Soluble CD26 is inversely Associated with Disease Severity in Patients with Chronic Eosinophilic Pneumonia

被引:0
作者
Matsuno, Osamu [1 ]
Miyazaki, Eishi [1 ]
Nureki, Shinichi [1 ]
Ueno, Takuya [1 ]
Ando, Masaru [1 ]
Kumamoto, Toshihide [1 ]
机构
[1] Oita Univ Fac Med, Dept Brain & Nerve Sci, Div Resp Dis, Ufu, Oita 8795593, Japan
关键词
CD26; eosinophilic pneumonia;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Backgrounds: CD26, a multifunctional T cell surface glycoprotein, is a type II transmembrane protein containing only six amino acid residues in its cytoplasmic region. In addition to its membrane form, CD26 exists in plasma in a soluble form (sCD26), which is thought to be the extracellular domain of the molecule cleaved from the cell surface. Recent studies indicated CD26 have an important role in the pathogenesis of asthma, known as Th2 like disease. The function of CD26 in the esosinophlic lung disease is not well understood. Methods: Serum sCD26 was determined by enzyme-linked immunosorbent assay in patients with acute eosinophilic pneumonia, chronic eosinophilic pneumonia (CEP), and sarcoidosis, and in healthy volunteers, to establish its value for discriminating between disease entities and as marker of disease activity. Results: Soluble CD26 was significantly reduced in CEP and was related to disease severity. In particular, sCD26 was inversely correlated with arterial oxygen tension in CEP. Conclusion: Serum levels of sCD26 might appear to be useful as a new marker of CEP disease activity.
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页码:201 / 204
页数:4
相关论文
共 19 条
[1]   ACUTE EOSINOPHILIC PNEUMONIA AS A REVERSIBLE CAUSE OF NONINFECTIOUS RESPIRATORY-FAILURE [J].
ALLEN, JN ;
PACHT, ER ;
GADEK, JE ;
DAVIS, WB .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (09) :569-574
[2]   Circulating CD26 is negatively associated with inflammation in human and experimental arthritis [J].
Busso, N ;
Wagtmann, N ;
Herling, C ;
Chobaz-Péclat, V ;
Bischof-Delaloye, A ;
So, A ;
Grouzmann, E .
AMERICAN JOURNAL OF PATHOLOGY, 2005, 166 (02) :433-442
[3]   CHRONIC EOSINOPHILIC PNEUMONIA [J].
CARRINGT.CB ;
ADDINGTO.WW ;
GOFF, AM ;
MADOFF, IM ;
MARKS, A ;
SCHWABER, JR ;
GAENSLER, EA .
NEW ENGLAND JOURNAL OF MEDICINE, 1969, 280 (15) :787-&
[4]   Interleukin-12-dependent activation of human lymphocyte subsets [J].
Cordero, OJ ;
Salgado, FJ ;
Viñuela, JE ;
Nogueira, M .
IMMUNOLOGY LETTERS, 1998, 61 (01) :7-13
[5]  
DANG NH, 1990, J IMMUNOL, V145, P3963
[6]   CD26, let it cut or cut it down [J].
De Meester, I ;
Korom, S ;
Van Damme, J ;
Scharpé, S .
IMMUNOLOGY TODAY, 1999, 20 (08) :367-375
[7]  
Dong RP, 1997, J IMMUNOL, V159, P6070
[8]   Endothelial catabolism of extracellular adenosine during hypoxia: the role of surface adenosine deaminase and CD26 [J].
Eltzschig, Holger K. ;
Faigle, Marion ;
Knapp, Simone ;
Karhausen, Jorn ;
Ibla, Juan ;
Rosenberger, Peter ;
Odegard, Kirsten C. ;
Laussen, Peter C. ;
Thompson, Linda F. ;
Colgan, Sean P. .
BLOOD, 2006, 108 (05) :1602-1610
[9]   Dipeptidyl peptidase IV (DP IV, CD26) in patients with inflammatory bowel disease [J].
Hildebrandt, M ;
Rose, N ;
Rüter, J ;
Salama, A ;
Mönnikes, H ;
Klapp, BF .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2001, 36 (10) :1067-1072
[10]   CD26-mediated signaling for T cell activation occurs in lipid rafts through its association with CD45RO [J].
Ishii, T ;
Ohnuma, K ;
Murakami, A ;
Takasawa, N ;
Kobayashi, S ;
Dang, NH ;
Schlossman, SF ;
Morimoto, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) :12138-12143