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Open AccessJournal ArticleDOI

Androgenic Hormones Modulate Autoantibody Responses and Improve Survival in Murine Lupus

Jirayr R. Roubinian, +2 more
- 01 Jun 1977 - 
- Vol. 59, Iss: 6, pp 1066-1070
TLDR
The results suggest that sex hormones modulate immunologic regulation and that androgenic hormones are protective in murine lupus.
Abstract
Evidence that andogenic hormones modulate autoantibody responses and improve survival in murine lupus is reported. Hybrid mice were either castrated or subjected to sham surgery at 2 weeks of age and studied for immunoglobulin class of antibodies to nucleic acids at 4 6 and 7 months postsurgery. Prepubertal male castation caused premature death in 60% of the mice. Castrated males had a marked decline in serum testosterone concentration. An increase in deoxyribonucleic acid and polyadenylic A (Poly A) binding and an accelerated switch from 19S to 7S antibodies to nucleic acids. Castrated females revealed no change in mortality however castrated females given maintained androgen treatment had a decreased mortality compared with castrasted females receiving estrogens (14 vs. 94%). The anticipated switch to 7S antibodies to Poly A was nearly eliminated in castrated females. These data suggest that sex hormones modulate immunologic regulation and that androgenic hormones are protective in murine lupus.

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Book ChapterDOI

Murine models of systemic lupus erythematosus.

TL;DR: This chapter reviews the histopathologic, serologic, lymphocytic, virological, hormonal, and genetic characteristics of murine models of systemic lupus erythematosus (SLE) to support the statement that the final immunopathologic perturbation in murine (and human) SLE is a B lymphocyte hyperactivity with corresponding enhancement of serum antibodies and autoantibodies, particularly IgG.
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Sex hormones, immune responses, and autoimmune diseases. Mechanisms of sex hormone action

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Systemic Lupus Erythematosus

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Gender differences in autoimmune disease.

TL;DR: Gender differences in systemic and organ-specific autoimmune diseases are considered, and human data is summarized that outlines the prevalence of common autoimmune diseases specific to adult males and females in countries commonly surveyed.
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Regulation of the Immune System by Sex Steroids

TL;DR: The present review will concentrate on only one aspect of the interaction between the immune and reproductive systems and involves interactions of pituitary hormones, gonadal steroid hormones and thymic hormones.
References
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Journal ArticleDOI

Immunochemical quantitation of antigens by single radial immunodiffusion

TL;DR: By standardizing the technical conditions of the experiment it is possible to use this principle for the immunochemical determination of antigens, and the lower limit of the method was found to correspond to 0·0025 μg of antigen, and to an antigen concentrations of 1·25 μg per ml.
Book ChapterDOI

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TL;DR: This chapter discusses the New Zealand Black (NZB) strain of mice that has attracted the attention of investigators throughout the world as an experimental model for human connective tissue disease and describes the patterns of development of the disease processes in the two groups of mice.
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Pathogenesis of the glomerulonephritis of nzb/w mice

TL;DR: Enhancement of the antinuclear antibody response by active immunization of young NZB/W mice with DNA-methylated BSA hastens the development and increases the severity of the glomerulonephritis.
Journal ArticleDOI

Studies of the regulatory effects of the sex hormones on antibody formation and stem cell differentiation

TL;DR: Changes in sex hormone levels exerted a marked influence on immune responsiveness and stem cell differentiation, by increasing numbers of functioning cells, by promoting cellular differentiation, as well as by promotes cellular function via hormonal effects.
Journal ArticleDOI

A Quantitative Difference in the Immune Response between Male and Female Mice

TL;DR: It was found that female mice developed a stronger and longer lasting immune response and thatfemale mice were more responsive to small doses of antigen.
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