Human small-intestinal epithelium contains functional natural killer lymphocytes

被引:86
作者
León, F
Roldán, E
Sanchez, L
Camarero, C
Bootello, A
Roy, G
机构
[1] Hosp Ramon & Cajal, Dept Immunol, Serv Inmunol, E-28034 Madrid, Spain
[2] Hosp Ramon & Cajal, Dept Paediat, E-28034 Madrid, Spain
关键词
D O I
10.1016/S0016-5085(03)00886-2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: CD3(-) non-T lymphocytes constitute the second most abundant lymphoid subset in the human small-bowel epithelium, and these CD3(-) intraepithelial lymphocytes are virtually absent in active celiac disease. Phenotypically, they resemble natural killer cells and have been termed natural killer-like intraepithelial lymphocytes. Because of the limited availability of appropriate human samples, functional studies have not yet been reported, and it is not yet clear whether these are true natural killer cells. Methods: We used magnetic bead-based purification and flow cytometry to study several aspects of normal human small-bowel natural killer-like intraepithelial lymphocytes: intracellular cytokine content (basally and after activation); ability to lyse natural killer-sensitive K562 target cells; and expression of perforins, Fas ligand, and other functional markers. Results: CD3(-) intraepithelial lymphocytes cultured in interleukin-2 showed a higher lymphokine-activated killer activity than CD3(+) intraepithelial lymphocytes (48%-83% lysis exerted by CD3(-) intraepithelial lymphocytes at an effector-target cell ratio of 2:1 vs. 8%-18% by CD3(+) intraepithelial lymphocytes). Perforin content correlated with this lytic potential (75% +/- 4% in CD3(-) vs. 5% +/- 4% in CD3(+) intraepithelial lymphocytes). Both CD3(-) and CD3+ cells displayed a type I cytokine profile (interferon-gamma > tumor necrosis factor-alpha > interleukin-2; undetectable interleukin-4 and interieukin-10). In addition to their activated phenotype, subsets of natural killer-like intraepithelial lymphocytes expressed CD8alphaalpha and intracellular CD3epsilon chain, showing the existence of heterogeneity within this cell lineage. Conclusions: This is the first demonstration of functional natural killer cells within the human gut epithelium. These cells might play an important role in innate mucosal immunity (host defense and tumor surveillance) and tolerance.
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页码:345 / 356
页数:12
相关论文
共 82 条
[1]   Increased HLA-DR and decreased CD3 on human intestinal intraepithelial lymphocytes: Evidence of activation? [J].
Abuzakouk, M ;
Kelleher, D ;
Feighery, C ;
OFarrelly, C .
GUT, 1996, 39 (03) :396-400
[2]   Definition of a natural killer NKR-P1A(+)/CD56(-)/CD16(-) functionally immature human NK cell subset that differentiates in vitro in the presence of interleukin 12 [J].
Bennett, IM ;
Zatsepina, O ;
Zamai, L ;
Azzoni, L ;
Mikheeva, T ;
Perussia, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (05) :1845-1856
[3]  
BuzoniGatel D, 1997, J IMMUNOL, V158, P5883
[4]   Intraepithelial lymphocytes and coeliac disease:: permanent changes in CD3-/CD7+ and T cell receptor γδ subsets studied by flow cytometry [J].
Camarero, C ;
Eiras, P ;
Asensio, A ;
Leon, F ;
Olivares, F ;
Escobar, H ;
Roy, G .
ACTA PAEDIATRICA, 2000, 89 (03) :285-290
[5]   Spontaneous secretion of interferon γ and interleukin 4 by human intraepithelial and lamina propria gut lymphocytes [J].
Carol, M ;
Lambrechts, A ;
Van Gossum, A ;
Libin, M ;
Goldman, M ;
Mascart-Lemone, F .
GUT, 1998, 42 (05) :643-649
[6]   Abnormal intestinal intraepithelial lymphocytes in refractory sprue [J].
Cellier, C ;
Patey, N ;
Mauvieux, L ;
Jabri, B ;
Delabesse, E ;
Cervoni, JP ;
Burtin, ML ;
Guy-Grand, D ;
Bouhnik, Y ;
Modigliani, R ;
Barbier, JP ;
Macintyre, E ;
Brousse, N ;
Cerf-Bensussan, N .
GASTROENTEROLOGY, 1998, 114 (03) :471-481
[7]  
CERFBENSUSSAN N, 1992, EUR J IMMUNOL, V22, P885
[8]   INTRAEPITHELIAL LYMPHOCYTES OF HUMAN GUT - ISOLATION, CHARACTERIZATION AND STUDY OF NATURAL-KILLER ACTIVITY [J].
CERFBENSUSSAN, N ;
GUYGRAND, D ;
GRISCELLI, C .
GUT, 1985, 26 (01) :81-88
[9]   A domain in TNF receptors that mediates ligand-independent receptor assembly and signaling [J].
Chan, FKM ;
Chun, HJ ;
Zheng, LX ;
Siegel, RM ;
Bui, KL ;
Lenardo, MJ .
SCIENCE, 2000, 288 (5475) :2351-2354
[10]  
CHANG L, 1993, J IMMUNOL METHODS, V166, P45