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Immunodeficiency Secondary to Prematurity, Pregnancy, and Aging

  • Johns Hopkins University

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

Abstract

In this chapter we address three common scenarios often faced by clinical immunologists. In the first case, we explore the approach to an abnormal newborn screening of T-cell receptor excision circles (TREC) and the challenges it presents specifically for secondary causes of T-cell lymphopenia including prematurity, low birth weight, stress, etc. We highlight the importance of prompt evaluation and initiation of therapy in newborns with “presumed” SCID based on abnormal TRECs. The second case addresses third trimester of pregnancy transplacental immunoglobulin G transfer. Mothers with primary antibody immune deficiency on replacement immunoglobulin therapy must have a dosing adjustment to account for plasma expansion. Failure to do so can result in not only suboptimal maternal IgG levels but also lower baseline IgG levels in newborns placing both the mother and child at risk for infections. Finally, comorbid conditions often seen after the sixth to seventh decade of life raise concern for increased risk of thromboembolic events in patients on immunoglobulin replacement. Here we review the use of anticoagulation and the mode of immunoglobulin replacement therapy.

Original languageEnglish
Title of host publicationPrimary and Secondary Immunodeficiency
Subtitle of host publicationA Case-Based Guide to Evaluation and Management
PublisherSpringer International Publishing
Pages381-395
Number of pages15
ISBN (Electronic)9783030571573
ISBN (Print)9783030571566
DOIs
StatePublished - Jan 1 2021

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