The NKp46 receptor contributes to NK cell lysis of mononuclear phagocytes infected with an intracellular bacterium

被引:117
|
作者
Vankayalapati, R
Wizel, B
Weis, SE
Safi, H
Lakey, DL
Mandelboim, O
Samten, B
Porgador, A
Barnes, PF
机构
[1] Univ Texas Hlth Ctr, Ctr Pulm & Infect Dis Control, Tyler, TX 75708 USA
[2] Univ Texas Hlth Ctr, Dept Microbiol & Immunol, Tyler, TX 75708 USA
[3] Univ Texas Hlth Ctr, Dept Med, Tyler, TX 75708 USA
[4] Univ N Texas, Hlth Sci Ctr, Dept Internal Med, Ft Worth, TX 76107 USA
[5] Hebrew Univ Jerusalem, Hadassah Med Sch, Lautenberg Ctr Gen & Tumor Immunol, Jerusalem, Israel
[6] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Microbiol & Immunol, IL-84105 Beer Sheva, Israel
[7] Ben Gurion Univ Negev, Canc Res Ctr, IL-84105 Beer Sheva, Israel
来源
JOURNAL OF IMMUNOLOGY | 2002年 / 168卷 / 07期
关键词
D O I
10.4049/jimmunol.168.7.3451
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We used human tuberculosis as a model to investigate the role of NK cytotoxic mechanisms in the immune response to intracellular infection. Freshly isolated NK cells and NK cell lines from healthy donors lysed Mycobacterium tuberculosis-infected monocytes to a greater extent than uninfected monocytes. Lysis of infected monocytes was associated with increased expression of mRNA for the NKp46 receptor, but not the NKp44 receptor. Antisera to NKp46 markedly inhibited lysis of infected monocytes. NK cell-mediated lysis was not due to reduced expression of MHC class I molecules on the surface of infected monocytes or to enhanced production of IL-18 or IFN-gamma. NK cell lytic activity against M. tuberculosis-infected monocytes and NKp46 mRNA expression were reduced in tuberculosis patients with ineffective immunity to M. tuberculosis compared with findings in healthy donors. These observations suggest that 1) the NKp46 receptor participates in NK cell-mediated lysis of cells infected with an intracellular pathogen, and 2) the reduced functional capacity of NK cells is associated with severe manifestations of infectious disease.
引用
收藏
页码:3451 / 3457
页数:7
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