Use of genetic profiling in leprosy to discriminate clinical forms of the disease

被引:127
作者
Bleharski, JR
Li, HY
Meinken, C
Graeber, TG
Ochoa, MT
Yamamura, M
Burdick, A
Sarno, EN
Wagner, M
Röllinghoff, M
Rea, TH
Colonna, M
Stenger, S
Bloom, BR
Eisenberg, D
Modlin, RL [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Div Dermatol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, UCLA Dept Energy Inst Genom & Proteom, Howard Hughes Med Inst, Dept Biol Chem, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[5] Univ Erlangen Nurnberg, Inst Klin Mikrobiol Immunol & Hyg, D-91054 Erlangen, Germany
[6] Okayama Univ, Grad Sch Med & Dent, Okayama, Japan
[7] Univ Miami, Dept Dermatol & Cutaneous Surg, Miami, FL 33101 USA
[8] Inst Oswaldo Cruz, Leprosy Lab, BR-20001 Rio De Janeiro, Brazil
[9] Klinikum Nurnberg, Med Klin 3, D-90340 Nurnberg, Germany
[10] Univ So Calif, Sch Med, Dermatol Sect, Los Angeles, CA 90033 USA
[11] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[12] Harvard Univ, Sch Publ Hlth, Off Dean, Boston, MA 02115 USA
关键词
D O I
10.1126/science.1087785
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
Leprosy presents as a clinical and immunological spectrum of disease. With the use of gene expression pro. ling, we observed that a distinction in gene expression correlates with and accurately classifies the clinical form of the disease. Genes belonging to the leukocyte immunoglobulin-like receptor (LIR) family were significantly up-regulated in lesions of lepromatous patients suffering from the disseminated form of the infection. In functional studies, LIR-7 suppressed innate host defense mechanisms by shifting monocyte production from interleukin-12 toward interleukin-10 and by blocking antimicrobial activity triggered by Toll-like receptors. Gene expression profiles may be useful in de. ning clinical forms of disease and providing insights into the regulation of immune responses to pathogens.
引用
收藏
页码:1527 / 1530
页数:4
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