Soluble donor HLA class I and β2m-free heavy chain in serum of lung transplant recipients:: Steady-state levels and increases in patients with recurrent CMV infection, acute rejection episodes, and poor outcome

被引:12
作者
De Vito-Haynes, LD
Jankowska-Gan, E
Meyer, KC
Cornwell, RD
Zeevi, A
Griffith, B
Dauber, J
Iacono, A
Burlingham, WJ
Love, RB
机构
[1] Univ Wisconsin, Dept Surg, Madison, WI 53792 USA
[2] Univ Wisconsin, Dept Med, Madison, WI USA
[3] Univ Pittsburgh, Dept Transplant Pathol, Pittsburgh, PA USA
关键词
acute rejection; CMV; HLA class I; lung transplantation;
D O I
10.1016/S0198-8859(00)00210-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We determined the concentration of donor sHLA/beta (2)m and total beta (2)m-free heavy chain (HC) in the serum of lung transplant recipients with ELISA assays. While we were unable to detect specific donor beta (2)m-free HCs due to a lack of available antibodies, we could determine if events chat led to an increase in the release of beta (2)m-free HC also led to an increase in the release of donor sHLA/beta (2)m, particularly the 36 kDa, proteolytically cleaved form. We found that lung transplants constituitively release donor sHLA/beta (2)m at ng/ml levels. The levels (bot-h of donor sHLA/beta (2)m and total beta (2)m-free HIC) were significantly increased in CMV-sero-negative recipients (but not in CMV-sero-positive recipients) at the onset of post-transplant CMV disease. Acute rejection episodes were also associated with an increased release of donor sHLA/beta (2)m, but not of beta (2)m-free HC. However, in patients with particularly poor outcome (i.e., graft loss within 1 year) there was a significant release of beta (2)m-free HC. Analysis of one such patient showed a predominance of 36 kDa forms of donor-sHLA/beta (2)m. Our data are consistent with the hypothesis that the metalloproteinase thar cleaves beta (2)m-free HC is active during uncontrolled CMV infection and acute rejection. However, recall responses to CMV and controlled immune responses to donor may result in little or no activation of sHLA class I release, (C) American Society for Histocompatibility and Immunogenetics, 2000. Published by Elsevier Science Inc.
引用
收藏
页码:1370 / 1382
页数:13
相关论文
共 53 条
[21]   BIOENGINEERED SOLUBLE HLA-B7 - GENESIS, CHARACTERIZATION, AND OCCURRENCE OF DIMERIZATION [J].
HIRAKI, DD ;
SEETHO, K ;
FILVAROFF, E ;
KRISHNASWAMY, S ;
DEBELLO, W ;
TAIDILASKOWSKI, B ;
GRUMET, FC .
HUMAN IMMUNOLOGY, 1994, 40 (03) :235-246
[22]   The application of human monoclonal antibodies for monitoring donor derived soluble HLA class I molecules in the serum of heart transplant recipients [J].
Koelman, CA ;
Mulder, A ;
Jutte, NHPM ;
Vaessen, LMB ;
Balk, AHMM ;
Weimar, W ;
Doxiadis, IIN ;
Claas, FHJ .
HUMAN IMMUNOLOGY, 1998, 59 (02) :106-114
[23]   SECRETION OF HLA-A AND HLA-B ANTIGENS VIA AN ALTERNATIVE RNA SPLICING PATHWAY [J].
KRANGEL, MS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 163 (05) :1173-1190
[24]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[25]   INDIRECT RECOGNITION BY HELPER-CELLS CAN INDUCE DONOR-SPECIFIC CYTOTOXIC T-LYMPHOCYTES IN-VIVO [J].
LEE, RS ;
GRUSBY, MJ ;
GLIMCHER, LH ;
WINN, HJ ;
AUCHINCLOSS, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (03) :865-872
[26]   Biochemical and immunological evaluation of donor-specific soluble HLA in the circulation of liver transplant recipients [J].
Mathew, JM ;
Shenoy, S ;
Phelan, D ;
Lowell, J ;
Howard, T ;
Mohanakumar, T .
TRANSPLANTATION, 1996, 62 (02) :217-223
[27]   Anti-HLA antibodies after solid organ transplantation [J].
McKenna, RM ;
Takemoto, SK ;
Terasaki, PI .
TRANSPLANTATION, 2000, 69 (03) :319-326
[28]   A MONOCLONAL-ANTIBODY THAT RECOGNIZES AN ANTIGENIC DETERMINANT SHARED BY HLA-A2 AND HLA-B17 [J].
MCMICHAEL, AJ ;
PARHAM, P ;
RUST, N ;
BRODSKY, F .
HUMAN IMMUNOLOGY, 1980, 1 (02) :121-129
[29]  
McMillan RW, 1997, CLIN TRANSPLANT, V11, P98
[30]   Human cytomegalovirus inhibits major histocompatibility complex class II expression by disruption of the Jak/Stat pathway [J].
Miller, DM ;
Rahill, BM ;
Boss, JM ;
Lairmore, MD ;
Durbin, JE ;
Waldman, WJ ;
Sedmak, DD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (05) :675-683