Extended histopathology in immunotoxicity testing: Interlaboratory validation studies

被引:27
作者
Germolec, DR
Nyska, A
Kashon, M
Kuper, CF
Portier, C
Kommineni, C
Johnson, KA
Luster, MI
机构
[1] NIEHS, Mol Toxicol Lab, Natl Toxicol Program, Res Triangle Pk, NC 27709 USA
[2] NIEHS, Lab Expt Pathol, Res Triangle Pk, NC 27709 USA
[3] NIOSH, Biostat Branch, Morgantown, WV USA
[4] TNO, Nutr & Food Res, NL-3700 AJ Zeist, Netherlands
[5] NIEHS, Lab Computat Biol & Risk Assessment, Res Triangle Pk, NC 27709 USA
[6] NIOSH, Pathol & Physiol Res Branch, Morgantown, WV USA
[7] Dow Chem Co USA, Toxicol & Environm Res & Consulting, Midland, MI 48674 USA
[8] NIOSH, Toxicol & Mol Biol Branch, Morgantown, WV USA
关键词
immunology; pathology; spleen; thymus; lymph node; histopathology; immunopathology; risk assessment;
D O I
10.1093/toxsci/kfh049
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
There has been considerable interest in the use of expanded histopathology as a primary screen for immunotoxicity assessment. To determine the utility of a semiquantitative histopathology approach for examining specific structural and architectural changes in lymphoid tissues, a validation effort was initiated. This study addresses the interlaboratory reproducibility of extended histopathology, using tissues from studies of ten test chemicals and both negative and positive controls from the National Toxicology Program's immunotoxicology testing program. We examined the consistency between experienced toxicologic pathologists, who had varied expertise in immunohistopathology in identifying lesions in immune tissues, and in the sensitivity of the individual and combined histopathological endpoints to detect chemical effects and dose response. Factor analysis was used to estimate the association of each pathologist with a so-called "common factor" and analysis-of-variance methods were used to evaluate biases. Agreement between pathologists was highest in the thymus, in particular, when evaluating cortical cellularity of the thymus; good in spleen follicular cellularity and in spleen and lymph node-germinal center development; and poorest in spleen red-pulp changes. In addition, the ability to identify histopathological change in lymphoid tissues was dependent upon the experience/training that the individual pathologist possessed in examining lymphoid tissue and the apparent severity of the specific lesion.
引用
收藏
页码:107 / 115
页数:9
相关论文
共 46 条
[1]  
Agresti A, 1992, Stat Methods Med Res, V1, P201, DOI 10.1177/096228029200100205
[2]   The relationship among microsomal enzyme induction, liver weight and histological change in rat toxicology studies [J].
Amacher, DE ;
Schomaker, SJ ;
Burkhardt, JE .
FOOD AND CHEMICAL TOXICOLOGY, 1998, 36 (9-10) :831-839
[3]   ALTERATIONS IN THE HEPATIC GLUCOCORTICOID RESPONSE TO MIREX TREATMENT [J].
BROWN, LD ;
WILSON, DE ;
YARBROUGH, JD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1988, 92 (02) :203-213
[4]  
BURNOUF T, 1994, ANIMAL CELL TECHNOLO, V6, P17
[5]   THE LYMPHOCYTE-B IS THE IMMUNE CELL TARGET FOR 2',3'-DIDEOXYADENOSINE [J].
CAO, W ;
SIKORSKI, EE ;
FUCHS, BA ;
STERN, ML ;
LUSTER, MI ;
MUNSON, AE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 105 (03) :492-502
[6]   HORMONAL CONSEQUENCES OF ORGANOPHOSHPATE POISONING [J].
CLEMENT, JG .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1985, 5 (06) :S61-S77
[7]  
Dayan AD, 1998, TOXICOLOGY, V125, P183
[8]   Differential effects of 2,3,7,8-tetrachlorodibenzo-P-dioxin, bis(tri-N-butyltin)oxide and cyclosporine on thymus histophysiology [J].
DeWaal, EJ ;
Schuurman, HJ ;
VanLoveren, H ;
Vos, JG .
CRITICAL REVIEWS IN TOXICOLOGY, 1997, 27 (04) :381-430
[9]  
Dunn G., 1989, Design and analysis of reliability studies: the statistical evaluation of measurement errors
[10]  
GREAVES P, 1990, HISTOPATHOLOGY PRECL, P77