A critical role for IL-21 in regulating immunoglobulin production

被引:793
作者
Ozaki, K
Spolski, R
Feng, CG
Qi, CF
Cheng, J
Sher, A
Morse, HC
Liu, CY
Schwartzberg, PL
Leonard, WJ
机构
[1] NHLBI, Lab Mol Immunol, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Transgen Facil, NIH, Bethesda, MD 20892 USA
[3] NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[4] NIAID, Immunopathol Lab, NIH, Bethesda, MD 20892 USA
[5] NHGRI, Genet Dis Res Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1126/science.1077002
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The cytokine interleukin-21 (IL-21) is closely related to IL-2 and IL-15, and their receptors all share the common cytokine receptor gamma chain, gamma(c), which is mutated in humans with X-linked severe combined immunodeficiency disease (XSCID). We demonstrate that, although mice deficient in the receptor for IL-21 (IL-21R) have normal lymphoid development, after immunization, these animals have higher production of the immunoglobulin IgE, but lower IgG1, than wild-type animals. Mice lacking both IL-4 and IL-21R exhibited a significantly more pronounced phenotype, with dysgammaglobulinemia, characterized primarily by a severely impaired IgG response. Thus, IL-21 has a significant influence on the regulation of B cell function in vivo and cooperates with IL-4. This suggests that these gamma(c)-dependent cytokines may be those whose inactivation is primarily responsible for the B cell defect in humans with XSCID.
引用
收藏
页码:1630 / 1634
页数:5
相关论文
共 32 条
[1]  
[Anonymous], UNPUB
[2]   Cutting edge:: The common γ-chain is an indispensable subunit of the IL-21 receptor complex [J].
Asao, H ;
Okuyama, C ;
Kumaki, S ;
Ishii, N ;
Tsuchiya, S ;
Foster, D ;
Sugamura, K .
JOURNAL OF IMMUNOLOGY, 2001, 167 (01) :1-5
[3]  
BUCKLEY R, 1993, FASEB J, V7, pA95
[4]   Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency [J].
Buckley, RH ;
Schiff, SE ;
Schiff, RI ;
Markert, ML ;
Williams, LW ;
Roberts, JL ;
Myers, LA ;
Ward, FE .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (07) :508-516
[5]   Human severe combined immunodeficiency: Genetic, phenotypic, and functional diversity in one hundred eight infants [J].
Buckley, RH ;
Schiff, RI ;
Schiff, SE ;
Markert, ML ;
Williams, LW ;
Harville, TO ;
Roberts, JL ;
Puck, JM .
JOURNAL OF PEDIATRICS, 1997, 130 (03) :378-387
[6]  
BUCKLEY RH, COMMUNICATION
[7]   DEFECTIVE LYMPHOID DEVELOPMENT IN MICE LACKING EXPRESSION OF THE COMMON CYTOKINE RECEPTOR-GAMMA CHAIN [J].
CAO, XQ ;
SHORES, EW ;
HULI, J ;
ANVER, MR ;
KELSALL, BL ;
RUSSELL, SM ;
DRAGO, J ;
NOGUCHI, M ;
GRINBERG, A ;
BLOOM, ET ;
PAUL, WE ;
KATZ, SI ;
LOVE, PE ;
LEONARD, WJ .
IMMUNITY, 1995, 2 (03) :223-238
[8]   Role of interleukin-2 (IL-2), IL-7, and IL-15 in natural killer cell differentiation from cord blood hematopoietic progenitor cells and from gamma c transduced severe combined immunodeficiency XI bone marrow cells [J].
CavazzanaCalvo, M ;
HaceinBey, S ;
Basile, GD ;
DeCoene, C ;
Selz, F ;
LeDeist, F ;
Fischer, A .
BLOOD, 1996, 88 (10) :3901-3909
[9]   NONRANDOM X-CHROMOSOME INACTIVATION IN B-CELLS FROM CARRIERS OF X-CHROMOSOME-LINKED SEVERE COMBINED IMMUNODEFICIENCY [J].
CONLEY, ME ;
LAVOIE, A ;
BRIGGS, C ;
BROWN, P ;
GUERRA, C ;
PUCK, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (09) :3090-3094
[10]   X-LINKED SEVERE COMBINED IMMUNODEFICIENCY [J].
CONLEY, ME .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1991, 61 (02) :S94-S99