Transgenic overexpression of human IL-17E results in eosinophilia, B-lymphocyte hyperplasia, and altered antibody production

被引:158
作者
Kim, MR
Manoukian, R
Yeh, R
Silbiger, SM
Danilenko, DM
Scully, S
Sun, JL
DeRose, ML
Stolina, M
Chang, D
Van, GY
Clarkin, K
Nguyen, HQ
Yu, YB
Jing, SQ
Senaldi, G
Elliott, G
Medlock, ES
机构
[1] Amgen Inc, Dept Pathol, Thousand Oaks, CA 91302 USA
[2] Amgen Inc, Dept Inflammat, Thousand Oaks, CA 91302 USA
[3] Amgen Inc, Dept Clin Immunol, Thousand Oaks, CA 91302 USA
[4] Amgen Inc, Dept Prot Sci, Thousand Oaks, CA 91302 USA
[5] Amgen Inc, Dept Functional Genom, Thousand Oaks, CA 91302 USA
关键词
D O I
10.1182/blood-2002-01-0012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have Identified and cloned a novel human cytokine with homology to cytokines of the Interleukin-17 (IL-17) family, which we have termed human IL-17E (hIL17E). With the identification of several IL-17 family members, it is critical to understand the in vivo function of these molecules. We have generated transgenic mice overexpressing hIL-17E using an apolipoprotein E (ApoE) hepatic promoter. These mice displayed changes In the peripheral blood, particularly, a 3-fold Increase in total leukocytes consisting of increases In eosinophils, lymphocytes, and neutrophils. Splenomegally and lymphoadenopathy were predominant and Included marked eosinophil Infiltrates and lymphoid hyperplasla. CCR3(+) eosinophils Increased In the blood and lymph nodes of the transgenic mice by 50- and 300-fold, respectively. Eosinophils also increased 8- to 18-fold In the bone marrow and spleen, respectively. In the bone marrow, most of the eosinophils had an Immature appearance. CD19(+) B cells Increased 2- to 5-fold In the peripheral blood, 2-fold In the spleen, and 10-fold In the lymph nodes of transgenic mice, whereas CD4(+) T lymphocytes Increased 2-fold In both blood and spleen. High serum levels of the cytokines IL-2, IL-4, IL-5, granulocyte colony-stimulating factor, eotaxin, and Interferon gamma were observed. Consistent with B-lymphocyte increases, serum immunoglobulin (1g) M, IgG, and IgE were significantly elevated. Antigenic challenge of the transgenic mice with keyhole limpet hemocyanin (KLH) resulted in a decrease In anti-KLH IgG accompanied by increases of anti-KLH IgA and IgE. In situ hybridization of transgenic tissues revealed that IL-11 7Rh1 (IL-17BR/Ev127), a receptor that binds IL-17E, Is up-regulated. Taken together, these data Indicate that IL-17E regulates hematopoietic and Immune functions, stimulating the development of eosinophils and B lymphocytes. The fact that hIL-17E overexpression results In high levels of circulating eosinophils, IL-4, IL-5, eotaxin, and IgE suggests that IL-17E may be a proinflammatory cytokine favoring Th2-type Immune responses. (C) 2002 by The American Society of Hematology.
引用
收藏
页码:2330 / 2340
页数:11
相关论文
共 60 条
[1]  
Aarvak T, 1999, J IMMUNOL, V162, P1246
[2]   Interleukin-17 is produced by both Th1 and Th2 lymphocytes, and modulates interferon-γ- and interleukin-4-induced activation of human keratinocytes [J].
Albanesi, C ;
Scarponi, CS ;
Cavani, A ;
Federici, M ;
Nasorri, F ;
Girolomoni, G .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 115 (01) :81-87
[3]  
Albanesi C, 1999, J IMMUNOL, V162, P494
[4]  
Antonysamy MA, 1999, J IMMUNOL, V162, P577
[5]   Interleukin-17 up-regulation of nitric oxide production in human osteoarthritis cartilage [J].
Attur, MG ;
Patel, RN ;
Abramson, SB ;
Amin, AR .
ARTHRITIS AND RHEUMATISM, 1997, 40 (06) :1050-1053
[6]  
Belov L, 2001, CANCER RES, V61, P4483
[7]   CD5 AND CD21 MOLECULES ARE A FUNCTIONAL UNIT IN THE CELL SUBSTRATE ADHESION OF B-CHRONIC LYMPHOCYTIC-LEUKEMIA CELLS [J].
BERGUI, L ;
TESIO, L ;
SCHENA, M ;
RIVA, M ;
MALAVASI, F ;
SCHULZ, T ;
MARCHISIO, PC ;
CALIGARISCAPPIO, F .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (01) :89-96
[8]   FACTORS AFFECTING THE EFFICIENCY OF INTRODUCING FOREIGN DNA INTO MICE BY MICROINJECTING EGGS [J].
BRINSTER, RL ;
CHEN, HY ;
TRUMBAUER, ME ;
YAGLE, MK ;
PALMITER, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (13) :4438-4442
[9]   Analysis of residual disease in chronic lymphocytic leukemia by flow cytometry [J].
Cabezudo, E ;
Matutes, E ;
Ramrattan, M ;
Morilla, R ;
Catovsky, D .
LEUKEMIA, 1997, 11 (11) :1909-1914
[10]   CYTOKINE REGULATION OF B-CELL GROWTH AND DIFFERENTIATION [J].
CALLARD, RE .
BRITISH MEDICAL BULLETIN, 1989, 45 (02) :371-388