When renal allografts turn darc.

被引:37
作者
Segerer, S
Böhmig, GA
Exner, M
Colin, Y
Cartron, JP
Kerjaschki, D
Schlöndorff, D
Regele, H
机构
[1] Univ Munich, Klinikum Innenstadt, Med Poliklin, D-80336 Munich, Germany
[2] Univ Vienna, Dept Internal Med 3, Vienna, Austria
[3] Univ Vienna, Dept Lab Med, Vienna, Austria
[4] Inst Natl Sante & Rech Med U76, Paris, France
[5] Univ Vienna, Clin Inst Pathol, Vienna, Austria
关键词
D O I
10.1097/01.TP.0000054679.91112.6F
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The Duffy antigen-receptor for chemokines (DARC) is a chemokine-binding protein that is up-regulated on peritubular capillaries (PTC) during cellular renal allograft rejection. C4d deposition and accumulation of inflammatory cells in PTC are indicators of humoral renal allograft rejection. Because DARC is expressed at the site of C4d deposition and might be involved. in inflammatory cell recruitment, the authors evaluated the expression of DARC in different forms of human renal allograft rejection. Methods. Deposition of C4d and DARC expression were evaluated by immunohistochemistry in 42 renal transplant biopsy specimens. Biopsy specimens were subdivided according to histologic and immunohistochemical results, that is, C4d-negative biopsy specimens with (Banff 1, n=8) or without signs of cellular rejection (n=16), and C4d-positive biopsies (humoral rejection) with (Banff 1 rejection, n=7) or without cellular rejection (n=11). Results. DARC expression was found on a small number of PTC and veins in patients without rejection. Cellular and humoral rejection led to a comparable increase in the number of DARC-positive PTC (9.7 and 8.7 vs. 2.6 vessels per high-power field [HPF], respectively). The highest numbers were found in biopsy specimens with signs of both humoral and cellular rejection (17.5 vessels per HPF). Conclusions. This is the first study that demonstrates an induction of a chemokine-binding protein at the site of C4d deposition in humoral allograft rejection. The additive effect of humoral and cellular rejection on DARC expression might imply different pathways of DARC induction for different forms of allograft rejection.
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收藏
页码:1030 / 1034
页数:5
相关论文
共 30 条
  • [1] Böhmig GA, 2002, J AM SOC NEPHROL, V13, DOI 10.1681/ASN.V1341091
  • [2] Bohmig Georg A, 2002, Curr Opin Urol, V12, P95, DOI 10.1097/00042307-200203000-00003
  • [3] Interleukin-8 expression in patients after renal transplantation
    Budde, K
    Waiser, J
    Ceska, M
    Katalinic, A
    Kurzdorfer, M
    Neumayer, HH
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1997, 29 (06) : 871 - 880
  • [4] Insights into the structure and function of membrane polypeptides carrying blood group antigens
    Cartron, JP
    Bailly, P
    Le van Kim, C
    Cherif-Zahar, B
    Matassi, G
    Bertrand, O
    Colin, Y
    [J]. VOX SANGUINIS, 1998, 74 : 29 - 64
  • [5] Collins AB, 1999, J AM SOC NEPHROL, V10, P2208
  • [6] Chemokines, their receptors, and transplant outcome
    Colvin, BL
    Thomson, AW
    [J]. TRANSPLANTATION, 2002, 74 (02) : 149 - 155
  • [7] RED-BLOOD-CELLS ARE A SINK FOR INTERLEUKIN-8, A LEUKOCYTE CHEMOTAXIN
    DARBONNE, WC
    RICE, GC
    MOHLER, MA
    APPLE, T
    HEBERT, CA
    VALENTE, AJ
    BAKER, JB
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (04) : 1362 - 1369
  • [8] Exaggerated response to endotoxin in mice lacking the Duffy antigen/receptor for chemokines (DARC)
    Dawson, TC
    Lentsch, AB
    Wang, ZX
    Cowhig, JE
    Rot, A
    Maeda, N
    Peiper, SC
    [J]. BLOOD, 2000, 96 (05) : 1681 - 1684
  • [9] CAPILLARY DEPOSITION OF C4D COMPLEMENT FRAGMENT AND EARLY RENAL GRAFT LOSS
    FEUCHT, HE
    SCHNEEBERGER, H
    HILLEBRAND, G
    BURKHARDT, K
    WEISS, M
    RIETHMULLER, G
    LAND, W
    ALBERT, E
    [J]. KIDNEY INTERNATIONAL, 1993, 43 (06) : 1333 - 1338
  • [10] Heterogeneity of endothelial cells - The specialized phenotype of human high endothelial venules characterized by suppression subtractive hybridization
    Girard, JP
    Baekkevold, ES
    Yamanaka, T
    Haraldsen, G
    Brandtzaeg, P
    Amalric, F
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (06) : 2043 - 2055