The Bone Marrow Functions as the Central Site of Proliferation for Long-Lived NK Cells

被引:35
作者
van Helden, Mary J. G.
de Graaf, Natascha
Boog, Claire J. P. [2 ]
Topham, David J. [3 ]
Zaiss, Dietmar M. W.
Sijts, Alice J. A. M. [1 ]
机构
[1] Univ Utrecht, Fac Vet Med, Dept Infect Dis & Immunol, Div Immunol, NL-3584 CL Utrecht, Netherlands
[2] Natl Inst Publ Hlth & Environm, Ctr Infect Dis Control, Dept Vaccinol, NL-3720 BA Bilthoven, Netherlands
[3] Univ Rochester, Med Ctr, D Smith Ctr Vaccine Biol & Immunol, Rochester, NY 14642 USA
基金
英国惠康基金;
关键词
RESPIRATORY SYNCYTIAL VIRUS; NATURAL-KILLER-CELLS; CD8; T-CELLS; HOMEOSTATIC PROLIFERATION; BACTERIAL-INFECTION; IFN-GAMMA; MEMORY; TRAFFICKING; RECRUITMENT; GENERATION;
D O I
10.4049/jimmunol.1200008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NK cells play an important role in the early defense against invading pathogens. Although it is well established that infection leads to a substantial, local increase in NK cell numbers, little is known about the mechanisms that trigger their proliferation and migration. In this study, we investigated the dynamics of NK cell responses after intranasal respiratory virus infection. We show that NK cell numbers increased in the airways after influenza virus infection but find no evidence of proliferation either at the site of infection or in the draining lymph nodes. Instead, we find that the bone marrow (BM) is the primary site of proliferation of both immature and mature NK cells during infection. Using an adoptive transfer model, we demonstrate that peripheral, long-lived and phenotypically mature NK cells migrate back to the BM and proliferate there, both homeostatically and in response to infection. Thus, the BM is not only a site of NK cell development but also an important site for proliferation of long-lived mature NK cells. The Journal of Immunology, 2012, 189: 2333-2337.
引用
收藏
页码:2333 / 2337
页数:5
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