic and immunologic effects of adding maraviroc to suppressive antiretroviral therapy in individuals with suboptimal CD4+ T-cell recovery [J].
Cillo, Anthony R. ;
Hilldorfer, Benedict B. ;
Lalama, Christina M. ;
McKinnon, John E. ;
Coombs, Robert W. ;
Tenorio, Allan R. ;
Fox, Lawrence ;
Gandhi, Rajesh T. ;
Ribaudo, Heather ;
Currier, Judith S. ;
Gulick, Roy M. ;
Wilkin, Timothy J. ;
Mellors, John W. .
AIDS, 2015, 29 (16) :2121-2129
[9]   Different biological significance of sCD14 and LPS in HIV-infection: Importance of the immunovirology stage and association with HIV-disease progression markers [J].
Concepcion Romero-Sanchez, Ma ;
Gonzalez-Serna, Alejandro ;
Pacheco, Yolanda M. ;
Ferrando-Martinez, Sara ;
Machmach, Kawthar ;
Garcia-Garcia, Maria ;
Isabel Alvarez-Rios, Ana ;
Vidal, Francisco ;
Leal, Manuel ;
Ruiz-Mateos, Ezequiel .
JOURNAL OF INFECTION, 2012, 65 (05) :431-438
[10]   A randomized controlled trial evaluating the efficacy and safety of intermittent 3-, 4-, and 5-day cycles of intravenous recombinant human interleukin-2 combined with antiretroviral therapy (ART) versus ART alone in HIV-seropositive patients with 100-300 CD4+ T cells [J].
de Boer, AW ;
Markowitz, N ;
Lane, HC ;
Saravolatz, LD ;
Koletar, SL ;
Donabedian, H ;
Yoshizawa, C ;
Duliege, AM ;
Fyfe, G ;
Mitsuyasu, RT .
CLINICAL IMMUNOLOGY, 2003, 106 (03) :188-196