SOLUBLE RECEPTORS FOR TUMOR-NECROSIS-FACTOR - A PUTATIVE MARKER OF DISEASE PROGRESSION IN HIV-INFECTION

被引:100
作者
GODFRIED, MH
VANDERPOLL, T
JANSEN, J
ROMIJIN, JA
SCHATTENKERK, JKME
ENDERT, E
VANDEVENTER, SJH
SAUERWEIN, HP
机构
[1] UNIV AMSTERDAM,ACAD MED CTR,DEPT ENDOCRINOL,1105 AZ AMSTERDAM,NETHERLANDS
[2] UNIV AMSTERDAM,ACAD MED CTR,CTR HAEMOSTASIS THROMBOSIS ATHEROSCLEROSIS & INFLAMMAT RES,1105 AZ AMSTERDAM,NETHERLANDS
[3] UNIV AMSTERDAM,ACAD MED CTR,DEPT INTENS CARE,1105 AZ AMSTERDAM,NETHERLANDS
关键词
TUMOR NECROSIS FACTOR (TNF); SOLUBLE TNF RECEPTORS P55 AND P75; HIV INFECTION; CD4+ LYMPHOCYTE COUNT;
D O I
10.1097/00002030-199301000-00005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To assess the value of concentrations of soluble receptors for tumour necrosis factor (sTNFR) as markers for disease progression in HIV infection. Design: We measured concentrations of sTNFR in the serum of 32 HIV-infected male patients in various stages of disease and in 12 healthy male control subjects. Correlations between the levels of sTNFR and CD4+ lymphocyte counts were calculated. Results: Serum levels of sTNFR p55 and p75 were elevated in parallel with severity of clinical stage. sTNFR p55 levels were higher at later stages of HIV infection (Centers for Disease Control stage IV) with or without concurrent illness, whereas sTNFR p75 was already elevated in asymptomatic carriers, compared with controls. There was an inverse correlation between sTNFR concentrations and CD4+ lymphocyte counts. Conclusions: Our results suggest that sTNFR concentrations could be potential markers for disease progression in HIV infection.
引用
收藏
页码:33 / 36
页数:4
相关论文
共 17 条
  • [1] ADERKA D, 1992, LYMPHOKINE CYTOK RES, V11, P157
  • [2] STABILIZATION OF THE BIOACTIVITY OF TUMOR-NECROSIS-FACTOR BY ITS SOLUBLE RECEPTORS
    ADERKA, D
    ENGELMANN, H
    MAOR, Y
    BRAKEBUSCH, C
    WALLACH, D
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (02) : 323 - 329
  • [3] IDENTIFICATION OF 2 TYPES OF TUMOR-NECROSIS-FACTOR RECEPTORS ON HUMAN CELL-LINES BY MONOCLONAL-ANTIBODIES
    BROCKHAUS, M
    SCHOENFELD, HJ
    SCHLAEGER, EJ
    HUNZIKER, W
    LESSLAUER, W
    LOETSCHER, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (08) : 3127 - 3131
  • [4] DEMBIC Z, 1990, Cytokine, V2, P231, DOI 10.1016/1043-4666(90)90022-L
  • [5] ENGELBERTS I, 1991, LYMPHOKINE CYTOK RES, V10, P69
  • [6] IMMUNOPATHOGENIC MECHANISMS IN HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) INFECTION
    FAUCI, AS
    SCHNITTMAN, SM
    POLI, G
    KOENIG, S
    PANTALEO, G
    [J]. ANNALS OF INTERNAL MEDICINE, 1991, 114 (08) : 678 - 693
  • [7] TUMOR-NECROSIS-FACTOR IN THE PATHOPHYSIOLOGY OF INFECTION AND SEPSIS
    FONG, Y
    LOWRY, SF
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1990, 55 (02): : 157 - 170
  • [8] GIRARDIN E, 1992, IMMUNOLOGY, V76, P20
  • [9] GRUNFELD C, 1992, NEW ENGL J MED, V327, P329, DOI 10.1056/NEJM199207303270506
  • [10] ELEVATED TNF RECEPTOR PLASMA-CONCENTRATIONS IN PATIENTS WITH RHEUMATOID-ARTHRITIS
    HEILIG, B
    WERMANN, M
    GALLATI, H
    BROCKHAUS, M
    BERKE, B
    EGEN, O
    PEZZUTTO, A
    HUNSTEIN, W
    [J]. CLINICAL INVESTIGATOR, 1992, 70 (01): : 22 - 27