RETRACTED: Analysis of Mycobacterium tuberculosis-Specific CD8 T-Cells in Patients with Active Tuberculosis and in Individuals with Latent Infection (Retracted Article)

被引:83
作者
Caccamo, Nadia
Guggino, Giuliana
Meraviglia, Serena
Gelsomino, Giuseppe
Di Carlo, Paola
Titone, Lucina
Bocchino, Marialuisa
Galati, Domenico
Matarese, Alessandro
Nouta, Jan
Klein, Michel R.
Salerno, Alfredo
Sanduzzi, Alessandro
Dieli, Francesco
Ottenhoff, Tom H. M.
机构
[1] Dipartimento di Biopatologia e Metodologie Biomediche, Università di Palermo, Palermo
[2] Dipartimento di Medicina Clinica e delle Patologie Emergenti, Università di Palermo, Palermo
[3] TB Infection Screening Unit, Department of Clinical and Experimental Medicine, University of Naples Federico II, Naples, Monaldi Hospital
[4] Department of Immunohematology and Blood Transfusion, Department of Infectious Diseases, Leiden University Medical Center, Leiden
[5] National Institute of Public Health and the Environment, Bilthoven
来源
PLOS ONE | 2009年 / 4卷 / 05期
关键词
D O I
10.1371/journal.pone.0005528
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
CD8 T-cells contribute to control of Mycobacterium tuberculosis infection, but little is known about the quality of the CD8 T-cell response in subjects with latent infection and in patients with active tuberculosis disease. CD8 T-cells recognizing epitopes from 6 different proteins of Mycobacterium tuberculosis were detected by tetramer staining. Intracellular cytokines staining for specific production of IFN-gamma and IL-2 was performed, complemented by phenotyping of memory markers on antigen-specific CD8 T-cells. The ex-vivo frequencies of tetramer-specific CD8 T-cells in tuberculous patients before therapy were lower than in subjects with latent infection, but increased at four months after therapy to comparable percentages detected in subjects with latent infection. The majority of CD8 T-cells from subjects with latent infection expressed a terminally-differentiated phenotype (CD45RA(+)CCR7(-)). In contrast, tuberculous patients had only 35% of antigen-specific CD8 T-cells expressing this phenotype, while containing higher proportions of cells with an effector memory-and a central memory-like phenotype, and which did not change significantly after therapy. CD8 T-cells from subjects with latent infection showed a codominance of IL-2(+)/IFN-gamma(+) and IL-2(-)/IFN-gamma(+) T-cell populations; interestingly, only the IL-2(+)/IFN-gamma(+) population was reduced or absent in tuberculous patients, highly suggestive of a restricted functional profile of Mycobacterium tuberculosis-specific CD8 T-cells during active disease. These results suggest distinct Mycobacterium tuberculosis specific CD8 T-cell phenotypic and functional signatures between subjects which control infection (subjects with latent infection) and those who do not (patients with active disease).
引用
收藏
页数:10
相关论文
共 39 条
[1]  
[Anonymous], 2008, Global tuberculosis control - surveillance, planning, financing
[2]   Phenotypical and functional analysis of memory and effector human CD8 T cells specific for mycobacterial antigens [J].
Caccamo, Nadia ;
Meraviglia, Serena ;
La Mendola, Carmela ;
Guggino, Giuliana ;
Dieli, Francesco ;
Salerno, Alfredo .
JOURNAL OF IMMUNOLOGY, 2006, 177 (03) :1780-1785
[3]   Use of a T cell-based assay for monitoring efficacy of antituberculosis therapy [J].
Carrara, S ;
Vincenti, D ;
Petrosillo, N ;
Amicosante, M ;
Girardi, E ;
Goletti, D .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (05) :754-756
[4]   Antimicrobial activity of MHC class I-restricted CD8+T cells in human tuberculosis [J].
Cho, S ;
Mehra, V ;
Thoma-Uszynski, S ;
Stenger, S ;
Serbina, N ;
Mazzaccaro, RJ ;
Flynn, JL ;
Barnes, PF ;
Southwood, S ;
Celis, E ;
Bloom, BR ;
Modlin, RL ;
Sette, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (22) :12210-12215
[5]   A COMPUTER-PROGRAM FOR PREDICTING POSSIBLE CYTOTOXIC T-LYMPHOCYTE EPITOPES BASED ON HLA CLASS-I PEPTIDE-BINDING MOTIFS [J].
DAMARO, J ;
HOUBIERS, JGA ;
DRIJFHOUT, JW ;
BRANDT, RMP ;
SCHIPPER, R ;
BAVINCK, JNB ;
MELIEF, CJM ;
KAST, WM .
HUMAN IMMUNOLOGY, 1995, 43 (01) :13-18
[6]   Decreased serum granulysin levels in childhood tuberculosis which reverse after therapy [J].
Di Liberto, Diana ;
Buccheri, Simona ;
Caccamo, Nadia ;
Meraviglia, Serena ;
Romano, Amelia ;
Di Carlo, Paola ;
Titone, Lucina ;
Dieli, Francesco ;
Krensky, Alan M. ;
Salerno, Alfredo .
TUBERCULOSIS, 2007, 87 (04) :322-328
[7]  
Dieli F, 2000, SCAND J IMMUNOL, V52, P96
[8]   Sequestration of T lymphocytes to body fluids in tuberculosis: Reversal of anergy following chemotherapy [J].
Dieli, F ;
Friscia, G ;
Di Sano, C ;
Ivanyi, J ;
Singh, M ;
Spallek, R ;
Sireci, G ;
Titone, L ;
Salerno, A .
JOURNAL OF INFECTIOUS DISEASES, 1999, 180 (01) :225-228
[9]   Selective depression of interferon-γ and granulysin production with increase of proliferative response by Vγ9/Vδ T cells in children with tuberculosis [J].
Dieli, F ;
Sireci, G ;
Caccamo, N ;
Di Sano, C ;
Titone, L ;
Romano, A ;
Di Carlo, P ;
Barera, A ;
Accardo-Palumbo, A ;
Krensky, AM ;
Salerno, A .
JOURNAL OF INFECTIOUS DISEASES, 2002, 186 (12) :1835-1839
[10]   Quiescence and functional reprogranuning of Epstein-Barr virus (EBV)-specific CD8+ T cells during persistent infection [J].
Dunne, PJ ;
Belaramani, L ;
Fletcher, JM ;
de Mattos, SF ;
Lawrenz, M ;
Soares, MVD ;
Rustin, MHA ;
Lam, EWF ;
Salmon, M ;
Akbar, AN .
BLOOD, 2005, 106 (02) :558-565