Impaired Th2 subset development in the absence of CD4

被引:103
作者
Fowell, DJ
Magram, J
Turck, CW
Killeen, N
Locksley, RM
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT MED,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,DEPT IMMUNOL & MICROBIOL,SAN FRANCISCO,CA 94143
[3] UNIV CALIF SAN FRANCISCO,HOWARD HUGHES MED INST,SAN FRANCISCO,CA 94143
[4] HOFFMANN LA ROCHE INC,DEPT INFLAMMAT AUTOIMMUNE DIS,NUTLEY,NJ 07110
关键词
D O I
10.1016/S1074-7613(00)80344-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Prior studies in CD4-deficient mice established the capacity of T helper (Th) lineage cells to mature into Th1 cells. Unexpectedly, challenge of these mice with Nippostrongylus brasiliensis, a Th2-inducing stimulus, failed to result in the development of Th2 cells. Additional studies were performed using CD4(+) or CD4(-)CD8(-) (double-negative) T cell receptor (TCR) transgenic T cells reactive to LACK antigen of Leishmania major. Double-negative T cells were unable to develop into Th2 cells in vivo, and, unlike CD4(+) T cells, could not be primed for interleukin-4 production in vitro. Similarly, CD4(+) TCR transgenic T cells primed on antigen-presenting cells expressing mutant MHC class II molecules unable to bind CD4 did not differentiate into Th2 cells. These data suggest that interactions between the TCR, MHC II-peptide complex and CD4 may be involved in Th2 development.
引用
收藏
页码:559 / 569
页数:11
相关论文
共 68 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]   A SUBSET OF CD4(+) THYMOCYTES SELECTED BY MHC CLASS-I MOLECULES [J].
BENDELAC, A ;
KILLEEN, N ;
LITTMAN, DR ;
SCHWARTZ, RH .
SCIENCE, 1994, 263 (5154) :1774-1778
[3]   EASILY PREPARED DEFINED MEDIUM FOR CULTIVATION OF LEISHMANIA-DONOVANI PROMASTIGOTES [J].
BERENS, RL ;
MARR, JJ .
JOURNAL OF PARASITOLOGY, 1978, 64 (01) :160-160
[4]   beta 2-microglobulin-dependent NK1.1(+) T cells are not essential for T helper cell 2 immune responses [J].
Brown, DR ;
Fowell, DJ ;
Corry, DB ;
Wynn, TA ;
Moskowitz, NH ;
Cheever, AW ;
Locksley, RM ;
Reiner, SL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (04) :1295-1304
[5]   The alpha beta T cell receptor can replace the gamma delta receptor in the development of gamma delta lineage cells [J].
Bruno, L ;
Fehling, HJ ;
vonBoehmer, H .
IMMUNITY, 1996, 5 (04) :343-352
[6]   IDENTIFICATION OF A CD4 BINDING-SITE ON THE BETA-2-DOMAIN OF HLA-DR MOLECULES [J].
CAMMAROTA, G ;
SCHEIRLE, A ;
TAKACS, B ;
DORAN, DM ;
KNORR, R ;
BANNWARTH, W ;
GUARDIOLA, J ;
SINIGAGLIA, F .
NATURE, 1992, 356 (6372) :799-801
[7]  
CAPONE M, 1995, J IMMUNOL, V154, P5165
[8]   DEMETHYLATED CD8 GENE IN CD4+ T-CELLS SUGGESTS THAT CD4+ CELLS DEVELOP FROM CD8+ PRECURSORS [J].
CARBONE, AM ;
MARRACK, P ;
KAPPLER, JW .
SCIENCE, 1988, 242 (4882) :1174-1176
[9]  
CHAN AC, 1994, J IMMUNOL, V152, P4758
[10]   EXTENT OF T-CELL RECEPTOR LIGATION CAN DETERMINE THE FUNCTIONAL-DIFFERENTIATION OF NAIVE CD4(+) T-CELLS [J].
CONSTANT, S ;
PFEIFFER, C ;
WOODARD, A ;
PASQUALINI, T ;
BOTTOMLY, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (05) :1591-1596