Temporal changes in cytokine expression of foals during the first month of life

被引:63
作者
Boyd, NK
Cohen, ND [1 ]
Lim, WS
Martens, RJ
Chaffin, MK
Ball, JM
机构
[1] Texas A&M Univ, Coll Vet Med, Dept Large Anim Med & Surg, College Stn, TX 77843 USA
[2] Texas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USA
关键词
cytokines; horse; interleukins; PBMC; immunodeficiency;
D O I
10.1016/S0165-2427(03)00021-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Foals are uniquely susceptible to a wide variety of opportunistic infections normally associated with immunodeficiencies. Little is understood about the immune system of foals during the neonatal period. An apparent age-related susceptibility predisposes neonatal foals to infectious diseases and hinders therapeutic and preventative interventions for these diseases. Cytokine expression is correlated with the type of immune response as well as the severity of a disease. In this study, we measured foal peripheral blood mononuclear cell (PBMC)-specific mRNA cytokine expression from 72 foals from three different farms during the first 4 weeks of life. Interleukin-1alpha (IL-1alpha), IL-1beta, IL-2, IL-4, IL-6 IL-8, IL-10, IL-12p35, IL-12p40, interferon-gamma (IFN-gamma), tumor necrosis factor-alpha (INF-alpha), and transforming growth factor-beta1 (TGF-beta1) were cloned and transcribed in vitro to generate antisense probes for ribonuclease protection assays. Using linear mixed-effect models, we determined that IFN-gamma, TGF-beta1, and IL-1alpha increased significantly (P < 0.05) with age. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:75 / 85
页数:11
相关论文
共 52 条
[1]  
ABBAS AK, 2000, CELLULAR MOL IMMUNOL, P332
[2]  
ABBAS AK, 2000, CELLULAR MOL IMMUNOL, P235
[3]   Adoptive transfer of immunity with intraepithelial lymphocytes in Cryptosporidium parvum-infected severe combined immunodeficient mice [J].
Adjei, AA ;
Shrestha, AK ;
Castro, M ;
Enriquez, FJ .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2000, 320 (05) :304-309
[4]  
Adkins B, 1998, J IMMUNOL, V160, P4217
[5]   T-cell function in newborn mice and humans [J].
Adkins, B .
IMMUNOLOGY TODAY, 1999, 20 (07) :330-335
[6]   The generation of th memory in neonates versus adults: Prolonged primary Th2 effector function and impaired development of Th1 memory effector function in murine neonates [J].
Adkins, P ;
Bu, YR ;
Guevara, P .
JOURNAL OF IMMUNOLOGY, 2001, 166 (02) :918-925
[7]  
Balkwill F., 2000, CYTOKINE NETWORK
[8]   Partial correction of the TH2/TH1 imbalance in neonatal murine responses to vaccine antigens through selective adjuvant effects [J].
Barrios, C ;
Brandt, C ;
Berney, M ;
Lambert, PH ;
Siegrist, CA .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (11) :2666-2670
[9]   Neonatal and early life immune responses to various forms of vaccine antigens qualitatively differ from adult responses: Predominance of a Th2-biased pattern which persists after adult boosting [J].
Barrios, C ;
Brawand, P ;
Berney, M ;
Brandt, C ;
Lambert, PH ;
Siegrist, CA .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (07) :1489-1496
[10]   FACTORS ASSOCIATED WITH FAILURE OF PASSIVE TRANSFER OF COLOSTRAL ANTIBODIES IN STANDARD-BRED FOALS [J].
CLABOUGH, DL ;
LEVINE, JF ;
GRANT, GL ;
CONBOY, HS .
JOURNAL OF VETERINARY INTERNAL MEDICINE, 1991, 5 (06) :335-340