NK cells, displaying early activation, cytotoxicity and adhesion molecules, are associated with mild dengue disease

被引:109
作者
Azeredo, EL
De Oliveira-Pinto, LM
Zagne, SM
Cerqueira, DIS
Nogueira, RMR
Kubelka, CF
机构
[1] Fiocruz MS, Inst Oswaldo Cruz, Dept Virol, BR-21040360 Rio De Janeiro, Brazil
[2] Fiocruz MS, Inst Oswaldo Cruz, Dept Immunol, BR-21040360 Rio De Janeiro, Brazil
[3] Hosp Univ Antonio Pedro, UFF, Niteroi, RJ, Brazil
关键词
dengue; NK cells; patients; activation; cytotoxicity; adhesion molecules;
D O I
10.1111/j.1365-2249.2006.02996.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During the innate immune response against infections, Natural Killer (NK) cells are as important effector cells as are Cytotoxic T lymphocytes (CTL) generated after antigenic stimulation in the adaptative response. NK cells increase in numbers, after viral infection or vaccination. We investigated the NK cell and CD8 T lymphocyte status in 55 dengue infected patients. The NK (CD56+CD3-) and CD56+ T cell (CD56+CD3+) rates rise during the acute phase of disease. The majority of NK cells from dengue patients display early markers for activation (CD69, HLA-DR, and CD38) and cell adhesion molecules (CD44, CD11a) during the acute phase of disease. The intracellular cytotoxic granule, TIA-1, is also up-regulated early in NK cells. Most of these markers appear also on CD8+ T lymphocytes but during the late acute phase. Circulating IL-15 is elevated in a significant number of patients during early acute infection and its values were statistically correlated with NK frequencies and cytotoxic markers on NKs. We have therefore shown that dengue virus infection is very likely stimulating a cytotoxic response that may be efficient in controlling the virus in synergism with CD8+ T lymphocytes. Interestingly, the heightened CD56+CD3-, CD56+CD3+, CD56+TIA-1+ and CD56+CD11a+ cell rates are associated with mild dengue clinical manifestations and might indicate a good prognosis of the disease.
引用
收藏
页码:345 / 356
页数:12
相关论文
共 78 条
[1]   MOLECULES AND STRUCTURES INVOLVED IN THE ADHESION OF NATURAL-KILLER-CELLS TO VASCULAR ENDOTHELIUM [J].
ALLAVENA, P ;
PAGANIN, C ;
MARTINPADURA, I ;
PERI, G ;
GABOLI, M ;
DEJANA, E ;
MARCHISIO, PC ;
MANTOVANI, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (02) :439-448
[2]  
ANDERSON P, 1990, J IMMUNOL, V144, P574
[3]  
[Anonymous], 1997, DENG HAEM FEV DIAGN, P13
[4]   Characterisation of lymphocyte response and cytokine patterns in patients with Dengue fever [J].
Azeredo, EL ;
Zagne, SMO ;
Santiago, MA ;
Gouvea, AS ;
Santana, AA ;
Neves-Souza, PCF ;
Nogueira, RMR ;
Miagostovich, MP ;
Kubelka, CF .
IMMUNOBIOLOGY, 2001, 204 (04) :494-507
[5]   THE ROLE OF NATURAL-KILLER-CELLS IN INNATE RESISTANCE TO INFECTION [J].
BANCROFT, GJ .
CURRENT OPINION IN IMMUNOLOGY, 1993, 5 (04) :503-510
[6]   Natural killer cells in antiviral defense: Function and regulation by innate cytokines [J].
Biron, CA ;
Nguyen, KB ;
Pien, GC ;
Cousens, LP ;
Salazar-Mather, TP .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :189-220
[7]   SEVERE HERPESVIRUS INFECTIONS IN AN ADOLESCENT WITHOUT NATURAL-KILLER CELLS [J].
BIRON, CA ;
BYRON, KS ;
SULLIVAN, JL .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (26) :1731-1735
[8]   INTERLEUKIN (IL)-15 IS A NOVEL CYTOKINE THAT ACTIVATES HUMAN NATURAL-KILLER-CELLS VIA COMPONENTS OF THE IL-2 RECEPTOR [J].
CARSON, WE ;
GIRI, JG ;
LINDEMANN, MJ ;
LINETT, ML ;
AHDIEH, M ;
PAXTON, R ;
ANDERSON, D ;
EISENMANN, J ;
GRABSTEIN, K ;
CALIGIURI, MA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) :1395-1403
[9]   NONRESTRICTED CYTO-TOXICITY MEDIATED BY INTERLEUKIN-2-EXPANDED LEUKOCYTES IS INHIBITED BY ANTI-LFA-1 MONOCLONAL-ANTIBODIES (MOAB) BUT POTENTIATED BY ANTI-CD3 MOAB [J].
CHEN, BP ;
MALKOVSKY, M ;
HANK, JA ;
SONDEL, PM .
CELLULAR IMMUNOLOGY, 1987, 110 (02) :282-293
[10]   The biology of human natural killer-cell subsets [J].
Cooper, MA ;
Fehniger, TA ;
Caligiuri, MA .
TRENDS IN IMMUNOLOGY, 2001, 22 (11) :633-640