Polyfunctional Mycobacterium tuberculosis-specific effector memory CD4+ T cells at sites of pleural TB

被引:25
作者
El Fenniri, L. [2 ]
Toossi, Z. [1 ]
Aung, H. [1 ]
El Iraki, G. [3 ]
Bourkkadi, J.
Benamor, J. [3 ]
Laskri, A.
Berrada, N. [4 ]
Benjouad, A. [4 ]
Mayanja-Kizza, H. [5 ]
Betts, M. R. [6 ]
El Aouad, R. [2 ]
Canaday, D. H. [1 ]
机构
[1] Case Western Reserve Univ, Sch Med, Div Infect Dis, Cleveland, OH 44106 USA
[2] Natl Inst Hyg, Dept Immunol Virol, Rabat, Morocco
[3] Hop Moulay Youssef, Rabat, Morocco
[4] Fac Sci Rabat, Dept Biol, Lab Biochim Immunol, Rabat, Morocco
[5] Makerere Univ, Dept Med, Kampala, Uganda
[6] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
关键词
Tuberculosis; Pleuritis; CD4+; T cells; Immunity; Polyfunctional; MESSENGER-RNA; INFECTION; DISEASE; LYMPHOCYTES; EFFUSION; EXPRESSION; CHEMOKINES; CXC;
D O I
10.1016/j.tube.2010.12.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pleural tuberculosis (TB) is a common presentation of Mycobacterium tuberculosis (MTB) infection, and despite spontaneous resolution remains a strong risk factor for reactivation pulmonary TB in a majority of individuals. This study was undertaken to further understand the characteristics of immune cells at sites of pleural TB. A significant shift toward memory CD4+ T cells with an effector phenotype and away from naive CD4+ T cells in pleural fluid as compared to blood mononuclear cells was found. These data suggest that effector T cells are capable of migrating to sites of active TB infection and/or the differentiation to effector phenotype T cells in situ is highly amplified. Using multi-parameter flow cytometry analysis, a significant portion of MTB-specific CD4+ T cells in the pleural space were polyfunctional demonstrating two, three or four simultaneous functions including IFN-gamma, IL-2, TNF-alpha, and or MIP-1 alpha production. A greater proportion of these polyfunctional cells were of effector memory rather than central memory phenotype. The role of these polyfunctional MTB-specific CD4+ T cells at sites of pleural TB requires further study. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:224 / 230
页数:7
相关论文
共 28 条
[11]   CD27low CD4 T lymphocytes that accumulate in the mouse lungs during mycobacterial infection differentiate from CD27high precursors in situ, produce IFN-γ, and protect the host against tuberculosis infection [J].
Kapina, Marina A. ;
Shepelkova, Galina S. ;
Mischenko, Vladimir V. ;
Sayles, Peter ;
Bogacheva, Polina ;
Winslow, Gary ;
Apt, Alexander S. ;
Lyadova, Irina V. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (02) :976-985
[12]   Sputum Mycobacterium tuberculosis mRNA as a Marker of Bacteriologic Clearance in Response to Antituberculosis Therapy [J].
Li, L. ;
Mahan, C. S. ;
Palaci, M. ;
Horter, L. ;
Loeffelholz, L. ;
Johnson, J. L. ;
Dietze, R. ;
Debanne, S. M. ;
Joloba, M. L. ;
Okwera, A. ;
Boom, W. H. ;
Eisenach, K. D. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2010, 48 (01) :46-51
[13]  
Luzze H, 2001, INT J TUBERC LUNG D, V5, P746
[14]   Polyfunctional analysis of human t cell responses: importance in vaccine immunogenicity and natural infection [J].
Makedonas, George ;
Betts, Michael R. .
SPRINGER SEMINARS IN IMMUNOPATHOLOGY, 2006, 28 (03) :209-219
[15]   Polarized helper T cells in tubercular pleural effusion: phenotypic identity and selective recruitment [J].
Mitra, DK ;
Sharma, SK ;
Dinda, AK ;
Bindra, MS ;
Madan, B ;
Ghosh, B .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (08) :2367-2375
[16]  
Ozvaran Mustafa Kursat, 2007, Ann Thorac Med, V2, P118, DOI 10.4103/1817-1737.33700
[17]  
PATIALA JORMA, 1954, ACTA TUBERC SCAND SUPPL, V36, P1
[18]   Expression of CXC and CC type of chemokines and its receptors in tuberculous and non-tuberculous effusions [J].
Pokkali, Supriya ;
Das, Sulochana D. ;
Logamurthy, R. .
CYTOKINE, 2008, 41 (03) :307-314
[19]  
Reiley WW, 2010, P NATL ACAD SCI US
[20]   Immunophenotypic characterization of peripheral T lymphocytes in Mycobacterium tuberculosis infection and disease [J].
Rodrigues, DSS ;
Medeiros, EAS ;
Weckx, LY ;
Bonnez, W ;
Salomao, R ;
Kallas, EG .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2002, 128 (01) :149-154