Quantitative analysis of serum free light chains - A new marker for the diagnostic evaluation of primary systemic amyloidosis

被引:142
作者
Abraham, RS
Katzmann, JA
Clark, RJ
Bradwell, AR
Kyle, RA
Gertz, MA
机构
[1] Mayo Clin & Mayo Fdn, Div Hematol & Internal Med, Rochester, MN 55905 USA
[2] Univ Birmingham, Div Clin Biochem & Immunol, Birmingham, W Midlands, England
[3] Univ Birmingham, Sch Med, Birmingham, W Midlands, England
关键词
amyloid; amyloidosis; monoclonal light chains; immunoglobulins; stem cell transplantation; monoclonal gammopathy; nelphelometry;
D O I
10.1309/LYWM47K2L8XYFFB3
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Primary systemic amyloidosis is a plasma cell dyscrasia characterized by the accumulation of excess free immunoglobulin light chains (FLCs) as amyloid. One of the diagnostic features of amyloidosis is the presence of circulating monoclonal FLCs in the serum and urine of the patients. The FLC usually is present in small amounts, and immunofixation is required for detection. A nephelometric method for quantitating FLCs in serum has been described using antibodies that recognize only FLC not bound to heavy chain. We describe a retrospective study using this quantitative FLC method for assessing monoclonal FLCs in 95 patients with amyloidosis. The sensitivity of nephelometric serum FLC measurements is particularly useful in patients with negative immunofixation results for serum, urine, or both. In addition, the FLC assay can be used for follow-up of patients with amyloidosis who have undergone stem cell transplantation.
引用
收藏
页码:274 / 278
页数:5
相关论文
共 19 条
  • [1] IMMUNOCHEMICAL IDENTIFICATION OF THE SERINE PROTEASE INHIBITOR ALPHA-1-ANTICHYMOTRYPSIN IN THE BRAIN AMYLOID DEPOSITS OF ALZHEIMERS-DISEASE
    ABRAHAM, CR
    SELKOE, DJ
    POTTER, H
    [J]. CELL, 1988, 52 (04) : 487 - 501
  • [2] Abraham RS, 2002, CLIN CHEM, V48, P655
  • [3] Bradwell AR, 2001, CLIN CHEM, V47, P673
  • [4] Comenzo RL, 1998, BLOOD, V91, P3662
  • [5] Serum free light-chain measurements for identifying and monitoring patients with nonsecretory multiple myeloma
    Drayson, M
    Tang, LX
    Drew, R
    Mead, GP
    Carr-Smith, H
    Bradwell, AR
    [J]. BLOOD, 2001, 97 (09) : 2900 - 2902
  • [6] AMYLOID PRODUCTION IN HUMAN MYELOMA STEM-CELL CULTURE, WITH MORPHOLOGIC EVIDENCE OF AMYLOID SECRETION BY ASSOCIATED MACROPHAGES
    DURIE, BGM
    PERSKY, B
    SOEHNLEN, BJ
    GROGAN, TM
    SALMON, SE
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1982, 307 (27) : 1689 - 1692
  • [7] THE PUTATIVE ROLE OF ALPHA-1-ANTITRYPSIN IN THE DISAGGREGATION OF AMYLOID-LAMBDA FIBRILS
    ERIKSSON, S
    JANCIAUSKIENE, S
    MERLINI, G
    [J]. JOURNAL OF INTERNAL MEDICINE, 1995, 237 (02) : 143 - 149
  • [8] GALLO G, 1994, AM J PATHOL, V145, P526
  • [9] Amyloidosis
    Gertz, MA
    Lacy, MQ
    Dispenzieri, A
    [J]. HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1999, 13 (06) : 1211 - +
  • [10] ALZHEIMERS-DISEASE - ITS PROTEINS AND GENES
    GLENNER, GG
    [J]. CELL, 1988, 52 (03) : 307 - 308