SEX STEROID REGULATION OF AUTOIMMUNITY

被引:145
作者
GROSSMAN, CJ
ROSELLE, GA
MENDENHALL, CL
机构
[1] VET ADM MED CTR, COLL MED, DEPT VET AFFAIRS MED CTR, RES & MED SERV, CINCINNATI, OH 45220 USA
[2] VET ADM MED CTR, COLL MED, DEPT PHYSIOL & BIOPHYS, CINCINNATI, OH 45220 USA
[3] XAVIER UNIV, DEPT BIOL, CINCINNATI, OH 45207 USA
关键词
D O I
10.1016/0960-0760(91)90287-F
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The immune response of males and females is not identical but instead has been shown to be dimorphic in its nature, with females generally demonstrating a greater overall response than males. This dimorphism extends to both the humoral and cell mediated systems and appears to be mechanistically based on the differences in type and concentration of sex steroids in males vs females. Furthermore, growth hormone and prolactin secretions which are different in males and females may also be partly responsible for the observed dimorphism. Because autoimmune disease results from a pathological perturbation of normal immune function, it follows that expression of these diseases will also demonstrate a dimorphic pattern. Examples of this autoimmune dimorphism include (but are not limited to) lupus, rheumatoid arthritis and multiple sclerosis with the two former more prevalent in females than males and the latter more severe during pregnancy. To explain autoimmune dimorphism it therefore becomes necessary firstly to describe the cellular and hormonal interactions found in normal immune regulation and thereafter extrapolate these to autoimmune phenomena.
引用
收藏
页码:649 / 659
页数:11
相关论文
共 53 条
[11]   T-CELL TOLERANCE BY CLONAL ANERGY IN TRANSGENIC MICE WITH NONLYMPHOID EXPRESSION OF MHC CLASS-II I-E [J].
BURKLY, LC ;
LO, D ;
KANAGAWA, O ;
BRINSTER, RL ;
FLAVELL, RA .
NATURE, 1989, 342 (6249) :564-566
[12]  
COULSON P, 1981, 63RD P END SOC ANN M, P255
[13]  
DAUPHINEE M J, 1981, Arthritis and Rheumatism, V24, pS64
[14]  
FRENCH SW, 1979, ARCH PATHOL LAB MED, V103, P146
[15]   CELLULAR SOURCES OF COLLAGEN AND REGULATION OF COLLAGEN PRODUCTION IN LIVER [J].
FRIEDMAN, SL .
SEMINARS IN LIVER DISEASE, 1990, 10 (01) :20-29
[16]  
GILBERT M, 1964, JAMA-J AM MED ASSOC, V190, P235
[17]   CELLULAR SOURCES OF NONCOLLAGENOUS MATRIX PROTEINS - ROLE OF FAT-STORING CELLS IN FIBROGENESIS [J].
GRESSNER, AM ;
BACHEM, MG .
SEMINARS IN LIVER DISEASE, 1990, 10 (01) :30-46
[18]   POSSIBLE UNDERLYING MECHANISMS OF SEXUAL DIMORPHISM IN THE IMMUNE-RESPONSE, FACT AND HYPOTHESIS [J].
GROSSMAN, C .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1989, 34 (1-6) :241-251
[19]  
Grossman C. J., 1990, PROG NEUROENDOCRINIM, V3, P75
[20]  
GROSSMAN CJ, 1989, NEUR CONT B, V3, P181