Summary of the animal homologue section of HLDA8

被引:66
作者
Saalmüller, A [1 ]
Lunney, JK
Daubenberger, C
Davis, W
Fischer, U
Göbel, TW
Griebel, P
Hollemweguer, E
Lasco, T
Meister, R
Schuberth, HJ
Sestak, K
Sopp, P
Steinbach, F
Wu, XW
Aasted, B
机构
[1] Vet Univ Vienna, A-1030 Vienna, Austria
[2] USDA, ARS, APDL, BARC, Beltsville, MD 20705 USA
[3] Swiss Trop Inst, CH-4002 Basel, Switzerland
[4] Washington State Univ, Pullman, WA 99164 USA
[5] Univ Munich, Munich, Germany
[6] Univ Saskatchewan, Saskatoon, SK, Canada
[7] BD Biosci Pharmingen, San Diego, CA USA
[8] Colorado State Univ, Ft Collins, CO 80523 USA
[9] Ohio State Univ, Columbus, OH 43210 USA
[10] Sch Vet Med, D-3000 Hannover, Germany
[11] Tulane Natl Primate Res Ctr, Covington, LA USA
[12] Inst Anim Hlth, Compton, England
[13] Leibniz Inst Zoo & Wildlife Res, Berlin, Germany
[14] Royal Vet & Agr Univ, Copenhagen, Denmark
关键词
animal homologues; CD molecules; cross-reactivity; veterinary immunology; evolution;
D O I
10.1016/j.cellimm.2005.08.009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Development of reagents against leukocyte differentiation antigens in veterinary immunology is slower compared to humans and mice. Cross-reactivity studies with monoclonal antibodies (mAb) generated against human molecules represent an excellent approach for the detection of new reagents for the minor characterised species. Three hundred seventy-seven commercially available mAb from different companies were tested for their reactivity with cells from 17 species-including non-human primates, ruminants, swine, horse, carnivores, rabbit, guinea pig, chicken and fish. In a first round of testing by flow cytometry (FCM) 182 mAb showed reactivity with atleast one of the species described above. Most of the cross-reactivity was found against non-human primate leukocytes, but also species in evolutionarily more distant from humans showed in some cases a clear staining pattern in flow cytometry (FCM). In a seeond round these FCM-results were confirmed by molecular analyses, by immunoprecipitation studies and analyses on transfectants. Interesting was the broad species-overlapping reactivity of mAb directed against CD9 (11 out of 17 species), CD11a (11/17), CD14 (11/17) CD18 (13/17), CD21 (7/17), CD29 (10/17), CD44 (13/17), CD45 (9/17), CD47 (10/17), and CD49d (13/17), CD61 (6/17), CD86 (7/17), CD91 (5/17), and CD172a (10/17), indicating evolutionary highly conserved epitopes on these surface molecules. Our results suggest the suitability of crossreactive mAb for the animal model studies. Moreover, these findings contribute to our understanding of the evolution of the immune system. Supported by the Veterinary Immunology Committee of IUIS. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:51 / 58
页数:8
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