Skip to main content Accessibility help
×
Hostname: page-component-7bb8b95d7b-nptnm Total loading time: 0 Render date: 2024-09-14T14:27:04.791Z Has data issue: false hasContentIssue false
This chapter is part of a book that is no longer available to purchase from Cambridge Core

39 - Autoimmune Disease in Pregnancy

from Section 5 - Late Pregnancy – Maternal Problems

T. Flint Porter
Affiliation:
Division of Maternal-Fetal Medicine, Department of Obstetrics & Gynecology, University of Utah Health Sciences, Salt Lake City, UT, USA
D. Ware Branch
Affiliation:
Department of Obstetrics & Gynecology, University of Utah Health Sciences Center & Intermountain Healthcare, Salt Lake City, UT, USA
Philip Steer
Affiliation:
Imperial College London
Carl Weiner
Affiliation:
University of Kansas
Bernard Gonik
Affiliation:
Wayne State University, Detroit
Stephen Robson
Affiliation:
University of Newcastle
Get access

Summary

Introduction

The immune system's remarkable ability to protect the body from invasion by foreign pathogens stems from its capacity to distinguish biologic “self” from “nonself.” An aberration in this normally wellregulated process leads to so-called autoimmunity, in which immune effector cells are directed against “self” tissues. Persistent abnormal immunologic activation results in autoimmune disease, each type characterized by a typical pattern of clinical signs and symptoms and confirmed by the presence of immune effector cells, usually autoantibodies. In some autoimmune conditions, serologically detected autoantibodies play an active role in tissue damage, while in others they serve only to confirm the existence of an autoimmune process. The pathophysiology leading to autoimmunity likely involves a failure of complex regulatory mechanisms, which normally control activation and deactivation of the immune system. Recent investigations suggest that full expression of autoimmune disease depends on a combination of environmental, genetic, and host factors. Autoimmune diseases have a predilection for reproductive-age women and are frequently encountered during pregnancy. More than 70% of patients with autoimmune disease are women of reproductive age. Both animal models and human studies support the role of sex hormones in the development of autoimmunity. Estrogens appear to accelerate disease, while androgens are protective.1–4 Not surprisingly, pregnancy-associated fluctuations in sex hormones may influence disease severity. Diseases with strong cellular pathophysiology, such as rheumatoid arthritis (RA) and multiple sclerosis, tend to improve during pregnancy, whereas those characterized by autoantibody production, such as systemic lupus erythematosus (SLE) and Graves’ disease, increase in severity. Still others are unique to pregnancy or have unique features associated with pregnancy.

Immunosuppressive Agents During Pregnancy

It is often necessary to continue immunosuppressive agents during pregnancy in women with preexisting autoimmune disease. Some of the most frequently prescribed immunosuppressive agents may be used safely during pregnancy while others are strictly contraindicated (Table 39.1). Still others have not been studied sufficiently during pregnancy. As with any drug during pregnancy, the goal of autoimmune treatment is to adequately control disease activity without placing undue risk on the mother and fetus. The decision to use any immunosuppressive agent during pregnancy should be based on the clinical context, risks associated with individual medications, and the stage of pregnancy.

Type
Chapter
Information
High-Risk Pregnancy: Management Options
Five-Year Institutional Subscription with Online Updates
, pp. 1108 - 1159
Publisher: Cambridge University Press
First published in: 2017

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×