Selective depression of interferon-γ and granulysin production with increase of proliferative response by Vγ9/Vδ T cells in children with tuberculosis

被引:46
作者
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
机构
[1] Univ Palermo, Dipartimento Biopatol, I-90134 Palermo, Italy
[2] Italian Natl Res Council, Ist Metodol Diagnost Avanzate, Palermo, Italy
[3] Hosp G Di Cristina, Ist Malattie Infett, Palermo, Italy
[4] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
关键词
D O I
10.1086/345766
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vgamma9/Vdelta2 T cells can contribute to protective immune response against Mycobacterium tuberculosis, although the extent to which and mechanisms by which they could actually protect against human tuberculosis remain unclear. We have previously reported that Vgamma9/Vdelta2 T cells from tuberculin purified protein derivative (PPD)-positive children, either healthy or affected by different clinical forms of tuberculosis, strongly proliferate to different phosphoantigens in vitro, whereas Vgamma9/Vdelta2 T cells from PPD-negative healthy subjects proliferate very poorly. We report here that Vgamma9/Vdelta2 T cells from tuberculous children have an increased proliferative activity, but decreased interferon (IFN)-gamma production and granulysin expression. After successful chemotherapy, the Vgamma9/Vdelta2 T cell proliferative response strongly decreased, whereas IFN-gamma and granulysin production consistently increased. Disease-associated changes in Vgamma9/Vdelta2 T cell effector functions in patients with tuberculosis are consistent with the possibility that these T cells may play a protective role in immune response against M. tuberculosis infection.
引用
收藏
页码:1835 / 1839
页数:5
相关论文
共 21 条
[1]   GAMMA-DELTA-LYMPHOCYTES-T IN HUMAN TUBERCULOSIS [J].
BARNES, PF ;
GRISSO, CL ;
ABRAMS, JS ;
BAND, H ;
REA, TH ;
MODLIN, RL .
JOURNAL OF INFECTIOUS DISEASES, 1992, 165 (03) :506-512
[2]  
Dieli F, 2000, EUR J IMMUNOL, V30, P1512, DOI 10.1002/(SICI)1521-4141(200005)30:5<1512::AID-IMMU1512>3.0.CO
[3]  
2-3
[4]   Granulysin-dependent killing of intracellular and extracellular Mycobacterium tuberculosis by Vγ9/Vδ2 T lymphocytes [J].
Dieli, F ;
Troye-Blomberg, M ;
Ivanyi, J ;
Fournié, JJ ;
Krensky, AM ;
Bonneville, M ;
Peyrat, MA ;
Caccamo, N ;
Sireci, G ;
Salerno, A .
JOURNAL OF INFECTIOUS DISEASES, 2001, 184 (08) :1082-1085
[5]   Ligand-specific αβ and γδ T cell responses in childhood tuberculosis [J].
Dieli, F ;
Sireci, G ;
Di Sano, C ;
Romano, A ;
Titone, L ;
Di Carlo, P ;
Ivanyi, J ;
Fourniè, JJ ;
Salerno, A .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (01) :294-301
[6]   Granulysin, a T cell product, kills bacteria by altering membrane permeability [J].
Ernst, WA ;
Thoma-Uszynski, S ;
Teitelbaum, P ;
Ko, C ;
Hanson, DA ;
Clayberger, C ;
Krensky, AM ;
Leippe, M ;
Bloom, BR ;
Ganz, T ;
Modlin, RL .
JOURNAL OF IMMUNOLOGY, 2000, 165 (12) :7102-7108
[7]  
Garcia VE, 1997, J IMMUNOL, V159, P1328
[8]   Lack of CD27-CD45RA-Vγ9Vδ2+ T cell effectors in immunocompromised hosts and during active pulmonary tuberculosis [J].
Gioia, C ;
Agrati, C ;
Casetti, R ;
Cairo, C ;
Borsellino, G ;
Battistini, L ;
Mancino, G ;
Goletti, D ;
Colizzi, V ;
Pucillo, LP ;
Poccia, F .
JOURNAL OF IMMUNOLOGY, 2002, 168 (03) :1484-1489
[9]   How can immunology contribute to the control of tuberculosis? [J].
Kaufmann, SHE .
NATURE REVIEWS IMMUNOLOGY, 2001, 1 (01) :20-30
[10]  
Li BQ, 1998, J IMMUNOL, V161, P1558