Development of a natural model of cutaneous leishmaniasis:: Powerful effects of vector saliva and saliva preexposure on the long-term outcome of Leishmania major infection in the mouse ear dermis

被引:334
作者
Belkaid, Y
Kamhawi, S
Modi, G
Valenzuela, J
Noben-Trauth, N
Rowton, E
Ribeiro, J
Sacks, DL
机构
[1] NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[3] Walter Reed Army Med Ctr, Walter Reed Army Inst Res, Dept Entomol, Washington, DC 20307 USA
关键词
Leishmania major; sand flies; saliva; skin; cytokines;
D O I
10.1084/jem.188.10.1941
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 have developed a model of cutaneous leishmaniasis due to Leishmania major that seeks to mimic the natural conditions of infection. 1,000 metacyclic promastigotes were coinoculated with a salivary gland sonicate (SGS) obtained from a natural vector, Phlebotomus payatasii, into the ear dermis of naive mice or of mice preexposed to SGS. The studies reveal a dramatic exacerbating effect of SGS on lesion development in the dermal site, and a complete abrogation of this effect in mice preexposed to salivary components. In both BALB/c and C57B1/6 (B/6) mice, the dermal lesions appeared earlier, were more destructive, and contained greater numbers of parasites after infection ill the presence of SGS. Furthermore, coinoculation of SGS converted B/6 mice into a nonhealing phenotype. No effect of SGS was seen in either IL-4-deficient or in SCID mice. Disease exacerbation in both BALB/c and B/6 mice was associated with an early (6 h) increase in the frequency of epidermal cells producing type 2 cytokines. SGS did not elicit type 2 cytokines in the epidermis of mice previously injected with SGS. These mice made antisaliva antibodies that were able to neutralize the ability of SGS to enhance infection and to elicit IL-4 and IL-5 responses in the epidermis. These results are the first to suggest that for individuals at risk of vector-borne infections, history of exposure to vector saliva, might influence the outcome of exposure to transmitted parasites.
引用
收藏
页码:1941 / 1953
页数:13
相关论文
共 42 条
[1]   A method to recover, enumerate and identify lymphomyeloid cells present in an inflammatory dermal site: A study in laboratory mice [J].
Belkaid, Y ;
Jouin, H ;
Milon, G .
JOURNAL OF IMMUNOLOGICAL METHODS, 1996, 199 (01) :5-25
[2]   THY-1 ANTIGEN-BEARING DENDRITIC CELLS POPULATE MURINE EPIDERMIS [J].
BERGSTRESSER, PR ;
TIGELAAR, RE ;
DEES, JH ;
STREILEIN, JW .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1983, 81 (03) :286-288
[3]   PARASITISM OF EPIDERMAL LANGERHANS CELLS IN EXPERIMENTAL CUTANEOUS LEISHMANIASIS WITH LEISHMANIA-MAJOR [J].
BLANK, C ;
FUCHS, H ;
RAPPERSBERGER, K ;
ROLLINGHOFF, M ;
MOLL, H .
JOURNAL OF INFECTIOUS DISEASES, 1993, 167 (02) :418-425
[4]   An innate view of gamma delta T cells [J].
Boismenu, R ;
Havran, WL .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) :57-63
[5]   ESTABLISHMENT OF STABLE, CELL-MEDIATED-IMMUNITY THAT MAKES SUSCEPTIBLE MICE RESISTANT TO LEISHMANIA-MAJOR [J].
BRETSCHER, PA ;
WEI, GJ ;
MENON, JN ;
BIELEFELDTOHMANN, H .
SCIENCE, 1992, 257 (5069) :539-542
[6]   Leishmania major: Effect of infectious dose on T cell subset development in BALB/c mice [J].
Doherty, TM ;
Coffman, RL .
EXPERIMENTAL PARASITOLOGY, 1996, 84 (02) :124-135
[7]   DIFFERENTIAL PRODUCTION OF INTERFERON-GAMMA AND INTERLEUKIN-4 IN RESPONSE TO TH1-STIMULATING AND TH2-STIMULATING PATHOGENS BY GAMMA-DELTA T-CELLS IN-VIVO [J].
FERRICK, DA ;
SCHRENZEL, MD ;
MULVANIA, T ;
HSIEH, B ;
FERLIN, WG ;
LEPPER, H .
NATURE, 1995, 373 (6511) :255-257
[8]  
GANAPAMO F, 1995, IMMUNOLOGY, V85, P120
[9]   The effect of anti-sandfly saliva antibodies on Phlebotomus argentipes and Leishmania donovani [J].
Ghosh, KN ;
Mukhopadhyay, J .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1998, 28 (02) :275-281
[10]   Recognition of stress-induced MHC molecules by intestinal epithelial γδ T cells [J].
Groh, V ;
Steinle, A ;
Bauer, S ;
Spies, T .
SCIENCE, 1998, 279 (5357) :1737-1740