An immunomodulatory function for neutrophils during the induction of a CD4+ Th2 response in BALB/c mice infected with Leishmania major

被引:237
作者
Tacchini-Cottier, F
Zweifel, C
Belkaid, Y
Mukankundiye, C
Vasei, M
Launois, P
Milon, G
Louis, JA
机构
[1] Univ Lausanne, Inst Biochem, WHO, Immunol Res & Training Ctr, CH-1066 Epalinges, Switzerland
[2] Inst Pasteur, Paris, France
关键词
D O I
10.4049/jimmunol.165.5.2628
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The possible immunomodulatory role of polymorphonuclear leukocytes (PMN) in CD4(+) T lymphocyte differentiation in mice was examined by studying the effect of transient depletion of PMN during the early phase after Leishmania major delivery. A single injection of the PMN-depleting NIMP-R14 mAb 6 h before infection with L. major prevented the early burst of IL-4 mRNA transcription otherwise occurring in the draining lymph node of susceptible BALB/c mice. Since this early burst of IL-4 mRNA transcripts had previously been shown to instruct Th2 differentiation in mice from this strain, we examined the effect of PMN depletion on Th subset differentiation at later time points after infection, The transient depletion of PR IN in BALB/c mice was sufficient to inhibit Th2 cell development otherwise occurring after L. major infection. Decreased Th2 responses were paralleled with partial resolution of the footpad lesions induced by L. major. Furthermore, draining lymph node-derived CD4(+) T cells from PMN-depleted mice remained responsive to IL-12 after L. major infection, unlike those of infected BALB/c mice receiving control Ab, PMN depletion had no effect when the NIMP-R14 mAb was injected 24 h postinfection. The protective effect of PMN depletion was shown to be IL-12 dependent, as concomitant neutralization of IL-12 reversed the protective effect of PMN depletion, These results suggest a role for an early wave of PMN in the development of the Th2 response characteristic of mice susceptible to infection with L. major.
引用
收藏
页码:2628 / 2636
页数:9
相关论文
共 51 条
[11]   Activation of human T cells by major histocompatability complex class II expressing neutrophils: Proliferation in the presence of superantigen, but not tetanus toxoid [J].
Fanger, NA ;
Liu, CL ;
Guyre, PM ;
Wardwell, K ;
ONeil, J ;
Guo, TL ;
Christian, TP ;
Mudzinski, SP ;
Gosselin, EJ .
BLOOD, 1997, 89 (11) :4128-4135
[12]   TRANSFORMING GROWTH-FACTOR BETA-1 (TGF-BETA-1) INDUCED NEUTROPHIL RECRUITMENT TO SYNOVIAL TISSUES - IMPLICATIONS FOR TGF-BETA-DRIVEN SYNOVIAL INFLAMMATION AND HYPERPLASIA [J].
FAVA, RA ;
OLSEN, NJ ;
POSTLETHWAITE, AE ;
BROADLEY, KN ;
DAVIDSON, JM ;
NANNEY, LB ;
LUCAS, C ;
TOWNES, AS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (05) :1121-1132
[13]  
FIORENTINO DF, 1991, J IMMUNOL, V146, P3444
[14]   Responsiveness of human neutrophils to interleukin-4: Induction of cytoskeletal rearrangements, de novo protein synthesis and delay of apoptosis [J].
Girard, D ;
Paquin, R ;
Beaulieu, AD .
BIOCHEMICAL JOURNAL, 1997, 325 :147-153
[15]   LUNG MYELOPEROXIDASE AS A MEASURE OF PULMONARY LEUKOSTASIS IN RABBITS [J].
GOLDBLUM, SE ;
WU, KM ;
JAY, M .
JOURNAL OF APPLIED PHYSIOLOGY, 1985, 59 (06) :1978-1985
[16]  
Gorham JD, 1998, J IMMUNOL, V161, P1664
[17]  
GOSSELIN EJ, 1993, J IMMUNOL, V151, P1482
[18]  
Guler ML, 1996, SCIENCE, V271, P984, DOI 10.1126/science.271.5251.984
[19]   RECOMBINANT INTERLEUKIN-12 CURES MICE INFECTED WITH LEISHMANIA-MAJOR [J].
HEINZEL, FP ;
SCHOENHAUT, DS ;
RERKO, RM ;
ROSSER, LE ;
GATELY, MK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (05) :1505-1509
[20]  
Himmelrich H, 1998, J IMMUNOL, V161, P6156