A Leishmania major response locus identified by interval-specific congenic mapping of a T helper type 2 cell bias-controlling quantitative trait locus

被引:22
作者
Baguet, A [1 ]
Epler, J [1 ]
Wen, KW [1 ]
Bix, M [1 ]
机构
[1] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
关键词
early IL-4; naive T cell; BALB/C; Dice; IL-4;
D O I
10.1084/jem.20040334
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 propensity of naive CD4 T cells to become T helper (Th) type 2 cells correlates with susceptibility to infection by the protozoal parasite Leishmania major. Using genetic linkage analysis, we earlier identified Dice 1 as a Th2 cell bias-controlling quantitative trait locus on chromosome 16. Using interval-specific congenic mapping, we now resolve Dice 1 into two independent genetic loci, Dice 1.1 and Dice 1.2, which control Il4 expression front naive Th cells and thereby indirectly control Th2 cell bias. Interestingly, only one of the two congenic intervals containing Dice 1.1 and Dice 1.2, respectively, also contained an L. major response locus, indicating that L. Major responsiveness can be insensitive to determinants that influence Th2 cell bias by controlling naive T cell Il4 expression. These results lay the groundwork for identifying the Dice 1.1 and Dice 1.2 genes controlling naive T cell Il4 expression and L. major responses, and for testing whether these control other Th2 cell-dependent processes such as worm expulsion, allergic asthma, and dermatitis.
引用
收藏
页码:1605 / 1612
页数:8
相关论文
共 29 条
[1]   Serial backcross mapping of multiple loci associated with resistance to Leishmania major in mice [J].
Beebe, AM ;
Mauze, S ;
Schork, NJ ;
Coffman, RL .
IMMUNITY, 1997, 6 (05) :551-557
[2]   Genetic regulation of commitment to interleukin 4 production by a CD4+ T cell-intrinsic mechanism [J].
Bix, M ;
Wang, ZE ;
Thiel, B ;
Schork, NJ ;
Locksley, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (12) :2289-2299
[3]   Interleukin 4, but not interleukin 5 or eosinophils, is required in a murine model of acute airway hyperreactivity [J].
Corry, DB ;
Folkesson, HG ;
Warnock, ML ;
Erle, DJ ;
Matthay, MA ;
WienerKronish, JP ;
Locksley, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (01) :109-117
[4]   Inhibition of Th1 differentiation by IL-6 is mediated by SOCS1 [J].
Diehl, S ;
Anguita, J ;
Hoffmeyer, A ;
Zapton, T ;
Ihle, JN ;
Fikrig, E ;
Rincón, M .
IMMUNITY, 2000, 13 (06) :805-815
[5]   Leishmaniasis host response loci (lmr1-3) modify disease severity through a Th1/Th2-independent pathway [J].
Elso, CM ;
Roberts, LJ ;
Smyth, GK ;
Thomson, RJ ;
Baldwin, TM ;
Foote, SJ ;
Handman, E .
GENES AND IMMUNITY, 2004, 5 (02) :93-100
[6]   Quantitative trait loci controlling allergen-induced airway hyperresponsiveness in inbred mice [J].
Ewart, SL ;
Kuperman, D ;
Schadt, E ;
Tankersley, C ;
Grupe, A ;
Shubitowski, DM ;
Peltz, G ;
Wills-Karp, M .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2000, 23 (04) :537-545
[7]  
Fang Nan, 2002, Curr Dir Autoimmun, V5, P161
[8]  
Finkelman FD, 2001, J ALLERGY CLIN IMMUN, V107, P772, DOI 10.1067/mai.2001.114989
[9]   Finding genes that underlie complex traits [J].
Glazier, AM ;
Nadeau, JH ;
Aitman, TJ .
SCIENCE, 2002, 298 (5602) :2345-2349
[10]  
Gordon BC, 2002, CONTRIB CIRCUMPOL AN, V2, P53