Decreased serum levels of Clara cell secretory protein (CC16) are associated with bronchiolitis obliterans and may permit early diagnosis in patients after allogeneic stem-cell transplantation

被引:39
作者
Mattsson, J [1 ]
Remberger, M
Andersson, O
Sundberg, B
Nord, M
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Ctr Allogeneic Stem Cell Transplantat, SE-14186 Stockholm, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Dept Clin Immunol, SE-14186 Stockholm, Sweden
[3] Karolinska Univ Hosp, Karolinska Inst, Dept Med Nutr, SE-14186 Stockholm, Sweden
[4] Karolinska Univ Hosp, Dept Lung Med, SE-14186 Stockholm, Sweden
关键词
Clara cell secretory protein (CC16); bronchiolitis obliterans; small airway disease; stem-cell transplantation; chronic graft-versus-host disease;
D O I
10.1097/01.TP.0000158354.39635.AB
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. Bronchiolitis obliterans (130) is a common complication and is associated with high mortality after allogeneic stem-cell transplantation (SCT). Early diagnosis of 130 may improve outcome. Low levels of Clara cell secretory protein (CC16) have previously been associated with 130 in lung transplant recipients. Methods. Serum samples were collected from eight patients with 130, eight patients with chronic graft-versus-host disease (GVHD), and eight control patients with neither 130 nor chronic GVHD in a matched patient analysis. Patients were matched for diagnosis, conditioning, donor match, and GVHD prophylaxis. Another seven patients with BO were also analyzed separately. CC 16 was measured with an enzyme-linked immunosorbent assay method. Results. In the matched analysis, eight patients were diagnosed with 130 at a median of 11.5 months (range, 4-13 months) after SCT and in nonmatched 130 patients at a median of 12 months (range, 9-36 months). In the matched patient analysis, patients with 130 had significantly lower (P=0.03) or decreasing (P=0.02) levels of CC16 compared with patients with only chronic GVHD or controls. In the matched patient analysis, measurement of CC16 showed a sensitivity of 88% and a specificity of 81%. With the criteria of low levels of CC16 or a decrease of more than 40% compared with the previous sample, BO was detected with analysis of CC16 in 13 of 15 patients. In 11 of the 13 patients, low or decreasing values of CC16 were detected at a median of 10 months (range, 1-30 months) before 130 was diagnosed clinically. Conclusions. Low levels of CC16 are associated with 130 after allogeneic SCT. Monitoring of CC16 in serum after SCT may have potential as an early marker for BO.
引用
收藏
页码:1411 / 1416
页数:6
相关论文
共 22 条
[1]   Bronchiolitis obliterans and other late onset non-infectious pulmonary complications in hematopoietic stem cell transplantation [J].
Afessa, B ;
Litzow, MR ;
Tefferi, A .
BONE MARROW TRANSPLANTATION, 2001, 28 (05) :425-434
[2]  
ASCHAN J, 1994, BONE MARROW TRANSPL, V14, P601
[3]  
BREUER R, 1993, RESP MED, V87, P571
[4]   Airflow obstruction after myeloablative allogeneic hematopoietic stem cell transplantation [J].
Chien, JW ;
Martin, PJ ;
Gooley, TA ;
Flowers, ME ;
Heckbert, SR ;
Nichols, WG ;
Clark, JG .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 168 (02) :208-214
[5]   Regression of metastatic renal-cell carcinoma after nonmyeloablative allogeneic peripheral-blood stem-cell transplantation [J].
Childs, R ;
Chernoff, A ;
Contentin, N ;
Bahceci, E ;
Schrump, D ;
Leitman, S ;
Read, EJ ;
Tisdale, J ;
Dunbar, C ;
Linehan, WM ;
Young, NS ;
Barrett, AJ ;
Clave, E ;
Epperson, D ;
Mayo, V .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (11) :750-758
[6]   OBSTRUCTIVE LUNG-DISEASE AFTER ALLOGENEIC MARROW TRANSPLANTATION - CLINICAL PRESENTATION AND COURSE [J].
CLARK, JG ;
CRAWFORD, SW ;
MADTES, DK ;
SULLIVAN, KM .
ANNALS OF INTERNAL MEDICINE, 1989, 111 (05) :368-376
[7]   POTENT INHIBITION OF BOTH HUMAN INTERFERON-GAMMA PRODUCTION AND BIOLOGIC ACTIVITY BY THE CLARA CELL PROTEIN CC16 [J].
DIERYNCK, I ;
BERNARD, A ;
ROELS, H ;
DELEY, M .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 12 (02) :205-210
[8]   Bronchiolitis obliterans in chronic graft-versus-host disease: Analysis of risk factors and treatment outcomes [J].
Dudek, AZ ;
Mahaseth, H ;
DeFor, TE ;
Weisdorf, DJ .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2003, 9 (10) :657-666
[9]   CLINICAL MANIFESTATIONS OF GRAFT VERSUS HOST DISEASE IN HUMAN RECIPIENTS OF MARROW FROM HL-A-MATCHED SIBLING DONORS [J].
GLUCKSBERG, H ;
STORB, R ;
FEFER, A ;
BUCKNER, CD ;
NEIMAN, PE ;
CLIFT, RA ;
LERNER, KG ;
THOMAS, ED .
TRANSPLANTATION, 1974, 18 (04) :295-304
[10]  
HAYRY P, 1994, TRANSPLANT P, V26, P3280