INTERFERON-GAMMA AND URINE NEOPTERIN IN ATTACKS OF THE HYPERIMMUNOGLOBULINEMIA-D AND PERIODIC FEVER SYNDROME

被引:23
作者
DRENTH, JPH
POWELL, RJ
BROWN, NS
VANDERMEER, JWM
机构
[1] UNIV NIJMEGEN HOSP, QUEENS MED CTR, DEPT IMMUNOL, NOTTINGHAM, ENGLAND
[2] UNIV NIJMEGEN HOSP, QUEENS MED CTR, DEPT CLIN CHEM, NOTTINGHAM, ENGLAND
关键词
HYPER-IGD SYNDROME; INTERFERON-GAMMA; URINE NEOPTERIN;
D O I
10.1111/j.1365-2362.1995.tb01986.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The hyperimmunoglobulinaemia D and periodic fever (hyper-IgD) syndrome is typified by recurrent unpredictable febrile attacks with abdominal pain, joint involvement (arthralgias/arthritis), headache, skin lesions and a polyclonal elevation of serum IgD(>100 U mL(-1)). Interferon-gamma (IFN-gamma) is a major proinflammatory cytokine which could play a role in the pathogenesis of the attacks. There is a need for parameters (if possible non-invasive) to monitor disease activity. A potential candidate is neopterin which is released by monocytes/macrophages when stimulated with IFN-gamma, excreted unchanged in urine, and appears to be an early and sensitive marker for activation of the immune system. We measured rectal body temperature, serum IFN-gamma, and urine neopterin in 10 hyper-IgD patients both during and between attacks. The body temperature rose to a mean of 38.9 degrees C on the first day of the attack and normalized within 5 days. Serum IFN-gamma during the first day of the attack was 2.98 IU mL(-1) and was significantly lower during remissions. The urine neopterin excretion was 268 +/- 170 mu mol mol(-1) creatinine between attacks and was significantly increased to 638 +/- 275 mu mol mol(-1) creatinine on the first day of symptoms. Maximal urine neopterin values were reached on the fourth day of the attack (1051 +/- 387 mu mol mol(-1) creatinine) and excretion gradually declined and attained values below 400 mu mol mol(-1) creatinine after 9 days. There was a good correlation between serum IFN-gamma and urine neopterin. The increases in serum IFN-gamma and urine neopterin suggest activation of the cellular immunity during the febrile attacks of the hyper-IgD syndrome. Furthermore, the activation of the cellular immune system appears to persist several days after normalization of the body temperature. The significant correlation between IFN-gamma and urine neopterin in the hyper-IgD syndrome accords with experimental data suggesting that IFN-gamma is the dominant factor in the release of neopterin. Our study shows that urinary neopterin is a good quantitative and qualitative parameter to monitor disease activity in patients with the hyper-IgD syndrome
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收藏
页码:683 / 686
页数:4
相关论文
共 15 条
[1]   COLCHICINE THERAPY FOR FAMILIAL MEDITERRANEAN FEVER - DOUBLE-BLIND TRIAL [J].
DINARELLO, CA ;
WOLFF, SM ;
GOLDFINGER, SE ;
DALE, DC ;
ALLING, DW .
NEW ENGLAND JOURNAL OF MEDICINE, 1974, 291 (18) :934-937
[2]  
DINARELLO CA, 1988, REV INFECT DIS, V10, P168
[3]   HYPERIMMUNOGLOBULINEMIA-D AND PERIODIC FEVER SYNDROME - THE CLINICAL SPECTRUM IN A SERIES OF 50 PATIENTS [J].
DRENTH, JPH ;
HAAGSMA, CJ ;
VANDERMEER, JWM ;
WEEMAES, CMR ;
BIJLSMA, JWJ ;
DEGRAEFFMEEDER, ER ;
ALCALAY, M ;
CHAPELONABRIC, C ;
KAHN, MF ;
PRIEUR, AM ;
SIBILIA, J ;
POWELL, RJ ;
TOPALOGLU, R ;
SAATCI, U ;
SCOLOZZI, R ;
LAZZARIN, P ;
MONCIOTTI, CM ;
DEMONTY, J ;
JILEK, D ;
MIYAGAWA, S ;
ESPANOL, T .
MEDICINE, 1994, 73 (03) :133-144
[4]   CUTANEOUS MANIFESTATIONS AND HISTOLOGIC-FINDINGS IN THE HYPERIMMUNOGLOBULINEMIA-D SYNDROME [J].
DRENTH, JPH ;
BOOM, BW ;
TOONSTRA, J ;
VANDERMEER, JWM .
ARCHIVES OF DERMATOLOGY, 1994, 130 (01) :59-65
[5]   LOCATION OF THE GENE CAUSING HYPERIMMUNOGLOBULINEMIA-D AND PERIODIC-FEVER-SYNDROME DIFFERS FROM THAT FOR FAMILIAL MEDITERRANEAN FEVER [J].
DRENTH, JPH ;
MARIMAN, ECM ;
VANDERVELDEVISSER, SD ;
ROPERS, HH ;
VANDERMEER, JWM ;
WEEMAES, CMR ;
BIJLSMA, JWJ ;
DEGRAEFFMEEDER, ER ;
ALCALAY, M ;
CHAPELONABRIC, C ;
KAHN, MF ;
PRIEUR, AM ;
SIBILIA, J ;
MORAND, C ;
POWELL, RJ ;
TOPALOGLU, R ;
SAATCI, U ;
SCOLOZZI, R ;
LAZZARIN, P ;
MONCIOTTI, CM ;
DEMONTY, J ;
JILEK, D ;
MIYAGAWA, S ;
ESPANOL, T .
HUMAN GENETICS, 1994, 94 (06) :616-620
[6]   THE MOLECULAR CELL BIOLOGY OF INTERFERON-GAMMA AND ITS RECEPTOR [J].
FARRAR, MA ;
SCHREIBER, RD .
ANNUAL REVIEW OF IMMUNOLOGY, 1993, 11 :571-611
[7]   THE ROLE OF NEOPTERIN AS A MONITOR OF CELLULAR IMMUNE ACTIVATION IN TRANSPLANTATION, INFLAMMATORY, INFECTIOUS, AND MALIGNANT DISEASES [J].
FUCHS, D ;
WEISS, G ;
REIBNEGGER, G ;
WACHTER, H .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 1992, 29 (3-4) :307-341
[8]   PROPHYLACTIC COLCHICINE THERAPY IN FAMILIAL MEDITERRANEAN FEVER - CONTROLLED, DOUBLE-BLIND STUDY [J].
GOLDSTEIN, RC ;
SCHWABE, AD .
ANNALS OF INTERNAL MEDICINE, 1974, 81 (06) :792-794
[9]   IMMUNE-RESPONSE ASSOCIATED PRODUCTION OF NEOPTERIN - RELEASE FROM MACROPHAGES PRIMARILY UNDER CONTROL OF INTERFERON-GAMMA [J].
HUBER, C ;
BATCHELOR, JR ;
FUCHS, D ;
HAUSEN, A ;
LANG, A ;
NIEDERWIESER, D ;
REIBNEGGER, G ;
SWETLY, P ;
TROPPMAIR, J ;
WACHTER, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (01) :310-316
[10]   URINE NEOPTERIN AS A PARAMETER OF DISEASE-ACTIVITY IN PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS - COMPARISONS WITH SERUM SIL-2R AND ANTIBODIES TO DSDNA, ERYTHROCYTE SEDIMENTATION-RATE, AND PLASMA-C3, C4, AND PLASMA-C3 DEGRADATION PRODUCTS [J].
LIM, KL ;
JONES, AC ;
BROWN, NS ;
POWELL, RJ .
ANNALS OF THE RHEUMATIC DISEASES, 1993, 52 (06) :429-435