Complex humoral immune response against a benign tumor: Frequent antibody response against specific antigens as diagnostic targets

被引:69
作者
Comtesse, N
Zippel, A
Walle, S
Monz, D
Backes, C
Fischer, U
Mayer, J
Ludwig, N
Hildebrandt, A
Keller, A
Steudel, WI
Lenhof, HP
Meese, E
机构
[1] Univ Saarland, Sch Med, Dept Human Genet, D-66421 Homburg, Germany
[2] Univ Saarland, Sch Med, Dept Neurosurg, D-66421 Homburg, Germany
[3] Univ Saarland, Dept Bioinformat, D-66041 Saarbrucken, Germany
关键词
meningioma;
D O I
10.1073/pnas.0500404102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
There are numerous studies on the immune response against malignant human tumors. This study was aimed to address the complexity and specificity of humoral immune response against a benign human tumor. We assembled a panel of 62 meningioma-expressed antigens that show reactivity with serum antibodies of meningioma patients, including 41 previously uncharacterized antigens by screening of a fetal brain expression library. We tested the panel for reactivity with 48sera, including sera of patients with common-type, atypical, and anaplastic meningioma, respectively. Meningioma sera detected an average of 14.6 antigens per serum and normal sera an average of 7.8 antigens per serum (P = 0.0001). We found a decline of seroreactivity with malignancy with a statistical significant difference between common-type and anaplastic meningioma (P < 0.05). We detected 17 antigens exclusively with patient sera, including 12 sera that were reactive against KIAA1344, 9 against natural killer tumor recognition (NKTR), and 7 against SRY (sex determining region Y)-box2 (SOX2). More than 80% of meningioma patients had antibodies against at least one of the antigens KIAA1344, SC65, SOX2, and C6orf153. Our results show a highly complex but specific humoral immune response against a benign tumor with a distinct serum reactivity pattern and a decline of complexity with malignancy. The frequent antibody response against specific antigens offers new diagnostic and therapeutic targets for meningioma. We developed a statistical learning method to differentiate sera of meningioma patients from sera of healthy donors.
引用
收藏
页码:9601 / 9606
页数:6
相关论文
共 35 条
[1]   A CYCLOPHILIN-RELATED PROTEIN INVOLVED IN THE FUNCTION OF NATURAL-KILLER-CELLS [J].
ANDERSON, SK ;
GALLINGER, S ;
RODER, J ;
FREY, J ;
YOUNG, HA ;
ORTALDO, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :542-546
[2]  
BACKES C, 2005, IN PRESS NUCL ACIDS, V33
[3]   Role of amplified genes in the production of autoantibodies [J].
Brass, N ;
Rácz, A ;
Bauer, C ;
Heckel, D ;
Sybrecht, G ;
Meese, E .
BLOOD, 1999, 93 (07) :2158-2166
[4]   Cleavage by granzyme B is strongly predictive of autoantigen status: Implications for initiation of autoimmunity [J].
Casciola-Rosen, L ;
Andrade, F ;
Ulanet, D ;
Wong, WB ;
Rosen, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (06) :815-825
[5]   Mgea6 is tumor-specific overexpressed and frequently recognized by patient-serum antibodies [J].
Comtesse N. ;
Niedermayer I. ;
Glass B. ;
Heckel D. ;
Maldener E. ;
Nastainczyk W. ;
Feiden W. ;
Meese E. .
Oncogene, 2002, 21 (2) :239-247
[6]   Identification of a nuclear variant of MGEA5, a cytoplasmic hyaluronidase and a β-N-acetylglucosaminidase [J].
Comtesse, N ;
Maldener, E ;
Meese, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 283 (03) :634-640
[7]  
Comtesse N, 1999, CLIN CANCER RES, V5, P3560
[8]   LONG CHARGE-RICH ALPHA-HELICES IN SYSTEMIC AUTOANTIGENS [J].
DOHLMAN, JG ;
LUPAS, A ;
CARSON, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 195 (02) :686-696
[9]  
DUMANSKI JP, 1990, CANCER RES, V50, P5863
[10]  
Friedman J., 2001, The elements of statistical learning, V1, DOI DOI 10.1007/978-0-387-21606-5