T-CELL RESPONSE IN MURINE LEISHMANIA-MEXICANA-AMAZONENSIS INFECTION - PRODUCTION OF INTERFERON-GAMMA BY CD8+ CELLS

被引:23
作者
CHAN, MMY [1 ]
机构
[1] RUTGERS UNIV,BUR BIOL RES,PISCATAWAY,NJ 08855
关键词
T-HELPER SUBSETS; CD8+ CELLS; INTERFERON-GAMMA; CUTANEOUS LEISHMANIASIS;
D O I
10.1002/eji.1830230532
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 immune response to Leishmania major has been the subject of many investigations. However. Leishmania includes many species with different clinical manifestations. In this report, we studied the T cell response to L. mexicana amazonensis, a New World species, in a murine model. We found that, similar to L. major, an Old World species, resistant C57BL/6 mice produced a high level of IFN-gamma and a low level of IL-4. Conversely, susceptible BALB/c mice produced a much lower level of IFN-gamma and higher level of IL-4. Although IFN-gamma is one of the important lymphokines that mediate macrophage activation and thus the destruction of the intracellular parasites, which lymphocyte subsets are producing the IFN-gamma is still a controversy. Much evidence including the isolation of protective, IFN-gamma-producing, CD4+ cell lines have confirmed the participation of CD4+ Th1 cells unequivocally. However, both CD4+ and CD8+ cells produced IFN-gamma. Recently, an increasing body of evidence has appeared suggesting that CD8+ cells also play a role in the resolution of murine L. major infection. We found that in the L. m. amazonensis model, when CD8+ lymphocytes from resistant C57BL/6 mice were eliminated by anti-CD8 antibody and complement-mediated lysis, the IFN-gamma production was reduced by 77%. This indicated that CD8+ cells produced a significant amount of the IFN-gamma. However, our results also indicate that IFN-gamma production by CD8+ cells was dependent on CD4+ cells.
引用
收藏
页码:1181 / 1184
页数:4
相关论文
共 30 条
[1]  
BELOSEVIC M, 1989, J IMMUNOL, V143, P266
[2]  
BRUNT LM, 1990, J IMMUNOL, V145, P3540
[3]  
CHAN MM, 1989, IMMUNOGENETICS, V28, P425
[4]  
CILLARI E, 1991, IMMUNOLOGY, V74, P25
[5]  
DIALYNAS DP, 1983, J IMMUNOL, V131, P2445
[6]  
FARRELL JP, 1989, J IMMUNOL, V142, P1426
[7]   RECIPROCAL EXPRESSION OF INTERFERON-GAMMA OR INTERLEUKIN-4 DURING THE RESOLUTION OR PROGRESSION OF MURINE LEISHMANIASIS - EVIDENCE FOR EXPANSION OF DISTINCT HELPER T-CELL SUBSETS [J].
HEINZEL, FP ;
SADICK, MD ;
HOLADAY, BJ ;
COFFMAN, RL ;
LOCKSLEY, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (01) :59-72
[8]   PRODUCTION OF INTERFERON-GAMMA, INTERLEUKIN-2, INTERLEUKIN-4, AND INTERLEUKIN-10 BY CD4+ LYMPHOCYTES INVIVO DURING HEALING AND PROGRESSIVE MURINE LEISHMANIASIS [J].
HEINZEL, FP ;
SADICK, MD ;
MUTHA, SS ;
LOCKSLEY, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7011-7015
[9]   ELIMINATION OF CD4+ SUPPRESSOR T-CELLS FROM SUSCEPTIBLE BALB/C MICE RELEASES CD8+ LYMPHOCYTE-T TO MEDIATE PROTECTIVE IMMUNITY AGAINST LEISHMANIA [J].
HILL, JO ;
AWWAD, M ;
NORTH, RJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (05) :1819-1827
[10]  
HOLADAY BJ, 1991, J IMMUNOL, V147, P1653